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Sample records for acid-coated magnetite nanoparticles

  1. Water-dispersible ascorbic-acid-coated magnetite nanoparticles for contrast enhancement in MRI

    NASA Astrophysics Data System (ADS)

    Sreeja, V.; Jayaprabha, K. N.; Joy, P. A.

    2015-04-01

    Superparamagnetic iron oxide nanoparticles of size ~5 nm surface functionalized with ascorbic acid (vitamin C) form a stable dispersion in water with a hydrodynamic size of ~30 nm. The anti-oxidant property of ascorbic acid is retained after capping, as evidenced from the capability of converting methylene blue to its reduced leuco form. NMR relaxivity studies show that the ascorbic-acid-coated superparamagnetic iron oxide aqueous nanofluid is suitable as a contrast enhancement agent for MRI applications, coupled with the excellent biocompatibility and medicinal values of ascorbic acid.

  2. Magnetic resonance imaging of folic acid-coated magnetite nanoparticles reflects tissue biodistribution of long-acting antiretroviral therapy

    PubMed Central

    Li, Tianyuzi; Gendelman, Howard E; Zhang, Gang; Puligujja, Pavan; McMillan, JoEllyn M; Bronich, Tatiana K; Edagwa, Benson; Liu, Xin-Ming; Boska, Michael D

    2015-01-01

    Regimen adherence, systemic toxicities, and limited drug penetrance to viral reservoirs are obstacles limiting the effectiveness of antiretroviral therapy (ART). Our laboratory’s development of the monocyte-macrophage-targeted long-acting nanoformulated ART (nanoART) carriage provides a novel opportunity to simplify drug-dosing regimens. Progress has nonetheless been slowed by cumbersome, but required, pharmacokinetic (PK), pharmacodynamics, and biodistribution testing. To this end, we developed a small magnetite ART (SMART) nanoparticle platform to assess antiretroviral drug tissue biodistribution and PK using magnetic resonance imaging (MRI) scans. Herein, we have taken this technique a significant step further by determining nanoART PK with folic acid (FA) decorated magnetite (ultrasmall superparamagnetic iron oxide [USPIO]) particles and by using SMART particles. FA nanoparticles enhanced the entry and particle retention to the reticuloendothelial system over nondecorated polymers after systemic administration into mice. These data were seen by MRI testing and validated by comparison with SMART particles and direct evaluation of tissue drug levels after nanoART. The development of alendronate (ALN)-coated magnetite thus serves as a rapid initial screen for the ability of targeting ligands to enhance nanoparticle-antiretroviral drug biodistribution, underscoring the value of decorated magnetite particles as a theranostic tool for improved drug delivery. PMID:26082630

  3. Simple polyol route to synthesize heptanoic acid coated magnetite (Fe{sub 3}O{sub 4}) nanoparticles

    SciTech Connect

    Gunay, M.; Kavas, H.; Baykal, A.

    2013-03-15

    Highlights: ► Heptanoic acid@Fe{sub 3}O{sub 4} nanocomposite has been prepared via simple polyol. ► Heptanoic acid used as both surfactant and solvents. ► Magneto polymer composite with adjustable Ea has a potential usage as functional composites. - Abstract: Magnetite (Fe{sub 3}O{sub 4}) nanoparticles were prepared via polyol method by using FeCl{sub 2} as only source of iron. As-prepared samples were characterized by powder X-ray diffractometer (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric analyzer (TGA) and vibrating sample magnetometer (VSM). Crystalline phase was identified as Fe{sub 3}O{sub 4} and the crystallite sizes were calculated as 19.1 ± 1.1 and 22 ± 1.3 nm for uncalcinated and calcinated products from X-ray line profile fitting. The capping of heptanoic acid around Fe{sub 3}O{sub 4} nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygen's of the carboxylate and the nanoparticle surface and also by TG analysis. VSM measurements showed that both samples exhibited typical superparamagnetic behavior at room temperature with different Ms values. The ε′ decreases with increasing frequency for both composites and permeability has almost same values for all temperatures at higher frequencies. As synthesized and calcinated samples conductivity increase linearly with the temperature.

  4. Cellular interactions of lauric acid and dextran-coated magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Pradhan, Pallab; Giri, Jyotsnendu; Banerjee, Rinti; Bellare, Jayesh; Bahadur, Dhirendra

    2007-04-01

    In vitro cytocompatibility and cellular interactions of lauric acid and dextran-coated magnetite nanoparticles were evaluated with two different cell lines (mouse fibroblast and human cervical carcinoma). Lauric acid-coated magnetite nanoparticles were less cytocompatible than dextran-coated magnetite nanoparticles and cellular uptake of lauric acid-coated magnetic nanoparticles was more than that of dextran-coated magnetite nanoparticles. Lesser cytocompatibility and higher uptake of lauric acid-coated magnetite nanoparticles as compared to dextran-coated magnetic nanoparticles may be due to different cellular interactions by coating material. Thus, coating plays an important role in modulation of biocompatibility and cellular interaction of magnetic nanoparticles.

  5. The synthesis and characterization of poly(γ-glutamic acid)-coated magnetite nanoparticles and their effects on antibacterial activity and cytotoxicity

    NASA Astrophysics Data System (ADS)

    Inbaraj, B. Stephen; Kao, T. H.; Tsai, T. Y.; Chiu, C. P.; Kumar, R.; Chen, B. H.

    2011-02-01

    Magnetite nanoparticles (MNPs) modified with sodium and calcium salts of poly(γ-glutamic acid) (NaPGA and CaPGA) were synthesized by the coprecipitation method, followed by characterization and evaluation of their antibacterial and cytotoxic effects. Superparamagnetic MNPs are particularly attractive for magnetic driving as well as bacterial biofilm and cell targeting in in vivo applications. Characterization of synthesized MNPs by the Fourier transform infrared spectra and magnetization curves confirmed the PGA coating on MNPs. The mean diameter of NaPGA- and CaPGA-coated MNPs as determined by transmission electron microscopy was 11.8 and 14 nm, respectively, while the x-ray diffraction pattern revealed the as-synthesized MNPs to be pure magnetite. Based on agar dilution assay, both NaPGA- and CaPGA-coated MNPs showed a lower minimum inhibitory concentration in Salmonella enteritidis SE 01 than the commercial antibiotics linezolid and cefaclor, but the former was effective against Escherichia coli ATCC 8739 and Staphylococcus aureus ATCC 10832, whereas the latter was effective against Escherichia coli O157:H7 TWC 01. An in vitro cytotoxicity study in human skin fibroblast cells as measured by MTT assay implied the as-synthesized MNPs to be nontoxic. This outcome demonstrated that both γ-PGA-modified MNPs are cytocompatible and possess antibacterial activity in vitro, and thereby should be useful in in vivo studies for biomedical applications.

  6. Synthesis of non-aggregated nicotinic acid coated magnetite nanorods via hydrothermal technique

    NASA Astrophysics Data System (ADS)

    Attallah, Olivia A.; Girgis, E.; Abdel-Mottaleb, Mohamed M. S. A.

    2016-02-01

    Non-aggregated magnetite nanorods with average diameters of 20-30 nm and lengths of up to 350 nm were synthesized via in situ, template free hydrothermal technique. These nanorods capped with different concentrations (1, 1.5, 2 and 2.5 g) of nicotinic acid (vitamin B3); possessed good magnetic properties and easy dispersion in aqueous solutions. Our new synthesis technique maintained the uniform shape of the nanorods even with increasing the coating material concentration. The effect of nicotinic acid on the shape, particle size, chemical structure and magnetic properties of the prepared nanorods was evaluated using different characterization methods. The length of nanorods increased from 270 nm to 350 nm in nicotinic acid coated nanorods. Goethite and magnetite phases with different ratios were the dominant phases in the coated samples while a pure magnetite phase was observed in the uncoated one. Nicotinic acid coated magnetic nanorods showed a significant decrease in saturation magnetization than uncoated samples (55 emu/g) reaching 4 emu/g in 2.5 g nicotinic acid coated sample. The novel synthesis technique proved its potentiality to prepare coated metal oxides with one dimensional nanostructure which can function effectively in different biological applications.

  7. Coating agents affected toward magnetite nanoparticles properties

    NASA Astrophysics Data System (ADS)

    Petcharoen, Karat; Sirivat, Anuvat

    2012-02-01

    Magnetite nanoparticles --MNPs-- are innovative materials used in biological and medical applications. They respond to magnetic field through the superparamagnetic behavior at room temperature. In this study, the MNPs were synthesized via the chemical co-precipitation method using various coating agents. Fatty acids, found naturally in the animal fats, can be used as a coating agent. Oleic acid and hexanoic acid were chosen as the surface modification agents to study the improvement in the suspension of MNPs in water and the magnetite properties. Suspension stability, particle size, and electrical conductivity of MNPs are critically affected by the modification process. The well-dispersed MNPs in water can be improved by the surface modification and the oleic acid coated MNPs possess excellent suspension stability over 1 week. The particle size of MNPs increases up to 40 nm using oleic acid coated MNPs. The electrical conductivity of the smallest particle size is 1.3x10-3 S/cm, which is 5 times higher than that of the largest particle, suggesting potential applications as a biomedical material under both of the electrical and magnetic fields.

  8. Thermal treatment of magnetite nanoparticles

    PubMed Central

    Wykowska, Urszula; Satula, Dariusz; Nordblad, Per

    2015-01-01

    Summary This paper presents the results of a thermal treatment process for magnetite nanoparticles in the temperature range of 50–500 °C. The tested magnetite nanoparticles were synthesized using three different methods that resulted in nanoparticles with different surface characteristics and crystallinity, which in turn, was reflected in their thermal durability. The particles were obtained by coprecipitation from Fe chlorides and decomposition of an Fe(acac)3 complex with and without a core–shell structure. Three types of ferrite nanoparticles were produced and their thermal stability properties were compared. In this study, two sets of unmodified magnetite nanoparticles were used where crystallinity was as determinant of the series. For the third type of particles, a Ag shell was added. By comparing the coated and uncoated particles, the influence of the metallic layer on the thermal stability of the nanoparticles was tested. Before and after heat treatment, the nanoparticles were examined using transmission electron microscopy, IR spectroscopy, differential scanning calorimetry, X-ray diffraction and Mössbauer spectroscopy. Based on the obtained results, it was observed that the fabrication methods determine, to some extent, the sensitivity of the nanoparticles to external factors. PMID:26199842

  9. Citric-acid-coated magnetite nanoparticles for biological applications

    NASA Astrophysics Data System (ADS)

    Răcuciu, M.; Creangă, D. E.; Airinei, A.

    2006-10-01

    Water-based magnetic fluids, generally intended for biomedical applications, often have various coating molecules that make them stable and compatible with biological liquids. Magnetic fluids containing iron oxide particles have been prepared by a co-precipitation method, using citric acid as stabilizer. The magnetic particles of the magnetic fluids were obtained by chemical precipitation from ferric ( FeCl3) and ferrous salts ( FeSO4 or FeCl2) in alkali medium (ammonia hydroxide). Citric acid was used to stabilize the magnetic-particle suspension. Physical tests were performed in order to determine various microstructural and rheological features. Transmission electron microscopy was the main investigation method for assessing the magnetic-particle size. The dimensional distribution of the magnetic-particle physical diameter was analyzed using the box-plot statistical method while infrared absorption spectra were used to study the colloidal particle structure. The magnetic-fluid density (picnometric method), viscosity (capillary method) and surface tension (stalagmometric method) were measured using standard methods.

  10. A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite

    PubMed Central

    Kahani, Seyed Abolghasem; Yagini, Zahra

    2014-01-01

    The preparation of Fe3O4 from ferrous salt by air in alkaline aqueous solution at various temperatures was proposed. The synthetic magnetites have different particle size distributions. We studied the properties of the magnetite prepared by chemical methods compared with magnetotactic bacterial nanoparticles. The results show that crystallite size, morphology, and particle size distribution of chemically prepared magnetite at 293 K are similar to biosynthesis of magnetite. The new preparation of Fe3O4 helps to explain the mechanism of formation of magnetosomes in magnetotactic bacteria. The products are characterized by X-ray powder diffraction (XRD), infrared (IR) spectra, vibrating sample magnetometry (VSM), and scanning electron microscopy (SEM). PMID:24982609

  11. A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite.

    PubMed

    Kahani, Seyed Abolghasem; Yagini, Zahra

    2014-01-01

    The preparation of Fe3O4 from ferrous salt by air in alkaline aqueous solution at various temperatures was proposed. The synthetic magnetites have different particle size distributions. We studied the properties of the magnetite prepared by chemical methods compared with magnetotactic bacterial nanoparticles. The results show that crystallite size, morphology, and particle size distribution of chemically prepared magnetite at 293 K are similar to biosynthesis of magnetite. The new preparation of Fe3O4 helps to explain the mechanism of formation of magnetosomes in magnetotactic bacteria. The products are characterized by X-ray powder diffraction (XRD), infrared (IR) spectra, vibrating sample magnetometry (VSM), and scanning electron microscopy (SEM). PMID:24982609

  12. Magnetite nanoparticles for nonradionuclide brachytherapy1

    PubMed Central

    Safronov, Victor; Sozontov, Evgeny; Polikarpov, Mikhail

    2015-01-01

    Magnetite nanoparticles possess several properties that can make them useful for targeted delivery of radiation to tumors for the purpose of brachytherapy. Such particles are biodegradable and magnetic and can emit secondary radiation when irradiated by an external source. In this work, the dose distribution around a magnetite particle of 10 nm diameter being irradiated by monochromatic X-rays with energies in the range 4–60 keV is calculated. PMID:26089761

  13. One-stop Genomic DNA Extraction by Salicylic Acid Coated Magnetic Nanoparticles

    PubMed Central

    Zhou, Zhongwu; Kadam, Ulhas; Irudayaraj, Joseph

    2014-01-01

    Salicylic acid coated magnetic nanoparticles were prepared via a modified, one-step synthesis and used for a one-stop extraction of genomic DNA from mammalian cells. The synthesized magnetic particles were used for magnetic separation of cells from the media by non-specific binding of the particles, as well as extraction of genomic DNA from the lysate. The quantity and quality were confirmed by agarose gel electrophoresis and polymerase chain reaction. The entire process of extraction and isolation can be completed within 30 min. Compared to traditional methods based on centrifugation and filtration, the established method is fast, simple, reliable, and environmentally-friendly. PMID:23911528

  14. Magnetite and magnetite/silver core/shell nanoparticles with diluted magnet-like behavior

    SciTech Connect

    Garza-Navarro, Marco; Gonzalez, Virgilio; Ortiz, Ubaldo; De la Rosa, Elder

    2010-01-15

    In the present work is reported the use of the biopolymer chitosan as template for the preparation of magnetite and magnetite/silver core/shell nanoparticles systems, following a two step procedure of magnetite nanoparticles in situ precipitation and subsequent silver ions reduction. The crystalline and morphological characteristics of both magnetite and magnetite/silver core/shell nanoparticles systems were analyzed by high resolution transmission electron microscopy (HRTEM) and nanobeam diffraction patterns (NBD). The results of these studies corroborate the core/shell morphology and the crystalline structure of the magnetite core and the silver shell. Moreover, magnetization temperature dependent, M(T), measurements show an unusual diluted magnetic behavior attributed to the dilution of the magnetic ordering in the magnetite and magnetite/silver core/shell nanoparticles systems. - Graphical abstract: Biopolymer chitosan was used as stabilization media to synthesize both magnetite and magnetite/silver core/shell nanoparticles. Results of HRTEM and NBD patterns confirm core/shell morphology of the obtained nanoparticles. It was found that the composites show diluted magnet-like behavior.

  15. One step facile synthesis of ferromagnetic magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Suppiah, Durga Devi; Abd Hamid, Sharifah Bee

    2016-09-01

    The ferromagnetic properties of magnetite (Fe3O4) were influenced by the nanoparticle size, hence importance were given to the synthesis method. This paper clearly shows that magnetite nanoparticles were successfully synthesized by employing one step controlled precipitation method using a single salt (Iron(II) sulfate) iron precursor. The acquired titration curve from this method provides vital information on the possible reaction mechanism leading to the magnetite (Fe3O4) nanoparticles formation. Goethite (α-FeOOH) was obtained at pH 4, while the continuous addition of hydroxyl ions (OH-) forms iron hydroxides (Fe(OH)2). This subsequently reacts with the goethite, producing magnetite (Fe3O4) at pH 10. Spectroscopy studies validate the magnetite phase existence while structural and morphology analysis illustrates cubic shaped magnetite with an average size of 35 nm was obtained. The synthesized magnetite might be superparamagnetic though lower saturation magnetization (67.5 emu/g) measured at room temperature as compared to bulk magnetite. However the nanoparticles surface anisotropy leads to higher remanence (12 emu/g) and coercivity (117.7 G) making the synthesized magnetite an excellent candidate to be utilized in recording devices. The understanding of the magnetite synthesis mechanism can not only be used to achieve even smaller magnetite nanoparticles but also to prepare different types of iron oxides hydroxides using different iron precursor source.

  16. Controlled cobalt doping in biogenic magnetite nanoparticles.

    PubMed

    Byrne, J M; Coker, V S; Moise, S; Wincott, P L; Vaughan, D J; Tuna, F; Arenholz, E; van der Laan, G; Pattrick, R A D; Lloyd, J R; Telling, N D

    2013-06-01

    Cobalt-doped magnetite (CoxFe3 -xO4) nanoparticles have been produced through the microbial reduction of cobalt-iron oxyhydroxide by the bacterium Geobacter sulfurreducens. The materials produced, as measured by superconducting quantum interference device magnetometry, X-ray magnetic circular dichroism, Mössbauer spectroscopy, etc., show dramatic increases in coercivity with increasing cobalt content without a major decrease in overall saturation magnetization. Structural and magnetization analyses reveal a reduction in particle size to less than 4 nm at the highest Co content, combined with an increase in the effective anisotropy of the magnetic nanoparticles. The potential use of these biogenic nanoparticles in aqueous suspensions for magnetic hyperthermia applications is demonstrated. Further analysis of the distribution of cations within the ferrite spinel indicates that the cobalt is predominantly incorporated in octahedral coordination, achieved by the substitution of Fe(2+) site with Co(2+), with up to 17 per cent Co substituted into tetrahedral sites. PMID:23594814

  17. Controlled cobalt doping in biogenic magnetite nanoparticles

    PubMed Central

    Byrne, J. M.; Coker, V. S.; Moise, S.; Wincott, P. L.; Vaughan, D. J.; Tuna, F.; Arenholz, E.; van der Laan, G.; Pattrick, R. A. D.; Lloyd, J. R.; Telling, N. D.

    2013-01-01

    Cobalt-doped magnetite (CoxFe3 −xO4) nanoparticles have been produced through the microbial reduction of cobalt–iron oxyhydroxide by the bacterium Geobacter sulfurreducens. The materials produced, as measured by superconducting quantum interference device magnetometry, X-ray magnetic circular dichroism, Mössbauer spectroscopy, etc., show dramatic increases in coercivity with increasing cobalt content without a major decrease in overall saturation magnetization. Structural and magnetization analyses reveal a reduction in particle size to less than 4 nm at the highest Co content, combined with an increase in the effective anisotropy of the magnetic nanoparticles. The potential use of these biogenic nanoparticles in aqueous suspensions for magnetic hyperthermia applications is demonstrated. Further analysis of the distribution of cations within the ferrite spinel indicates that the cobalt is predominantly incorporated in octahedral coordination, achieved by the substitution of Fe2+ site with Co2+, with up to 17 per cent Co substituted into tetrahedral sites. PMID:23594814

  18. Soft X-ray Spectroscopy Study of the Electronic Structure of Oxidized and Partially Oxidized Magnetite Nanoparticles

    SciTech Connect

    Gilbert, Benjamin; Katz, Jordan E.; Denlinger, Jonathan D.; Yin, Yadong; Falcone, Roger; Waychunas, Glenn A.

    2010-10-24

    The crystal structure of magnetite nanoparticles may be transformed to maghemite by complete oxidation, but under many relevant conditions the oxidation is partial, creating a mixed-valence material with structural and electronic properties that are poorly characterized. We used X-ray diffraction, Fe K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy, and soft X-ray absorption and emission spectroscopy to characterize the products of oxidizing uncoated and oleic acid-coated magnetite nanoparticles in air. The oxidization of uncoated magnetite nanoparticles creates a material that is structurally and electronically indistinguishable from maghemite. By contrast, while oxidized oleic acid-coated nanoparticles are also structurally indistinguishable from maghemite, Fe L-edge spectroscopy revealed the presence of interior reduced iron sites even after a 2-year period. We used X-ray emission spectroscopy at the O K-edge to study the valence bands (VB) of the iron oxide nanoparticles, using resonant excitation to remove the contributions from oxygen atoms in the ligands and from low-energy excitations that obscured the VB edge. The bonding in all nanoparticles was typical of maghemite, with no detectable VB states introduced by the long-lived, reduced-iron sites in the oleic acid-coated sample. However, O K-edge absorption spectroscopy observed a 0.2 eV shift in the position of the lowest unoccupied states in the coated sample, indicating an increase in the semiconductor band gap relative to bulk stoichiometric maghemite that was also observed by optical absorption spectroscopy. The results show that the ferrous iron sites within ferric iron oxide nanoparticles coated by an organic ligand can persist under ambient conditions with no evidence of a distinct interior phase and can exert an effect on the global electronic and optical properties of the material. This phenomenon resembles the band gap enlargement caused by electron accumulation in the

  19. Caffeic acid-coated multifunctional magnetic nanoparticles for the treatment and bimodal imaging of tumours.

    PubMed

    Lee, Jun; Kim, Kyoung Sub; Na, Kun

    2016-07-01

    Accurate theragnosis of tumour is essential for improving the life rate of tumour patients. Superparamagnetic iron oxide nanoparticles (SPIONs) have been used as both diagnostic and therapeutic agents. However, their application is often limited because of a lack of water solubility, lack of cancer treatment efficacy, and ineffective targeting of tumour cells. In this report, a double ligand (caffeic acid-polyethylene glycol-folic acid; FA-PEG-CA, caffeic acid-polyethylene glycol-pheophorbide-a; PheoA-PEG-CA) coated iron oxide nanoparticle has been fabricated that overcomes the limitations of conventional SPION. Photosensitizer and tumour targeting ligands were coated on SPION using a ligand-substitution method. We confirmed the successful substitution of oleic acid ligands with FA-PEG-CA and PheoA-PEG-CA ligands by FT-IR spectroscopy. The caffeic acid coated iron oxide nanoparticles (CAMNPs) also demonstrated high water solubility in an aqueous environment and folate-mediated active tumour targeting. The water solubility of CAMNPs was evaluated by DLS measurement and TEM images. The cytotoxicity of CAMNPs increased two-fold in MDA-MB-231 cells at a laser irradiation condition. The fabricated CAMNPs retained their ability to function as both MRI diagnostic and tumour-selective therapeutic agents. These results suggest that these efficient characteristics of CAMNPs can be incorporated into applications, thus enhancing the efficacy of clinical cancer treatment. PMID:27107705

  20. Synthesis, characterization and applications of magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Kanmukhla, Vikram Kumar

    In the past few years, the synthesis of magnetic nanoparticles has received considerable attention due to their potential use in clinical applications. Since the properties of these nanoparticles depend strongly on their size, shape and crystallinity, there is a need for a general method to produce these particles with a controlled size, shape and crystal type. Of the many magnetic materials (Co, Ni, and Fe), the magnetite (Fe3O 4) is least toxic and hence most promising for applications in medical diagnostics. Microemulsion-based synthesis utilizes the local aqueous environment within a reverse micelle as a nano-scale reactor and allows synthesizing nanoparticles with a hydrophilic surface for subsequent functionalization. By controlling the water-to-surfactant ratio, the type of surfactants, and the ionic strength of the aqueous core, one can control the size and shape of the resulting particles. We developed such a system that allows the multi-step synthesis of surface-functionalized, magnetic nanoparticles in a one-pot synthesis reaction. By altering the system chemistry, we were further able to produce either spheres or cylinders of controlled dimension in the size range of 5 nm to 30 nm. Using standard bio-conjugation techniques, we successfully immobilized an enzyme onto the nanoparticles. We also developed a theoretical model for the separation and fractionation of nanoparticles based on their size and magnetic properties. Using the multiphysics and finite element modeling capabilities of FEMLAB(TM), we solved the coupled system of PDEs describing the interaction of magnetic particles within a magnetic field for either static (cylindrical beaker) or convective flow (capillary) conditions. A net retention time as high as 310 s is achieved for 200 nm particles at field strength of 1250 kA/m. The model allows the design of a magnetic, field-flow fractionation (MFFF) system to separate nanoparticles by size.

  1. Magnetic Properties of Bio-Synthesized Magnetite Nanoparticles

    SciTech Connect

    Rawn, Claudia J; Yeary, Lucas W; Moon, Ji Won; Love, Lonnie J; Thompson, James R; Phelps, Tommy Joe

    2005-01-01

    Magnetic nanoparticles, which are unique because of both structural and functional elements, have various novel applications. The popularity and practicality of nanoparticle materials create a need for a synthesis method that produces quality particles in sizable quantities. This paper describes such a method, one that uses bacterial synthesis to create nanoparticles of magnetite. The thermophilic bacterial strain Thermoanaerobacter ethanolicus TOR-39 was incubated under anaerobic conditions at 65 C for two weeks in aqueous solution containing Fe ions from a magnetite precursor (akaganeite). Magnetite particles formed outside of bacterial cells. We verified particle size and morphology by using dynamic light scattering, X-ray diffraction, and transmission electron microscopy. Average crystallite size was 45 nm. We characterized the magnetic properties by using a superconducting quantum interference device magnetometer; a saturation magnetization of 77 emu/g was observed at 5 K. These results are comparable to those for chemically synthesized magnetite nanoparticles.

  2. Poly(methacrylic acid)-Coated Gold Nanoparticles: Functional Platforms for Theranostic Applications.

    PubMed

    Yilmaz, Gokhan; Demir, Bilal; Timur, Suna; Becer, C Remzi

    2016-09-12

    The integration of drugs with nanomaterials have received significant interest in the efficient drug delivery systems. Conventional treatments with therapeutically active drugs may cause undesired side effects and, thus, novel strategies to perform these treatments with a combinatorial approach of therapeutic modalities are required. In this study, polymethacrylic acid coated gold nanoparticles (AuNP-PMAA), which were synthesized with reversible addition-fragmentation chain transfer (RAFT) polymerization, were combined with doxorubicin (DOX) as a model anticancer drug by creating a pH-sensitive hydrazone linkage in the presence of cysteine (Cys) and a cross-linker. Drug-AuNP conjugates were characterized via spectrofluorimetry, dynamic light scattering and zeta potential measurements as well as X-ray photoelectron spectroscopy. The particle size of AuNP-PMAA and AuNP-PMAA-Cys-DOX conjugate were calculated as found as 104 and 147 nm, respectively. Further experiments with different pH conditions (pH 5.3 and 7.4) also showed that AuNP-PMAA-Cys-DOX conjugate could release the DOX in a pH-sensitive way. Finally, cell culture applications with human cervix adenocarcinoma cell line (HeLa cells) demonstrated effective therapeutic impact of the final conjugate for both chemotherapy and radiation therapy by comparing free DOX and AuNP-PMAA independently. Moreover, cell imaging study was also an evidence that AuNP-PMAA-Cys-DOX could be a beneficial candidate as a diagnostic agent. PMID:27447298

  3. Effective Removal of Tetracycline from Aqueous Solution by Organic Acid-Coated Magnetic Nanoparticles.

    PubMed

    Guo, Liang; Liang, Yuyan; Chen, Xuelan; Xu, Wei; Wu, Kesheng; Wei, Hua; Xiong, Yonghua

    2016-03-01

    Self-assembled iron oxide nanocomposites are good magnetic nano-adsorbents that can be prepared using simple methods. Four types of organic acid-functionalised (oleic acid, undecenoic acid, caprylic acid or hexanoic acid) magnetic nanoparticles (MNPs) were synthesised through a one-pot chemisorption method for the removal of tetracycline (TC) from aqueous solution. The undecenoic acid-coated MNPs (UA-MNPs) exhibited the highest adsorption efficiency and can be easily retrieved with a low-gradient magnetic separator (0.4 Tesla) at pH 5.0 aqueous solution. The TC adsorption process on the UA-MNPs followed the Langmuir isotherm and the maximum adsorption capacities increased from 86.96 mg g(-1) to 222.2 mg g(-1) with the increase in temperature from 288 K to 318 K. The kinetics of adsorption fits pseudo-second-order model perfectly with a rate constant, 5.946 g mg(-1) min(-1) at 298 K. The positive values of the enthalpy (AH) and the negative value of the free energy (AG) indicated an endothermic and spontaneous adsorption process of TC on the UA-MNPs. Moreover, the UA-MNPs possessed excellent ability to adsorb the other three major types of TC antibiotics, including chlortetracycline, oxytetracycline and doxycycline. PMID:27455621

  4. Structure and superparamagnetic behaviour of magnetite nanoparticles in cellulose beads

    SciTech Connect

    Correa, Jose R.; Bordallo, Eduardo; Canetti, Dora; Leon, Vivian; Otero-Diaz, Luis C.; Negro, Carlos; Gomez, Adrian; Saez-Puche, Regino

    2010-08-15

    Superparamagnetic magnetite nanoparticles were obtained starting from a mixture of iron(II) and iron(III) solutions in a preset total iron concentration from 0.04 to 0.8 mol l{sup -1} with ammonia at 25 and 70 {sup o}C. The regeneration of cellulose from viscose produces micrometrical spherical cellulose beads in which synthetic magnetite were embedded. The characterization of cellulose-magnetite beads by X-ray diffraction, Scanning and Transmission Electron Microscopy and magnetic measurement is reported. X-ray diffraction patterns indicate that the higher is the total iron concentration and temperature the higher is the crystal size of the magnetite obtained. Transmission Electron Microscopy studies of cellulose-magnetite beads revealed the distribution of magnetite nanoparticles inside pores of hundred nanometers. Magnetite as well as the cellulose-magnetite composites exhibit superparamagnetic characteristics. Field cooling and zero field cooling magnetic susceptibility measurements confirm the superparamagnetic behaviour and the blocking temperature for the magnetite with a mean size of 12.5 nm, which is 200 K.

  5. Synthesis and characterization of magnetite/PLGA/chitosan nanoparticles

    NASA Astrophysics Data System (ADS)

    Ibarra, Jaime; Melendres, Julio; Almada, Mario; Burboa, María G.; Taboada, Pablo; Juárez, Josué; Valdez, Miguel A.

    2015-09-01

    In this work, we report the synthesis and characterization of a new hybrid nanoparticles system performed by magnetite nanoparticles, loaded in a PLGA matrix, and stabilized by different concentrations of chitosan. Magnetite nanoparticles were hydrophobized with oleic acid and entrapped in a PLGA matrix by the emulsion solvent evaporation method, after that, magnetite/PLGA/chitosan nanoparticles were obtained by adding dropwise magnetite/PLGA nanoparticles in chitosan solutions. Magnetite/PLGA nanoparticles produced with different molar ratios did not show significant differences in size and the 3:1 molar ratio showed best spherical shapes as well as uniform particle size. Isothermal titration calorimetry studies demonstrated that the first stage of PLGA-chitosan interaction is mostly regulated by electrostatic forces. Based on a single set of identical sites model, we obtained for the average number of binding sites a value of 3.4, which can be considered as the number of chitosan chains per nanoparticle. This value was confirmed by using a model based on the DLVO theory and fitting zeta potential measurements of magnetite/PLGA/chitosan nanoparticles. From the adjusted parameters, we found that an average number of chitosan molecules of 3.6 per nanoparticle are attached onto the surface of the PLGA matrix. Finally, we evaluated the effect of surface charge of nanoparticles on a membrane model of endothelial cells performed by a mixture of three phospholipids at the air-water interface. Different isotherms and adsorption curves show that cationic surface of charged nanoparticles strongly interact with the phospholipids mixture and these results can be the basis of future experiments to understand the nanoparticles- cell membrane interaction.

  6. Synthesis of stabilized myrrh-capped hydrocolloidal magnetite nanoparticles.

    PubMed

    Atta, Ayman M; Al-Lohedan, Hamad A; Al-Hussain, Sami A

    2014-01-01

    Herein we report a new method for synthesizing stabilized magnetic nanoparticle (MNP) colloids. A new class of monodisperse water-soluble magnetite nano-particles was prepared by a simple and inexpensive co-precipitation method. Iron ions and iodine were prepared by the reaction between ferric chloride and potassium iodide. The ferrous and ferric ions were hydrolyzed at low temperature at pH 9 in the presence of iodine to produce iron oxide nanoparticles. The natural product myrrh gum was used as capping agent to produce highly dispersed coated magnetite nanoparticles. The structure and morphology of the magnetic nanogel was characterized by Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM), and X-ray diffraction (XRD) was used to examine the crystal structure of the produced magnetite nanoparticles. PMID:25090117

  7. In Vitro Sustained Release Study of Gallic Acid Coated with Magnetite-PEG and Magnetite-PVA for Drug Delivery System

    PubMed Central

    Kura, Aminu Umar; Hussein-Al-Ali, Samer Hasan; Bin Hussein, Mohd Zobir; Fakurazi, Sharida; Shaari, Abdul Halim; Ahmad, Zalinah

    2014-01-01

    The efficacy of two nanocarriers polyethylene glycol and polyvinyl alcohol magnetic nanoparticles coated with gallic acid (GA) was accomplished via X-ray diffraction, infrared spectroscopy, magnetic measurements, thermal analysis, and TEM. X-ray diffraction and TEM results showed that Fe3O4 nanoparticles were pure iron oxide having spherical shape with the average diameter of 9 nm, compared with 31 nm and 35 nm after coating with polyethylene glycol-GA (FPEGG) and polyvinyl alcohol-GA (FPVAG), respectively. Thermogravimetric analyses proved that after coating the thermal stability was markedly enhanced. Magnetic measurements and Fourier transform infrared (FTIR) revealed that superparamagnetic iron oxide nanoparticles could be successfully coated with two polymers (PEG and PVA) and gallic acid as an active drug. Release behavior of gallic acid from two nanocomposites showed that FPEGG and FPVAG nanocomposites were found to be sustained and governed by pseudo-second-order kinetics. Anticancer activity of the two nanocomposites shows that the FPEGG demonstrated higher anticancer effect on the breast cancer cell lines in almost all concentrations tested compared to FPVAG. PMID:24737969

  8. Functionalization of magnetite nanoparticles as oil spill collector.

    PubMed

    Atta, Ayman M; Al-Lohedan, Hamad A; Al-Hussain, Sami A

    2015-01-01

    In the present study, a new magnetic powder based on magnetite can be used as a petroleum crude oil collector. Amidoximes based on rosin as a natural product can be prepared from a reaction between hydroxylamine and rosin/acrylonitrile adducts. The produced rosin amidoximes were used as capping agents for magnetite nanoparticles to prepare hydrophobic coated magnetic powders. A new class of monodisperse hydrophobic magnetite nanoparticles was prepared by a simple and inexpensive co-precipitation method. Iron ions and iodine were prepared by the reaction between ferric chloride and potassium iodide. The structure and morphology of magnetite capped with rosin amidoxime were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), zeta potential, thermogravimetric analysis (TGA) and dynamic light scattering (DLS). The magnetic properties were determined from vibrating sample magnetometer (VSM) analyses. These prepared magnetite nanoparticles were tested as bioactive nanosystems and their antimicrobial effects were investigated. The prepared nanomaterials were examined as a crude oil collector using magnetic fields. The results show promising data for the separation of the petroleum crude oil from aqueous solution in environmental pollution cleanup. PMID:25822876

  9. Functionalization of Magnetite Nanoparticles as Oil Spill Collector

    PubMed Central

    Atta, Ayman M.; Al-Lohedan, Hamad A.; Al-Hussain, Sami A.

    2015-01-01

    In the present study, a new magnetic powder based on magnetite can be used as a petroleum crude oil collector. Amidoximes based on rosin as a natural product can be prepared from a reaction between hydroxylamine and rosin/acrylonitrile adducts. The produced rosin amidoximes were used as capping agents for magnetite nanoparticles to prepare hydrophobic coated magnetic powders. A new class of monodisperse hydrophobic magnetite nanoparticles was prepared by a simple and inexpensive co-precipitation method. Iron ions and iodine were prepared by the reaction between ferric chloride and potassium iodide. The structure and morphology of magnetite capped with rosin amidoxime were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), zeta potential, thermogravimetric analysis (TGA) and dynamic light scattering (DLS). The magnetic properties were determined from vibrating sample magnetometer (VSM) analyses. These prepared magnetite nanoparticles were tested as bioactive nanosystems and their antimicrobial effects were investigated. The prepared nanomaterials were examined as a crude oil collector using magnetic fields. The results show promising data for the separation of the petroleum crude oil from aqueous solution in environmental pollution cleanup. PMID:25822876

  10. Lanthanide sorbent based on magnetite nanoparticles functionalized with organophosphorus extractants

    NASA Astrophysics Data System (ADS)

    Basualto, Carlos; Gaete, José; Molina, Lorena; Valenzuela, Fernando; Yañez, Claudia; Marco, Jose F.

    2015-06-01

    In this work, an adsorbent was prepared based on the attachment of organophosphorus acid extractants, namely, D2EHPA, CYANEX 272, and CYANEX 301, to the surface of superparamagnetic magnetite (Fe3O4) nanoparticles. The synthesized nanoparticles were coated with oleic acid, first by a chemisorption mechanism and later by the respective extractant via physical adsorption. The obtained core-shell functionalized magnetite nanoparticle composites were characterized by dynamic light scattering, scanning electron microscopy, transmission electron microscopy, thermogravimetry, infrared absorption and vibrating sample magnetometry. All the prepared nanoparticles exhibited a high saturation magnetization capacity that varied between 72 and 46 emu g-1 and decreased as the magnetite nanoparticle was coated with oleic acid and functionalized. The scope of this study also included adsorption tests for lanthanum, cerium, praseodymium, and neodymium and the corresponding analysis of their results. Sorption tests indicated that the functionalized nanoparticles were able to extract the four studied lanthanide metal ions, although the best extraction performance was observed when the sorbent was functionalized with CYANEX 272, which resulted in a loading capacity of approximately 12-14 mgLa/gMNP. The magnetization of the synthesized nanoparticles was verified during the separation of the lanthanide-loaded sorbent from the raffinate by using a conventional magnet.

  11. Raman spectroscopy investigation of magnetite nanoparticles in ferrofluids

    NASA Astrophysics Data System (ADS)

    Slavov, L.; Abrashev, M. V.; Merodiiska, T.; Gelev, Ch.; Vandenberghe, R. E.; Markova-Deneva, I.; Nedkov, I.

    2010-07-01

    Raman spectroscopy is used to investigate magnetite nanoparticles dispersed in two types of β-cyclodextrin suspensions. An approach is presented for characterization of the magnetic core in liquid surrounding at room temperature and atmospheric pressure. The effect of elevating laser power on the structural stability and chemical composition of magnetite in the ferrofluids is discussed. The data are compared with data from dry by-products from the fluids. Powder samples undergo total phase transition from magnetite to hematite at laser power of 1.95 mW. The same nanoparticles in the fluid undergo transformation at 9 mW, but no hematite positions appear throughout that investigation. The Raman spectra revealed that the main phase of the magnetic core in the fluids is magnetite. That is indicated by a strong and non-diminishing in intensity peak at 670 cm -1. A second phase is present at the nanoparticle's surface with Raman spectroscopy unveiling maghemite-like and small fractions of goethite-like structures. The Fourier transform infrared spectroscopy investigations confirm deviations in the surface structure and also point to the fact that the oxidation process starts at an early stage after formation of the nanoparticles. The analyses of the infrared data also show that β-cyclodextrin molecules retain their cyclic character and the coating does not affect the oxidation process once the particles are evicted from the fluids. A Mössbauer spectroscopy measurement on a ferrofluidic sample is also presented.

  12. Prolonged in vivo circulation time by zwitterionic modification of magnetite nanoparticles for blood pool contrast agents.

    PubMed

    Xiao, Wangchuan; Lin, Jiang; Li, Mingli; Ma, Yongjie; Chen, Yuxin; Zhang, Chunfu; Li, Dan; Gu, Hongchen

    2012-01-01

    Long circulation time is critical for blood pool contrast agents used in high-resolution magnetic resonance angiography. For iron oxide particle contrast agents, size and surface properties significantly influence their in vivo performance. We developed a novel long-circulating blood pool contrast agent by introducing zwitterionic structure onto the particle surface. Zwitterionic structure was fabricated by 3-(diethylamino)propylamine (DEAPA) grafted onto the surface of ployacrylic acid coated magnetite nanoparticles via EDC/NHS [N-(3-dimethylaminopropyl)-N'-ethylcarbo-diimide hydrochloride/N-hydroxysuccinimide] coupling chemistry. Zwitterionic particles demonstrated five times lower macrophage cell uptake than the original particles and low cell toxicity. Magnetic resonance angiography indicated that zwitterionic nanoparticles had much longer in vivo circulation time than the original particles and were an ideal candidate for blood pool contrast agent. We suppose that zwitterionic modification by DEAPA and EDC/NHS can be used generally for coating nanoparticles with carboxyl surface and to prolong their circulating time. PMID:22539402

  13. Magnetite-Alginate-AOT nanoparticles based drug delivery platform

    NASA Astrophysics Data System (ADS)

    Regmi, R.; Sudakar, C.; Dixit, A.; Naik, R.; Lawes, G.; Toti, U.; Panyam, J.; Vaishnava, P. P.

    2008-03-01

    Iron oxide having the magnetite structure is a widely used biomaterial, having applications ranging from cell separation and drug delivery to hyperthermia. In order to increase the efficacy of drug treatments, magnetite nanoparticles can be incorporated into a composite system with a surfactant-polymer nanoparticle, which can act as a platform for sustained and enhanced cellular delivery of water-soluble molecules. Here we report a composite formulation based on magnetite and Alginate-aerosol OT (AOT) nanoparticles formulated using an emulsion-cross-linking process loaded with Rhodamine 6G [1]. We prepared two set of nanoparticles by using Ca^2+ or Fe^2+ to cross-link the alginate polymer. Additionally, we added ˜8 nm diameter Fe3O4 magnetic nanoparticles prepared by a soft chemical method to these alginate-AOT nanoparticles. The resulting composites were superparamagnetic at room temperature, with a saturation magnetization of approximately 0.006 emu/g of solution. We will present detailed studies on the structural and magnetic properties of these samples. We will also discuss HPLC measurements on Rhodamine uploading in these composites. [1] M.D.Chavanpatil, Pharmaceutical Research, vol.24, (2007) 803.

  14. Relaxometry imaging of superparamagnetic magnetite nanoparticles at ambient conditions

    NASA Astrophysics Data System (ADS)

    Finkler, Amit; Schmid-Lorch, Dominik; Häberle, Thomas; Reinhard, Friedemann; Zappe, Andrea; Slota, Michael; Bogani, Lapo; Wrachtrup, Jörg

    We present a novel technique to image superparamagnetic iron oxide nanoparticles via their fluctuating magnetic fields. The detection is based on the nitrogen-vacancy (NV) color center in diamond, which allows optically detected magnetic resonance (ODMR) measurements on its electron spin structure. In combination with an atomic-force-microscope, this atomic-sized color center maps ambient magnetic fields in a wide frequency range from DC up to several GHz, while retaining a high spatial resolution in the sub-nanometer range. We demonstrate imaging of single 10 nm sized magnetite nanoparticles using this spin noise detection technique. By fitting simulations (Ornstein-Uhlenbeck process) to the data, we are able to infer additional information on such a particle and its dynamics, like the attempt frequency and the anisotropy constant. This is of high interest to the proposed application of magnetite nanoparticles as an alternative MRI contrast agent or to the field of particle-aided tumor hyperthermia.

  15. Glucose oxidase-magnetite nanoparticle bioconjugate for glucose sensing.

    PubMed

    Rossi, Liane M; Quach, Ashley D; Rosenzweig, Zeev

    2004-10-01

    Immobilization of bioactive molecules on the surface of magnetic nanoparticles is of great interest, because the magnetic properties of these bioconjugates promise to greatly improve the delivery and recovery of biomolecules in biomedical applications. Here we present the preparation and functionalization of magnetite (Fe3O4) nanoparticles 20 nm in diameter and the successful covalent conjugation of the enzyme glucose oxidase to the amino-modified nanoparticle surface. Functionalization of the magnetic nanoparticle surface with amino groups greatly increased the amount and activity of the immobilized enzyme compared with immobilization procedures involving physical adsorption. The enzymatic activity of the glucose oxidase-coated magnetic nanoparticles was investigated by monitoring oxygen consumption during the enzymatic oxidation of glucose using a ruthenium phenanthroline fluorescent complex for oxygen sensing. The glucose oxidase-coated magnetite nanoparticles could function as nanometric glucose sensors in glucose solutions of concentrations up to 20 mmol L(-1). Immobilization of glucose oxidase on the nanoparticles also increased the stability of the enzyme. When stored at 4 degrees C the nanoparticle suspensions maintained their bioactivity for up to 3 months. PMID:15448967

  16. Synthesis and characterization of magnetite nanoparticles coated with lauric acid

    SciTech Connect

    Mamani, J.B.; Costa-Filho, A.J.; Cornejo, D.R.; Vieira, E.D.; Gamarra, L.F.

    2013-07-15

    Understanding the process of synthesis of magnetic nanoparticles is important for its implementation in in vitro and in vivo studies. In this work we report the synthesis of magnetic nanoparticles made from ferrous oxide through coprecipitation chemical process. The nanostructured material was coated with lauric acid and dispersed in aqueous medium containing surfactant that yielded a stable colloidal suspension. The characterization of magnetic nanoparticles with distinct physico-chemical configurations is fundamental for biomedical applications. Therefore magnetic nanoparticles were characterized in terms of their morphology by means of TEM and DLS, which showed a polydispersed set of spherical nanoparticles (average diameter of ca. 9 nm) as a result of the protocol. The structural properties were characterized by using X-ray diffraction (XRD). XRD pattern showed the presence of peaks corresponding to the spinel phase of magnetite (Fe{sub 3}O{sub 4}). The relaxivities r{sub 2} and r{sub 2}* values were determined from the transverse relaxation times T{sub 2} and T{sub 2}* at 3 T. Magnetic characterization was performed using SQUID and FMR, which evidenced the superparamagnetic properties of the nanoparticles. Thermal characterization using DSC showed exothermic events associated with the oxidation of magnetite to maghemite. - Highlights: • Synthesis of magnetic nanoparticles coated with lauric acid • Characterization of magnetic nanoparticles • Morphological, structural, magnetic, calorimetric and relaxometric characterization.

  17. Sticking polydisperse hydrophobic magnetite nanoparticles to lipid membranes.

    PubMed

    Paulus, Michael; Degen, Patrick; Brenner, Thorsten; Tiemeyer, Sebastian; Struth, Bernd; Tolan, Metin; Rehage, Heinz

    2010-10-19

    The formation of a layer of hydrophobic magnetite (Fe(3)O(4)) nanoparticles stabilized by lauric acid is analyzed by in situ X-ray reflectivity measurements. The data analysis shows that the nanoparticles partially disperse their hydrophobic coating. Consequently, a Langmuir layer was formed by lauric acid molecules that can be compressed into an untilted condensed phase. A majority of the nanoparticles are attached to the Langmuir film integrating lauric acid residue on their surface into the Langmuir film. Hence, the particles at the liquid-gas interface can be identified as so-called Janus beads, which are amphiphilic solids having two sides with different functionality. PMID:20873726

  18. Preparation of size-controlled nanoparticles of magnetite

    NASA Astrophysics Data System (ADS)

    Andrade, Ângela L.; Valente, Manuel A.; Ferreira, José M. F.; Fabris, José D.

    2012-05-01

    Samples of ferrofluids containing chemically stabilized nanoparticles of magnetite (Fe3O4) with tetramethylammonium hydroxide (TMAOH) were prepared by a direct reduction-precipitation method. The influences of aging time and temperature on the size and monodispersion characteristics of the produced nanoparticles were investigated. Transmission electron microscopy, powder X-ray diffraction, Fourier-transform infrared, and magnetization measurements with applied magnetic field up to 2 T were used to characterize the synthesized iron oxides. Raising the temperature of the synthesized material in autoclave affects positively the monodispersion of the nanoparticles, but it was not found to significantly influence the size itself of individual particles.

  19. Functionalized magnetite particles for adsorption of colloidal noble metal nanoparticles.

    PubMed

    Lopes, Joana L; Marques, Karine L; Girão, Ana V; Pereira, Eduarda; Trindade, Tito

    2016-08-01

    Magnetite (inverse spinel type) particles have been surface-modified with siliceous shells enriched in dithiocarbamate groups. The deposition of colloidal noble metal nanoparticles (Au, Ag, Pt, Pd) onto the modified magnetites can be performed by treating the respective hydrosols with the magnetic sorbents, thus allowing their uptake from water under a magnetic gradient. In particular, for Au colloids, these magnetic particles are very efficient sorbents that we ascribe to the strong affinity of sulfur-containing groups at the magnetite surfaces for this metal. Considering the extensive use of Au colloids in laboratorial and industrial contexts, the approach described here might have an impact on the development of nanotechnologies to recover this precious metal. En route to these findings, we varied several operational parameters in order to investigate this strategy as a new bottom-up assembly method for producing plasmonic-magnetic nanoassemblies. PMID:27156089

  20. Stable ferrofluids of magnetite nanoparticles in hydrophobic ionic liquids.

    PubMed

    Mestrom, Luuk; Lenders, Jos J M; de Groot, Rick; Hooghoudt, Tonnis; Sommerdijk, Nico A J M; Artigas, Marcel Vilaplana

    2015-07-17

    Ferrofluids (FFs) of metal oxide nanoparticles in ionic liquids (ILs) are a potentially useful class of magnetic materials for many applications because of their properties related to temperature/pressure stability, hydrophobicity, viscosity and recyclability. In this work, the screening of several designer surfactants for their stabilizing capabilities has resulted in the synthesis of stable FFs of superparamagnetic 7 ± 2 nm magnetite (Fe3O4) nanoparticles in the hydrophobic IL 1-alkyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C(R)MIM][NTf2]). The designed and synthesized 1-butyl-3-(10-carboxydecyl)-1H-imidazol-3-ium bromide (ILC10-COOH) surfactant that combines the same imidazole moiety as the IL with a long alkyl chain ensured compatibility with the IL and increased the steric repulsion between the magnetite nanoparticles sufficiently such that stable dispersions of up to 50 wt% magnetite were obtained according to stability tests in the presence of a magnetic field (0.5-1 Tesla). Cryo-transmission electron microscopy (cryo-TEM) of the IL-based FFs allowed direct visualization of the surfactant-stabilized nanoparticles in the ILs and the native, hardly aggregated state of their dispersion. PMID:26118409

  1. Stable ferrofluids of magnetite nanoparticles in hydrophobic ionic liquids

    NASA Astrophysics Data System (ADS)

    Mestrom, Luuk; Lenders, Jos J. M.; de Groot, Rick; Hooghoudt, Tonnis; Sommerdijk, Nico A. J. M.; Vilaplana Artigas, Marcel

    2015-07-01

    Ferrofluids (FFs) of metal oxide nanoparticles in ionic liquids (ILs) are a potentially useful class of magnetic materials for many applications because of their properties related to temperature/pressure stability, hydrophobicity, viscosity and recyclability. In this work, the screening of several designer surfactants for their stabilizing capabilities has resulted in the synthesis of stable FFs of superparamagnetic 7 ± 2 nm magnetite (Fe3O4) nanoparticles in the hydrophobic IL 1-alkyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([CRMIM][NTf2]). The designed and synthesized 1-butyl-3-(10-carboxydecyl)-1H-imidazol-3-ium bromide (ILC10-COOH) surfactant that combines the same imidazole moiety as the IL with a long alkyl chain ensured compatibility with the IL and increased the steric repulsion between the magnetite nanoparticles sufficiently such that stable dispersions of up to 50 wt% magnetite were obtained according to stability tests in the presence of a magnetic field (0.5-1 Tesla). Cryo-transmission electron microscopy (cryo-TEM) of the IL-based FFs allowed direct visualization of the surfactant-stabilized nanoparticles in the ILs and the native, hardly aggregated state of their dispersion.

  2. Polypyrrole coated magnetite nanoparticles from water based nanofluids

    NASA Astrophysics Data System (ADS)

    Turcu, R.; Pana, O.; Nan, A.; Craciunescu, I.; Chauvet, O.; Payen, C.

    2008-12-01

    The synthesis and characterization of hybrid structures obtained by coating Fe3O4 magnetic nanoparticles from water based nanofluid with a polypyrrole (PPy) layer are reported. The thin amorphous layer of polypyrrole surrounding the crystalline magnetic core was observed by HRTEM. The FTIR spectra of the nanocomposites show that the absorption bands characteristic for pyrrole ring vibrations significantly shifted to lower frequencies in the nanocomposite spectra, which indicates a higher degree of oxidation of the PPy shell covering the magnetite as compared with conventional PPy. The existence of superparamagnetism in the investigated nanocomposites is evidenced by the missing hysterezis loop in the magnetization versus applied magnetic field dependences. The comparison between the physical size of nanoparticles determined from TEM analysis and the magnetic size deduced from magnetization measurements is discussed. The surface modification of magnetite by polypyrrole coating results in an increase in the saturation magnetization and of the apparent magnetic diameter of the nanoparticles. This novel effect is attributed to a charge transfer process from the conducting polymer to the surface iron ions of magnetite, producing an increase in the surface contribution to the overall magnetic moment of the nanoparticles.

  3. Synthesis, Magnetic Properties, Map Images, and Water Proton Relaxivities of D-Glucuronic Acid Coated Ln2O3 Nanoparticles (Ln = Ho and Er).

    PubMed

    Kattel, Krishna; Kim, Cho Rong; Xu, Wenlong; Kim, Tae Jeong; Park, Jang Woo; Chang, Yongmin; Lee, Gang Ho

    2015-09-01

    T2 MRI contrast agents cannot be synthesized by using molecules but nanoparticles because appreciable magnetic moments at room temperature are needed. Recently, some of lanthanide (Ln) oxide nanoparticles have shown decent magnetic moments at room temperature and even at ultrasmall particle diameters. In this study, we explored D-glucuronic acid coated Ln2O3 nanoparticles (Ln = Ho and Er) with ultrasmall particle diameters. They showed decent magnetic moments at room temperature and as a result, appreciable transverse water proton relaxivities (r2s) at 1.5 tesla MR field. Clear dose-dependent contrast enhancements in R2 map images were observed in both samples. These results showed that D-glucuronic acid coated Ln2O3 nanoparticles (Ln = Ho and Er) would be potential T2 MRI contrast agents at high MR fields. PMID:26716328

  4. Growth mechanism and magnetic properties of magnetite nanoparticles during solution process

    NASA Astrophysics Data System (ADS)

    Iwamoto, Takashi; Kinoshita, Toshiya; Takahashi, Kazuma

    2016-05-01

    We investigated the growth mechanism of magnetite nanoparticles during chemical synthesis by analyzing their physicochemical properties. The transformation from metallic precursor to particles and the growth of the particle occurred during chemical synthesis. During the transformation process, Fe(acac)3, which was used as a metallic precursor, was decomposed, fabricating an Fe oleate. The Fe oleates then agglomerated to each other to form Fe oleate clusters. Finally, the Fe oleate cluster was reduced, and a magnetite nanoparticle was fabricated. During the growth process of the magnetite nanoparticle, the diameter of the magnetite nanoparticles increased as the reaction temperature increased. Then, the Fe oleates on the surface of the magnetite nanoparticle were reduced at a constant rate, and as a result, the magnetite nanoparticle grew significantly.

  5. Homo- and co-polymerization of polysytrene-block-poly(acrylic acid)-coated metal nanoparticles.

    PubMed

    Wang, Hong; Song, Xiaohui; Liu, Cuicui; He, Jiating; Chong, Wen Han; Chen, Hongyu

    2014-08-26

    Amphiphilic block copolymers such as polystyrene-block-poly(acrylic acid) (PSPAA) give micelles that are known to undergo sphere-to-cylinder shape transformation. Exploiting this polymer property, core-shell nanoparticles coated in PSPAA can be "polymerized" into long chains following the chain-growth polymerization mode. This method is now extended to include a variety of different nanoparticles. A case study on the assembly process was carried out to understand the influence of the PAA block length, the surface ligand, and the size and morphology of the monomer nanoparticles. Shortening the PAA block promotes the reorganization of the amphiphilic copolymer in the micelles, which is essential for assembling large Au nanoparticles. Small Au nanoparticles can be directly "copolymerized" with empty PSPAA micelles into chains. The reaction time, acid quantity, and the [Au nanoparticles]/[PSPAA micelles] concentration ratio played important roles in controlling the sphere-cylinder-vesicle conversion of the PSPAA micelles, giving rise to different kinds of random "copolymers". With this knowledge, a general method is then developed to synthesize homo, random, and block "copolymers", where the basic units include small Au nanoparticles (d = 16 nm), large Au nanoparticles (d = 32 nm), Au nanorods, Te nanowires, and carbon nanotubes. Given the lack of means for assembling nanoparticles, advancing synthetic capabilities is of crucial importance. Our work provides convenient routes for combining nanoparticles into long-chain structures, facilitating rational design of complex nanostructures in the future. PMID:25000121

  6. Aqueous ferrofluid of magnetite nanoparticles: Fluorescence labeling and magnetophoretic control.

    PubMed

    Sahoo, Yudhisthira; Goodarzi, Alireza; Swihart, Mark T; Ohulchanskyy, Tymish Y; Kaur, Navjot; Furlani, Edward P; Prasad, Paras N

    2005-03-10

    A method is presented for the preparation of a biocompatible ferrofluid containing dye-functionalized magnetite nanoparticles that can serve as fluorescent markers. This method entails the surface functionalization of magnetite nanoparticles using citric acid to produce a stable aqueous dispersion and the subsequent binding of fluorescent dyes to the surface of the particles. Several ferrofluid samples were prepared and characterized using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), BET surface area analysis, transmission electron microscopy (TEM), and SQUID magnetometry. In addition, confocal fluorescence microscopy was used to study the response of the fluorescent nanoparticles to an applied magnetic field and their uptake by cells in vitro. Results are presented on the distribution of particle sizes, the fluorescent and magnetic properties of the nanoparticles, and the nature of their surface bonds. Biocompatible ferrofluids with fluorescent nanoparticles enable optical tracking of basic processes at the cellular level combined with magnetophoretic manipulation and should be of substantial value to researchers engaged in both fundamental and applied biomedical research. PMID:16851439

  7. Enhanced thermal stability of phosphate capped magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Muthukumaran, T.; Philip, John

    2014-06-01

    We have studied the effect of phosphate capping on the high temperature thermal stability and magnetic properties of magnetite (Fe3O4) nanoparticles synthesized through a single-step co-precipitation method. The prepared magnetic nanoparticles are characterized using various techniques. When annealed in air, the phosphate capped nanoparticle undergoes a magnetic to non-magnetic phase transition at a temperature of 689 °C as compared to 580 °C in the uncoated nanoparticle of similar size. The observed high temperature phase stability of phosphate capped nanoparticle is attributed to the formation of a phosphocarbonaceous shell over the nanoparticles, which acts as a covalently attached protective layer and improves the thermal stability of the core material by increasing the activation energy. The phosphocarbonaceous shell prevents the intrusion of heat, oxygen, volatiles, and mass into the magnetic core. At higher temperatures, the coalescence of nanoparticles occurs along with the restructuring of the phosphocarbonaceous shell into a vitreous semisolid layer on the nanoparticles, which is confirmed from the small angle X-ray scattering, Fourier transform infra red spectroscopy, and transmission electron microscopy measurements. The probable mechanism for the enhancement of thermal stability of phosphocarbonaceous capped nanoparticles is discussed.

  8. Enhanced thermal stability of phosphate capped magnetite nanoparticles

    SciTech Connect

    Muthukumaran, T.; Philip, John

    2014-06-14

    We have studied the effect of phosphate capping on the high temperature thermal stability and magnetic properties of magnetite (Fe{sub 3}O{sub 4}) nanoparticles synthesized through a single-step co-precipitation method. The prepared magnetic nanoparticles are characterized using various techniques. When annealed in air, the phosphate capped nanoparticle undergoes a magnetic to non-magnetic phase transition at a temperature of 689 °C as compared to 580 °C in the uncoated nanoparticle of similar size. The observed high temperature phase stability of phosphate capped nanoparticle is attributed to the formation of a phosphocarbonaceous shell over the nanoparticles, which acts as a covalently attached protective layer and improves the thermal stability of the core material by increasing the activation energy. The phosphocarbonaceous shell prevents the intrusion of heat, oxygen, volatiles, and mass into the magnetic core. At higher temperatures, the coalescence of nanoparticles occurs along with the restructuring of the phosphocarbonaceous shell into a vitreous semisolid layer on the nanoparticles, which is confirmed from the small angle X-ray scattering, Fourier transform infra red spectroscopy, and transmission electron microscopy measurements. The probable mechanism for the enhancement of thermal stability of phosphocarbonaceous capped nanoparticles is discussed.

  9. Some Properties of Magnetite Nanoparticles Produced Under Different Conditions

    NASA Astrophysics Data System (ADS)

    Khan, Umar Saeed; Khattak, Nazir Shah; Manan, Abdul; Rahman, Aminur; Khan, Faridullah; Rahim, Abdur

    2015-01-01

    Temperature, stirring rate, stirring time, reaction pH, and concentration of precursors during synthesis were found to be crucial in determining the size of the magnetite nanoparticles (NPs) obtained. The relationship between synthetic conditions and the crystal structure, particle size, and size distribution of the NPs was studied. Surface coating of iron oxide NPs was performed in two steps. Magnetite NPs were prepared by coprecipitation then coated with silica by use of a sol-gel process. Saturation magnetization of the magnetite NPs increased from 47.23 to 49.12 emu/g when their size was increased from 8.89 to 9.39 nm. Magnetite NPs in the size range 11-12 nm, coated with silica, are monodispersed and their corresponding saturation magnetization is 40.67 emu/g (11 nm) and 34.65 emu/g (12 nm). The decrease in the saturation magnetization of the coated samples is attributed to the increase in the amount of tetraethyl orthosilicate.

  10. Structural and magnetic properties of sonoelectrocrystallized magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Mosivand, S.; Monzon, L. M. A.; Ackland, K.; Kazeminezhad, I.; Coey, J. M. D.

    2014-02-01

    The effect of ultrasound power on the morphology, structure and magnetic properties of magnetite nanoparticles synthesized from iron electrodes by the electro-oxidation method was investigated. Samples made in aqueous solution in the absence or presence of an organic stabilizer (thiourea, tetramethylammonium chloride, sodium butanoate or β-cyclodextrine) were characterized by x-ray diffraction, transmission and scanning electron microscopy, magnetometry and Mössbauer spectrometry. The iron is almost all in the form of 20-85 nm particles of slightly nonstoichiometric Fe3-δO4, with δ ≈ 0.10. Formation of a paramagnetic secondary phase in the presence of sodium butanoate or β-cyclodextrine is supressed by ultrasound. Specific magnetization of the magnetite nanoparticles ranges from 19 to 90 A m2 kg-1 at room temperature, and it increases with particle size in each series. The particles show no sign of superparamagnetism, and the anhysteretic and practically temperature-independent magnetization curves are associated with a stable magnetic vortex state throughout the size range. The spin structure of the particles and the use of magnetization measurements to detect magnetite in unknown mixtures are discussed.

  11. Fabrication and characterization of superparamagnetic and thermoresponsive hydrogels based on oleic-acid-coated Fe 3O 4 nanoparticles, hexa(ethylene glycol) methyl ether methacrylate and 2-(acetoacetoxy)ethyl methacrylate

    NASA Astrophysics Data System (ADS)

    Papaphilippou, Petri C.; Pourgouris, Antonis; Marinica, Oana; Taculescu, Alina; Athanasopoulos, George I.; Vekas, Ladislau; Krasia-Christoforou, Theodora

    2011-03-01

    Stimuli-responsive hydrogel nanocomposites comprised of swollen polymer networks, in which magnetic nanoparticles are embedded, are a relatively new class of "smart" soft materials presenting a significant impact on various technological and biomedical applications. A novel approach for the fabrication of hydrogel nanocomposites exhibiting temperature- and magneto-responsive behavior involves the random copolymerization of hexa(ethylene glycol) methyl ether methacrylate (HEGMA, hydrophilic, thermoresponsive) and 2-(acetoacetoxy)ethyl methacrylate (AEMA, hydrophobic, metal-chelating) in the presence of preformed oleic-acid-coated magnetite nanoparticles (OA·Fe 3O 4). In total, two series of hydrogel nanocomposites have been prepared in two different solvent systems: ethyl acetate (series A) and tetrahydrofuran (series B). The degrees of swelling (DSs) of all conetworks were determined in organic and in aqueous media. The nanocrystalline phase adopted by the embedded magnetic nanoparticles was investigated by X-ray diffraction (XRD) spectroscopy. The obtained diffraction patterns indicated the presence of magnetite (Fe 3O 4). Deswelling kinetic studies that were carried out at ˜60 °C in water demonstrated the thermoresponsive properties of the hydrogel nanocomposites, attributed to the presence of the hexaethylene glycol side chains within the conetworks. Moreover, thermal gravimetric analysis (TGA) measurements showed that these materials exhibited superior thermal stability compared to the pristine hydrogels. Further to the characterization of compositional and thermal properties, the assessment of magnetic characteristics by vibrational sample magnetometry (VSM) disclosed superparamagnetic behavior. The tunable superparamagnetic behavior exhibited by these materials depending on the amount of magnetic nanoparticles incorporated within the networks combined with their thermoresponsive properties may allow for their future exploitation in the biomedical field.

  12. Magnetite Nanoparticles for Medical MR Imaging

    PubMed Central

    Stephen, Zachary R.; Kievit, Forrest M.; Zhang, Miqin

    2011-01-01

    Nanotechnology has given scientists new tools for the development of advanced materials for the detection and diagnosis of disease. Iron oxide nanoparticles (SPIONs) in particular have been extensively investigated as novel magnetic resonance imaging (MRI) contrast agents due to a combination of favorable superparamagnetic properties, biodegradability, and surface properties of easy modification for improved in vivo kinetics and multifunctionality. This review discusses the basics of MR imaging, the origin of SPION’s unique magnetic properties, recent developments in MRI acquisition methods for detection of SPIONs, synthesis and post-synthesis processes that improve SPION’s imaging characteristics, and an outlook on the translational potential of SPIONs. PMID:22389583

  13. Transport in Porous Media of Poly(Acrylic Acid) Coated Ferrihydrite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Jaffe, P. R.; Xiang, A.; Koel, B. E.

    2012-12-01

    Augmentation of soils with iron to enhance biological processes such as uranium reduction via iron reducing bacteria, e.g., Geobacter sp., might be achieved via the injection of iron nanoparticles into the subsurface. The challenge is to make these nanoparticles transportable in the subsurface while not affecting the iron bioavailability. Poorly crystallized 2-line ferrihydrite iron oxide nanoparticles were synthesized and coated with different amounts of poly(acrylic acid) polymers (Na-PAA6K or Na-PAA140K). Analyses were then performed on these particles, including sorption/desorption of the polymer onto the iron nanoparticles, particle size, zeta potential, transport in sand and soil columns, and bioavailabity of the Fe(III) in the absence and presence of the coating to iron reducing organisms. Results showed that at pH values of environmental relevance, the zeta potential of the particles varied from about 3 mV (pH=8.2) for the non-coated particles to about -30 mV for the particles coated with the polymers to their highest sorption capacity. The coated particle diameter was shown to be in the range of 200 nm. Column transport experiments showed that for the highest polymer coating the nanoparticle breakthrough was virtually identical to that of bromide, while significant filtration was observed for particles with an intermediate coating, and complete particle removal via filtration was observed for the non-coated particles. These results held for sand as well as for soil, which had been previously characterized, from a field site at Rifle, CO. Bioavailability experiments showed no difference in the iron reduction rate between the untreated and treated nanoparticles. These results show that it is possible to manufacture iron nanoparticles to enhance biological iron reduction, and that the transport properties of these treated particles is tunable so that a desired retention in the porous medium can be achieved.

  14. Plasma amino acid coatings for a conformal growth of titania nanoparticles.

    PubMed

    Anderson, Kyle D; Marczewski, Kamil; Singamaneni, Srikanth; Slocik, Joseph M; Jakubiak, Rachel; Naik, Rajesh R; Bunning, Timothy J; Tsukruk, Vladimir V

    2010-08-01

    We report on the conformal synthesis of ultrathin films from the amino acid histidine on flat silicon substrates and 3D periodic polymer structures via plasma enhanced chemical vapor deposition. We demonstrate the efficient utilization of this functional amino acid nanocoating for the formation of individual titania nanoparticles with dimensions from 2 to 15 nm depending upon reduction conditions. The titania nanoparticles were grown directly on histidine-functionalized planar and 3D polymer substrates by a wet-chemistry method that showed uniform surface coverage that reached approximately 75%. This approach demonstrates the potential for modifying the optical properties of periodic porous polymeric structures via direct conformal growth of titania nanoparticles. PMID:20735097

  15. Simple and facile approach to synthesize magnetite nanoparticles and assessment of their effects on blood cells

    NASA Astrophysics Data System (ADS)

    Cótica, Luiz F.; Freitas, Valdirlei F.; Dias, Gustavo S.; Santos, Ivair A.; Vendrame, Sheila C.; Khalil, Najeh M.; Mainardes, Rubiana M.; Staruch, Margo; Jain, Menka

    2012-02-01

    In this paper, a very simple and facile approach for the large scale synthesis of uniform and size-controllable single-domain magnetite nanoparticles is reported. These magnetite nanoparticles were synthesized via thermal decomposition of a ferric nitrate/ethylene glycol solution. The structural and morphological properties of the synthesized nanoparticles were carefully studied. Nearly spherical nanoparticles with inverted spinel structure and average particle and crystallite sizes smaller than 20 nm were obtained. The magnetic measurements revealed that magnetite nanoparticles have a magnetic saturation value near that of the bulk magnetite. The erythrocyte cytotoxicity assays showed no hemolytic potential of the samples containing magnetite nanoparticles, indicating no cytotoxic activity on human erythrocytes, which makes these interesting for biotechnological applications.

  16. Magnetite nanoparticles for biosensor model based on bacteria fluorescence

    NASA Astrophysics Data System (ADS)

    Poita, A.; Creanga, D.-E.; Airinei, A.; Tupu, P.; Goiceanu, C.; Avadanei, O.

    2009-06-01

    Fluorescence emission of pyoverdine - the siderophore synthesized by iron scavenger bacteria - was studied using in vitro cultures of Pseudomonas aeruginosa with the aim to design a biosensor system for liquid sample iron loading. Diluted suspensions of colloidal magnetite nanoparticles were supplied in the culture medium (10 microl/l and 100 microl/l) to simulate magnetic loading with iron oxides of either environmental waters or human body fluids. The electromagnetic exposure to radiofrequency waves of bacterial samples grown in the presence of magnetic nanoparticles was also carried out. Cell density diminution but fluorescence stimulation following 10 microl/l ferrofluid addition and simultaneous exposure to radiofrequency waves was evidenced. The inhibitory influence of 100 microl/l ferrofluid combined with RF exposure was evidenced by fluorescence data. Mathematical model was proposed to approach quantitatively the dynamics of cell density and fluorescence emission in relation with the consumption of magnetite nanoparticle supplied medium. The biosensor scheme was shaped based on the response to iron loading of bacterial sample fluorescence.

  17. Novel humic acid-bonded magnetite nanoparticles for protein immobilization.

    PubMed

    Bayrakci, Mevlut; Gezici, Orhan; Bas, Salih Zeki; Ozmen, Mustafa; Maltas, Esra

    2014-09-01

    The present paper is the first report that introduces (i) a useful methodology for chemical immobilization of humic acid (HA) to aminopropyltriethoxysilane-functionalized magnetite iron oxide nanoparticles (APS-MNPs) and (ii) human serum albumin (HSA) binding to the obtained material (HA-APS-MNPs). The newly prepared magnetite nanoparticle was characterized by using Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and elemental analysis. Results indicated that surface modification of the bare magnetite nanoparticles (MNPs) with aminopropyltriethoxysilane (APS) and HA was successfully performed. The protein binding studies that were evaluated in batch mode exhibited that HA-APS-MNPs could be efficiently used as a substrate for the binding of HSA from aqueous solutions. Usually, recovery values higher than 90% were found to be feasible by HA-APS-MNPs, while that value was around 2% and 70% in the cases of MNPs and APS-MNPs, respectively. Hence, the capacity of MNPs was found to be significantly improved by immobilization of HA. Furthermore, thermal degradation of HA-APS-MNPs and HSA bonded HA-APS-MNPs was evaluated in terms of the Horowitz-Metzger equation in order to determine kinetic parameters for thermal decomposition. Activation energies calculated for HA-APS-MNPs (20.74 kJmol(-1)) and HSA bonded HA-APS-MNPs (33.42 kJmol(-1)) implied chemical immobilization of HA to APS-MNPs, and tight interactions between HA and HA-APS-MNPs. PMID:25063152

  18. Magnetite nanoparticle interactions with insulin amyloid fibrils.

    PubMed

    Chen, Yun-Wen; Chang, Chiung-Wen; Hung, Huey-Shan; Kung, Mei-Lang; Yeh, Bi-Wen; Hsieh, Shuchen

    2016-10-14

    Accumulation of amyloid fibrils is one of the likely key factors leading to the development of Alzheimer's disease and other amyloidosis associated diseases. Magnetic nanoparticles (NPs) have been developed as promising medical materials for many medical applications. In this study, we have explored the effects of Fe3O4 NPs on the fibrillogenesis process of insulin fibrils. When Fe3O4 NPs were co-incubated with insulin, Fe3O4 NPs had no effect on the structural transformation into amyloid-like fibrils but had higher affinity toward insulin fibrils. We demonstrated that the zeta potential of insulin fibrils and Fe3O4 NPs were both positive, suggesting the binding forces between Fe3O4 NPs and insulin fibrils were van der Waals forces but not surface charge. Moreover, a different amount of Fe3O4 NPs added had no effect on secondary structural changes of insulin fibrils. These results propose the potential use of Fe3O4 NPs as therapeutic agents against diseases related to protein aggregation or contrast agents for magnetic resonance imaging. PMID:27585675

  19. Effects of magnetite nanoparticles on soybean chlorophyll.

    PubMed

    Ghafariyan, Mohammad H; Malakouti, Mohammad J; Dadpour, Mohammad R; Stroeve, Pieter; Mahmoudi, Morteza

    2013-09-17

    Nanoparticles (NPs) have emerged as one of the most innovative and promising application in agriculture. Since plants are recognized as essential component of all ecosystems, the effects of NPs on plants may pave a new insight to the ecosystems. Here, uptake and translocation of superparamagnetic iron oxide NPs (SPIONs), with various surface charges, on soybean has been probed; in addition, the effects of SPIONs on variations of chlorophyll, in hydroponic condition, together with their ability for reduction of iron deficiency chlorosis were explored. We find that SPIONs, which were entered and translocated in the soybean, increased chlorophyll levels, with no trace of toxicity. Furthermore, it was found that physicochemical characteristics of the SPIONs had a crucial role on the enhancement of chlorophyll content in subapical leaves of soybean. The equivalent ratio of chlorophyll a to b, in all treatments with conventional growth medium iron chelate and SPIONs (as iron source), indicated no significant difference on the photosynthesis efficiency. Finally, it was observed that the effect of SPIONs on the soybean chlorophyll content may have influence on both biochemical and enzymatic efficiency in different stages of the photosynthesis reactions. PMID:23951999

  20. Rheological Study of Dextran-Modified Magnetite Nanoparticle Water Suspension

    NASA Astrophysics Data System (ADS)

    Józefczak, A.; Hornowski, T.; Rozynek, Z.; Skumiel, A.; Fossum, J. O.

    2013-04-01

    The aim of this work is to investigate the effect of surface modification of superparamagnetic magnetite nanoparticles (sterically stabilized by sodium oleate) by the dextran biocompatible layer on the rheological behavior of water-based magnetic fluids. The flow curves were measured as a function of the magnetic field strength by means of rheometry. The measured viscosity is generally dependent on both the particle concentration and the geometrical factors such as the particle shape and thickness of the adsorbed layers. The rheological properties of the magnetic fluids studied show the effect of the magnetic field strength and the presence of the surfactant second layer (dextran) on their viscosity.

  1. Interaction of polyacrylic acid coated and non-coated iron oxide nanoparticles with human neutrophils.

    PubMed

    Couto, Diana; Freitas, Marisa; Vilas-Boas, Vânia; Dias, Irene; Porto, Graça; Lopez-Quintela, M Arturo; Rivas, José; Freitas, Paulo; Carvalho, Félix; Fernandes, Eduarda

    2014-02-10

    Iron oxide nanoparticles (ION), with different coatings and sizes, have attracted extensive interest in the last years to be applied in drug delivery, cancer therapy and as contrast agents in imagiologic techniques such as magnetic resonance imaging. However, the safety of these nanoparticles is still not completely established, particularly to host defense systems that are usually recruited for their clearance from the body. In this paper, given the importance of neutrophils in the immune response of the organism to nanoparticles, the effect of polyacrylic acid (PAA)-coated and non-coated ION on human neutrophils was evaluated in vitro, namely their capacity to activate the oxidative burst and to modify their lifespan. The obtained results showed that the studied PAA-coated and non-coated ION triggered neutrophils' oxidative burst in a NADPH oxidase dependent manner, and that PAA-coated ION increased - while non-coated ION prevented - apoptotic signaling and apoptosis. These effects may have important clinical implications in biomedical applications of ION. PMID:24291037

  2. Water dispersible oleic acid-coated Fe3O4 nanoparticles for biomedical applications

    NASA Astrophysics Data System (ADS)

    Shete, P. B.; Patil, R. M.; Tiwale, B. M.; Pawar, S. H.

    2015-03-01

    Fe3O4 magnetic nanoparticles (MNPs) have proved their tremendous potential to be used for various biomedical applications. Oleic acid (OA) is widely used in ferrite nanoparticle synthesis because it can form a dense protective monolayer, thereby producing highly uniform and monodispersed particles. Capping agents such as oleic acid are often used because they form a protective monolayer, which is strongly bonded to the surface of nanoparticles. This is necessary for making monodisperse and highly uniform MNPs. Coating of Fe3O4 MNPs with OA makes the particles dispersible only in organic solvents and consequently limits their use for biomedical applications. Hence, in this work, the OA coated MNPs were again functionalized with chitosan (CS), in order to impart hydrophilicity on their surface. All the morphological, magnetic, colloidal and cytotoxic characteristics of the resulting core-shells were studied thoroughly. Their heating induction ability was studied to predict their possible use in hyperthermia therapy of cancer. Specific absorption rate was found to be increased than that of bare MNPs.

  3. Arsenate removal with 3-mercaptopropanoic acid-coated superparamagnetic iron oxide nanoparticles.

    PubMed

    Morillo, D; Uheida, A; Pérez, G; Muhammed, M; Valiente, M

    2015-01-15

    In the present work, superparamagnetic iron oxide nanoparticles (SPION) surface-coated with 3-mercaptopropanoic acid (3-MPA) were prepared and their feasibility for the removal of arsenate from dilute aqueous solutions was demonstrated. The synthesized 3-MPA-coated SPION was characterized using transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Fourier transform infra-red spectrometry (FTIR). Separation efficiency of the coated nanoparticles and the equilibrium isotherm of arsenate adsorption were investigated. The obtained results reveal the arsenate adsorption to be highly pH-dependent, and the maximum adsorption was attained in less than 60 min. The resulting increase of 3-MPA-coated SPION adsorption capacity to twice the adsorption capacity of SPION alone under the same conditions is attributed to the increase of active adsorption sites. An adsorption reaction is proposed. On the other hand, efficient recovery of arsenate from the loaded nanoparticles was achieved using nitric acid (HNO3) solution, which also provides a concentration over the original arsenate solution. PMID:25454446

  4. Synthesis, magnetic and ethanol gas sensing properties of semiconducting magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Al-Ghamdi, Ahmed A.; Al-Hazmi, Faten; Al-Tuwirqi, R. M.; Alnowaiser, F.; Al-Hartomy, Omar A.; El-Tantawy, Farid; Yakuphanoglu, F.

    2013-05-01

    The superparamagnetic magnetite (Fe3O4) nanoparticles with an average size of 7 nm were synthesized using a rapid and facile microwave hydrothermal technique. The structure of the magnetite nanoparticles was characterized by X-ray diffraction (X-ray), field effect scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), and transmission electron microscopy (TEM). The prepared Fe3O4 was shown to have a cubic phase of pure magnetite. Magnetization hysteresis loop shows that the synthesized magnetite exhibits no hysteretic features with a superparamagnetic behavior. The ethanol gas sensing properties of the synthesized magnetite were investigated, and it was found that the responsibility time is less than 10 s with good reproducibility for ethanol sensor. Accordingly, it is evaluated that the magnetite nanoparticles can be effectively used as a solid state ethanol sensor in industrial commercial product applications.

  5. Temperature-dependent structure of Tb-doped magnetite nanoparticles

    SciTech Connect

    Rice, Katherine P.; Russek, Stephen E. Shaw, Justin M.; Usselman, Robert J.; Evarts, Eric R.; Silva, Thomas J.; Nembach, Hans T.; Geiss, Roy H.; Arenholz, Elke; Idzerda, Yves U.

    2015-02-09

    High quality 5 nm cubic Tb-doped magnetite nanoparticles have been synthesized by a wet-chemical method to investigate tailoring of magnetic properties for imaging and biomedical applications. We show that the Tb is incorporated into the octahedral 3+ sites. High-angle annular dark-field microscopy shows that the dopant is well-distributed throughout the particle, and x-ray diffraction measurements show a small lattice parameter shift with the inclusion of a rare-earth dopant. Magnetization and x-ray magnetic circular dichroism data indicate that the Tb spins are unpolarized and weakly coupled to the iron spin lattice at room temperature, and begin to polarize and couple to the iron oxide lattice at temperatures below 50 K. Broadband ferromagnetic resonance measurements show no increase in magnetic damping at room temperature for Tb-doped nanoparticles relative to undoped nanoparticles, further confirming weak coupling between Fe and Tb spins at room temperature. The Gilbert damping constant, α, is remarkably low for the Tb-doped nanoparticles, with α = 0.024 ± 0.003. These nanoparticles, which have a large fixed moment, a large fluctuating moment and optically active rare-earth elements, are potential high-relaxivity T1 and T2 MRI agents with integrated optical signatures.

  6. Linear birefringence and dichroism in citric acid coated Fe3O4 magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Lin, Jing-Fung; Tsai, Chun-Chin; Lee, Meng-Zhe

    2014-12-01

    To prepare highly dispersed water-based Fe3O4 magnetic nanoparticles (MNPs), we adopted the co-precipitation method and used citric acid (CA) as the surfactant. Via transmission electronic microscopy, dynamic light scattering, and X-ray diffractometry, we characterized the dispersibility and size of the products. Through two single-parameter experiments, including the pH value of suspension and the action of double centrifugations, the appropriate parameters' values were determined. Further, to produce CA coated MNPs with good magneto-optical properties as high retardance and low dichroism, the orthogonal design method was used to find the optimal parameters' values, including pH value of suspension after coating was 5, molar ratio of CA to Fe3O4 MNPs was 0.06, volume of CA was 40 ml, and coating temperature was 70 °C. Above all, the linear birefringence and dichroism of the best CA coated ferrofluid we produced were measured by a Stokes polarimeter as 23.6294° and 0.3411 under 64.5 mT, respectively. Thus, the biomedical applications could be performed hereafter.

  7. Cell type-specific response to high intracellular loading of polyacrylic acid-coated magnetic nanoparticles.

    PubMed

    Lojk, Jasna; Bregar, Vladimir B; Rajh, Maruša; Miš, Katarina; Kreft, Mateja Erdani; Pirkmajer, Sergej; Veranič, Peter; Pavlin, Mojca

    2015-01-01

    Magnetic nanoparticles (NPs) are a special type of NP with a ferromagnetic, electron-dense core that enables several applications such as cell tracking, hyperthermia, and magnetic separation, as well as multimodality. So far, superparamagnetic iron oxide NPs (SPIONs) are the only clinically approved type of metal oxide NPs, but cobalt ferrite NPs have properties suitable for biomedical applications as well. In this study, we analyzed the cellular responses to magnetic cobalt ferrite NPs coated with polyacrylic acid (PAA) in three cell types: Chinese Hamster Ovary (CHO), mouse melanoma (B16) cell line, and primary human myoblasts (MYO). We compared the internalization pathway, intracellular trafficking, and intracellular fate of our NPs using fluorescence and transmission electron microscopy (TEM) as well as quantified NP uptake and analyzed uptake dynamics. We determined cell viability after 24 or 96 hours' exposure to increasing concentrations of NPs, and quantified the generation of reactive oxygen species (ROS) upon 24 and 48 hours' exposure. Our NPs have been shown to readily enter and accumulate in cells in high quantities using the same two endocytic pathways; mostly by macropinocytosis and partially by clathrin-mediated endocytosis. The cell types differed in their uptake rate, the dynamics of intracellular trafficking, and the uptake capacity, as well as in their response to higher concentrations of internalized NPs. The observed differences in cell responses stress the importance of evaluation of NP-cell interactions on several different cell types for better prediction of possible toxic effects on different cell and tissue types in vivo. PMID:25733835

  8. Oleic Acid Coated Gelatin Nanoparticles Impregnated Gel for Sustained Delivery of Zaltoprofen: Formulation and Textural Characterization

    PubMed Central

    Pawar, Savita; Pande, Vishal

    2015-01-01

    Purpose: In the present study, we have formulated zaltoprofen loaded, surface decorated, biodegradable gelatin nanogel and evaluated its texture characterization. Methods: The method used to prepare gelatin nanoparticles (GNP) was ‘two step desolvation’ and its surface decoration was performed with oleic acid (OA). The GNP was optimized by DOE software. Nanogels were evaluated for particle size entrapment efficiency, texture properties, SEM, in-vitro, ex-vivo drug release studies, in-vitro characterization, stability and in vivo evaluation of nanogel for anti-inflammatory activity was carried out by carrageenan induced rat paw edema method as an anti-inflammatory experimental model. Results: The formulated GNP with particle size and entrapment efficiency of optimized batch was found to be 247.1 nm and 76.21% respectively. The SEM of GNP shows smooth and spherical shape. In-vitro and Ex-vivo drug release shows that there was 69.47% and 78.59% drug released within 48 hrs. It follows Ritger peppas model, which indicates sustained drug release. The good texture properties of nanogel were observed from texture analysis graphs.In vivo studies of our formulation give significant results compared to the marketed nanogel. Stability data revealed stability of nanogel formulation up to 3 months. Conclusion: The present approach can provide us promising results of the sustained analgesic activity and the stability of drug within the GNP. PMID:26819927

  9. Cell type-specific response to high intracellular loading of polyacrylic acid-coated magnetic nanoparticles

    PubMed Central

    Lojk, Jasna; Bregar, Vladimir B; Rajh, Maruša; Miš, Katarina; Kreft, Mateja Erdani; Pirkmajer, Sergej; Veranič, Peter; Pavlin, Mojca

    2015-01-01

    Magnetic nanoparticles (NPs) are a special type of NP with a ferromagnetic, electron-dense core that enables several applications such as cell tracking, hyperthermia, and magnetic separation, as well as multimodality. So far, superparamagnetic iron oxide NPs (SPIONs) are the only clinically approved type of metal oxide NPs, but cobalt ferrite NPs have properties suitable for biomedical applications as well. In this study, we analyzed the cellular responses to magnetic cobalt ferrite NPs coated with polyacrylic acid (PAA) in three cell types: Chinese Hamster Ovary (CHO), mouse melanoma (B16) cell line, and primary human myoblasts (MYO). We compared the internalization pathway, intracellular trafficking, and intracellular fate of our NPs using fluorescence and transmission electron microscopy (TEM) as well as quantified NP uptake and analyzed uptake dynamics. We determined cell viability after 24 or 96 hours’ exposure to increasing concentrations of NPs, and quantified the generation of reactive oxygen species (ROS) upon 24 and 48 hours’ exposure. Our NPs have been shown to readily enter and accumulate in cells in high quantities using the same two endocytic pathways; mostly by macropinocytosis and partially by clathrin-mediated endocytosis. The cell types differed in their uptake rate, the dynamics of intracellular trafficking, and the uptake capacity, as well as in their response to higher concentrations of internalized NPs. The observed differences in cell responses stress the importance of evaluation of NP–cell interactions on several different cell types for better prediction of possible toxic effects on different cell and tissue types in vivo. PMID:25733835

  10. Polyacrylic acid-coated cerium oxide nanoparticles: An oxidase mimic applied for colorimetric assay to organophosphorus pesticides.

    PubMed

    Zhang, Shi-Xiang; Xue, Shi-Fan; Deng, Jingjing; Zhang, Min; Shi, Guoyue; Zhou, Tianshu

    2016-11-15

    It is important and urgent to develop reliable and highly sensitive methods that can provide on-site and rapid detection of extensively used organophosphorus pesticides (OPs) for their neurotoxicity. In this study, we developed a novel colorimetric assay for the detection of OPs based on polyacrylic acid-coated cerium oxide nanoparticles (PAA-CeO2) as an oxidase mimic and OPs as inhibitors to suppress the activity of acetylcholinesterase (AChE). Firstly, highly dispersed PAA-CeO2 was prepared in aqueous solution, which could catalyze the oxidation of TMB to produce a color reaction from colorless to blue. And the enzyme of AChE was used to catalyze the substrate of acetylthiocholine (ATCh) to produce thiocholine (TCh). As a thiol-containing compound with reducibility, TCh can decrease the oxidation of TMB catalyzed by PAA-CeO2. Upon incubated with OPs, the enzymatic activity of AChE was inhibited to produce less TCh, resulting in more TMB catalytically oxidized by PAA-CeO2 to show an increasing blue color. The two representative OPs, dichlorvos and methyl-paraoxon, were tested using our proposed assay. The novel assay showed notable color change in a concentration-dependent manner, and as low as 8.62 ppb dichlorvos and 26.73 ppb methyl-paraoxon can be readily detected. Therefore, taking advantage of such oxidase-like activity of PAA-CeO2, our proposed colorimetric assay can potentially be a screening tool for the precise and rapid evaluation of the neurotoxicity of a wealth of OPs. PMID:27208478

  11. The potential application of hyaluronic acid coated chitosan nanoparticles in ocular delivery of dexamethasone.

    PubMed

    Kalam, Mohd Abul

    2016-08-01

    This study investigates in-vitro transcorneal permeation on excised-rabbit cornea and its effect on corneal hydration-level, in-vivo ocular irritation, tear and aqueous humor dexamethasone-sodium-phosphate (DEX) concentration after topical administration of chitosan-nanoparticles (CS-NPs), hyaluronan-coated-CS-NPs (HA-CS-NPs) and DEX-aqueous-solution in rabbit eyes. The permeation parameters and irritation results indicated the ocular safety of NPs. The developed UPLC-method was successfully applied for DEX quantification in tears and aqueous-humors. Tear samples were collected and DEX-concentration was analyzed by UPLC. A statistically significantly (p<0.05) high DEX-concentration in the inferior conjunctival-sulcus from NPs treated eyes was found as compared to DEX-solution treated eyes. Similarly, DEX-concentration in aqueous-humor was estimated. The drug was detected sufficiently high in aqueous-humor till 24h following topical administration of NPs. The NPs have shown significantly (p<0.05) higher bioavailability of DEX compared to DEX-solution. About 1.83- and 2.14-fold higher AUC0-24h was observed with the CS-NPs and HA-CS-NPs, respectively compared to DEX-solution. The reason for higher tear concentration and higher bioavailability of DEX from uncoated and HA-coated CS-NPs was assumed due to their prolonged precorneal-retention because of highly mucoadhesive characteristics of CS and HA. Moreover, presence of HA on CS-NPs, speed-up cellular-uptake by receptor-mediated-endocytosis could be another reason for enhanced bioavailability. PMID:27164496

  12. Introduction of biotin or folic acid into polypyrrole magnetite core-shell nanoparticles

    SciTech Connect

    Nan, Alexandrina; Turcu, Rodica; Liebscher, Jürgen

    2013-11-13

    In order to contribute to the trend in contemporary research to develop magnetic core shell nanoparticles with better properties (reduced toxicity, high colloidal and chemical stability, wide scope of application) in straightforward and reproducible methods new core shell magnetic nanoparticles were developed based on polypyrrole shells functionalized with biotin and folic acid. Magnetite nanoparticles stabilized by sebacic acid were used as magnetic cores. The morphology of magnetite was determined by transmission electron microscopy TEM, while the chemical structure investigated by FT-IR.

  13. Synthesis and evaluation of poly(Sodium 2-Acrylamido-2-Methylpropane Sulfonate-co-Styrene)/magnetite nanoparticle composites as corrosion inhibitors for steel.

    PubMed

    El-Mahdy, Gamal A; Atta, Ayman M; Al-Lohedan, Hamad A

    2014-01-01

    Self-stabilized magnetic polymeric composite nanoparticles of coated poly-(sodium 2-acrylamido-2-methylpropane sulfonate-co-styrene)/magnetite (PAMPS-Na-co-St/Fe3O4) were prepared by emulsifier-free miniemulsion polymerization using styrene (St) as a monomer, 2-acrylamido-2-methylpropane sulfonic acid sodium salt (AMPS-Na) as an ionic comonomer, N,N-methylenebisacrylamide (MBA) as crosslinker, hexadecane (HD) as a hydrophobic solvent, and 2,2-azodiisobutyronitrile (AIBN) as an initiator in the presence of hydrophobic oleic acid coated magnetite particles. Hydrophobic oleic acid coated magnetite particles with an average size of about 7-10 nm were prepared with the new modified water-based magnetite ferrofluid, synthesized by a chemical modified coprecipitation method. The morphology and the particle size distributions of the crosslinked PAMPS-Na-co-St/Fe3O4 composite were observed and analyzed by transmission electron microscopy (TEM). The average Fe3O4 content of PAMPS-Na-co-St/Fe3O4 was determined by thermogravimetric analysis (TGA). The inhibitory action of PAMPS-Na-co-St/Fe3O4 towards steel corrosion in 1 M HCl solutions has been investigated by polarization and electrochemical impedance spectroscopy (EIS) methods. Polarization measurements indicate that PAMPS-Na-co-St/Fe3O4 acts as a mixed type-inhibitor and the inhibition efficiency increases with inhibitor concentration. The results of potentiodynamic polarization and EIS measurements clearly showed that the inhibition mechanism involves blocking of the steel surface by inhibitor molecules via adsorption. PMID:24487568

  14. Influence of Magnetite Nanoparticles on Human Leukocyte Activity

    NASA Astrophysics Data System (ADS)

    Džarová, Anežka; Dubničková, Martina; Závišová, Vlasta; Koneracká, Martina; Kopčanský, Peter; Gojzewski, Hubert; Timko, Milan

    2010-12-01

    Chemically synthesized magnetite particles coated by sodium oleate and PEG (MNP), and magnetosomes (MS) influence the process of phagocytosis and the metabolic activity (lysozyme and peroxidase activity) in leukocytes. Lysozyme activity is oxygen-independent liquidation mechanisms of engulfed microorganism, peroxidase activity is an oxygen-dependent mechanism. Both tested types of nanoparticles lysed leukocyte cells during incubation. MNP at concentrations of 10 and 20 μg/mL lysed almost all leukocytes and their cell viability was in the 14±0.05% range. On the other hand MS begin to influence leukocytes activity at the concentration of 1 μg/ml and this influence grows with increasing concentration up to 20 μg/ml. MS are more suitable for biological applications than MNP which are more aggressive material than MS. MS should not be used above 10 μg/mL.

  15. Surface modification of magnetite nanoparticles using lactobionic acid and their interaction with hepatocytes.

    PubMed

    Kamruzzaman Selim, K M; Ha, Yong-Soo; Kim, Sun-Jung; Chang, Yongmin; Kim, Tae-Jeong; Ho Lee, Gang; Kang, Inn-Kyu

    2007-02-01

    In the current study, superparamagnetic magnetite nanoparticles were surface-modified with lactobionic acid (LA) to improve their intracellular uptake and ability to target hepatocytes. Maltotrionic acid (MA)-modified nanoparticles were also synthesized as a control. Cell culture experiment showed that LA-modified nanoparticles were internalized into hepatocytes and atomic absorption spectrometer (AAS) measurement indicated that the uptake amount of LA-modified magnetite into hepatocytes was higher than that of unmodified and MA-modified nanoparticles. LA-modified nanoparticle solution was injected in rabbit and the magnetic resonance (MR) images obtained showed that LA-coated nanoparticles were selectively accumulated onto the hepatocytes. This result demonstrates that the LA-modified magnetite nanoparticles have a great potential to be used as contrast agent for liver diagnosis. PMID:17049979

  16. Influence of synthesis experimental parameters on the formation of magnetite nanoparticles prepared by polyol method

    NASA Astrophysics Data System (ADS)

    Vega-Chacón, Jaime; Picasso, Gino; Avilés-Félix, Luis; Jafelicci, Miguel, Jr.

    2016-03-01

    In this paper we present a modified polyol method for synthesizing magnetite nanoparticles using iron (III) nitrate, a low toxic and cheap precursor salt. The influence of the precursor salt nature and initial ferric concentration in the average particle size and magnetic properties of the obtained nanoparticles were investigated. Magnetite nanoparticles have received much attention due to the multiple uses in the biomedical field; for these purposes nanoparticles with monodisperse size distribution, superparamagnetic behavior and a combination between small average size and high saturation magnetization are required. The polyol conventional method allows synthesizing water-dispersible magnetite nanoparticles with these features employing iron (III) acetylacetonate as precursor salt. Although the particle sizes of samples synthesized from the conventional polyol method (denoted CM) are larger than those of samples synthesized from the modified method (denoted MM), they display similar saturation magnetization. The differences in the nanoparticles average sizes of samples CM and samples MM were explained though the known nanoparticle formation mechanism.

  17. Synthesis of functionalized magnetite nanoparticles to use as liver targeting MRI contrast agent

    NASA Astrophysics Data System (ADS)

    Yazdani, Farshad; Fattahi, Bahare; Azizi, Najmodin

    2016-05-01

    The aim of this research was the preparation of functionalized magnetite nanoparticles to use as a liver targeting contrast agent in magnetic resonance imaging (MRI). For this purpose, Fe3O4 nanoparticles were synthesized via the co-precipitation method. The synthesized nanoparticles were coated with silica via the Stober method and finally the coated nanoparticles were functionalized with mebrofenin. Formation of crystalline magnetite particles was confirmed by X-ray diffraction (XRD) analysis. The Fourier transform infrared spectroscopy (FTIR) and energy dispersive X-ray analyzer (EDX) of the final product showed that silica had been effectively bonded onto the surface of the magnetite nanoparticles and the coated nanoparticles functionalized with mebrofenin. The magnetic resonance imaging of the functional nanoparticles showed that the Fe3O4-SiO2-mebrofenin composite is an effective MRI contrast agent for liver targeting.

  18. Biodistribution of polyacrylic acid-coated iron oxide nanoparticles is associated with proinflammatory activation and liver toxicity.

    PubMed

    Couto, Diana; Freitas, Marisa; Costa, Vera Marisa; Chisté, Renan Campos; Almeida, Agostinho; Lopez-Quintela, M Arturo; Rivas, José; Freitas, Paulo; Silva, Paula; Carvalho, Félix; Fernandes, Eduarda

    2016-10-01

    Iron oxide nanoparticles (IONs) have physical and chemical properties that render them useful for several new biomedical applications. Still, so far, in vivo safety studies of IONs with coatings of biomedical interest are still scarce. The aim of this study, therefore, was to clarify the acute biological effects of polyacrylic acid (PAA)-coated IONs, by determining their biodistribution and their potential proinflammatory and toxic effects in CD-1 mice. The biodistribution of PAA-coated IONs in several organs (liver, spleen, kidneys, brain, heart, testes and lungs), the plasma cytokines, chemokine and aminotransferases levels, white blood cell count, oxidative stress parameters, adenosine triphosphate and histologic features of liver, spleen and kidneys were evaluated 24 h after a single acute (8, 20 or 50 mg kg(-1) ) intravenous administration of PAA-coated IONs in magnetite form. The obtained results showed that these IONs accumulate mainly in the liver and spleen and, to a lesser extent, in the lungs. Although our data showed that PAA-coated IONs do not cause severe organ damage, an inflammatory process was triggered in vivo, as evidenced by as evidenced by increased neutrophils and large lymphocytes in the differential blood count. Moreover, an accumulation of iron in macrophages of the liver and spleen was observed and hepatic lipid peroxidation was elicited, showing that the IONs are able to induce oxidative stress. The effects of these nanoparticles need to be further investigated regarding the mechanisms involved and the long-term consequences of intravenous administration of PAA-coated IONs. Copyright © 2016 John Wiley & Sons, Ltd. PMID:27102234

  19. Optimizing Magnetite Nanoparticles for Mass Sensitivity in Magnetic Particle Imaging

    SciTech Connect

    Ferguson, R Matthew; Minard, Kevin R; Khandhar, Amit P; Krishnan, Kannan M

    2011-03-01

    Purpose: Magnetic particle imaging (MPI), using magnetite nanoparticles (MNPs) as tracer material, shows great promise as a platform for fast tomographic imaging. To date, the magnetic properties of MNPs used in imaging have not been optimized. As nanoparticle magnetism shows strong size dependence, we explore how varying MNP size impacts imaging performance in order to determine optimal MNP characteristics for MPI at any driving field frequency f0. Methods: Monodisperse MNPs of varying size were synthesized and their magnetic properties characterized. Their MPI response was measured experimentally, at an arbitrarily chosen f0 = 250 kHz, using a custom-built MPI transceiver designed to detect the third harmonic of MNP magnetization. Results were interpreted using a model of dynamic MNP magnetization that is based on the Langevin theory of superparamagnetism and accounts for sample size distribution, and size-dependent magnetic relaxation. Results: Our experimental results show clear variation in the MPI signal intensity as a function of MNP size that is in good agreement with modeled results. A maxima in the plot of MPI signal vs. MNP size indicates there is a particular size that is optimal for the chosen frequency of 250 kHz. Conclusions: For MPI at any chosen frequency, there will exist a characteristic particle size that generates maximum signal amplitude. We illustrate this at 250 kHz with particles of 15 nm core diameter.

  20. Lipolytic biocatalyst based on recyclable magnetite-polysiloxane nanoparticles

    NASA Astrophysics Data System (ADS)

    Durdureanu-Angheluta, Anamaria; Ignat, Maurusa-Elena; Maier, Stelian Sergiu; Pricop, Lucia; Coroaba, Adina; Fifere, Adrian; Pinteala, Mariana; Chiriac, Anca

    2014-02-01

    This work presents a novel hydrophobic magnetizable nanosupport able to load and valorize the lipase derived from Candida cylindracea (CCL). Nude magnetite nanoparticles (MP) were coated by covalent binding with an ester-polysiloxane (PS). The chemical composition, dimensions, morphology and magnetic properties of the resulted core-shell nanoparticles (MP-PS-CCL) are analyzed. The amount of immobilized lipase increase when loaded from aqueous solutions of up to 12.8 mg/mL CCL, when a lipolytic activity of 74.76 U/g is achieved. For higher concentrations of the loading solution, the activity of immobilized lipase decreases, probably due to the enzyme steric hindrance. MP-PS-CCL exhibits a good lipolytic activity against 4-nitrophenyl laurate (4-NPL), which allows the kinetic study of lipolysis reaction by measuring the amount of released 4-nitrophenol (4-NP), when working at room temperature, in TRIS buffer (pH 8.2). Even after three months of storage, the product is able to sustain up to 4 reusing cycles.

  1. Usefulness of palladium impregnated magnetite nanoparticles for polyphenol determination.

    PubMed

    Godoy-Navajas, Juan; Aguilar-Caballos, María Paz; Gómez-Hens, Agustina

    2016-07-01

    Palladium impregnated magnetite nanoparticles (Pd-Fe3O4NPs) have been synthesized and used as reusable catalyst for the fluorometric determination of polyphenols in wines. The method is based on the decrease of the indocyanine green fluorescence, which is ascribed to its oxidation by dissolved oxygen in the presence of the nanoparticles, and the inhibition of the fluorescence decrease by polyphenols, which is proportional to the polyphenol concentration. The dynamic range of the calibration graph is 0.1-10.0µM gallic acid, which was chosen as model analyte, and the detection limit is 0.02µM. Precision data, expressed as relative standard deviation, ranged between 3.3% and 5.4%. The method was applied to the analysis of several wine samples, obtaining recovery values in the range of 79.7-102.0%. The results obtained were compared with those obtained using the Folin-Ciocalteu and laccase methods, finding that Pd-Fe3O4NPs provide a better selectivity than the first method and show a catalytic behavior similar to that of laccase. PMID:27154689

  2. Improving biohydrogen production using Clostridium beijerinckii immobilized with magnetite nanoparticles.

    PubMed

    Seelert, Trevor; Ghosh, Dipankar; Yargeau, Viviane

    2015-05-01

    In order to supplement the need for alternative energy resources within the near future, enhancing the production of biohydrogen with immobilized Clostridium beijerinckii NCIMB8052 was investigated. Magnetite nanoparticles were functionalized, with chitosan and alginic acid polyelectrolytes using a layer-by-layer method, to promote bacterial attachment. Cultivating C. beijerinckii with these nanoparticles resulted in a shorter lag growth phase and increased total biohydrogen production within 100-ml, 250-ml and 3.6-L reactors compared with freely suspended organisms. The greatest hydrogen yield was obtained in the 250-ml reactor with a value of 2.1 ± 0.7 mol H2/mol glucose, corresponding to substrate conversion and energy conversion efficiencies of 52 ± 18 and 10 ± 3 %, respectively. The hydrogen yields obtained using the immobilized bacteria are comparable to values found in literature. However, to make this process viable, further improvements are required to increase the substrate and energy conversion efficiencies. PMID:25728446

  3. The effect of two novel amino acid-coated magnetic nanoparticles on survival in vascular endothelial cells, bone marrow stromal cells, and macrophages

    NASA Astrophysics Data System (ADS)

    Wu, Qinghua; Meng, Ning; Zhang, Yanru; Han, Lei; Su, Le; Zhao, Jing; Zhang, Shangli; Zhang, Yun; Zhao, Baoxiang; Miao, Junying

    2014-09-01

    Magnetic nanoparticles (MNPs) have been popularly used in many fields. Recently, many kinds of MNPs are modified as new absorbents, which have attracted considerable attention and are promising to be applied in waste water. In our previous study, we synthesized two novel MNPs surface-coated with glycine or lysine, which could efficiently remove many anionic and cationic dyes under severe conditions. It should be considered that MNP residues in water may exert some side effects on human health. In the present study, we evaluated the potential nanotoxicity of MNPs in human endothelial cells, macrophages, and rat bone marrow stromal cells. The results showed that the two kinds of nanoparticles were consistently absorbed into the cell cytoplasm. The concentration of MNPs@Gly that could distinctly decrease survival was 15 μg/ml in human umbilical vascular endothelial cells (HUVECs) or bone marrow stromal cells (BMSCs) and 10 μg/ml in macrophages. While the concentration of MNPs@Lys that obviously reduced viability was 15 μg/ml in HUVECs or macrophages and 50 μg/ml in BMSCs. Furthermore, cell nucleus staining and cell integrity assay indicated that the nanoparticles induced cell apoptosis, but not necrosis even at a high concentration. Altogether, these data suggest that the amino acid-coated magnetic nanoparticles exert relatively high cytotoxicity. By contrast, lysine-coated magnetic nanoparticles are more secure than glycine-coated magnetic nanoparticles.

  4. Novel hybrid nanostructured materials of magnetite nanoparticles and pectin

    NASA Astrophysics Data System (ADS)

    Sahu, Saurabh; Dutta, Raj Kumar

    2011-04-01

    A novel hybrid nanostructured material comprising superparamagnetic magnetite nanoparticles (MNPs) and pectin was synthesized by crosslinking with Ca2+ ions to form spherical calcium pectinate nanostructures, referred as MCPs, which were typically found to be 100-150 nm in size in dried condition, confirmed from transmission electron microscopy and scanning electron microscopy. The uniform size distribution was revealed from dynamic light scattering measurement. In aqueous medium the MCPs showed swelling behavior with an average size of 400 nm. A mechanism of formation of spherical MCPs is outlined constituting a MNP-pectin interface encapsulated by calcium pectinate at the periphery, by using an array of characterization techniques like zeta potential, thermogravimetry, Fourier transformed infrared and X-ray photoelectron spectroscopy. The MCPs were stable in simulated gastrointestinal fluid and ensured minimal loss of magnetic material. They exhibited superparamagnetic behavior, confirmed from zero field cooled and field cooled profiles and showed high saturation magnetization (Ms) of 46.21 emu/g at 2.5 T and 300 K. Ms decreased with increasing precursor pectin concentrations, attributed to quenching of magnetic moments by formation of a magnetic dead layer on the MNPs.

  5. Optimizing magnetite nanoparticles for mass sensitivity in magnetic particle imaging

    PubMed Central

    Ferguson, R. Matthew; Minard, Kevin R.; Khandhar, Amit P.; Krishnan, Kannan M.

    2011-01-01

    Purpose: Magnetic particle imaging (MPI), using magnetite nanoparticles (MNPs) as tracer material, shows great promise as a platform for fast tomographic imaging. To date, the magnetic properties of MNPs used in imaging have not been optimized. As nanoparticle magnetism shows strong size dependence, the authors explore how varying MNP size impacts imaging performance in order to determine optimal MNP characteristics for MPI at any driving field frequency f0. Methods: Monodisperse MNPs of varying size were synthesized and their magnetic properties characterized. Their MPI response was measured experimentally using a custom-built MPI transceiver designed to detect the third harmonic of MNP magnetization. The driving field amplitude H0=6 mT μ0−1 and frequency f0=250 kHz were chosen to be suitable for imaging small animals. Experimental results were interpreted using a model of dynamic MNP magnetization that is based on the Langevin theory of superparamagnetism and accounts for sample size distribution and size-dependent magnetic relaxation. Results: The experimental results show a clear variation in the MPI signal intensity as a function of MNP diameter that is in agreement with simulated results. A maximum in the plot of MPI signal vs MNP size indicates there is a particular size that is optimal for the chosen f0. Conclusions: The authors observed that MNPs 15 nm in diameter generate maximum signal amplitude in MPI experiments at 250 kHz. The authors expect the physical basis for this result, the change in magnetic relaxation with MNP size, will impact MPI under other experimental conditions. PMID:21520874

  6. High stable suspension of magnetite nanoparticles in ethanol by using sono-synthesized nanomagnetite in polyol medium

    SciTech Connect

    Bastami, Tahereh Rohani; Entezari, Mohammad H.

    2013-09-01

    Graphical abstract: - Highlights: • The sonochemical synthesis of magnetite nanoparticles was carried out in EG without any surfactant. • The nanoparticles with sizes ∼24 nm were composed of small building blocks with sizes ∼2 nm. • The hydrophilic magnetite nanoparticles were stable in ethanol even after 8 months. • Ultrasonic intensity showed a crucial role on the obtained high stable magnetite nanoparticles in ethanol. - Abstract: The sonochemical synthesis of magnetite nanoparticles was carried out at relatively low temperature (80 °C) in ethylene glycol (EG) as a polyol solvent. The particle size was determined by transmission electron microscopy (TEM). The magnetite nanoparticles with an average size of 24 nm were composed of small building blocks with an average size of 2–3 nm and the particles exhibited nearly spherical shape. The surface characterization was investigated by using Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The stability of magnetite nanoparticles was studied in ethanol as a polar solvent. The nanoparticles showed an enhanced stability in ethanol which is due to the hydrophilic surface of the particles. The colloidal stability of magnetite nanoparticles in ethanol was monitored by UV–visible spectrophotometer. According to the results, the nanoparticles synthesized in 30 min of sonication with intensity of 35 W/cm{sup 2} (50%) led to a maximum stability in ethanol as a polar solvent with respect to the other applied intensities. The obtained magnetite nanoparticles were stable for more than12 months.

  7. Covalently modified magnetite nanoparticles with PEG: preparation and characterization as nano-adsorbent for removal of lead from wastewater

    PubMed Central

    2014-01-01

    Background Lead is one of the hazardous materials which is associated with pollution and toxicity problems. This paper describes a novel approach for removal of lead from wastewater. Although naked magnetic nanoparticles have been applied for removal of different pollutants from wastewater, there was no research on employment of covalently PEG modified magnetic nanoparticles for such purpose. Results A magnetic nano-adsorbent was prepared by chemically modification of magnetite nanoparticles (MNPs) with polyethylene glycol (PEG) for removal of lead ions. The surface of MNPs was coated covalently with 3-aminopropyltriethoxysilane (APTES) and PEG. Modified MNPs (MNPs-APTES-PEG) were characterized by FT-IR, XRD, SEM, and particle size analysis. Compared to the oleic acid coated MNPs, MNPs-APTES-PEG exhibited significant higher uptake capability for Pb(II) ions. The effective parameters on the extent of adsorption (time, temperature, Pb(II) concentration, contact time and pH) were studied and optimized by response surface methodology. Maximum uptake of MNPs-APTES-PEG for Pb(II) was determined to be 81.39 ± 2.5%. The results showed that the kinetic data was best described by Pseudo-second order model as evidenced by the relatively high value of determination coefficient (R2 = 0.9998). Successful removal of Pb(II) from industrial wastewater was also accomplished by MNPs-APTES-PEG. Conclusions The results revealed high capability and excellent efficiency of developed nano-adsorbents in removal of lead contaminants from industrial wastewater. PMID:26413305

  8. Antimicrobial Properties of Lysosomal Enzymes Immobilized on NH₂Functionalized Silica-Encapsulated Magnetite Nanoparticles.

    PubMed

    Bang, Seung Hyuck; Sekhon, Simranjeet Singh; Cho, Sung-Jin; Kim, So Jeong; Le, Thai-Hoang; Kim, Pil; Ahn, Ji-Young; Kim, Yang-Hoon; Min, Jiho

    2016-01-01

    The immobilization efficiency, antimicrobial activity and recovery of lysosomal enzymes on NH2 functionalized magnetite nanoparticles have been studied under various conditions. The immobi- lization efficiency depends upon the ratio of the amount of enzyme and magnetite and it shows an increase with magnetite concentration which is due to the presence of amine group at the magnetite surface that leads to a strong attraction. The optimized reaction time to immobilize the lysosomal enzymes on magnetite was determined by using a rolling method. The immobilization efficiency increases with reaction time and reached a plateau after 5 minutes and then remained constant for 10 minutes. However, after 30 minutes the immobilization efficiency decreased to 85%, which is due to the weaker electrostatic interactions between magnetite and detached lysosomal enzymes. The recovery and stability of immobilized lysosomal enzymes has also been studied. The antimicrobial activity was almost 100% but it decreased upon reuse and no activity was observed after its reuse for seven times. The storage stability of lysosomal enzymes as an antimicrobial agent was about 88%, which decreased to 53% after one day and all activity of immobilized lysosomal enzymes was maintained after five days. Thus, the lysosomal enzymes immobilized on magnetite nanoparticles could potentially be used as antimicrobial agents to remove bacteria. PMID:27398573

  9. A comparison between acoustic properties and heat effects in biogenic (magnetosomes) and abiotic magnetite nanoparticle suspensions

    NASA Astrophysics Data System (ADS)

    Józefczak, A.; Leszczyński, B.; Skumiel, A.; Hornowski, T.

    2016-06-01

    Magnetic nanoparticles show unique properties and find many applications because of the possibility to control their properties using magnetic field. Magnetic nanoparticles are usually synthesized chemically and modification of the particle surface is necessary. Another source of magnetic nanoparticles are various magnetotactic bacteria. These biogenic nanoparticles (magnetosomes) represent an attractive alternative to chemically synthesized iron oxide particles because of their unique characteristics and a high potential for biotechnological and biomedical applications. This work presents a comparison between acoustic properties of biogenic and abiotic magnetite nanoparticle suspensions. Experimental studies have shown the influence of a biological membrane on the ultrasound properties of magnetosomes suspension. Finally the heat effect in synthetic and biogenic magnetite nanoparticles is also discussed. The experimental study shows that magnetosomes present good heating efficiency.

  10. Magnetic properties of magnetite nanoparticles coated with mesoporous silica by sonochemical method

    SciTech Connect

    Ursachi, Irina; Vasile, Aurelia; Chiriac, Horia; Postolache, Petronel; Stancu, Alexandru

    2011-12-15

    Highlights: Black-Right-Pointing-Pointer MCM-41-coating of magnetite nanoparticles performed under ultrasonic irradiation. Black-Right-Pointing-Pointer Ultrasonic irradiation accelerates the formation of the MCM-41 framework. Black-Right-Pointing-Pointer The hysteretic response to an applied field was investigated applying FORC diagram. Black-Right-Pointing-Pointer The average coercive field of the Fe{sub 3}O{sub 4} nanoparticles increased after coating. -- Abstract: In this paper we present the magnetic properties of mesoporous silica-coated Fe{sub 3}O{sub 4} nanoparticles. The coating of magnetite nanoparticles with mesoporous silica shell was performed under ultrasonic irradiation. The obtained mesoporous silica-coated magnetite nanoparticles were characterized by powder X-ray diffraction, focused ion beam-scanning electron microscopy, nitrogen adsorption-desorption isotherms and vibrating sample magnetometer. The hysteretic behavior was studied using first-order reversal curves diagrams. The X-ray diffraction result indicates that the extreme chemical and physical conditions created by acoustic cavitations have an insignificant effect on crystallographic structural characteristic of magnetite nanoparticles. Changes in the coercivity distributions of the magnetite nanoparticles were observed on the first-order reversal curves diagrams for the samples with coated particles compared with the samples containing uncoated particles of magnetite. The coated particles show an increased most probable coercivity of about 20% compared with the uncoated particles which can be associated with an increased anisotropy due to coating even if the interaction field distribution measured on the diagrams are virtually identical for coated/uncoated samples.

  11. Visible Light-Driven Photocatalytic Activity of Oleic Acid-Coated TiO2 Nanoparticles Synthesized from Absolute Ethanol Solution

    NASA Astrophysics Data System (ADS)

    Li, Huihui; Liu, Bin; Yin, Shu; Sato, Tsugio; Wang, Yuhua

    2015-10-01

    The one-step synthesis of oleic acid-coated TiO2 nanoparticles with visible light-driven photocatalytic activity was reported by this manuscript, using oleic acid-ethanol as crucial starting materials. The photocatalytic degradation of nitrogen monoxide (deNOx) in the gas phase was investigated in a continuous reactor using a series of TiO2 semiconductors, prepared from oleic acid- or acetic acid-ethanol solution. The surface modification on TiO2 by organic fatty acid, oleic acid, could reinvest TiO2 photocatalyst with the excellent visible light response. The deNOx ability is almost as high as 30 % destruction in the visible light region ( λ > 510 nm) which is similar to the nitrogen-doped TiO2. Meanwhile, acetic acid, a monobasic acid, has a weaker ability on visible light modification of TiO2.

  12. Controlled release study of an anti-carcinogenic agent, gallate from the surface of magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Ghotbi, Mohammad Yeganeh; bin Hussein, Mohd Zobir

    2012-07-01

    Immobilization of gallate anion, an anti-carcinogenic, anti-mutagenic, and anti-microbial agent on the surface of magnetite nanoparticles was accomplished by adsorption technique for the formation of a core-shell nanocomposite. A simple co-precipitation technique in the presence of poly vinyl pyrrolidone was successfully applied for the preparation of magnetite nanoparticles as core beads with narrow size distribution. The powders were characterized by X-ray diffraction, particle size analysis, magnetic measurements, atomic force microscope and also infrared spectroscopy. FTIR and CHNS results indicated that the gallate anion was actually adsorbed onto the surface of the magnetite nanoparticles. The release of the anion from the surface of the nanocomposite was found to be controllable by the selection of the release media.

  13. Smart hollow microspheres of chondroitin sulfate conjugates and magnetite nanoparticles for magnetic vector.

    PubMed

    Guilherme, Marcos R; Reis, Adriano V; Alves, Bruno R V; Kunita, Marcos H; Rubira, Adley F; Tambourgi, Elias B

    2010-12-01

    Smart hollow microspheres composed of vinyled-chondroitin sulfate conjugates (CSπ) and magnetite nanoparticles were obtained by the intermediate of a multiple emulsion in absence of a surfactant, attributable to stabilizing properties of the CS. It was formed an oil-water multiple emulsion in which the CS played a role as an anionic stabilizer for magnetite nanoparticles via complexation. Iron oxides were bonded to the microspheres by the formation of a complex of Fe(3+) ions on the crystalline phase with oxygen atoms at the carboxyl groups without their magnetic properties being affected. The average crystal size of embedded magnetite nanoparticles was approximately 16.5nm, indicative of a good dispersion in microspheres. Furthermore, the introduction of iron oxides resulted in microspheres with a higher diameter and a narrower particle size distribution. PMID:20832809

  14. Magnetite nanoparticles as-prepared and dispersed in Copaiba oil: study using magnetic measurements and Mössbauer spectroscopy

    NASA Astrophysics Data System (ADS)

    Oshtrakh, Michael I.; Ushakov, Mikhail V.; Semenova, Anna S.; Kellerman, Dina G.; Šepelák, Vladimir; Rodriguez, Alfonso F. R.; Semionkin, Vladimir A.; Morais, Paulo C.

    2013-04-01

    Study of magnetite nanoparticles, as-prepared and dispersed in Copaiba oil as magnetic fluid, by means of magnetic measurement and Mössbauer spectroscopy at various temperatures demonstrated differences in the saturation magnetization and Mössbauer hyperfine parameters which were related to the interactions of Copaiba oil polar molecules with iron cations on magnetite nanoparticle's surface.

  15. Fabrication of magnetite-based core-shell coated nanoparticles with antibacterial properties.

    PubMed

    Grumezescu, A M; Cristescu, R; Chifiriuc, M C; Dorcioman, G; Socol, G; Mihailescu, I N; Mihaiescu, D E; Ficai, A; Vasile, O R; Enculescu, M; Chrisey, D B

    2015-01-01

    We report the fabrication of biofunctionalized magnetite core/sodium lauryl sulfate shell/antibiotic adsorption-shell nanoparticles assembled thin coatings by matrix assisted pulsed laser evaporation for antibacterial drug-targeted delivery. Magnetite nanoparticles have been synthesized and subsequently characterized by transmission electron microscopy and x-ray diffraction. The obtained thin coatings have been investigated by FTIR and scanning electron microscope, and tested by in vitro biological assays, for their influence on in vitro bacterial biofilm development and cytotoxicity on human epidermoid carcinoma (HEp2) cells. PMID:25797361

  16. Stability of uncoated and fulvic acids coated manufactured CeO2 nanoparticles in various conditions: From ultrapure to natural Lake Geneva waters.

    PubMed

    Oriekhova, Olena; Stoll, Serge

    2016-08-15

    Understanding the behavior of engineered nanoparticles in natural water and impact of water composition in changing conditions is of high importance to predict their fate once released into the environment. In this study we investigated the stability of uncoated and Suwannee River fulvic acids coated CeO2 manufactured nanoparticles in various environmental conditions. The effect of pH changes on the nanoparticle and coating stability was first studied in ultrapure water as well as the variation of zeta potentials and sizes with time in presence of fulvic acids at environmental pH. Then the stability of CeO2 in synthetic and natural Lake Geneva waters was investigated as a function of fulvic acids concentration. Our results indicate that the adsorption of environmentally relevant concentrations of Suwannee River fulvic acids promotes CeO2 stabilization in ultrapure water as well as synthetic water and that the coating stability is high upon pH variations. On the other hand in natural Lake Geneva water CeO2 NPs are found in all cases aggregated due to the effect of heterogeneous organic and inorganic compounds. PMID:27100013

  17. Removal of hexavalent chromium [Cr(VI)] from aqueous solutions by the diatomite-supported/unsupported magnetite nanoparticles.

    PubMed

    Yuan, Peng; Liu, Dong; Fan, Mingde; Yang, Dan; Zhu, Runliang; Ge, Fei; Zhu, JianXi; He, Hongping

    2010-01-15

    Diatomite-supported/unsupported magnetite nanoparticles were prepared by co-precipitation and hydrosol methods, and characterized by X-ray diffraction, nitrogen adsorption, elemental analysis, differential scanning calorimetry, transmission electron microscopy and X-ray photoelectron spectroscopy. The average sizes of the unsupported and supported magnetite nanoparticles are around 25 and 15 nm, respectively. The supported magnetite nanoparticles exist on the surface or inside the pores of diatom shells, with better dispersing and less coaggregation than the unsupported ones. The uptake of hexavalent chromium [Cr(VI)] on the synthesized magnetite nanoparticles was mainly governed by a physico-chemical process, which included an electrostatic attraction followed by a redox process in which Cr(VI) was reduced into trivalent chromium [Cr(III)]. The adsorption of Cr(VI) was highly pH-dependent and the kinetics of the adsorption followed a pseudo-second-order model. The adsorption data of diatomite-supported/unsupported magnetite fit well with the Langmuir isotherm equation. The supported magnetite showed a better adsorption capacity per unit mass of magnetite than unsupported magnetite, and was more thermally stable than their unsupported counterparts. These results indicate that the diatomite-supported/unsupported magnetite nanoparticles are readily prepared, enabling promising applications for the removal of Cr(VI) from aqueous solution. PMID:19748178

  18. Control of nanoparticle size, reactivity and magnetic properties during the bioproduction of magnetite by Geobacter sulfurreducens

    NASA Astrophysics Data System (ADS)

    Byrne, J. M.; Telling, N. D.; Coker, V. S.; Pattrick, R. A. D.; van der Laan, G.; Arenholz, E.; Tuna, F.; Lloyd, J. R.

    2011-11-01

    The bioproduction of nanoscale magnetite by Fe(III)-reducing bacteria offers a potentially tunable, environmentally benign route to magnetic nanoparticle synthesis. Here, we demonstrate that it is possible to control the size of magnetite nanoparticles produced by Geobacter sulfurreducens by adjusting the total biomass introduced at the start of the process. The particles have a narrow size distribution and can be controlled within the range of 10-50 nm. X-ray diffraction analysis indicates that controlled production of a number of different biominerals is possible via this method including goethite, magnetite and siderite, but their formation is strongly dependent upon the rate of Fe(III) reduction and total concentration and rate of Fe(II) produced by the bacteria during the reduction process. Relative cation distributions within the structure of the nanoparticles have been investigated by x-ray magnetic circular dichroism and indicate the presence of a highly reduced surface layer which is not observed when magnetite is produced through abiotic methods. The enhanced Fe(II)-rich surface, combined with small particle size, has important environmental applications such as in the reductive bioremediation of organics, radionuclides and metals. In the case of Cr(VI), as a model high-valence toxic metal, optimized biogenic magnetite is able to reduce and sequester the toxic hexavalent chromium very efficiently to the less harmful trivalent form.

  19. Aqueous dispersions of magnetite nanoparticles complexed with copolyether dispersants: experiments and theory.

    PubMed

    Zhang, Qian; Thompson, M Shane; Carmichael-Baranauskas, Anita Y; Caba, Beth L; Zalich, Michael A; Lin, Yin-Nian; Mefford, O Thompson; Davis, Richey M; Riffle, Judy S

    2007-06-19

    Magnetite (Fe3O4) nanoparticles have been synthesized and complexed with carboxylate-functional block copolymers, and then aqueous dispersions of the complexes were investigated as functions of their chemical and morphological structures. The block copolymer dispersants had either poly(ethylene oxide), poly(ethylene oxide-co-propylene oxide), or poly(ethylene oxide-b-propylene oxide) outer blocks, and all of them had a polyurethane center block that contained pendent carboxylate groups. The complexes were formed through interactions of the carboxylates with the surfaces of the magnetite nanoparticles. The magnetite cores of the magnetite-copolymer complexes were near 10 nm in diameter, and the particles were superparamagnetic. Complexes with mass ratios of polymer to magnetite varying from 50:50 to 85:15 were studied. One of our objectives is to design complexes that form stable dispersions of discrete particles in water, yet that can be actuated (moved together) upon exposure to a uniform magnetic field. DLVO calculations that accounted for magnetic attractive interparticle forces, as well as van der Waals, steric, and electrostatic forces are presented. Compositions were identified wherein a shallow, attractive interparticle potential minimum appears once the magnetic term is applied. This suggests that it may be possible to tune the structures of superparamagnetic nanoparticle shells to allow discrete dispersions without a field, yet weak flocculation could be induced upon exposure to a field. PMID:17521205

  20. Control of nanoparticle size, reactivity and magnetic properties during the bioproduction of magnetite by Geobacter sulfurreducens

    SciTech Connect

    Byrne, J. M.; Telling, N. D.; Coker, V. S.; Pattrick, R. A. D.; Laan, G. van der; Arenholz, E.; Tuna, F.; Lloyd, J. R.

    2011-08-02

    The bioproduction of nano-scale magnetite by Fe(III)-reducing bacteria offers a potentially tunable, environmentally benign route to magnetic nanoparticle synthesis. Here, we demonstrate that it is possible to control the size of magnetite nanoparticles produced by Geobacter sulfurreducens, by adjusting the total biomass introduced at the start of the process. The particles have a narrow size distribution and can be controlled within the range of 10-50 nm. X-ray diffraction analysis indicates that controlled production of a number of different biominerals is possible via this method including goethite, magnetite and siderite, but their formation is strongly dependent upon the rate of Fe(III) reduction and total concentration and rate of Fe(II) produced by the bacteria during the reduction process. Relative cation distributions within the structure of the nanoparticles has been investigated by X-ray magnetic circular dichroism and indicates the presence of a highly reduced surface layer which is not observed when magnetite is produced through abiotic methods. The enhanced Fe(II)-rich surface, combined with small particle size, has important environmental applications such as in the reductive bioremediation of organics, radionuclides and metals. In the case of Cr(VI), as a model high-valence toxic metal, optimised biogenic magnetite is able to reduce and sequester the toxic hexavalent chromium very efficiently in the less harmful trivalent form.

  1. Magnetite nanoparticles coated glass wool for As(V) removal from drinking water

    SciTech Connect

    Kango, Sarita; Kumar, Rajesh

    2015-08-28

    Arsenic (As) removal from contaminated groundwater is a key environmental concern worldwide. In this study, glass wool was coated with magnetite nanoparticles under argon gas flow and magnetite coated glass wool have been investigated for application as an adsorbent for As(V) removal from water. The adsorbent was characterized by using Scanning Electron Microscopy (SEM) and arsenic contaminated water treated with adsorbent was analyzed by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The ICP-MS results showed that 10 g/L of adsorbent removed 99.4% of As(V) within 5 hours at pH-7 and initial arsenic concentration of 360µg/L. Adsorption kinetics data fitted well in pseudo-first-order kinetics model with high correlation coefficient (R{sup 2} = 0.995). As magnetite nanoparticles coated glass wool showed favorable adsorption behavior for As(V), it can be a promising tool for water purification.

  2. Surface Enhanced Raman Spectroscopy of Organic Molecules on Magnetite (Fe3O4) Nanoparticles.

    PubMed

    Lee, Namhey; Schuck, P James; Nico, Peter S; Gilbert, Benjamin

    2015-03-19

    Surface-enhanced Raman spectroscopy (SERS) of species bound to environmentally relevant oxide nanoparticles is largely limited to organic molecules structurally related to catechol that facilitate a chemical enhancement of the Raman signal. Here, we report that magnetite (Fe3O4) nanoparticles provide a SERS signal from oxalic acid and cysteine via an electric field enhancement. Magnetite thus likely provides an oxide substrate for SERS study of any adsorbed organic molecule. This substrate combines benefits from both metal-based and chemical SERS by providing an oxide surface for studies of environmentally and catalytically relevant detailed chemical bonding information with fewer restrictions of molecular structure or binding mechanisms. Therefore, the magnetite-based SERS demonstrated here provides a new approach to establishing the surface interactions of environmentally relevant organic ligands and mineral surfaces. PMID:26262854

  3. Magnetite nanoparticles coated glass wool for As(V) removal from drinking water

    NASA Astrophysics Data System (ADS)

    Kango, Sarita; Kumar, Rajesh

    2015-08-01

    Arsenic (As) removal from contaminated groundwater is a key environmental concern worldwide. In this study, glass wool was coated with magnetite nanoparticles under argon gas flow and magnetite coated glass wool have been investigated for application as an adsorbent for As(V) removal from water. The adsorbent was characterized by using Scanning Electron Microscopy (SEM) and arsenic contaminated water treated with adsorbent was analyzed by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The ICP-MS results showed that 10 g/L of adsorbent removed 99.4% of As(V) within 5 hours at pH-7 and initial arsenic concentration of 360µg/L. Adsorption kinetics data fitted well in pseudo-first-order kinetics model with high correlation coefficient (R2 = 0.995). As magnetite nanoparticles coated glass wool showed favorable adsorption behavior for As(V), it can be a promising tool for water purification.

  4. Keeping Nanoparticles Fully Functional: Long-Term Storage and Alteration of Magnetite

    PubMed Central

    Widdrat, Marc; Kumari, Monika; Tompa, Éva; Pósfai, Mihály; Hirt, Ann M; Faivre, Damien

    2014-01-01

    Magnetite is an iron oxide found in rocks. Its magnetic properties are used for paleoclimatic reconstructions. It can also be synthesized in the laboratory to exploit its magnetic properties for bio- and nanotechnological applications. However, although the magnetic properties depend on particle size in a well-understood manner, they also depend on the structure of the oxide, because magnetite oxidizes to maghemite under environmental conditions. The dynamics of this process have not been well described. Here, a study of the alteration of magnetite particles of different sizes as a function of their storage conditions is presented. Smaller nanoparticles are shown to oxidize more rapidly than larger ones, and that the lower the storage temperature, the lower the measured oxidation. In addition, the magnetic properties of the altered particles are not decreased dramatically, thus suggesting that this alteration will not impact the use of such nanoparticles as medical carriers. PMID:26366334

  5. Synthesis of superparamagnetic silica-coated magnetite nanoparticles for biomedical applications

    SciTech Connect

    Kaur, Navjot Chudasama, Bhupendra

    2015-05-15

    Multifunctional superparamagnetic iron oxide nanoparticles (SPIONs) coated with silica are widely researched for biomedical applications such as magnetic resonance imaging, tissue repair, cell separation, hyperthermia, drug delivery, etc. In this article synthesis of magnetite (Fe{sub 3}O{sub 4}) nanoparticles and their coating with SiO{sub 2} is reported. Fe{sub 3}O{sub 4} nanoparticles were synthesized by chemical co-precipitation and it was coated with silica by hydrolysis and condensation of tetraethylorthosilicate. XRD, FTIR, TEM and VSM techniques were used to characterize bare and coated nanoparticles. Results indicated that the average size of SPIONS was 8.4 nm. X-ray diffraction patterns of silica coated SPIONS were identical to that of SPIONS confirming the inner spinal structure of SPIONS. FTIR results confirmed the binding of silica with the magnetite and the formation of the silica shell around the magnetite core. Magnetic properties of SPIONS and silica coated SPIONS are determined by VSM. They are superparamagnetic. The major conclusion drawn from this study is that the synthesis route yields stable, non-aggregated magnetite-silica core-shell nanostructures with tailored morphology and excellent magnetic properties.

  6. Investigations on the interactions of proteins with polyampholyte-coated magnetite nanoparticles.

    PubMed

    Zhao, Tao; Chen, Kaimin; Gu, Hongchen

    2013-11-14

    Magnetite nanoparticles have been widely used in biomedical applications, especially as contrast agents in magnetic resonance imaging. In this work, the antifouling property of polyampholyte-coating (poly(acrylic acid) (PAA)-co-3-(diethylamino)-propylamine (DEAPA)) is systematically demonstrated. Polyampholyte-coated magnetite nanoparticles (NP1) and PAA-coated magnetite nanoparticles (NP2) were synthesized to investigate their interactions with BSA and lysozyme (LYZ) by high-resolution turbidimetric titration, dynamic light scattering (DLS), and isothermal titration calorimetry (ITC) in phosphate buffer saline (PBS) buffer with pH 7.4. The abundant carboxyl groups of NP2 and polyampholyte coating of NP1 were well proven by TGA, ζ-potential, and titration methods. Turbidity change shows that NP1 have no interaction with both proteins other than NP2 having adsorption with LYZ, which was further confirmed by DLS. Besides, ITC gives the exact enthalpy change and unveils the binding stoichiometry for each interaction. All characterizations demonstrate the antifouling property of NP1 to both negatively charged protein BSA and positively charged protein LYZ. The polyampholyte-coated magnetite nanoparticles were shown to be a promising material to eliminate the strong interaction with proteins in complex medium, for example, when it is applied for MRA contrast agents with long in vivo circulation time. PMID:24063374

  7. Self-heating of magnetite nanoparticles for a potential hyperthermia application

    NASA Astrophysics Data System (ADS)

    Kim, Chang-Yeoul; Xu, Lixing; Lee, Eun-Hee

    2014-07-01

    A comparative study of heat generation in superparamagnetic magnetite nanoparticles in aqueous and hexane solutions in the presence of external magnetic field is presented. The field strength dependence of the specific absorption rate (SAR) complies with the power law of second order. The concave-convex change of SAR-H curves substantially illustrates the importance of particle dispersion in the fluid.

  8. The facile fabrication of magnetite nanoparticles and their enhanced catalytic performance in Fischer-Tropsch synthesis.

    PubMed

    Zheng, Shenke; Sun, Jiaqiang; Song, Dechen; Chen, Zheng; Chen, Jiangang

    2015-07-14

    Uniform and crystalline magnetite nanoparticles are facilely fabricated and utilized as an efficient catalyst in Fischer-Tropsch synthesis (FTS). The catalyst exhibits a high and stable activity with low methane selectivity, attributed to its remarkable structural and chemical stability at the realistic conditions of FTS. PMID:26074335

  9. Synthesis of superparamagnetic silica-coated magnetite nanoparticles for biomedical applications

    NASA Astrophysics Data System (ADS)

    Kaur, Navjot; Chudasama, Bhupendra

    2015-05-01

    Multifunctional superparamagnetic iron oxide nanoparticles (SPIONs) coated with silica are widely researched for biomedical applications such as magnetic resonance imaging, tissue repair, cell separation, hyperthermia, drug delivery, etc. In this article synthesis of magnetite (Fe3O4) nanoparticles and their coating with SiO2 is reported. Fe3O4 nanoparticles were synthesized by chemical co-precipitation and it was coated with silica by hydrolysis and condensation of tetraethylorthosilicate. XRD, FTIR, TEM and VSM techniques were used to characterize bare and coated nanoparticles. Results indicated that the average size of SPIONS was 8.4 nm. X-ray diffraction patterns of silica coated SPIONS were identical to that of SPIONS confirming the inner spinal structure of SPIONS. FTIR results confirmed the binding of silica with the magnetite and the formation of the silica shell around the magnetite core. Magnetic properties of SPIONS and silica coated SPIONS are determined by VSM. They are superparamagnetic. The major conclusion drawn from this study is that the synthesis route yields stable, non-aggregated magnetite-silica core-shell nanostructures with tailored morphology and excellent magnetic properties.

  10. Antagonistic effects between magnetite nanoparticles and a hydrophobic surfactant in highly concentrated Pickering emulsions.

    PubMed

    Vílchez, Alejandro; Rodríguez-Abreu, Carlos; Menner, Angelika; Bismarck, Alexander; Esquena, Jordi

    2014-05-13

    Herein we present a systematic study of the antagonistic interaction between magnetite nanoparticles (Fe3O4) and nonionic hydrophobic surfactant in Pickering highly concentrated emulsions. Interfacial tension measurements, phase behavior, and emulsion stability studies, combined with electron microscopy observations in polymerized systems and magnetometry, are used to support the discussion. First, stable W/O highly concentrated emulsions were obtained using partially hydrophobized magnetite nanoparticles. These emulsions experienced phase separation when surfactant is added at concentrations as low as 0.05 wt %. Such phase separation arises from the preferential affinity of the surfactant for the nanoparticle surfaces, which remarkably enhances their hydrophobicity, leading to a gradual desorption of nanoparticles from the interface. W/O emulsions were obtained at higher surfactant concentrations, but in this case, these emulsions were mainly stabilized by surfactant molecules. Therefore, stable emulsions could be prepared in two separate ranges of surfactant concentrations. After polymerization, low-density macroporous polymers were obtained, and the adsorption and aggregation of nanoparticles was analyzed by transmission electron microscopy. The progressive displacement of the nanoparticles was revealed: from the oil-water interface, in which aggregated nanoparticles were adsorbed, forming dense layers, to the continuous phase of the emulsions, where small nanoparticle aggregates were randomly dispersed. Interestingly, the results also show that the blocking temperature of the iron oxide superparamagnetic nanoparticles embedded in the macroporous polymers could be modulated by appropriate control of the concentrations of both surfactant and nanoparticles. PMID:24738961

  11. 4-aminobenzoic acid-coated maghemite nanoparticles as potential anticancer drug magnetic carriers: a case study on highly cytotoxic Cisplatin-like complexes involving 7-azaindoles.

    PubMed

    Starha, Pavel; Stavárek, Martin; Tuček, Jiří; Trávníček, Zdeněk

    2014-01-01

    This study describes a one-pot synthesis of superparamagnetic maghemite-based 4-aminobenzoic acid-coated spherical core-shell nanoparticles (PABA@FeNPs) as suitable nanocomposites potentially usable as magnetic carriers for drug delivery. The PABA@FeNPs system was subsequently functionalized by the activated species (1* and 2*) of highly in vitro cytotoxic cis-[PtCl2(3Claza)2] (1; 3Claza stands for 3-chloro-7-azaindole) or cis-[PtCl2(5Braza)2] (2; 5Braza stands for 5-bromo-7-azaindole), which were prepared by a silver(I) ion assisted dechlorination of the parent dichlorido complexes. The products 1*@PABA@FeNPs and 2*@PABA@FeNPs, as well as an intermediate PABA@FeNPs, were characterized by a combination of various techniques, such as Mössbauer, FTIR and EDS spectroscopy, thermal analysis, SEM and TEM. The results showed that the products consist of well-dispersed maghemite-based nanoparticles of 13 nm average size that represent an easily obtainable system for delivery of highly cytotoxic cisplatin-like complexes in oncological practice. PMID:24476602

  12. Synthesis of environmentally friendly highly dispersed magnetite nanoparticles based on rosin cationic surfactants as thin film coatings of steel.

    PubMed

    Atta, Ayman M; El-Mahdy, Gamal A; Al-Lohedan, Hamad A; Al-Hussain, Sami A

    2014-01-01

    This work presents a new method to prepare monodisperse magnetite nanoparticles capping with new cationic surfactants based on rosin. Core/shell type magnetite nanoparticles were synthesized using bis-N-(3-levopimaric maleic acid adduct-2-hydroxy) propyl-triethyl ammonium chloride (LPMQA) as capping agent. Fourier transform infrared spectroscopy (FTIR) was employed to characterize the nanoparticles chemical structure. Transmittance electron microscopies (TEM) and X-ray powder diffraction (XRD) were used to examine the morphology of the modified magnetite nanoparticles. The magnetite dispersed aqueous acid solution was evaluated as an effective anticorrosion behavior of a hydrophobic surface on steel. The inhibition effect of magnetite nanoparticles on steel corrosion in 1 M HCl solution was investigated using potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). Results obtained from both potentiodynamic polarisation and EIS measurements reveal that the magnetite nanoparticle is an effective inhibitor for the corrosion of steel in 1.0 M HCl solution. Polarization data show that magnetite nanoparticles behave as a mixed type inhibitor. The inhibition efficiencies obtained from potentiodynamic polarization and EIS methods are in good agreement. PMID:24758936

  13. Synthesis of Environmentally Friendly Highly Dispersed Magnetite Nanoparticles Based on Rosin Cationic Surfactants as Thin Film Coatings of Steel

    PubMed Central

    Atta, Ayman M.; El-Mahdy, Gamal A.; Al-Lohedan, Hamad A.; Al-Hussain, Sami A.

    2014-01-01

    This work presents a new method to prepare monodisperse magnetite nanoparticles capping with new cationic surfactants based on rosin. Core/shell type magnetite nanoparticles were synthesized using bis-N-(3-levopimaric maleic acid adduct-2-hydroxy) propyl-triethyl ammonium chloride (LPMQA) as capping agent. Fourier transform infrared spectroscopy (FTIR) was employed to characterize the nanoparticles chemical structure. Transmittance electron microscopies (TEM) and X-ray powder diffraction (XRD) were used to examine the morphology of the modified magnetite nanoparticles. The magnetite dispersed aqueous acid solution was evaluated as an effective anticorrosion behavior of a hydrophobic surface on steel. The inhibition effect of magnetite nanoparticles on steel corrosion in 1 M HCl solution was investigated using potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). Results obtained from both potentiodynamic polarisation and EIS measurements reveal that the magnetite nanoparticle is an effective inhibitor for the corrosion of steel in 1.0 M HCl solution. Polarization data show that magnetite nanoparticles behave as a mixed type inhibitor. The inhibition efficiencies obtained from potentiodynamic polarization and EIS methods are in good agreement. PMID:24758936

  14. Synthesis and characterization of ultrafine poly(vinylalcohol phosphate) coated magnetite nanoparticles.

    PubMed

    Mohapatra, Sasmita; Pramanik, Nabakumar; Ghosh, Sudip K; Pramanik, Panchanan

    2006-03-01

    Nanosized magnetite (Fe3O4) particles showing superparamagnetism at room temperature have been prepared by controlled coprecipitation of Fe2+ and Fe3+ in presence of highly hydrophilic poly(vinylalcohol phosphate)(PVAP). The impact of polymer concentration on particle size, size distribution, colloidal stability, and magnetic property has been extensively studied. The aqueous suspension of magnetite, prepared using 1% PVAP solution is stable for four weeks at pH 5-8. X-ray diffractograms show the formation of nanocrystalline inverse spinel phase magnetite. Transmission Electron Microscopy confirmed well dispersed cubic magnetite particles of size of about 5.8 nm. Dynamic Light Scattering measurement shows narrow distribution of hydrodynamic size of particle aggregates. Infrared spectra of samples show strong Fe--O--P bond on the oxide surface. UV-visible studies show aqueous dispersion of magnetite formed by using 1% PVAP solution is stable at least for four weeks without any detoriation of particle size. Magnetization measurements at room temperature show superparamagnetic nature of polymer coated magnetite nanoparticles. PMID:16573145

  15. Incorporation of magnetite nanoparticle clusters in fluorescent silica nanoparticles for high-performance brain tumor delineation.

    PubMed

    Wan, Jiaqi; Meng, Xiangxi; Liu, Enzhong; Chen, Kezheng

    2010-06-11

    Bifunctional nanoprobes with both magnetic and optical contrast have been developed for ultra-sensitive brain tumor imaging at the cellular level. The nanoprobes were synthesized by simultaneously incorporating a magnetite nanoparticle cluster and fluorescence dyes into silica encapsulation by a sol-gel approach under ultrasonic treatment. The nanoprobes maintain superparamagnetic behavior at room temperature and possess enhanced transverse relaxivity and good photostability. As a glioma targeting ligand, chlorotoxin was covalently bonded to the surface of the nanoprobes. In vitro cellular uptake assays demonstrated that the nanoprobes were highly specific, taken up by human U251-MG glioma cells via receptor-mediated endocytosis. The labeled glioma cells were readily detectable by both MR imager and confocal laser scanning microscopy. PMID:20472942

  16. Nitrilotriacetic acid-coated magnetic nanoparticles as affinity probes for enrichment of histidine-tagged proteins and phosphorylated peptides.

    PubMed

    Li, Yi-Cheng; Lin, Ya-Shiuan; Tsai, Pei-Jane; Chen, Cheng-Tai; Chen, Wei-Yu; Chen, Yu-Chie

    2007-10-01

    We herein demonstrate superparamagnetic Fe3O4 nanoparticles coated with nitrilotriacetic acid derivative (NTA) that can bind with different immobilized metal ions are capable of probing diverse target species. Immobilized Ni(II) on the surfaces of the NTA-magnetic nanoparticles have the capability of selectively trapping histidine (His)-tagged proteins such as a mutated streptopain tagged with 6x His, i.e., C192S (MW approximately 42 kDa), from cell lysates. Enrichment was achieved by vigorously mixing the sample solution and the nanoparticles by pipetting in and out of a sample vial for only 30 s. After enrichment, the probe-target species could be readily isolated by magnetic separation. We also characterized the proteins enriched on the affinity probes using on-probe tryptic digestion under microwave irradiation for only 2 min, followed by matrix-assisted laser desorption/ionization mass spectrometry analysis. Using this enrichment and tryptic digestion, the target species can be rapidly enriched and characterized, reducing the time required for carrying out the complete analysis to less than 10 min. Furthermore, when either Zr(IV) or Ga (III) ions are immobilized on the surfaces of the NTA-magnetic nanoparticles, the nanoparticles have the capability of selectively enriching phosphorylated peptides from tryptic digests of alpha-, beta-caseins, and diluted milk. The detection limit for the tryptic digests of alpha- and beta-caseins is approximately 50 fmol. PMID:17784733

  17. Silver or gold deposition onto magnetite nanoparticles by using plant extracts as reducing and stabilizing agents.

    PubMed

    Norouz Dizaji, Araz; Yilmaz, Mehmet; Piskin, Erhan

    2016-06-01

    In this paper, we describe an environmentally friendly procedure to produce silver (Ag) or gold (Au)-deposited magnetite nanoparticles by using plant extracts (Ligustrum vulgare) as reducing and stabilizing agents. Firstly, magnetite nanoparticles (∼6 nm) with superparamagnetic properties - SPIONs - were synthesized by co-precipitation of Fe(+ 2) and Fe(+ 3) ions. Color changes indicated the differing amounts of Au and Ag ions reduced and deposited on to the SPIONs when the plant extracts were used. UV-vis and transmission electron microscope (TEM) with energy dispersive X-ray (EDX) apparatus confirmed the metallic deposition. Magnetic saturation decreased when the amount of the metallic deposition increased, which was measured by vibrating sample magnetometry (VSM). Due to the molecules coming into contact with - and even remaining on - the surface of the nanoparticles after aggressive washing procedures, the Ag/Au-deposited SPIONs were stable, and almost no agglomeration was observed for months. Fourier Transform Infrared (FTIR) spectra depicted that functional groups such as carboxylic and ketone groups, which are most probably responsible for the reduction and stabilization of Ag/Au- carrying magnetite nanoparticles, originated from the plant extract. The proposed route was facile, viable, and reproducible, and it should be stressed that nanoparticles do contain only safe biomolecules as stabilizing agents on their surfaces. PMID:25801040

  18. Lunar soil simulant and synthesized nanoparticles of magnetite exhibit diverse neurotoxic potential

    NASA Astrophysics Data System (ADS)

    Borisova, Tatiana; Krisanova, Natalia; Sivko, Roman; Nazarova, Anastasiya; Borysov, Arseniy

    Lunar soli simulant can be deleterious to human physiology and the components of lunar soil may be internalized by lung epithelium and may overcome the blood-brain barrier. Nanoparticles of ferric oxide are one of the components of Lunar soil simulants. Neurotoxic potential of lunar soil simulant and synthesized nanoparticles of magnetite was analyzed. The size of particles, their effects on membrane potential, acidification of synaptic vesicles, uptake and ambient level of glutamate, which is the major excitatory neurotransmitter in the CNS, were studied in isolated rat brain nerve terminals (synaptosomes) using photon correlation spectroscopy, spectrofluorimetry, radiolabeled assay, respectively. No significant effect of Lunar soil simulant and synthesized nanoparticles of magnetite on acidification of synaptic vesicles were found in synaptosomes. Also, nanoparticles did not influence the potential of the plasma membrane of synaptosomes. Unspecific binding of L-[14C]glutamate to synaptosomes was not altered by nanoparticles of magnetite, whereas in the presence of Lunar soil simulant this parameter was changed. Thus, it was suggested that Lunar soil simulant might disturb glutamate homeostasis in the mammalian CNS.

  19. Magnetite Nanoparticles Coated with Rifampicin and Chlortetracycline for Drug Delivery Applications

    NASA Astrophysics Data System (ADS)

    Nǎdejde, Claudia; Ciurlicǎ, Ecaterina Foca-nici; Creangǎ, Dorina; Cârlescu, Aurelian; Bǎdescu, Vasile

    2010-12-01

    Four types of biocompatible magnetic fluids based on superparamagnetic nanoparticles with Fe3O4 cores were functionalized with antibiotics (rifampicin or chlortetracycline) as potential candidates for in vivo biomedical applications, such as magnetically controlled drug delivery. The synthesis consisted in coprecipitation of iron oxide in basic, as well as in acid medium, followed by the dispersion of the resulted magnetite nanoparticles in aqueous solution containing the antibiotic. The chosen method to prepare the magnetite-core/drug-shell systems avoided intermediate organic coating of the magnetic nanoparticles. Comparative analysis of the rheological features of the aqueous magnetic fluid samples was performed. The structural features of the coated magnetic particles were investigated by X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Vibrating Sample Magnetometry (VSM). Good crystallinity and adequate stability in time were evidenced. Drug delivery curves were spectrophotometrically provided.

  20. Magnetite Nanoparticles Coated with Rifampicin and Chlortetracycline for Drug Delivery Applications

    SciTech Connect

    Nadejde, Claudia; Ciurlica, Ecaterina Foca-nici; Creanga, Dorina; Carlescu, Aurelian; Badescu, Vasile

    2010-12-02

    Four types of biocompatible magnetic fluids based on superparamagnetic nanoparticles with Fe{sub 3}O{sub 4} cores were functionalized with antibiotics (rifampicin or chlortetracycline) as potential candidates for in vivo biomedical applications, such as magnetically controlled drug delivery. The synthesis consisted in coprecipitation of iron oxide in basic, as well as in acid medium, followed by the dispersion of the resulted magnetite nanoparticles in aqueous solution containing the antibiotic. The chosen method to prepare the magnetite-core/drug-shell systems avoided intermediate organic coating of the magnetic nanoparticles. Comparative analysis of the rheological features of the aqueous magnetic fluid samples was performed. The structural features of the coated magnetic particles were investigated by X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Vibrating Sample Magnetometry (VSM). Good crystallinity and adequate stability in time were evidenced. Drug delivery curves were spectrophotometrically provided.

  1. Magnetic properties of magnetite nanoparticles crystallized in sodium-aluminoborosilicate glass matrix

    NASA Astrophysics Data System (ADS)

    Georgieva, M.; Tzankov, D.; Harizanova, R.; Avdeev, G.; Rüssel, C.

    2016-03-01

    Magnetite (Fe3O4) nanoparticles were crystallized from soda alumina borosilicate glasses with the composition (24- y)Na2O· yAl2O3·14B2O3·37SiO2·25Fe2O3, where y = 8, 12, 14, 16 mol%. All samples are phase separated into magnetite core, enriched in iron oxide, and a glass shell. The magnetic core phase consists of nanocrystallites with sizes ranging between 25 and 40 nm, depending on the respective glass composition. All samples show characteristic well-defined hysteresis loops at room temperature, indicating that the magnetite particles are ferrimagnetic. No evidence for the existence of superparamagnetic particles is found by measuring the ZFC and FC thermomagnetic curves.

  2. Gold-magnetite nanoparticle-biomolecule conjugates: Synthesis, properties and toxicity studies

    NASA Astrophysics Data System (ADS)

    Pariti, Akshay

    This thesis study focuses on synthesizing and characterizing gold-magnetite optically active magnetic nanoparticle and its conjugation with biomolecules for biomedical applications, especially magnetic fluid hyperthermia treatment for cancerous tissue. Gold nanoparticles have already displayed their potential in the biomedical field. They exhibit excellent optical properties and possess strong surface chemistry which renders them suitable for various biomolecule attachments. Studies have showed gold nanoparticles to be a perfect biocompatible vector. However, clinical trials for gold mediated drug delivery and treatment studied in rat models identified some problems. Of these problems, the low retention time in bloodstream and inability to maneuver externally has been the consequential. To further enhance their potential applications and overcome the problems faced in using gold nanoparticles alone, many researchers have synthesized multifunctional magnetic materials with gold at one terminal. Magnetite, among the investigated magnetic materials is a promising and reliable candidate because of its high magnetic saturation moment and low toxicity. This thesis showcases a simple and facile one pot synthesis of gold-magnetite nanoparticles with an average particle size of 80 nm through hot injection method. The as-synthesized nanoparticles were characterized by XRD, TEM, Mossbauer spectroscopy, SQUID and MTS toxicity studies. The superparamagnetism of the as-synthesized nanoparticles has an interestingly high saturation magnetization moment and low toxicity than the literature values reported earlier. L-cysteine and (-)-EGCG (epigallacatechin-3-gallate) were attached to this multifunctional nanoparticles through the gold terminal and characterized to show the particles applicability through Raman, FTIR and UV-Vis spectroscopy.

  3. Hyaluronic acid-coated solid lipid nanoparticles for targeted delivery of vorinostat to CD44 overexpressing cancer cells.

    PubMed

    Tran, Tuan Hiep; Choi, Ju Yeon; Ramasamy, Thiruganesh; Truong, Duy Hieu; Nguyen, Chien Ngoc; Choi, Han-Gon; Yong, Chul Soon; Kim, Jong Oh

    2014-12-19

    Hyaluronic acid (HA)-decorated solid lipid nanoparticles (SLNs) were developed for tumor-targeted delivery of vorinostat (VRS), a histone deacetylase inhibitor. HA, a naturally occurring polysaccharide, which specifically binds to the CD44 receptor, was coated on a cationic lipid core through electrostatic interaction. After the optimization process, HA-coated VRS-loaded SLNs (HA-VRS-SLNs) were spherical, core-shell nanoparticles, with small size (∼100 nm), negative charge (∼-9 mV), and narrow size distribution. In vitro release profile of HA-VRS-SLNs showed a typical bi-phasic pattern. In addition, the intracellular uptake of HA-VRS-SLNs was significantly enhanced in CD44 overexpressing cells, A549 and SCC-7 cells, but reduced when HA-VRS-SLNs were incubated with SCC-7 cells pretreated with HA or MCF-7 cells with low over-expressed CD44. Of particular importance, HA-VRS-SLNs were more cytotoxic than the free drug and VRS-SLNs in A549 and SCC-7 cells. In addition, HA shell provided longer blood circulation and reduced VRS clearance rate in rats, resulting in enhanced higher plasma concentration and bioavailability. These results clearly indicated the potential of the HA-functionalized lipid nanoparticle as a nano-sized drug formulation for chemotherapy. PMID:25263908

  4. Influence of cobalt doping on the hyperthermic efficiency of magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Fantechi, Elvira; Innocenti, Claudia; Albino, Martin; Lottini, Elisabetta; Sangregorio, Claudio

    2015-04-01

    Magnetite nanoparticles (NPs) are extensively investigated for biomedical applications, particularly as contrast agents for Magnetic Resonance Imaging and as heat mediators in Magnetic Fluid Hyperthermia. For the latter, one of the goal of the research is to obtain materials with improved hyperthermic properties. A valuable strategy is the increase of the magnetic anisotropy of commonly employed magnetite through the total or partial substitution of Fe2+ ions with Co2+ ions. Here we present a study on a family of 8 nm Co-doped magnetite NPs (CoxFe3-xO4), with composition ranging from pure magnetite (x=0) to stoichiometric cobalt ferrite (x=1), aimed to investigate the evolution of the hyperthermic properties with the increase of Co content. We found that the addition of a small amount of Co is enough to sharply increase the Specific Absorption Rate (SAR). The SAR further increases with x but it reaches a maximum for an intermediate value (x=0.6). Such anomalous behavior is ascribed to the intrinsic magnetic properties of the material, and, in particular, to the magnetic anisotropy, which displays the same peculiar trend. The Co-doping thus may represent an effective strategy to improve the poor hyperthermic efficiency of very small magnetite NPs (<10 nm).

  5. Hydroxyl-modified magnetite nanoparticles as novel carrier for delivery of methotrexate.

    PubMed

    Farjadian, Fatemeh; Ghasemi, Sahar; Mohammadi-Samani, Soliman

    2016-05-17

    In this work, novel hydroxyl-modified magnetite nanocarriers are introduced as efficient host for methotrexate conjugation. The modification was based on the Micheal type addition reaction between tris(hydroxymethyl) aminomethane and acrylamidopropyl functionalized, silica-coated magnetite nanoparticle. The chemical structure characterization was carried out by FT-IR and the organic content was determined by CHN analysis. The topography was studied by SEM, TEM, AFM. DLS was performed to show particles' mean diameter. Furthermore, the magnetite properties of modified particles were evaluated by VSM and the crystallinity was proved by XRD. To illustrate the efficiency of the modified particles, the anti-cancer drug methotrexate was conjugated to hydroxyl groups through estric bond formation. The controlled release activity of established nanoparticles was evaluated in simulated cellular fluid. Later, the anti-cancer behavior of drug conjugated nanoparticles was evaluated in vitro in MCF-7 cell line which showed enhanced toxicity after 48 h. Conclusively, the modified nanoparticles have remarked as powerful carrier to be applied as an anti-cancer agent. PMID:26994523

  6. Magnetite nanoparticles facilitate methane production from ethanol via acting as electron acceptors

    NASA Astrophysics Data System (ADS)

    Yang, Zhiman; Shi, Xiaoshuang; Wang, Chuanshui; Wang, Lin; Guo, Rongbo

    2015-11-01

    Potential for interspecies hydrogen transfer within paddy soil enrichments obtained via addition of magnetite nanoparticles and ethanol (named as PEM) was investigated. To do this, PEM derived from rice field of Hangzhou (named as PEM-HZ) was employed, because it offered the best methane production performance. Methane production and Fe (III) reduction proceeded in parallel in the presence of magnetite. Inhibition experiments with 2-bromoethane sulfonate (BES) or phosphate showed that interspecies hydrogen transfer and Fe (III) reduction also occurred in methane production from ethanol. 16S rRNA-based Illumina sequencing results showed that Dechloromonas, Thauera, Desulfovibrio and Clostridium were the dominant putative Fe (III) -reducers, and that hydrogenotrophic Methanobacterium accounted for about 88% of the total archaeal community. These results indicated that magnetite nanoparticles that acted as electron acceptor could facilitate rapid oxidation of ethanol by members of the Fe (III) -reducers in PEM-HZ and establishment of the syntrophic relationship of Fe (III) -reducers with Methanobacterium via interspecies hydrogen transfer. Our results could offer a model to understand the microbial interaction with magnetite from a novel angle during methanogenesis.

  7. Magnetite nanoparticles facilitate methane production from ethanol via acting as electron acceptors.

    PubMed

    Yang, Zhiman; Shi, Xiaoshuang; Wang, Chuanshui; Wang, Lin; Guo, Rongbo

    2015-01-01

    Potential for interspecies hydrogen transfer within paddy soil enrichments obtained via addition of magnetite nanoparticles and ethanol (named as PEM) was investigated. To do this, PEM derived from rice field of Hangzhou (named as PEM-HZ) was employed, because it offered the best methane production performance. Methane production and Fe (III) reduction proceeded in parallel in the presence of magnetite. Inhibition experiments with 2-bromoethane sulfonate (BES) or phosphate showed that interspecies hydrogen transfer and Fe (III) reduction also occurred in methane production from ethanol. 16S rRNA-based Illumina sequencing results showed that Dechloromonas, Thauera, Desulfovibrio and Clostridium were the dominant putative Fe (III) -reducers, and that hydrogenotrophic Methanobacterium accounted for about 88% of the total archaeal community. These results indicated that magnetite nanoparticles that acted as electron acceptor could facilitate rapid oxidation of ethanol by members of the Fe (III) -reducers in PEM-HZ and establishment of the syntrophic relationship of Fe (III) -reducers with Methanobacterium via interspecies hydrogen transfer. Our results could offer a model to understand the microbial interaction with magnetite from a novel angle during methanogenesis. PMID:26559132

  8. Magnetite nanoparticles facilitate methane production from ethanol via acting as electron acceptors

    PubMed Central

    Yang, Zhiman; Shi, Xiaoshuang; Wang, Chuanshui; Wang, Lin; Guo, Rongbo

    2015-01-01

    Potential for interspecies hydrogen transfer within paddy soil enrichments obtained via addition of magnetite nanoparticles and ethanol (named as PEM) was investigated. To do this, PEM derived from rice field of Hangzhou (named as PEM-HZ) was employed, because it offered the best methane production performance. Methane production and Fe (III) reduction proceeded in parallel in the presence of magnetite. Inhibition experiments with 2-bromoethane sulfonate (BES) or phosphate showed that interspecies hydrogen transfer and Fe (III) reduction also occurred in methane production from ethanol. 16S rRNA-based Illumina sequencing results showed that Dechloromonas, Thauera, Desulfovibrio and Clostridium were the dominant putative Fe (III) -reducers, and that hydrogenotrophic Methanobacterium accounted for about 88% of the total archaeal community. These results indicated that magnetite nanoparticles that acted as electron acceptor could facilitate rapid oxidation of ethanol by members of the Fe (III) -reducers in PEM-HZ and establishment of the syntrophic relationship of Fe (III) -reducers with Methanobacterium via interspecies hydrogen transfer. Our results could offer a model to understand the microbial interaction with magnetite from a novel angle during methanogenesis. PMID:26559132

  9. Monodisperse magnetite nanoparticles coupled with nuclear localization signal peptide for cell-nucleus targeting.

    PubMed

    Xu, Chenjie; Xie, Jin; Kohler, Nathan; Walsh, Edward G; Chin, Y Eugene; Sun, Shouheng

    2008-03-01

    Functionalization of monodisperse superparamagnetic magnetite (Fe(3)O(4)) nanoparticles for cell specific targeting is crucial for cancer diagnostics and therapeutics. Targeted magnetic nanoparticles can be used to enhance the tissue contrast in magnetic resonance imaging (MRI), to improve the efficiency in anticancer drug delivery, and to eliminate tumor cells by magnetic fluid hyperthermia. Herein we report the nucleus-targeting Fe(3)O(4) nanoparticles functionalized with protein and nuclear localization signal (NLS) peptide. These NLS-coated nanoparticles were introduced into the HeLa cell cytoplasm and nucleus, where the particles were monodispersed and non-aggregated. The success of labeling was examined and identified by fluorescence microscopy and MRI. The work demonstrates that monodisperse magnetic nanoparticles can be readily functionalized and stabilized for potential diagnostic and therapeutic applications. PMID:18080259

  10. Computer enhancement of ESR spectra of magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Dobosz, B.; Krzyminiewski, R.; Koralewski, M.; Hałupka-Bryl, M.

    2016-06-01

    We present ESR measurements of non-interacting magnetic nanoparticle systems. Temperature and orientational dependence of ESR spectra were measured for Fe3O4 nanoparticle coated by dextran or oleic acid, frozen in different magnetic field. Several parameters describing magnetic properties such as g-factor, line width, the anisotropy constant were calculated and discussed. The ESR spectra of investigated nanoparticles were also subjected to Computer Resolution Enhancement Method (CREM). This procedure allows to separate a narrow line on the background of the broad line, which presence in this type of materials was recognized in the recent literature and have been further discussed in the paper. CREM is a valuable tool for monitoring of changes on the surface of magnetic core of nanoparticles.

  11. Magnetofection of human somatic cells with magnetite and cobalt ferrospinel nanoparticles.

    PubMed

    Sukoyan, M A; Khrapov, E A; Voronina, E N; Boyarskikh, U A; Gubanov, A I; Itin, V I; Magaeva, A A; Nayden, E P; Terekhova, O G; Filipenko, M L

    2013-03-01

    Superparamagnetic nanoparticles varying by their chemical composition and synthesis method were used to transfer DNA into somatic cells under the influence of constant magnetic field (method of magnetofection). Magnetite particles obtained by mechanochemical synthesis ensured higher expression of the marker gene GFP (evaluated by fluorescence intensity of the cell lysate) then particles of ferric oxide obtained by chemical co-precipitation and cobalt ferrospinel particles obtained by the mechanochemical method. PMID:23658896

  12. Self-assembled MmsF proteinosomes control magnetite nanoparticle formation in vitro.

    PubMed

    Rawlings, Andrea E; Bramble, Jonathan P; Walker, Robyn; Bain, Jennifer; Galloway, Johanna M; Staniland, Sarah S

    2014-11-11

    Magnetotactic bacteria synthesize highly uniform intracellular magnetite nanoparticles through the action of several key biomineralization proteins. These proteins are present in a unique lipid-bound organelle (the magnetosome) that functions as a nanosized reactor in which the particle is formed. A master regulator protein of nanoparticle formation, magnetosome membrane specific F (MmsF), was recently discovered. This predicted integral membrane protein is essential for controlling the monodispersity of the nanoparticles in Magnetospirillum magneticum strain AMB-1. Two MmsF homologs sharing over 60% sequence identity, but showing no apparent impact on particle formation, were also identified in the same organism. We have cloned, expressed, and used these three purified proteins as additives in synthetic magnetite precipitation reactions. Remarkably, these predominantly α-helical membrane spanning proteins are unusually highly stable and water-soluble because they self-assemble into spherical aggregates with an average diameter of 36 nm. The MmsF assembly appears to be responsible for a profound level of control over particle size and iron oxide (magnetite) homogeneity in chemical precipitation reactions, consistent with its indicated role in vivo. The assemblies of its two homologous proteins produce imprecise various iron oxide materials, which is a striking difference for proteins that are so similar to MmsF both in sequence and hierarchical structure. These findings show MmsF is a significant, previously undiscovered, protein additive for precision magnetite nanoparticle production. Furthermore, the self-assembly of these proteins into discrete, soluble, and functional "proteinosome" structures could lead to advances in fields ranging from membrane protein production to drug delivery applications. PMID:25349410

  13. Self-assembled MmsF proteinosomes control magnetite nanoparticle formation in vitro

    PubMed Central

    Rawlings, Andrea E.; Bramble, Jonathan P.; Walker, Robyn; Bain, Jennifer; Galloway, Johanna M.; Staniland, Sarah S.

    2014-01-01

    Magnetotactic bacteria synthesize highly uniform intracellular magnetite nanoparticles through the action of several key biomineralization proteins. These proteins are present in a unique lipid-bound organelle (the magnetosome) that functions as a nanosized reactor in which the particle is formed. A master regulator protein of nanoparticle formation, magnetosome membrane specific F (MmsF), was recently discovered. This predicted integral membrane protein is essential for controlling the monodispersity of the nanoparticles in Magnetospirillum magneticum strain AMB-1. Two MmsF homologs sharing over 60% sequence identity, but showing no apparent impact on particle formation, were also identified in the same organism. We have cloned, expressed, and used these three purified proteins as additives in synthetic magnetite precipitation reactions. Remarkably, these predominantly α-helical membrane spanning proteins are unusually highly stable and water-soluble because they self-assemble into spherical aggregates with an average diameter of 36 nm. The MmsF assembly appears to be responsible for a profound level of control over particle size and iron oxide (magnetite) homogeneity in chemical precipitation reactions, consistent with its indicated role in vivo. The assemblies of its two homologous proteins produce imprecise various iron oxide materials, which is a striking difference for proteins that are so similar to MmsF both in sequence and hierarchical structure. These findings show MmsF is a significant, previously undiscovered, protein additive for precision magnetite nanoparticle production. Furthermore, the self-assembly of these proteins into discrete, soluble, and functional “proteinosome” structures could lead to advances in fields ranging from membrane protein production to drug delivery applications. PMID:25349410

  14. Preparation and application of crosslinked poly(sodium acrylate)--coated magnetite nanoparticles as corrosion inhibitors for carbon steel alloy.

    PubMed

    Atta, Ayman M; El-Mahdy, Gamal A; Al-Lohedan, Hamad A; El-Saeed, Ashraf M

    2015-01-01

    This work presents a new method to prepare poly(sodium acrylate) magnetite composite nanoparticles. Core/shell type magnetite nanocomposites were synthesized using sodium acrylate as monomer and N,N-methylenebisacrylamide (MBA) as crosslinker. Microemulsion polymerization was used for constructing core/shell structures with magnetite nanoparticles as core and poly(sodium acrylate) as shell. Fourier transform infrared spectroscopy (FTIR) was employed to characterize the nanocomposite chemical structure. Transmittance electron microscopy (TEM) was used to examine the morphology of the modified poly(sodium acrylate) magnetite composite nanoparticles. These particle will be evaluated for effective anticorrosion behavior as a hydrophobic surface on stainless steel. The composite nanoparticles has been designed by dispersing nanocomposites which act as a corrosion inhibitor. The inhibition effect of AA-Na/magnetite composites on steel corrosion in 1 M HCl solution was investigated using potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). Polarization measurements indicated that the studied inhibitor acts as mixed type corrosion inhibitor. EIS spectra exhibit one capacitive loop. The different techniques confirmed that the inhibition efficiency reaches 99% at 50 ppm concentration. This study has led to a better understanding of active anticorrosive magnetite nanoparticles with embedded nanocomposites and the factors influencing their anticorrosion performance. PMID:25594340

  15. Impact of magnetite nanoparticle incorporation on the eigenfrequencies of nanocomposite microcapsules

    NASA Astrophysics Data System (ADS)

    Glukhova, O. E.; Grishina, O. A.

    2015-03-01

    Modern researches showed that nanocomposite films with magnetite nanoparticle incorporation have good perspectives for applications in electronics to create antireflective coatings and also for biomedical applications to create coatings with remote control of physical properties using alternative magnetic field or microwave radiation, which is very important for fabrication of new generation substrates in tissue engineering and advanced drug delivery systems. In particular, the unique properties of advanced nanocomposite microcapsules allowed developing of the supramolecular system of targeted drug delivery. A study of the behavior of the nanocomposite shell of microcapsules, which consists of alternate layers of negatively charged iron oxide nanoparticles and cationic polyallylamine hydrochloride molecules, was carried out. The aim of the present study was to investigate the effect of the number of nanoparticle layers on magnetic properties of polyelectrolyte/nanoparticles nanocomposite microcapsules prepared via layer-by-layer technique using iron oxide colloids. In result of numerical simulation using ANSYS Workbench software the behavior of the nanocomposite shell of microcapsules depending on the concentration of magnetite particles in it was investigated. Modal and harmonic analysis of behavior of the microcapsules shell was conducted in water at a temperature of 37°. As a result of numerical experiment the eigenfrequencies and mode shape were first time defined for any modifications of the nanocomposite microcapsules. It has been established that the magnetic permeability value depends on the number of iron oxide nanoparticle layers in a nanocomposite microcapsule.

  16. Magnetite-containing spherical silica nanoparticles for biocatalysis and bioseparations.

    PubMed

    Yang, Huang-Hao; Zhang, Shu-Qiong; Chen, Xiao-Lan; Zhuang, Zhi-Xia; Xu, Jin-Gou; Wang, Xiao-Ru

    2004-03-01

    The simultaneous entrapment of biological macromolecules and nanostructured silica-coated magnetite in sol-gel materials using a reverse-micelle technique leads to a bioactive, mechanically stable, nanometer-sized, and magnetically separable particles. These spherical particles have a typical diameter of 53 +/- 4 nm, a large surface area of 330 m(2)/g, an average pore diameter of 1.5 nm, a total pore volume of 1.427 cm(3)/g and a saturated magnetization (M(S)) of 3.2 emu/g. Peroxidase entrapped in these particles shows Michaelis-Mentan kinetics and high activity. The catalytic reaction will take place immediately after adding these particles to the reaction solution. These enzyme entrapping particles catalysts can be easily separated from the reaction mixture by simply using an external magnetic field. Experiments have proved that these catalysts have a long-term stability toward temperature and pH change, as compared to free enzyme molecules. To further prove the application of this novel magnetic biomaterial in analytical chemistry, a magnetic-separation immunoassay system was also developed for the quantitative determination of gentamicin. The calibration for gentamicin has a working range of 200-4000 ng/mL, with a detection limit of 160 ng/mL, which is close to that of the fluorescent polarization immunoassay (FPIA) using the same reactants. PMID:14987087

  17. Magnetite nanoparticle (NP) uptake by wheat plants and its effect on cadmium and chromium toxicological behavior.

    PubMed

    López-Luna, J; Silva-Silva, M J; Martinez-Vargas, S; Mijangos-Ricardez, O F; González-Chávez, M C; Solís-Domínguez, F A; Cuevas-Díaz, M C

    2016-09-15

    The aim of this work was to assess the uptake of citrate-coated magnetite nanoparticles (NPs) by wheat plants and its effect on the bioaccumulation and toxicity of individual and joint Cd(2+) and Cr(6+) levels. Seven-day assays were conducted using quartz sand as the plant growth substrate. The endpoints measured were seed germination, root and shoot lengths, and heavy metal accumulation. Magnetite exhibited very low toxicity, regardless of the wheat seedling NP uptake and distribution into roots and shoots. The seed germination and shoot length were not sensitive enough, while the root length was a more sensitive toxicity endpoint. The root length of wheat seedlings exposed to individual metals decreased by 50% at 2.67mgCd(2)(+)kg(-1) and 5.53mgCr(6+)kg(-1). However, when magnetite NPs (1000mgkg(-1)) were added, the root length of the plants increased by 25 and 50%. Cd(2+) and Cr(6+) showed similar and noninteractive joint action, but strongly impaired the wheat seedlings. In contrast, an interactive infra-additive or antagonistic effect was observed upon adding magnetite NPs. Thus, cadmium and chromium accumulation in vegetable tissues was considerately diminished and the toxicity alleviated. PMID:26806072

  18. Study of the electrochemical properties of magnetite, maghemite and hematite nanoparticles for their applications in lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Chen, Linfeng; Wang, Gaojun; Xie, Jining; Rai, Pratyush; Lee, Jungmin; Mathur, Gyanesh N.; Varadan, Vijay K.

    2013-04-01

    Iron oxide nanoparticles, including magnetite, maghemite and hematite, are promising electrode active materials for lithium ion batteries due to their low cost, high capacity and environmental friendliness. Though the electrochemical properties of each kind of iron oxide nanoparticles have been intensively studied, systematic comparison of the three kinds of iron oxides is hardly reported. This paper reports the study and comparison of the electrochemical properties of magnetite, maghemite and hematite nanoparticles with the same shape and size. In this work, hematite and maghemite nanoparticles were obtained from commercial magnetite nanoparticles by thermal treatments at different conditions. Their crystalline structures were characterized by X-ray diffraction (XRD), their magnetic properties were measured by a vibration sample magnetometer (VSM), and their particle morphologies were analyzed by scanning electron microscopy (SEM). Composite electrodes were made from iron oxide nanoparticles with carbon black as the conducting material and PVDF as the binding material (iron oxide : carbon black : PVDF = 70 : 15 : 15). Prototype lithium ion batteries (CR2032 button cells) were assembled with iron oxide composite electrodes as cathodes, metal lithium as anodes, and Celgard 2400 porous membrane as separators. The impedance and discharge-charge behaviors were characterized by a Solartron electrochemical workstation and an Arbin battery tester, respectively. It was found that at the same shape and size, hematite nanoparticles has higher specific discharge and charge capacities than magnetite and maghemite nanoparticles.

  19. MAPLE fabrication of thin films based on kanamycin functionalized magnetite nanoparticles with anti-pathogenic properties

    NASA Astrophysics Data System (ADS)

    Grumezescu, Valentina; Andronescu, Ecaterina; Holban, Alina Maria; Mogoantă, Laurenţiu; Mogoşanu, George Dan; Grumezescu, Alexandru Mihai; Stănculescu, Anca; Socol, Gabriel; Iordache, Florin; Maniu, Horia; Chifiriuc, Mariana Carmen

    2015-05-01

    In this study we aimed to evaluate the biocompatibility and antimicrobial activity of kanamycin functionalized 5 nm-magnetite (Fe3O4@KAN) nanoparticles thin films deposited by Matrix Assisted Pulsed Laser Evaporation (MAPLE) technique. A laser deposition regime was established in order to stoichiometrically transfer Fe3O4@KAN thin films on silicone and glass substrates. Morphological and physico-chemical properties of powders and coatings were characterized by XRD, TEM, SEM, AFM and IR microscopy (IRM). Our nanostructured thin films have proved efficiency in the prevention of microbial adhesion and mature biofilms development as a result of antibiotic release in its active form. Furthermore, kanamycin functionalized nanostructures exhibit a good biocompatibility, both in vivo and in vitro, demonstrating their potential for implants application. This is the first study reporting the assessment of the in vivo biocompatibility of a magnetite-antimicrobial thin films produced by MAPLE technique.

  20. Composition controlled synthesis of PCL-PEG Janus nanoparticles: magnetite nanoparticles prepared from one-pot photo-click reaction.

    PubMed

    Khoee, S; Bagheri, Y; Hashemi, A

    2015-03-01

    The aim of this study is to investigate the effect of polymer nature on the morphology of synthesized nanoparticles. Super paramagnetic iron oxide nanoparticles (SPIONs) were prepared by co-precipitation method and then reacted with (3-mercaptopropyl) trimethoxysilane to obtain thiol-decorated SPIONs. Acrylated poly(caprolactone) and methoxy poly(ethylene glycol) were prepared, and then "thiol-ene click" reaction was performed under UV irradiation to attach two types of polymers on the surface of magnetite nanoparticles via the "photo-click" reaction method. Computational modelling was used for the prediction of the self-assembly of polymers on the surface of SPIONs, which determines the morphology of polymer coated nanoparticles. PMID:25666985

  1. Composition controlled synthesis of PCL-PEG Janus nanoparticles: magnetite nanoparticles prepared from one-pot photo-click reaction

    NASA Astrophysics Data System (ADS)

    Khoee, S.; Bagheri, Y.; Hashemi, A.

    2015-02-01

    The aim of this study is to investigate the effect of polymer nature on the morphology of synthesized nanoparticles. Super paramagnetic iron oxide nanoparticles (SPIONs) were prepared by co-precipitation method and then reacted with (3-mercaptopropyl) trimethoxysilane to obtain thiol-decorated SPIONs. Acrylated poly(caprolactone) and methoxy poly(ethylene glycol) were prepared, and then ``thiol-ene click'' reaction was performed under UV irradiation to attach two types of polymers on the surface of magnetite nanoparticles via the ``photo-click'' reaction method. Computational modelling was used for the prediction of the self-assembly of polymers on the surface of SPIONs, which determines the morphology of polymer coated nanoparticles.

  2. Polyelectrolyte/magnetite nanoparticle multilayers: preparation and structure characterization.

    PubMed

    Grigoriev, D; Gorin, D; Sukhorukov, G B; Yashchenok, A; Maltseva, E; Möhwald, H

    2007-11-20

    Polyelectrolyte composite planar films containing a different number of iron oxide (Fe3O4) nanoparticle layers have been prepared using the layer-by-layer adsorption technique. The nanocomposite assemblies were characterized by ellipsometry, UV-vis spectroscopy, and AFM. Linear growth of the multilayer thickness with the increase of the layer number, N, up to 12 reflects an extensive character of this parameter in this range. A more complicated behavior of the refractive index is caused by changes in the multilayer structure, especially for the thicker nanocomposites. A quantitative analysis of the nanocomposite structure is provided comparing a classical and a modified effective medium approach taking into account the influence of light absorption by the Fe3O4 nanoparticles on the complex refractive index of the nanocomposite and contributions of all components to film thickness. Dominant influence of co-adsorbed water on their properties was found to be another interesting peculiarity of the nanocomposite film. This effect, as well as possible film property modulation by light, is discussed. PMID:17958452

  3. U(VI) removal kinetics in presence of synthetic magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Huber, F.; Schild, D.; Vitova, T.; Rothe, J.; Kirsch, R.; Schäfer, T.

    2012-11-01

    The interaction of hexavalent U with a freshly synthesized nanoparticulate magnetite (FeIIFeIII2O4) (stochiometric ratio x(Fe(II)/FeTOT) = 0.25-0.33), a partly oxidized synthetic nanoparticulate magnetite (x = 0.11-0.27) and maghemite nanoparticles (x = 0-1) under anoxic conditions and exclusion of CO2 as function of pH, contact time and total U concentration (3 × 10-5 M and 1 × 10-7 M) has been examined. Short term kinetic batch experiments (contact time of 90 d) for four different pH values have been conducted. Moreover, classical batch pH sorption edges have been prepared for two different uranium concentrations for a contact time of 550 d. Spectroscopic techniques (XPS, XAS) were applied to probe for the presence and amount of reduced U on the magnetite surface. Batch kinetic studies revealed a fast initial U removal from aqueous solution with >90% magnetite associated U after 24 h within the pH range 5-11. Long-term contact time batch experiments (550 d) showed neither a U removal below pH < 3 nor a decrease in the magnetite associated U at pH ⩾ 9. Redox speciation by XPS verifies the presence of reduced U (both U(IV) and U(V) were resolved if the satellite structures were used in the fitting procedure) at the near surface of magnetite up to a contact time of 550 d and a clear correlation of the amount of available Fe(II) on the magnetite surface and the amount of reduced U is observed. XANES investigation supports presence of U(V)/U(VI) uranate and U(IV). Interpretation of the EXAFS for one sample is consistent with incorporation of U into an Fe oxide phase, after long reaction times. Thermodynamic calculations based on the experimentally determined redox potentials corroborate the spectroscopic findings of U oxidation states. Overall, the results reflect the importance of structurally bound Fe(II) as redox partner for uranyl reduction.

  4. The influence of colloidal parameters on the specific power absorption of PAA-coated magnetite nanoparticles

    PubMed Central

    2011-01-01

    The suitability of magnetic nanoparticles (MNPs) to act as heat nano-sources by application of an alternating magnetic field has recently been studied due to their promising applications in biomedicine. The understanding of the magnetic relaxation mechanism in biocompatible nanoparticle systems is crucial in order to optimize the magnetic properties and maximize the specific absorption rate (SAR). With this aim, the SAR of magnetic dispersions containing superparamagnetic magnetite nanoparticles bio-coated with polyacrylic acid of an average particle size of ≈10 nm has been evaluated separately by changing colloidal parameters such as the MNP concentration and the viscosity of the solvent. A remarkable decrease of the SAR values with increasing particle concentration and solvent viscosity was found. These behaviours have been discussed on the basis of the magnetic relaxation mechanisms involved. PACS: 80; 87; 87.85jf PMID:21711915

  5. Synthesis and microwave absorption properties of magnetite nanoparticles.

    PubMed

    Shao, XiaoPing; Dai, Bo; Zhang, XiaoWei; Ma, YongJun

    2012-02-01

    Nanoparticles of Fe3O4 with various sizes were synthesized from FeCl3 x 6H2O, FeCl2 x 4H2O and NaOH by coprecipitation process. The crystal structure, morphology, particle size and magnetic property of the products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). It was found that the molar ratio of ferrous to ferric played an important role in the formation of Fe3O4 nanoparticles. The particle mean diameter swelled from approximately 10 to approximately 20 nm with the molar ratio range from 1:2 to 6:1. The saturation magnetization and the coercivity increased correspondingly. The complex permittivity epsilon(r) and permeability mu(r) of the Fe3O4 mixture with paraffin were measured using vector network analysis. Values of epsilon(r), and mu(r) were used to determine the reflection loss at various sample thicknesses, based on a model of microwave absorbing layer backed by a metal plate. The minimal reflection loss or the dip shifts to a lower frequency region with increasing thickness. When the thickness is 5 mm, the minimal reflection loss of Fe3O4 synthesized with the molar ratio of 6:1 and paraffin wax composites reaches -35.1 dB at 5.2 GHz and -30.2 dB at 17.6 GHz, respectively. The minimal reflection loss is attributed to the thickness of the absorber approximates an odd number multiple of a quarter of the propagation wavelength. PMID:22629906

  6. Studies of magnetite nanoparticles synthesized by thermal decomposition of iron (III) acetylacetonate in tri(ethylene glycol)

    NASA Astrophysics Data System (ADS)

    Maity, Dipak; Kale, S. N.; Kaul-Ghanekar, Ruchika; Xue, Jun-Min; Ding, Jun

    2009-10-01

    In this paper, water-soluble magnetite nanoparticles have been directly synthesized by thermal decomposition of iron (III) acetylacetonate, Fe(acac) 3 in tri(ethyleneglycol). Size and morphology of the nanoparticles are determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements while the crystal structure is identified using X-ray diffraction (XRD). Surface charge and surface coating of the nanoparticles are recognized using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectra (XPS) and zeta potential measurements. Magnetic properties are determined using vibrating sample magnetometer (VSM) and superconducting quantum interference device (SQUID) measurements. The results show that as-prepared magnetite nanoparticles are relatively monodisperse, single crystalline and superparamagnetic in nature with the blocking temperature at around 100 K. The magnetite nanoparticles are found to be highly soluble in water due to steric and electrostatic interactions between the particles arising by the surface adsorbed tri(ethyleneglycol) molecules and associated positive charges, respectively. Cytotoxicity studies on human cervical (SiHa), mouse melanoma (B16F10) and mouse primary fibroblast cells demonstrate that up to a dose of 80 μg/ml, the magnetic nanoparticles are nontoxic to the cells. Specific absorption rate (SAR) value has been calculated to be 885 and 539 W/gm for samples with the iron concentration of 1 and 0.5 mg/ml, respectively. The high SAR value upon exposure to 20 MHz radiofrequency signifies the applicability of as-prepared magnetite nanoparticles for a feasible magnetic hyperthermia treatment.

  7. Effects of uncoated and citric acid coated cerium oxide nanoparticles, bulk cerium oxide, cerium acetate, and citric acid on tomato plants.

    PubMed

    Barrios, Ana Cecilia; Rico, Cyren M; Trujillo-Reyes, Jesica; Medina-Velo, Illya A; Peralta-Videa, Jose R; Gardea-Torresdey, Jorge L

    2016-09-01

    Little is known about the physiological and biochemical responses of plants exposed to surface modified nanomaterials. In this study, tomato (Solanum lycopersicum L.) plants were cultivated for 210days in potting soil amended with uncoated and citric acid coated cerium oxide nanoparticles (nCeO2, CA+nCeO2) bulk cerium oxide (bCeO2), and cerium acetate (CeAc). Millipore water (MPW), and citric acid (CA) were used as controls. Physiological and biochemical parameters were measured. At 500mg/kg, both the uncoated and CA+nCeO2 increased shoot length by ~9 and ~13%, respectively, while bCeO2 and CeAc decreased shoot length by ~48 and ~26%, respectively, compared with MPW (p≤0.05). Total chlorophyll, chlo-a, and chlo-b were significantly increased by CA+nCeO2 at 250mg/kg, but reduced by bCeO2 at 62.5mg/kg, compared with MPW. At 250 and 500mg/kg, nCeO2 increased Ce in roots by 10 and 7 times, compared to CA+nCeO2, but none of the treatments affected the Ce concentration in above ground tissues. Neither nCeO2 nor CA+nCeO2 affected the homeostasis of nutrient elements in roots, stems, and leaves or catalase and ascorbate peroxidase in leaves. CeAc at 62.5 and 125mg/kg increased B (81%) and Fe (174%) in roots, while at 250 and 500mg/kg, increased Ca in stems (84% and 86%, respectively). On the other hand, bCeO2 at 62.5 increased Zn (152%) but reduced P (80%) in stems. Only nCeO2 at 62.5mg/kg produced higher total number of tomatoes, compared with control and the rest of the treatments. The surface coating reduced Ce uptake by roots but did not affect its translocation to the aboveground organs. In addition, there was no clear effect of surface coating on fruit production. To our knowledge, this is the first study comparing the effects of coated and uncoated nCeO2 on tomato plants. PMID:26672385

  8. Monodisperse sodium oleate coated magnetite high susceptibility nanoparticles for hyperthermia applications

    NASA Astrophysics Data System (ADS)

    Araújo-Neto, R. P.; Silva-Freitas, E. L.; Carvalho, J. F.; Pontes, T. R. F.; Silva, K. L.; Damasceno, I. H. M.; Egito, E. S. T.; Dantas, Ana L.; Morales, Marco A.; Carriço, Artur S.

    2014-09-01

    We report a simple and low cost methodology to synthesize sodium oleate coated magnetite nanoparticles for hyperthermia applications. The system consists of oleate coated magnetite nanoparticles with large susceptibility (1065 emu/gT), induced by the dipolar inter-particle interaction, with a magnetic core diameter in the 6 nm-12 nm size range. In aqueous medium, the nanoparticles agglomerate to form a monodisperse system, exhibiting a mean hydrodynamic diameter of 60.6 nm±4.1 nm, with a low average polydispersity index of 0.128±0.003, as required for intravenous applications. The system exhibits promising efficiency for magnetic hyperthermia, with a specific absorption rate of 14 W/g at a low field amplitude of 15.9 kA/m and frequency of 62 kHz. In a 50 mg/mL density in 1 mL, the temperature rises to 42.5 °C in 1.9 min.

  9. Reduction of iron by decarboxylation in the formation of magnetite nanoparticles.

    PubMed

    Pérez, Nicolás; López-Calahorra, Francisco; Labarta, Amílcar; Batlle, Xavier

    2011-11-21

    The process of formation of magnetite nanoparticles has been investigated by liquid chromatography and mass spectroscopy in the liquid phase decomposition of either Fe(III) acetylacetonate with decanoic acid or Fe(III) decanoate. In both cases, the dissociation into radicals of the iron carboxylate bonds provides the reduction of the Fe(III) cations and the oxygen atoms required for the formation of the mixed-valence inverse spinel magnetite structure. A reaction mechanism is proposed. It is also shown that the reaction of free decanoic acid with the Fe(III) cations in solution promotes the growth of faceted particles at the reflux temperature of the solvent (ca. 280 °C), while, under the same conditions, the stepwise decomposition of the Fe(III) decanoate generates smaller and pseudo-spherical particles. The latter also yields faceted particles when the temperature is increased above that of the total decomposition of the salt. Magnetic measurements make evident that the reaction starting from Fe(III) acetylacetonate yields nanoparticles with higher magnetization and lower spin disorder, due to the improved regularity of the surface crystal structure. The starting conditions for the decarboxylation process thus affect the morphology and magnetic properties of the resulting nanoparticles. PMID:21960123

  10. Laser spectroscopy of finite size and covering effects in magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Nikiforov, V. N.; Ignatenko, A. N.; Ivanov, A. V.; Irkhin, V. Yu

    2016-02-01

    Experiments on the impact of the size of magnetite clusters on various magnetic properties (magnetic moment, Curie temperature, blocking temperature etc) have been carried out. The methods of magnetic separation and centrifugation of water suspensions of biocompatible iron oxide nanoparticles (NPs) allow one to produce fractions with diameters of nanoparticles in the range of 4-22 nm. The size of the NPs is controlled by the methods of dynamic light scattering (DLS), transmission electron microscopy (TEM) and atomic force microscopy (AFM). For the first time the DLS method is applied in real time to control the size during the process of the separation of the NPs in aqueous suspensions. The changes of the size of NPs cause a shift in the Curie temperature and changes in the specific magnetic properties of the iron NPs. The experimental data is interpreted on the basis of Monte Carlo simulations for the classical Heisenberg model with different bulk and surface magnetic moments. It is demonstrated experimentally and by theoretical modeling that the magnetic properties of magnetite NPs are determined not only by their sizes, but also by their surface spin states, while both growing and falling dependences of the magnetic moment (per Fe3O4 formula unit) are possible, depending on the number of magnetic atoms in the nanoparticle. NPs that are both clean and covered with bioresorbable layer clusters have been investigated.

  11. Preparation and characterization of chondroitin-sulfate-A-coated magnetite nanoparticles for biomedical applications

    NASA Astrophysics Data System (ADS)

    Tóth, Ildikó Y.; Illés, Erzsébet; Szekeres, Márta; Tombácz, Etelka

    2015-04-01

    Polysaccharides are promising candidates for manufacturing biocompatible core-shell nanoparticles with potential in vivo use. Superparamagnetic magnetite nanoparticles (MNPs) have prospective application in both diagnosis and therapy, and so developing a novel polysaccharide shell on MNP core is of great challenge. MNPs were prepared by co-precipitation, then the surface of purified MNPs was coated with chondroitin-sulfate-A (CSA) to obtain core-shell structured magnetite nanoparticles (CSA@MNP). The effect of the added amount of CSA on the surface charging and the aggregation state of MNPs at various pHs and 10 mM NaCl was measured by electrophoresis and dynamic light scattering. The amphoteric behavior of MNPs was fundamentally modified by adsorption of CSA polyanions. A very low CSA-loading induces the aggregation of MNPs, while four times more stabilizes the dispersions over the whole pH-range studied. The coagulation kinetics experiments measured at pH=6.3±0.3 showed that salt tolerance of CSA@MNPs rises up to ~150 mM NaCl.

  12. Size-dependent reactivity of magnetite nanoparticles: a field-laboratory comparison

    USGS Publications Warehouse

    Swindle, Andrew L.; Elwood Madden, Andrew S.; Cozzarelli, Isabelle M.; Benamara, Mourad

    2014-01-01

    Logistic challenges make direct comparisons between laboratory- and field-based investigations into the size-dependent reactivity of nanomaterials difficult. This investigation sought to compare the size-dependent reactivity of nanoparticles in a field setting to a laboratory analog using the specific example of magnetite dissolution. Synthetic magnetite nanoparticles of three size intervals, ∼6 nm, ∼44 nm, and ∼90 nm were emplaced in the subsurface of the USGS research site at the Norman Landfill for up to 30 days using custom-made subsurface nanoparticle holders. Laboratory analog dissolution experiments were conducted using synthetic groundwater. Reaction products were analyzed via TEM and SEM and compared to initial particle characterizations. Field results indicated that an organic coating developed on the particle surfaces largely inhibiting reactivity. Limited dissolution occurred, with the amount of dissolution decreasing as particle size decreased. Conversely, the laboratory analogs without organics revealed greater dissolution of the smaller particles. These results showed that the presence of dissolved organics led to a nearly complete reversal in the size-dependent reactivity trends displayed between the field and laboratory experiments indicating that size-dependent trends observed in laboratory investigations may not be relevant in organic-rich natural systems.

  13. On the adsorption of magnetite nanoparticles on lysozyme amyloid fibrils.

    PubMed

    Majorosova, Jozefina; Petrenko, Viktor I; Siposova, Katarina; Timko, Milan; Tomasovicova, Natalia; Garamus, Vasil M; Koralewski, Marceli; Avdeev, Mikhail V; Leszczynski, Błażej; Jurga, Stefan; Gazova, Zuzana; Hayryan, Shura; Hu, Chin-Kun; Kopcansky, Peter

    2016-10-01

    An adsorption of magnetic nanoparticles (MNP) from electrostatically stabilized aqueous ferrofluids on amyloid fibrils of hen egg white lysozyme (HEWL) in 2mg/mL acidic dispersions have been detected for the MNP concentration range of 0.01-0.1vol.%. The association of the MNP with amyloid fibrils has been characterized by transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS) and magneto-optical measurements. It has been observed that the extent of adsorption is determined by the MNP concentration. When increasing the MNP concentration the formed aggregates of magnetic particles repeat the general rod-like structure of the fibrils. The effect is not observed when MNP are mixed with the solution of lysozyme monomers. The adsorption has been investigated with the aim to clarify previously found disaggregation activity of MNP in amyloid fibrils dispersions and to get deeper insight into interaction processes between amyloids and MNP. The observed effect is also discussed with respect to potential applications for ordering lysozyme amyloid fibrils in a liquid crystal phase under external magnetic fields. PMID:27451367

  14. Synthesis of magnetite magnetic nanoparticles and measurement of magneto-optical effects

    NASA Astrophysics Data System (ADS)

    Lin, Jing-Fung; Lee, Meng-Zhe

    2014-06-01

    In the present study, magnetite (Fe3O4) magnetic nanoparticles (MNPs) were prepared by an improved chemical co-precipitation method. The effects of the pH value of the solution after titration, the reaction temperature in surface coating, and the molar concentration of Fe3+/Fe2+ salts in dispersibility and size of MNPs are studied. Characterization of the dispersibility and size in MNPs involved using transmission electronic microscope and X-ray diffractometry. Above all, the measurement of magneto-optical effect including the linear birefringence and dichroism of magnetic fluid are executed by a Stokes polarimeter.

  15. Biodistribution and pharmacokinetics of uniform magnetite nanoparticles chemically modified with polyethylene glycol

    NASA Astrophysics Data System (ADS)

    Ruiz, A.; Hernández, Y.; Cabal, C.; González, E.; Veintemillas-Verdaguer, S.; Martínez, E.; Morales, M. P.

    2013-11-01

    The influence of polyethylene glycol (PEG) grafting on the pharmacokinetics, biodistribution and elimination of iron oxide nanoparticles is studied in this work. Magnetite nanoparticles (12 nm) were obtained via thermal decomposition of an iron coordination complex as a precursor. Particles were coated with meso-2,3-dimercaptosuccinic acid (DMSA) and conjugated to PEG-derived molecules by 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide (EDC) chemistry. Using a rat model, we explored the nanoparticle biodistribution pattern in blood and in different organs (liver, spleen and lungs) after intravenous administration of the product. The time of residence in blood was measured from the evolution of water proton relaxivities with time and Fe analysis in blood samples. The results showed that the residence time was doubled for PEG coated nanoparticles and consequently particle accumulation in liver and spleen was reduced. Post-mortem histological analyses showed no alterations in the liver and confirm heterogeneous distribution of NPs in the organ, in agreement with magnetic measurements and iron analysis. Finally, by successive magnetic resonance images we studied the evolution of contrast in the liver and measured the absorption, time of residence and excretion of nanoparticles in the liver during a one month period. On the basis of these results we propose different metabolic routes that determine the fate of magnetic nanoparticles.

  16. Modeling and prediction of retardance in citric acid coated ferrofluid using artificial neural network

    NASA Astrophysics Data System (ADS)

    Lin, Jing-Fung; Sheu, Jer-Jia

    2016-06-01

    Citric acid coated (citrate-stabilized) magnetite (Fe3O4) magnetic nanoparticles have been conducted and applied in the biomedical fields. Using Taguchi-based measured retardances as the training data, an artificial neural network (ANN) model was developed for the prediction of retardance in citric acid (CA) coated ferrofluid (FF). According to the ANN simulation results in the training stage, the correlation coefficient between predicted retardances and measured retardances was found to be as high as 0.9999998. Based on the well-trained ANN model, the predicted retardance at excellent program from Taguchi method showed less error of 2.17% compared with a multiple regression (MR) analysis of statistical significance. Meanwhile, the parameter analysis at excellent program by the ANN model had the guiding significance to find out a possible program for the maximum retardance. It was concluded that the proposed ANN model had high ability for the prediction of retardance in CA coated FF.

  17. Effect of concentration of sodium silicate solution in the synthesis of silica-coated magnetite nanoparticles by ultrasonication

    NASA Astrophysics Data System (ADS)

    Fajaroh, Fauziatul; Sumari, Nazriati

    2016-02-01

    An ex-situ silica coating of magnetite nanoparticles synthesized electrochemically had been successfully carried out by ultrasonication. An aqueous solution of sodium silicate had been used as silica source.The Si-O-Si, Si-O and Fe-O-Si bonds on the surface of the silica-coated magnetite had been successfully identified using FTIR. Reduction in particle size due to the influence of ultrasound was studied using SEM. Enhancement in the specific surface area of the particles due to the silica coating and reduction in particle size was learned through BET analysis. The Characters of the resulting silica-coated magnetite were influenced by the concentration of sodium silicate solution. The greater the concentration of sodium silicate solution, the smaller the particle crystallinity and the larger the particles surface area was produced. The resulting silica-coated magnetite has a surface area of 38.171 to 67.993 m2/g, otherwise the non-coated particles only has a surface area of 27.894 m2/g. This silica-coated magnetite nanoparticles has more potent as an adsorbent than that of the bare magnetite. Besides that, the presence of silanol groups on its surface makes an opportunity for further functionalization needed for some applications.

  18. AC susceptibility and EPR investigations of superspin dynamics in magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Price, Alex D.

    In this investigation we use two complementary techniques to distinguish between superparamagnetic blocking (SPB) and superspin-glass (SSG) freezing phenomena in magnetite nanoparticles. While these manifestations of the superspin dynamics are fundamentally different, they have similar "signatures", especially in dc-magnetization experiments. Even if ac-susceptibility measurements are employed, careful use of mathematical models to analyze the data are needed to uncover which type of phenomena (SPB or SSG freezing) occurs within the material. Yet, by utilizing electron paramagnetic resonance (EPR) on a 10 nm Fe3O4 nano-powder as well as on a ferrofluid (based on the same nanoparticle ensemble) we found a very distinct difference in the absorption spectra between the two samples, which indicates markedly different EPR signatures from SPB and SSG freezing behaviors.

  19. Influence of nanoparticle size on the nonlinear optical properties of magnetite ferrofluids

    NASA Astrophysics Data System (ADS)

    Espinosa, D.; Carlsson, L. B.; Neto, A. M. Figueiredo; Alves, S.

    2013-09-01

    The nonlinear index of refraction (n2) and the two-photon absorption coefficient (β) of water-based ferrofluids made of magnetite nanocrystals of different sizes and with different coatings have been measured through the Z-scan technique, with ultrashort (femtoseconds) laser pulses. Their third-order susceptibility is calculated from the values of n2 and β. The influence of different particles' coatings and sizes on these nonlinear optical properties are investigated. The values of n2 and β depend more significantly on the nanoparticles' size than on the particular coating. We observe a decrease of β as the nanoparticles' diameters decrease, although the optical gap is found to be the same for all samples. The results are interpreted considering modifications in the electronic orbital shape due to the particles' nanosize effect.

  20. Comparative Cytogenetic Study on the Toxicity of Magnetite and Zinc Ferrite Nanoparticles in Sunflower Root Cells

    NASA Astrophysics Data System (ADS)

    Foca-nici, Ecaterina; Capraru, Gabriela; Creanga, Dorina

    2010-12-01

    In this experimental study the authors present their results regarding the cellular division rate and the percentage of chromosomal aberrations in the root meristematic cells of Helianthus annuus cultivated in the presence of different volume fractions of magnetic nanoparticle suspensions, ranging between 20 and 100 microl/l. The aqueous magnetic colloids were prepared from chemically co-precipitated ferrites coated in sodium oleate. Tissue samples from the root meristeme of 2-3 day old germinated seeds were taken to prepare microscope slides following Squash method combined with Fuelgen techniques. Microscope investigation (cytogenetic tests) has resulted in the evaluation of mitotic index and chromosomal aberration index that appeared diminished and respectively increased following the addition of magnetic nanoparticles in the culture medium of the young seedlings. Zinc ferrite toxic influence appeared to be higher than that of magnetite, according to both cytogenetic parameters.

  1. Influence of nanoparticle size on the nonlinear optical properties of magnetite ferrofluids.

    PubMed

    Espinosa, D; Carlsson, L B; Neto, A M Figueiredo; Alves, S

    2013-09-01

    The nonlinear index of refraction (n_{2}) and the two-photon absorption coefficient (β) of water-based ferrofluids made of magnetite nanocrystals of different sizes and with different coatings have been measured through the Z-scan technique, with ultrashort (femtoseconds) laser pulses. Their third-order susceptibility is calculated from the values of n_{2} and β. The influence of different particles' coatings and sizes on these nonlinear optical properties are investigated. The values of n_{2} and β depend more significantly on the nanoparticles' size than on the particular coating. We observe a decrease of β as the nanoparticles' diameters decrease, although the optical gap is found to be the same for all samples. The results are interpreted considering modifications in the electronic orbital shape due to the particles' nanosize effect. PMID:24125263

  2. In vivo MRI of single-wall carbon nanohorns through magnetite nanoparticle attachment

    NASA Astrophysics Data System (ADS)

    Miyawaki, Jin; Yudasaka, Masako; Imai, Hideto; Yorimitsu, Hideki; Isobe, Hiroyuki; Nakamura, Eiichi; Iijima, Sumio

    2006-03-01

    Superparamagnetic magnetite (SPM) is used as a contrast agent in magnetic resonance imaging (MRI). Thus, the SPM-attachment to carbon nanotubes (CNTs) will enable to visualize motional behaviors of CNTs in the living body through MRI. We found that the strong attachment of the SPM nanoparticles (ca. 6 nm size) to one type of CNTs, single-wall carbon nanohorns (SWNHs), could be achieved through a deposition of iron acetate clusters on SWNHs in ethanol at room temperature, followed by heat-treatment in Ar. In vivo MRI visualized that the SWNHs attached with the SPM nanoparticles accumulated in several organs of mice when injected into mice via tail veins. This simple method for the SPM-attaching on CNTs would facilitate the toxicity assessment of CNTs and the applications of CNTs in bioscience and biotechnology.

  3. Influence of Growth Conditions on Magnetite Nanoparticles Electro-Crystallized in the Presence of Organic Molecules

    PubMed Central

    Mosivand, Saba; Monzon, Lorena M. A.; Kazeminezhad, Iraj; Coey, J. Michael D.

    2013-01-01

    Magnetite nanoparticles were synthesized by electrocrystallization in the presence of thiourea or sodium butanoate as an organic stabilizer. The synthesis was performed in a thermostatic electrochemical cell containing two iron electrodes with an aqueous solution of sodium sulfate as electrolyte. The effects of organic concentration, applied potential and growth temperature on particle size, morphology, structure and magnetic properties were investigated. The magnetite nanoparticles were characterized by X-ray diffraction, electron microscopy, magnetometry and Mössbauer spectrometry. When the synthesis is performed in the presence of sodium butanoate at 60 °C, a paramagnetic ferric salt is obtained as a second phase; it is possible to avoid formation of this phase, increase the specific magnetization and improve the structure of the oxide particles by tuning the growth conditions. Room-temperature magnetization values range from 45 to 90 Am2kg−1, depending on the particle size, type of surfactant and synthesis conditions. Mössbauer spectra, which were recorded at 290 K for all the samples, are typical of nonstoichiometric Fe3−δO4, with a small excess of Fe3+, 0.05 ≤ δ ≤ 0.15. PMID:23685871

  4. Removal of aqueous perfluorooctanoic acid (PFOA) using starch-stabilized magnetite nanoparticles.

    PubMed

    Gong, Yanyan; Wang, Lin; Liu, Juncheng; Tang, Jingchun; Zhao, Dongye

    2016-08-15

    Fully stabilized magnetite (Fe3O4) nanoparticles were prepared with a water-soluble starch as a stabilizer and tested for removal of aqueous perfluorooctanoic acid (PFOA). The presence of starch at ≥0.2wt% can fully stabilize 0.1g/L as Fe of the Fe3O4 nanoparticles. The particle stabilization technique resulted in 2.4 times higher PFOA uptake. Fourier transform infrared spectra suggested that the main PFOA removal mechanism was inner-sphere complexation. Batch kinetic experiments revealed that the starch-stabilized nanoparticles facilitated a rapid PFOA uptake with a sorption equilibrium time of 30min, and the sorption process followed a pseudo-second-order kinetic model. The Langmuir model was able to well interpret the adsorption isotherm, with a maximum adsorption capacity of 62.5mg/g. Increasing pH from 4.7 to 9.6 led to a sharp increase (by 2.6 times) in PFOA uptake. The presence of 12mg/L humic acid inhibited PFOA uptake by 96%, while effect of ionic strength (CaCl2=0-2mmol/L) was negligible. The nanoparticles significantly reduced the biological toxicity of PFOA. The results demonstrated promise of starch-stabilized Fe3O4 nanoparticles as a "green" adsorbent for effective removal of PFOA in soil and groundwater. PMID:27100000

  5. A facile approach to enhance the high temperature stability of magnetite nanoparticles with improved magnetic property

    NASA Astrophysics Data System (ADS)

    Pati, S. S.; Philip, John

    2013-01-01

    We study the effect of Zn2+ doping on crystal structure, magnetic properties, blocking and Curie temperatures, and the high temperature phase stability of magnetite nanoparticles under air and vacuum annealing. The Zn2+ doped nanoparticles (ZnxFe3-xO4 with x = 0, 0.2, 0.4, and 0.6) are prepared by simple co-precipitation technique and are characterized by high temperature X-ray powder diffraction (HTXRD), vibrating sample magnetometer, small angle X-ray scattering, thermogravimetry, differential scanning calorimetry (DSC), and transmission electron microscopy. Our HTXRD studies show that the decomposition temperature of pure magnetite (Fe3O4) in vacuum is increased by 300 °C (from 700 to 1000 °C), with 0.2 fraction of Zn2+ doping. The DSC studies under air environment also show that the γ-Fe2O3 to α-Fe2O3 phase transition temperature increases with the zinc fraction. The increase in transition temperature is attributed to the increase in the activation energy of the maghemite to hematite phase transition after the replacement of Fe3+ with larger diameter Zn2+ in the A site. Interestingly, the saturation magnetization increases from 61 to 69 emu/g upon 0.2 fraction of Zn2+, which augments the utility of the doped compound for practical applications. While the Curie temperature is found to increase with doping concentration, the blocking temperature shows an opposite trend. The blocking temperature values were found to be 262, 196, 144, and 153 K for 0, 0.2, 0.4, and 0.6 fraction of zinc, respectively. The reduction in TB is attributed to weak dipole-dipole interactions and local exchange coupling between nanoparticles. All the Zn2+ doped samples show superparamagnetic nature. These findings are extremely useful in producing superparamagnetic nanoparticles with enhanced magnetic properties for high temperature applications.

  6. Characterization of Single-core Magnetite Nanoparticles for Magnetic Imaging by SQUID-relaxometry

    PubMed Central

    Adolphi, Natalie L.; Huber, Dale L.; Bryant, Howard C.; Monson, Todd C.; Fegan, Danielle L.; Lim, JitKang; Trujillo, Jason E.; Tessier, Trace E.; Lovato, Debbie M.; Butler, Kimberly S.; Provencio, Paula P.; Hathaway, Helen J.; Majetich, Sara A.; Larson, Richard S.; Flynn, Edward R.

    2013-01-01

    Optimizing the sensitivity of SQUID (superconducting quantum interference device)-relaxometry for detecting cell-targeted magnetic nanoparticles for in vivo diagnostics requires nanoparticles with a narrow particle size distribution to ensure that the Néel relaxation times fall within the measurement timescale (50 ms - 2 s, in this work). To determine the optimum particle size, single-core magnetite nanoparticles (with nominal average diameters 20, 25, 30, and 35 nm) were characterized by SQUID-relaxometry, transmission electron microscopy (TEM), SQUID-susceptometry, dynamic light scattering, and zeta potential analysis. The SQUID-relaxometry signal (detected magnetic moment/kg) from both the 25 nm and 30 nm particles was an improvement over previously-studied multi-core particles. However, the detected moments were an order of magnitude lower than predicted based on a simple model that takes into account the measured size distributions (but neglects dipolar interactions and polydispersity of the anisotropy energy density), indicating that improved control of several different nanoparticle properties (size, shape, coating thickness) will be required to achieve the highest detection sensitivity. Antibody conjugation and cell incubation experiments show that single-core particles enable a higher detected moment per cell, but also demonstrate the need for improved surface treatments to mitigate aggregation and improve specificity. PMID:20858918

  7. The effect of humic acid adsorption on pH-dependent surface charging and aggregation of magnetite nanoparticles

    SciTech Connect

    Illes, E.; Tombacz, E.

    2006-03-01

    The pH-dependent adsorption of humic acid (HA) on magnetite and its effect on the surface charging and the aggregation of oxide particles were investigated. HA was extracted from brown coal. Synthetic magnetite was prepared by alkaline hydrolysis of iron(II) and iron(III) salts. The pH-dependent particle charge and aggregation, and coagulation kinetics at pH around to 4 were measured by laser Doppler electrophoresis and dynamic light scattering. The charge of pure magnetite reverses from positive to negative at pH around 8, which may consider as isoelectric point (IEP). Near this pH, large aggregates form, while stable sols exist further from it. In the presence of increasing HA loading, the IEP shifts to lower pH, then at higher loading, magnetite becomes negatively charged even at low pHs, which indicate the neutralization and gradual recharging positive charges on surface. In acidic region, the trace HA amounts are adsorbed on magnetite surface as oppositely charged patches, systems become highly unstable due to heterocoagulation. Above the adsorption saturation, however, the nanoparticles are stabilized in a way of combined steric and electrostatic effects. The HA coated magnetite particles form stable colloidal dispersion, particle aggregation does not occur in a wide range of pH and salt tolerance is enhanced.

  8. Magnetite nanoparticles for functionalized textile dressing to prevent fungal biofilms development

    PubMed Central

    2012-01-01

    The purpose of this work was to investigate the potential of functionalized magnetite nanoparticles to improve the antibiofilm properties of textile dressing, tested in vitro against monospecific Candida albicans biofilms. Functionalized magnetite (Fe3O4/C18), with an average size not exceeding 20 nm, has been synthesized by precipitation of ferric and ferrous salts in aqueous solution of oleic acid (C18) and NaOH. Transmission electron microscopy, X-ray diffraction analysis, and differential thermal analysis coupled with thermo gravimetric analysis were used as characterization methods for the synthesized Fe3O4/C18. Scanning electron microscopy was used to study the architecture of the fungal biofilm developed on the functionalized textile dressing samples and culture-based methods for the quantitative assay of the biofilm-embedded yeast cells. The optimized textile dressing samples proved to be more resistant to C. albicans colonization, as compared to the uncoated ones; these functionalized surfaces-based approaches are very useful in the prevention of wound microbial contamination and subsequent biofilm development on viable tissues or implanted devices. PMID:22950367

  9. Magnetite nanoparticles for functionalized textile dressing to prevent fungal biofilms development

    NASA Astrophysics Data System (ADS)

    Anghel, Ion; Grumezescu, Alexandru Mihai; Andronescu, Ecaterina; Anghel, Alina Georgiana; Ficai, Anton; Saviuc, Crina; Grumezescu, Valentina; Vasile, Bogdan Stefan; Chifiriuc, Mariana Carmen

    2012-09-01

    The purpose of this work was to investigate the potential of functionalized magnetite nanoparticles to improve the antibiofilm properties of textile dressing, tested in vitro against monospecific Candida albicans biofilms. Functionalized magnetite (Fe3O4/C18), with an average size not exceeding 20 nm, has been synthesized by precipitation of ferric and ferrous salts in aqueous solution of oleic acid (C18) and NaOH. Transmission electron microscopy, X-ray diffraction analysis, and differential thermal analysis coupled with thermo gravimetric analysis were used as characterization methods for the synthesized Fe3O4/C18. Scanning electron microscopy was used to study the architecture of the fungal biofilm developed on the functionalized textile dressing samples and culture-based methods for the quantitative assay of the biofilm-embedded yeast cells. The optimized textile dressing samples proved to be more resistant to C. albicans colonization, as compared to the uncoated ones; these functionalized surfaces-based approaches are very useful in the prevention of wound microbial contamination and subsequent biofilm development on viable tissues or implanted devices.

  10. Tegafur loading and release properties of magnetite/poly(alkylcyanoacrylate) (core/shell) nanoparticles.

    PubMed

    Arias, José L; Ruiz, M Adolfina; Gallardo, Visitación; Delgado, Angel V

    2008-01-01

    In this work, we describe a reproducible method to prepare polymeric colloidal nanospheres of poly(ethyl-2-cyanoacrylate), poly(butylcyanoacrylate), poly(hexylcyanoacrylate) and poly(octylcyanoacrylate) with a magnetite core, and loaded with the anticancer drug Tegafur. The method is based on the emulsion polymerization procedure, often used in the synthesis of poly(alkylcyanoacrylate) nanospheres for drug delivery. The heterogeneous structure of the particles confer them both magnetic-field responsiveness and potential applicability as drug carriers. In order to investigate to what extent is this target achieved, we compare the surface electrical properties of the core/shell particles with those of both the nucleus and the coating material. The hysteresis cycles of both magnetite and composite particles demonstrate that the polymer shell reduces the magnetic responsiveness of the particles, but keeps their soft ferrimagnetic character unchanged. A detailed investigation of the capabilities of the core/shell particles to load this drug is shown. We found, by means of spectrophotometric and electrophoretic measurements, the existence of two drug loading mechanisms: absorption or entrapment in the polymeric network, and surface adsorption. The type of polymer, the pH and the drug concentration are the main factors determining the drug incorporation to the nanoparticles. The release studies showed a biphasic profile affected by the type of polymeric shell, the type of drug incorporation and the amount of drug loaded. PMID:17949844

  11. TEA controllable preparation of magnetite nanoparticles (Fe3O4 NPs) with excellent magnetic properties

    NASA Astrophysics Data System (ADS)

    Han, Chengliang; Zhu, Dejie; Wu, Hanzhao; Li, Yao; Cheng, Lu; Hu, Kunhong

    2016-06-01

    A fast and controllable synthesis method for superparamagnetic magnetite nanoparticles (Fe3O4 NPs) was developed in Fe(III)-triethanolamine (TEA) solution. The phase structure, morphology and particle size of the as-synthesized samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the magnetic particles were pure Fe3O4 with mean sizes of approximately 10 nm. The used TEA has key effects on the formation of well dispersing Fe3O4 NPs. Vibrating sample magnetometer (VSM) result indicated that the as-obtained Fe3O4 NPs exhibited superparamagnetic behavior and the saturation magnetization (Ms) was about 70 emu/g, which had potential applications in magnetic science and technology.

  12. Photothermally driven fast responding photo-actuators fabricated with comb-type hydrogels and magnetite nanoparticles

    PubMed Central

    Lee, Eunsu; Kim, Dowan; Kim, Haneul; Yoon, Jinhwan

    2015-01-01

    To overcome the slow kinetics of the volume phase transition of stimuli-responsive hydrogels as platforms for soft actuators, thermally responsive comb-type hydrogels were prepared using synthesized poly(N-isopropylacrylamide) macromonomers bearing graft chains. Fast responding light-responsive hydrogels were fabricated by combining a comb-type hydrogel matrix with photothermal magnetite nanoparticles (MNP). The MNPs dispersed in the matrix provide heat to stimulate the volume change of the hydrogel matrix by converting absorbed visible light to thermal energy. In this process, the comb-type hydrogel matrix exhibited a rapid response due to the free, mobile grafted chains. The comb-type hydrogel exhibited significantly enhanced light-induced volume shrinkage and rapid recovery. The comb-type hydrogels containing MNP were successfully used to fabricate a bilayer-type photo-actuator with fast bending motion. PMID:26459918

  13. Radiation effects in polyisobutylene succinic anhydride modified with silica and magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Zaharescu, T.; Borbath, I.; Vékás, L.

    2014-12-01

    Polyisobutylene succinic anhydride (PIBSA) was modified with nanoparticles of magnetite and silica for the appraising the modification in the thermal stability of organic component after gamma irradiation. Pristine anhydride was loaded with different amounts of nanofiller (1, 2 and 5 wt% of each oxide). Gamma exposure was performed in air at several doses: 10, 20, 50 and 100 kGy. The stability determinations were carried out by nonisothermal chemiluminescence in stationary air atmosphere. The presence of these oxides induces an increase in the oxidation level corresponding to their chemical availability as the filler amounts and exposure doses are enhanced. The oxidation takes essentially place on quaternary carbon atoms and double bonds, which was demonstrated by the presence of two chemiluminescence intensity peaks. The comparative analysis on the radiation oxidation of PIBSA modified with Fe3O4 and SiO2 is presented.

  14. Recyclable magnetite nanoparticle coated with cationic polymers for adsorption of DNA.

    PubMed

    Rutnakornpituk, B; Theppaleak, T; Rutnakornpituk, M; Vilaivan, T

    2016-08-01

    Magnetite nanoparticle (MNP) grafted with a cationic copolymer between poly(2-(N,N-diethylamino) ethyl methacrylate) and poly(poly(ethylene glycol) methyl ether methacrylate)) for efficient and recyclable adsorption of 5'-fluorescein-tagged DNA (FAM-dT9) was prepared. MNP having highest degree of positive charge (+32.1 ± 1.9 mV) retained 100% adsorption of FAM-dT9 during eight adsorption-separation-desorption cycles. The MNP having lower degree of positive charge showed a slight decrease in adsorption percentages (94-98% adsorption) after multiple recycling processes. This biocompatible hybrid material with charged surface and magnetic-responsive properties might be applicable for use as a nanosolid support for efficient and facile separation of various bioentities. PMID:27206488

  15. Assemblies of magnetite nanoparticles extracted from magnetotactic bacteria: A magnetic study

    NASA Astrophysics Data System (ADS)

    Huízar-Félix, A. M.; Muñoz, D.; Orue, I.; Magén, C.; Ibarra, A.; Barandiarán, J. M.; Muela, A.; Fdez-Gubieda, M. L.

    2016-02-01

    Self-assembly has emerged as a suitable technique for tuning the properties of nanoparticles. In this work, we report the self-assembly of magnetosomes assisted by an external magnetic field. The magnetosomes are magnetite nanoparticles biomineralized by magnetotactic bacteria Magnetospirillum gryphiswaldense. These nanoparticles present truncated cubo-octahedral morphology with a mean diameter of ≈36 nm and are surrounded by a lipid bilayer membrane with a thickness ≈2-4 nm. The use of the appropriate preparation conditions, such as initial colloidal concentration and magnetic fields applied during deposition allowed us to obtain very reproducible self-assembled 2D patterns. Homogeneous ensembles of magnetosomes onto silicon and carbon surfaces are composed of elongated structures in the form of wide chains that cover a large area of the substrates. Transmission electron microscopy image and off-axis electron holography showed the map of the stray magnetic fields produced by these assemblies. The induced magnetic anisotropy was analyzed by measuring the hysteresis loops of the assemblies at different angles in a magneto-optical Kerr effect magnetometer. The evolution of the coercive field and remanence verified the presence of well-defined patterns. The experimental results were analyzed on the based of a biaxial model.

  16. Structural and magnetic characterization of electro-crystallized magnetite nanoparticles under constant current

    SciTech Connect

    Mosivand, Saba; Kazeminezhad, Iraj

    2015-10-15

    Graphical abstract: Structural and magnetic properties of electro-crystallized magnetite nanoparticles under constant current were studied. All samples were characterized using XRD, SEM, VSM, and Mössbauer spectrometry. - Highlights: • The effect of applied current on morphology and properties of Fe{sub 3}O{sub 4} is studied. • The particle size and morphology are controllable by adjusting the current. • The magnetization depends on particle size, type of surfactant and applied current. • The clear correlation between magnetization and the mean particle size is observed. - Abstract: The effect of applied current on the morphology, particle size, structure, and magnetic properties of magnetite nanoparticles prepared by electro-crystallization method was studied. The synthesis was performed in an electrochemical cell containing two iron electrodes and an aqueous solution of sodium sulfate, and either thiourea, sodium butanoate, or β-cyclodextrine as organic stabilizer. All the samples were characterized by XRD, SEM, VSM, and Mössbauer spectroscopy. X-ray diffraction patterns, clearly confirmed that all products have the cubic spinel Fe{sub 3}O{sub 4} crystal structure. Electron microscope images of the samples showed that their mean particle size is in the range 20–80 nm, and depends critically on the applied current and type of the organic additives. Specific magnetization of the samples at room temperature ranges from 60 to 90 A m{sup 2} kg{sup −1}, depending on the growth conditions. Room temperature Mössbauer spectra are typical of nonstoichiometric Fe{sub 3−δ}O{sub 4}, with a small excess of Fe{sup 3+}, 0.06 ≤ δ ≤ 0.17.

  17. Structural determination of Bi-doped magnetite multifunctional nanoparticles for contrast imaging.

    PubMed

    Laguna-Marco, M A; Piquer, C; Roca, A G; Boada, R; Andrés-Vergés, M; Veintemillas-Verdaguer, S; Serna, C J; Iadecola, A; Chaboy, J

    2014-09-14

    To determine with precision how Bi atoms are distributed in Bi-doped iron oxide nanoparticles their structural characterization has been carried out by X-ray absorption spectroscopy (XAS) recorded at the K edge of Fe and at the L3 edge of Bi. The inorganic nanoparticles are nominally hybrid structures integrating an iron oxide core and a bismuth oxide shell. Fe K-edge XAS indicates the formation of a structurally ordered, non-stoichiometric magnetite (Fe3-δO4) phase for all the nanoparticles. The XAS spectra show that, in the samples synthesized by precipitation in aqueous media and laser pyrolysis, the Bi atoms neither enter into the iron oxide spinel lattice nor form any other mixed Bi-Fe oxides. No modification of the local structure around the Fe atoms induced by the Bi atoms is observed at the Fe K edge. In addition, contrary to expectations, our results indicate that the Bi atoms do not form a well-defined Bi oxide structure. The XAS study at the Bi L3 edge indicates that the environment around Bi atoms is highly disordered and only a first oxygen coordination shell is observed. Indefinite [BiO6-x(OH)x] units (isolated or aggregated forming tiny amorphous clusters) bonded through hydroxyl bridges to the nanoparticle, rather than a well defined Bi2O3 shell, surround the nanoparticle. On the other hand, the XAS study indicates that, in the samples synthesized by thermal decomposition, the Bi atoms are embedded in a longer range ordered structure showing the first and second neighbors. PMID:25057849

  18. Hybrid magnetite nanoparticles/Rosmarinus officinalis essential oil nanobiosystem with antibiofilm activity.

    PubMed

    Chifiriuc, Carmen; Grumezescu, Valentina; Grumezescu, Alexandru Mihai; Saviuc, Crina; Lazăr, Veronica; Andronescu, Ecaterina

    2012-01-01

    Biofilms formed by fungal organisms are associated with drastically enhanced resistance against most antimicrobial agents, contributing to the persistence of the fungi despite antifungal therapy. The purpose of this study is to combine the unique properties of nanoparticles with the antimicrobial activity of the Rosmarinus officinalis essential oil in order to obtain a nanobiosystem that could be pelliculised on the surface of catheter pieces, in order to obtain an improved resistance to microbial colonization and biofilm development by Candida albicans and C. tropicalis clinical strains. The R. officinalis essential oils were extracted in a Neo-Clevenger type apparatus, and its chemical composition was settled by GC-MS analysis. Functionalized magnetite nanoparticles of up to 20 nm size had been synthesized by precipitation method adapted for microwave conditions, with oleic acid as surfactant. The catheter pieces were coated with suspended core/shell nanoparticles (Fe3O4/oleic acid:CHCl3), by applying a magnetic field on nanofluid, while the CHCl3 diluted essential oil was applied by adsorption in a secondary covering treatment. The fungal adherence ability was investigated in six multiwell plates, in which there have been placed catheters pieces with and without hybrid nanoparticles/essential oil nanobiosystem pellicle, by using culture-based methods and confocal laser scanning microscopy (CLSM). The R. officinalis essential oil coated nanoparticles strongly inhibited the adherence ability and biofilm development of the C. albicans and C. tropicalis tested strains to the catheter surface, as shown by viable cell counts and CLSM examination. Due to the important implications of Candida spp. in human pathogenesis, especially in prosthetic devices related infections and the emergence of antifungal tolerance/resistance, using the new core/shell/coated shell based on essential oil of R. officinalis to inhibit the fungal adherence could be of a great interest for the

  19. Hybrid magnetite nanoparticles/ Rosmarinus officinalis essential oil nanobiosystem with antibiofilm activity

    NASA Astrophysics Data System (ADS)

    Chifiriuc, Carmen; Grumezescu, Valentina; Grumezescu, Alexandru Mihai; Saviuc, Crina; Lazăr, Veronica; Andronescu, Ecaterina

    2012-04-01

    Biofilms formed by fungal organisms are associated with drastically enhanced resistance against most antimicrobial agents, contributing to the persistence of the fungi despite antifungal therapy. The purpose of this study is to combine the unique properties of nanoparticles with the antimicrobial activity of the Rosmarinus officinalis essential oil in order to obtain a nanobiosystem that could be pelliculised on the surface of catheter pieces, in order to obtain an improved resistance to microbial colonization and biofilm development by Candida albicans and C. tropicalis clinical strains. The R. officinalis essential oils were extracted in a Neo-Clevenger type apparatus, and its chemical composition was settled by GC-MS analysis. Functionalized magnetite nanoparticles of up to 20 nm size had been synthesized by precipitation method adapted for microwave conditions, with oleic acid as surfactant. The catheter pieces were coated with suspended core/shell nanoparticles (Fe3O4/oleic acid:CHCl3), by applying a magnetic field on nanofluid, while the CHCl3 diluted essential oil was applied by adsorption in a secondary covering treatment. The fungal adherence ability was investigated in six multiwell plates, in which there have been placed catheters pieces with and without hybrid nanoparticles/essential oil nanobiosystem pellicle, by using culture-based methods and confocal laser scanning microscopy (CLSM). The R. officinalis essential oil coated nanoparticles strongly inhibited the adherence ability and biofilm development of the C. albicans and C. tropicalis tested strains to the catheter surface, as shown by viable cell counts and CLSM examination. Due to the important implications of C andida spp. in human pathogenesis, especially in prosthetic devices related infections and the emergence of antifungal tolerance/resistance, using the new core/shell/coated shell based on essential oil of R. officinalis to inhibit the fungal adherence could be of a great interest for the

  20. Aqueous suspensions of polymer coated magnetite nanoparticles: Colloidal stability, specific absorption rate, and transverse relaxivity

    NASA Astrophysics Data System (ADS)

    Saville, Steven Lee

    The design, functionalization, characterization, and applications of magnetic nanoparticles have garnered significant interest over the past several decades. While this area has garnered increasing attention, several questions remain unanswered about the stability of these systems and it's influence on their biomedical applications. To help answer these questions about the stability of these, a novel tri(nitroDOPA) terminated polymer based ligand has been developed for the stabilization of magnetite nanoparticles. The synthesis involves a process in which ethylene oxide is polymerized using a trivinyl initiator, modified with carboxylic acid using a free radical addition of mercaptoundecanoic acid, and then functionalized with nitroDOPA using N,N-dicyclohexylcarbodiimide (DCC) and N-hydroxysuccinimide (NHS) chemistry. This polymer has displayed robust adhesion even in harsh chemical environments, out performing many polymers used today for the stabilization of magnetite. Along these same lines, the effects of instability of these systems were analyzed in both MRI and magnetic hyperthermia applications. It is widely known that formation of linear aggregates (i.e. chains) occurs in more concentrated ferrofluids systems and that this has an affect on the ferrofluid properties. It has been recently reported that for some suspensions of magnetic nanoparticles the transverse proton relaxation rate, R2, is dependent on the time that the sample is exposed to an applied magnetic field. This time dependence has been linked to the formation of linear aggregates or chains in an applied magnetic field via numerical modeling. In this work the relationships between colloidal stability, the formation of these linear structures, and changes observed in the proton transverse relaxation rate and heating rate in magnetic hyperthermia of aqueous suspensions of magnetic particles are examined. The results indicate that varying the ligand length has a direct effect on the colloidal

  1. Direct synthesis of magnetite nanoparticles from iron(II) carboxymethylcellulose and their performance as NMR contrast agents

    NASA Astrophysics Data System (ADS)

    da Silva, Delmarcio Gomes; Hiroshi Toma, Sergio; de Melo, Fernando Menegatti; Carvalho, Larissa Vieira C.; Magalhães, Alvicler; Sabadini, Edvaldo; dos Santos, Antônio Domingues; Araki, Koiti; Toma, e. Henrique E.

    2016-01-01

    Iron(II) carboxymethylcellulose (CMC) has been successfully employed in the synthesis of hydrophylic magnetite nanoparticles stabilized with a biopolymer coating, aiming applications in NMR imaging. The new method encompasses a convenient one-step synthetic procedure, allowing a good size control and yielding particles of about 10 nm (core size). In addition to the biocompatibility, the nanoparticles have promoted a drastic reduction in the transverse relaxation time (T2) of the water protons. The relaxivity rates have been investigated as a function of the nanoparticles concentration, showing a better performance in relation to the common NMR contrast agents available in the market.

  2. Simple synthesis of functionalized superparamagnetic magnetite/silica core/shell nanoparticles and their application as magnetically separable high-performance biocatalysts

    SciTech Connect

    Lee, Jinwoo; Lee, Youjin; Youn, Jongkyu; Na, Hyon Bin; Yu, Taekyung; Kim, Hwan O.; Lee, Sang-mok; Koo, Yoon-mo; Kwak, Ja Hun; Park, Hyun-Gyu; Chang, Ho Nam; Hwang, Misun; Park, Je-Geun; Kim, Jungbae; Hyeon, Taeghwan

    2008-01-01

    We report on the facile large-scale synthesis of magnetite@silica core-shell nanoparticles by a simple addition of tetraethyl orthosilicate (TEOS) into reverse micelles during the formation of uniformly-sized magnetite nanoparticles. The size of magnetic core was determined by the ratio of solvent and surfactant in reverse micelle solution while the thickness of silica shell could be easily controlled by adjusting the amount of added TEOS. Amino group functional groups were grafted to the magnetic nanoparticles, and crosslinked enzyme clusters (CEC) were fabricated on the surface of magnetite@silica nanoparticles. The resulting hybrid materials of magnetite and CEC were magnetically separable, highly active, and stable enough to show no decrease of enzyme activity under rigorous shaking for more than 15 days.

  3. Green Synthesis of Magnetite (Fe3O4) Nanoparticles Using Seaweed (Kappaphycus alvarezii) Extract.

    PubMed

    Yew, Yen Pin; Shameli, Kamyar; Miyake, Mikio; Kuwano, Noriyuki; Bt Ahmad Khairudin, Nurul Bahiyah; Bt Mohamad, Shaza Eva; Lee, Kar Xin

    2016-12-01

    In this study, a simple, rapid, and eco-friendly green method was introduced to synthesize magnetite nanoparticles (Fe3O4-NPs) successfully. Seaweed Kappaphycus alvarezii (K. alvarezii) was employed as a green reducing and stabilizing agents. The synthesized Fe3O4-NPs were characterized with X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) techniques. The X-ray diffraction planes at (220), (311), (400), (422), (511), (440), and (533) were corresponding to the standard Fe3O4 patterns, which showed the high purity and crystallinity of Fe3O4-NPs had been synthesized. Based on FT-IR analysis, two characteristic absorption peaks were observed at 556 and 423 cm(-1), which proved the existence of Fe3O4 in the prepared nanoparticles. TEM image displayed the synthesized Fe3O4-NPs were mostly in spherical shape with an average size of 14.7 nm. PMID:27251326

  4. Green Synthesis of Magnetite (Fe3O4) Nanoparticles Using Seaweed ( Kappaphycus alvarezii) Extract

    NASA Astrophysics Data System (ADS)

    Yew, Yen Pin; Shameli, Kamyar; Miyake, Mikio; Kuwano, Noriyuki; Bt Ahmad Khairudin, Nurul Bahiyah; Bt Mohamad, Shaza Eva; Lee, Kar Xin

    2016-06-01

    In this study, a simple, rapid, and eco-friendly green method was introduced to synthesize magnetite nanoparticles (Fe3O4-NPs) successfully. Seaweed Kappaphycus alvarezii ( K. alvarezii) was employed as a green reducing and stabilizing agents. The synthesized Fe3O4-NPs were characterized with X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) techniques. The X-ray diffraction planes at (220), (311), (400), (422), (511), (440), and (533) were corresponding to the standard Fe3O4 patterns, which showed the high purity and crystallinity of Fe3O4-NPs had been synthesized. Based on FT-IR analysis, two characteristic absorption peaks were observed at 556 and 423 cm-1, which proved the existence of Fe3O4 in the prepared nanoparticles. TEM image displayed the synthesized Fe3O4-NPs were mostly in spherical shape with an average size of 14.7 nm.

  5. Taking a hard line with biotemplating: cobalt-doped magnetite magnetic nanoparticle arrays.

    PubMed

    Bird, Scott M; Galloway, Johanna M; Rawlings, Andrea E; Bramble, Jonathan P; Staniland, Sarah S

    2015-04-28

    Rapid advancements made in technology, and the drive towards miniaturisation, means that we require reliable, sustainable and cost effective methods of manufacturing a wide range of nanomaterials. In this bioinspired study, we take advantage of millions of years of evolution, and adapt a biomineralisation protein for surface patterning of biotemplated magnetic nanoparticles (MNPs). We employ soft-lithographic micro-contact printing to pattern a recombinant version of the biomineralisation protein Mms6 (derived from the magnetotactic bacterium Magnetospirillum magneticum AMB-1). The Mms6 attaches to gold surfaces via a cysteine residue introduced into the N-terminal region. The surface bound protein biotemplates highly uniform MNPs of magnetite onto patterned surfaces during an aqueous mineralisation reaction (with a mean diameter of 90 ± 15 nm). The simple addition of 6% cobalt to the mineralisation reaction maintains the uniformity in grain size (with a mean diameter of 84 ± 14 nm), and results in the production of MNPs with a much higher coercivity (increased from ≈ 156 Oe to ≈ 377 Oe). Biotemplating magnetic nanoparticles on patterned surfaces could form a novel, environmentally friendly route for the production of bit-patterned media, potentially the next generation of ultra-high density magnetic data storage devices. This is a simple method to fine-tune the magnetic hardness of the surface biotemplated MNPs, and could easily be adapted to biotemplate a wide range of different nanomaterials on surfaces to create a range of biologically templated devices. PMID:25825205

  6. Aqueous U(VI) interaction with magnetite nanoparticles in a mixed flow reactor system: HR-XANES study

    NASA Astrophysics Data System (ADS)

    Pidchenko, I.; Heberling, F.; Kvashnina, KO; Finck, N.; Schild, D.; Bohnert, E.; Schäfer, T.; Rothe, J.; Geckeis, H.; Vitova, T.

    2016-05-01

    The redox variations and changes in local atomic environment of uranium (U) interacted with the magnetite nanoparticles were studied in a proof of principle experiment by the U L3 and M4 edges high energy resolution X-ray absorption near edge structure (HR-XANES) technique. We designed and applied a mixed flow reactor (MFR) set-up to maintain dynamic flow conditions during U-magnetite interactions. Formation of hydrolyzed, bi- and poly-nuclear U species were excluded by slow continuous injection of U(VI) (10-6 M) and pH control integrated in the MFR set-up. The applied U HR-XANES technique is more sensitive to minor changes in the U redox states and bonding compared to the conventional XANES method. Major U(VI) contribution in uranyl type of bonding is found in the magnetite nanoparticles after three days operation time of the MFR. Indications for shortening of the U-Oaxial bond length for the magnetite compared to the maghemite system are present too.

  7. Fabrication and study of properties of magnetite nanoparticles in hybrid micelles of polystyrene- block-polyethylene oxide and sodium dodecyl sulfate

    NASA Astrophysics Data System (ADS)

    Loginova, T. P.; Timofeeva, G. I.; Lependina, O. L.; Shandintsev, V. A.; Matyushin, A. A.; Khotina, I. A.; Shtykova, E. V.

    2016-01-01

    Magnetite nanoparticles have been formed for the first time in hybrid micelles of polystyrene- block-polyethylene oxide and sodium dodecyl sulfate in water by ultrasonic treatment at room temperature. An analysis by small-angle X-ray scattering and transmission electron microscopy (TEM) showed that magnetite nanoparticles in hybrid micelles of block copolymer and sodium dodecyl sulfate are polydesperse (have sizes from 0.5 to 20 nm). The specific magnetization of solid samples has been measured.

  8. Aloe vera plant-extracted solution hydrothermal synthesis and magnetic properties of magnetite (Fe3O4) nanoparticles

    NASA Astrophysics Data System (ADS)

    Phumying, Santi; Labuayai, Sarawuth; Thomas, Chunpen; Amornkitbamrung, Vittaya; Swatsitang, Ekaphan; Maensiri, Santi

    2013-06-01

    Magnetite (Fe3O4) nanoparticles have been successfully synthesized by a novel hydrothermal method using ferric acetylacetonate (Fe(C5H8O2)3) and aloe vera plant-extracted solution. The influences of different reaction temperatures and times on the structure and magnetic properties of the synthesized Fe3O4 nanoparticles were investigated. The synthesized nanoparticles are crystalline and have particle sizes of ˜6-30 nm, as revealed by transmission electron microscopy (TEM). The results of X-ray diffraction (XRD), High resolution TEM (HRTEM) and selected area electron diffraction (SAED) indicate that the synthesized Fe3O4 nanoparticles have the inverse cubic spinel structure without the presence of any other phase impurities. The hysteresis loops of the Fe3O4 nanoparticles at room temperature show superparamagnetic behavior and the saturation magnetization of the Fe3O4 samples increases with increasing reaction temperature and time.

  9. Preparation and Cytotoxic Evaluation of Magnetite (Fe3O4) Nanoparticles on Breast Cancer Cells and its Combinatory Effects with Doxorubicin used in Hyperthermia

    PubMed Central

    Sadeghi-Aliabadi, Hojjat; Mozaffari, Morteza; Behdadfar, Behshid; Raesizadeh, Maryam; Zarkesh-Esfahani, Hamid

    2013-01-01

    Background Magnetic nanoparticles in a variable magnetic field are able to produce heat. This heat (42-45°C) has more selective effect on fast dividing cancer cells than normal tissues. Methods In this work magnetite nanoparticles have been prepared via co-precipitation and phase identification was performed by powder x-ray diffraction (XRD). Magnetic parameters of the prepared nanoparticles were measured by a Vibrating Sample Magnetometer (VSM). A sensitive thermometer has been used to measure the increase of temperature in the presence of an alternating magnetic field. To evaluate the cytotoxicity of nanoparticles, the suspended magnetite nanoparticles in liquid paraffin, doxorubicin and a mixture of both were added to the MDA-MB-468 cells in separate 15 ml tubes and left either in the RT or in the magnetic field for 30 min. Cell survival was measured by trypan blue exclusion assay and flow cytometer. Particle size distribution of the nanoparticles was homogeneous with a mean particles size of 10 nm. A 15°C temperature increase was achieved in presence of an AC magnetic field after 15 min irradiation. Results Biological results showed that magnetite nanoparticles alone were not cytotoxic at RT, while in the alternative magnetic filed more than 50% of cells were dead. Doxorubicin alone was not cytotoxic during 30 min, but in combination with magnetite more than 80% of the cells were killed. Conclusion It could be concluded that doxorubicin and magnetite nanoparticles in an AC magnetic field had combinatory effects against cells. PMID:23799178

  10. [Role of mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate) in the obtaining of stabilized magnetite nanoparticles for biomedical application].

    PubMed

    Vazhnichaya, Ye M; Mokliak, Ye V; Kurapov, Yu A; Zabozlaev, A A

    2015-01-01

    Magnetite nanoparticles (NPs) are studied as agents for magnetic resonance imaging, hyperthermia of malignant tumors, targeted drug delivery as well as anti-anemic action. One of the main problems of such NPs is their aggregation that requires creation of methods for magnetite NPs stabilization during preparation of liquid medicinal forms on their basis. The present work is devoted to the possibility of mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate) use for solubilization of magnetite NPs in hydrophilic medium. For this purpose, the condensate produced by electron-beam evaporation and condensation, with magnetite particles of size 5-8 nm deposited into the crystals of sodium chloride were used in conjunction with substance of mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate), and low molecular weight polyvinylpyrrolidone (PVP). The NP condensate was dispersed in distilled water or PVP or mexidol solutions. NPs size distribution in the liquid phase of the systems was determined by photon correlation spectroscopy, iron (Fe) concentration was evaluated by atomic emission spectrometry. It is shown that in the dispersion prepared in distilled water, the major amount of NPs was of 13-120 nm in size, in mexidol solution - 270-1700 nm, in PVP solution - 30-900 nm. In the fluid containing magnetite NPs together with mexidol and PVP, the main fraction (99.9%) was characterized by the NPs size of 14-75 nm with maximum of 25 nm. This system had the highest iron concentration: it was similar to that in the sample with mexidol solution and 6.6-7.3 times higher than the concentration in the samples with distilled water or PVP. Thus, in the preparation of aqueous dispersions based on magnetite NPs condensate, mexidol provides a transition of Fe to the liquid phase in amount necessary to achieve its biological activity, and PVP stabilizes such modified NPs. PMID:26215417

  11. Taking a hard line with biotemplating: cobalt-doped magnetite magnetic nanoparticle arrays

    NASA Astrophysics Data System (ADS)

    Bird, Scott M.; Galloway, Johanna M.; Rawlings, Andrea E.; Bramble, Jonathan P.; Staniland, Sarah S.

    2015-04-01

    Rapid advancements made in technology, and the drive towards miniaturisation, means that we require reliable, sustainable and cost effective methods of manufacturing a wide range of nanomaterials. In this bioinspired study, we take advantage of millions of years of evolution, and adapt a biomineralisation protein for surface patterning of biotemplated magnetic nanoparticles (MNPs). We employ soft-lithographic micro-contact printing to pattern a recombinant version of the biomineralisation protein Mms6 (derived from the magnetotactic bacterium Magnetospirillum magneticum AMB-1). The Mms6 attaches to gold surfaces via a cysteine residue introduced into the N-terminal region. The surface bound protein biotemplates highly uniform MNPs of magnetite onto patterned surfaces during an aqueous mineralisation reaction (with a mean diameter of 90 +/- 15 nm). The simple addition of 6% cobalt to the mineralisation reaction maintains the uniformity in grain size (with a mean diameter of 84 +/- 14 nm), and results in the production of MNPs with a much higher coercivity (increased from ~156 Oe to ~377 Oe). Biotemplating magnetic nanoparticles on patterned surfaces could form a novel, environmentally friendly route for the production of bit-patterned media, potentially the next generation of ultra-high density magnetic data storage devices. This is a simple method to fine-tune the magnetic hardness of the surface biotemplated MNPs, and could easily be adapted to biotemplate a wide range of different nanomaterials on surfaces to create a range of biologically templated devices.Rapid advancements made in technology, and the drive towards miniaturisation, means that we require reliable, sustainable and cost effective methods of manufacturing a wide range of nanomaterials. In this bioinspired study, we take advantage of millions of years of evolution, and adapt a biomineralisation protein for surface patterning of biotemplated magnetic nanoparticles (MNPs). We employ soft

  12. Determination of sulfonamides in soil samples based on alumina-coated magnetite nanoparticles as adsorbents.

    PubMed

    Sun, Lei; Sun, Xin; Du, Xiaobo; Yue, Yanshan; Chen, Ligang; Xu, Haoyan; Zeng, Qinglei; Wang, Hui; Ding, Lan

    2010-04-30

    In this study, alumina-coated magnetite nanoparticles (Fe(3)O(4)/Al(2)O(3) NPs) were synthesized, and they were applied to the analysis of sulfonamides (SAs) including sulfadiazine (SDZ), sulfamerazine (SMR), sulfamethoxazole (SMX), sulfamonomethoxine (SMM), sulfamethoxydiazine (SMD), sulfadimethoxine (SDM) and sulfaquinoxaline (SQX) in different soil samples based on magnetic solid-phase extraction (MSPE). The extraction and concentration process was carried out in a single step by mixing the extraction solvent, magnetic adsorbents and soil sample under ultrasonic action. Then, the adsorbents were isolated from the complicated matrix easily with an external magnetic field. The SAs desorbed from the adsorbents were determined by liquid chromatography-tandem mass spectrometry. Compared with traditional methods, the MSPE method simplified the operation procedure and reduced the analysis time. Under the optimum conditions, the recoveries of SDZ, SMR, SMX, SMM, SMD and SDM by analyzing the five spiked soil samples were between 71% and 93% except for SQX (42-60%). This may be due to the stronger hydrophobic property of SQX. Detection limits of SAs were between 0.37 and 6.74 ng g(-1). It was also found that the "aging" effect of SAs contaminated soil could cause the recoveries to decrease. PMID:20417329

  13. Hybrid optoacoustic and ultrasound biomicroscopy monitors’ laser-induced tissue modifications and magnetite nanoparticle impregnation

    NASA Astrophysics Data System (ADS)

    Estrada, Héctor; Sobol, Emil; Baum, Olga; Razansky, Daniel

    2014-12-01

    Tissue modification under laser radiation is emerging as one of the advanced applications of lasers in medicine, with treatments ranging from reshaping and regeneration of cartilage to normalization of the intraocular pressure. Laser-induced structural alterations can be studied using conventional microscopic techniques applied to thin specimen. Yet, development of non-invasive imaging methods for deep tissue monitoring of structural alterations under laser radiation is of great importance, especially for attaining efficient feedback during the procedures. We developed a fast scanning biomicroscopy system that can simultaneously deliver both optoacoustic and pulse-echo ultrasound contrast from intact tissues and show that both modalities allow manifesting the laser-induced changes in cartilage and sclera. Furthermore, images of the sclera samples reveal a crater developing around the center of the laser-irradiated spot as well as a certain degree of thickening within the treated zone, presumably due to pore formation. Finally, we were able to observe selective impregnation of magnetite nanoparticles into the cartilage, thus demonstrating a possible contrast enhancement approach for studying specific treatment effects. Overall, the new imaging approach holds promise for development of noninvasive feedback control systems that could guarantee efficacy and safety of laser-based medical procedures.

  14. Monodispersed magnetite nanoparticles optimized for magnetic fluid hyperthermia: Implications in biological systems

    NASA Astrophysics Data System (ADS)

    Khandhar, Amit P.; Ferguson, R. Matthew; Krishnan, Kannan M.

    2011-04-01

    Magnetite (Fe3O4) nanoparticles (MNPs) are suitable materials for Magnetic Fluid Hyperthermia (MFH), provided their size is carefully tailored to the applied alternating magnetic field (AMF) frequency. Since aqueous synthesis routes produce polydisperse MNPs that are not tailored for any specific AMF frequency, we have developed a comprehensive protocol for synthesizing highly monodispersed MNPs in organic solvents, specifically tailored for our field conditions (f = 376 kHz, H0 = 13.4 kA/m) and subsequently transferred them to water using a biocompatible amphiphilic polymer. These MNPs (σavg. = 0.175) show truly size-dependent heating rates, indicated by a sharp peak in the specific loss power (SLP, W/g Fe3O4) for 16 nm (diameter) particles. For broader size distributions (σavg. = 0.266), we observe a 30% drop in overall SLP. Furthermore, heating measurements in biological medium [Dulbecco's modified Eagle medium (DMEM) + 10% fetal bovine serum] show a significant drop for SLP (˜30% reduction in 16 nm MNPs). Dynamic Light Scattering (DLS) measurements show particle hydrodynamic size increases over time once dispersed in DMEM, indicating particle agglomeration. Since the effective magnetic relaxation time of MNPs is determined by fractional contribution of the Neel (independent of hydrodynamic size) and Brownian (dependent on hydrodynamic size) components, we conclude that agglomeration in biological medium modifies the Brownian contribution and thus the net heating capacity of MNPs.

  15. Efficient functionalization of magnetite nanoparticles with phosphonate using a one-step continuous hydrothermal process.

    PubMed

    Thomas, Guillaume; Demoisson, Frédéric; Boudon, Julien; Millot, Nadine

    2016-06-28

    For the first time, phosphonate-functionalized magnetite nanoparticles (Fe3O4 NPs) were synthesized using a one-step continuous hydrothermal process. The NP surface was modified using a hydrophilic organic molecule, namely 6-phosphonohexanoic acid (PHA). NPs were fully characterized (TEM, XRD, DLS, ζ-potential, TGA, FTIR, XPS and specific surface area measurements) in order to investigate PHA effect on size, oxidation state, anchoring and colloidal stability. PHA reduced the crystallite size and size distribution and improved greatly colloidal stability when compared with bare Fe3O4 NPs. Moreover, PHA was grafted on the NP surface according to three different conformations: as mononuclear monodendates, as binuclear bidentates or as lying-down complexes. This report is very promising regarding the stabilization and functionalization of Fe3O4 NPs by phosphonate molecules under continuous hydrothermal conditions. The post-grafting of polymers such as polyethylene glycol can be considered owing to the presence of free carboxyl groups (-COOH) on the surface of Fe3O4 NPs. PMID:27295502

  16. Superoxide mediated production of hydroxyl radicals by magnetite nanoparticles: demonstration in the degradation of 2-chlorobiphenyl.

    PubMed

    Fang, Guo-Dong; Zhou, Dong-Mei; Dionysiou, Dionysios D

    2013-04-15

    Increasing attention has been paid to magnetite nanoparticles (MNPs) due to their highly reductive reactivity toward environmental contaminants. However, there is little information related to the generation of reactive oxygen species (ROS) by MNPs, which in fact plays a vital role for the transformation of contaminants. In this paper, the degradation of 2-chlorobiphenyl (2-CB) by MNPs was investigated. The role of ROS generated by MNPs in this process was elucidated. The results demonstrated that hydroxyl radicals (OH) generated by MNPs at low pH could efficiently degrade 2-CB. The mechanism of the formation of OH by MNPs was divided into two steps: (i) the superoxide radical anion (O2(-)) mediated production of hydrogen peroxide (H2O2), and (ii) the reaction of formed H2O2 with Fe(II) dissolved from MNPs to produce OH through Fenton reaction. Comparison of the degradation products of 2-CB by MNPs with MNPs/ethanol and Fenton reagents further supported the involvement of OH in the degradation of 2-CB. The degradation efficiency of 2-CB by MNPs under acidic conditions was higher than that in alkaline solution. These findings provide a new insight into the understanding of reactivity of MNPs for the transformation of 2-CB and possibly other relevant environmental contaminants. PMID:23434481

  17. Remediation of mercury contaminated saltwater with functionalized silica coated magnetite nanoparticles.

    PubMed

    Mohmood, Iram; Lopes, Cláudia B; Lopes, Isabel; Tavares, Daniela S; Soares, Amadeu M V M; Duarte, Armando C; Trindade, Tito; Ahmad, Iqbal; Pereira, Eduarda

    2016-07-01

    The study aimed to evaluate the efficiency of dithiocarbamate functionalized silica coated magnetite nanoparticles (NPs) for Hg decontamination of saltwater either contaminated with Hg alone or with As and Cd. For this, the residual levels of Hg in seawater were assessed and Hg-contaminated or Hg+As+Cd-contaminated seawater toxicity to aquatic biota, before and after the sorption process, was compared. The results showed that under highly competitive conditions (water salts, Cd and As), the removal of Hg from seawater, by using these magnetic NPs, for the lowest concentration (50μg/L) was superior to 98% and for the highest concentration (500μg/L) ranged between 61% to 67%. Despite the great affinity of the magnetic NPs for Hg, they were not effective at removing As and Cd from seawater. In relation to the ecotoxicity endpoints after remediation, the mixture with lower Hg concentration exhibited no toxicity to rotifer Brachionus plicatilis and bacteria Vibrio fischeri ; however, the mixture with higher concentration revealed toxicity. In addition, the toxicity of bacteria V. fischeri, rotifer B. plicatilis and algae Phaeodactylum tricornutum, whose responses where inhibited during its exposure to the non-remediate sample was considerably reduced after treatment with NPs. Furthermore, microalgae P. tricornutum appears to be most sensitive species while Artemia franciscana showed no toxic effects to the tested solutions. Both chemical and ecotoxicological approaches revealed a high efficiency for the remediation of Hg-contaminated saltwater. PMID:27039062

  18. Mechanism of Arsenic Adsorption on Magnetite Nanoparticles from Water: Thermodynamic and Spectroscopic Studies.

    PubMed

    Liu, Cheng-Hua; Chuang, Ya-Hui; Chen, Tsan-Yao; Tian, Yuan; Li, Hui; Wang, Ming-Kuang; Zhang, Wei

    2015-07-01

    Removal of arsenic (As) from water supplies is needed to reduce As exposure through drinking water and food consumption in many regions of the world. Magnetite nanoparticles (MNPs) are promising and novel adsorbents for As removal because of their great adsorption capacity for As and easy separation. This study aimed to investigate the adsorption mechanism of arsenate, As(V), and arsenite, As(III), on MNPs by macroscopic adsorption experiments in combination with thermodynamic calculation and microspectroscopic characterization using synchrotron-radiation-based X-ray absorption spectroscopy (XAS) and X-ray photoelectron spectroscopy (XPS). Adsorption reactions are favorable endothermic processes as evidenced by increased adsorption with increasing temperatures, and high positive enthalpy change. EXAFS spectra suggested predominant formation of bidentate binuclear corner-sharing complexes ((2)C) for As(V), and tridentate hexanuclear corner-sharing ((3)C) complexes for As(III) on MNP surfaces. The macroscopic and microscopic data conclusively identified the formation of inner-sphere complexes between As and MNP surfaces. More intriguingly, XANES and XPS results revealed complex redox transformation of the adsorbed As on MNPs exposed to air: Concomitant with the oxidation of MNPs, the oxidation of As(III) and MNPs was expected, but the observed As(V) reduction was surprising because of the role played by the reactive Fe(II). PMID:26055623

  19. Influences of surface coating, UV irradiation and magnetic field on the algae removal using magnetite nanoparticles.

    PubMed

    Ge, Shijian; Agbakpe, Michael; Wu, Zhiyi; Kuang, Liyuan; Zhang, Wen; Wang, Xianqin

    2015-01-20

    Magnetophoretic separation is a promising and sustainable technology for rapid algal separation or removal from water. This work demonstrated the application of magnetic magnetite nanoparticles (MNPs) coated with a cationic polymer, polyethylenimine (PEI), toward the separation of Scenedesmus dimorphus from the medium broth. The influences of surface coating, UV irradiation, and magnetic field on the magnetophoretic separation were systematically examined. After PEI coating, zeta potential of MNPs shifted from −7.9 ± 2.0 to +39.0 ± 3.1 mV at a pH of 7.0, which improved MNPs-algae interaction and helped reduce the dose demand of MNPs (e.g., from 0.2 to 0.1 g·g(–1) while the harvesting efficiency (HE) of over 80% remained unchanged). The extended Derjaguin–Landau–Verwey–Overbeek theory predicted a strong attractive force between PEI-coated MNPs and algae, which supported the improved algal harvesting. Moreover, the HE was greater under the UV365 irradiation than that under the UV254, and increased with the irradiation intensity. Continuous application of the external magnetic field at high strength remarkably improved the algal harvesting. Finally, the reuse of MNPs for multiple cycles of algal harvesting was studied, which aimed at increasing the sustainability and lowering the cost. PMID:25486124

  20. Phosphate removal and recovery from water using nanocomposite of immobilized magnetite nanoparticles on cationic polymer.

    PubMed

    Abo Markeb, Ahmad; Alonso, Amanda; Dorado, Antonio David; Sánchez, Antoni; Font, Xavier

    2016-08-01

    A novel nanocomposite (NC) based on magnetite nanoparticles (Fe3O4-NPs) immobilized on the surface of a cationic exchange polymer, C100, using a modification of the co-precipitation method was developed to obtain magnetic NCs for phosphate removal and recovery from water. High-resolution transmission electron microscopy-energy-dispersive spectroscopy, scanning electron microscopy , X-ray diffraction, and inductively coupled plasma optical emission spectrometry were used to characterize the NCs. Continuous adsorption process by the so-called breakthrough curves was used to determine the adsorption capacity of the Fe3O4-based NC. The adsorption capacity conditions were studied under different conditions (pH, phosphate concentration, and concentration of nanoparticles). The optimum concentration of iron in the NC for phosphate removal was 23.59 mgFe/gNC. The sorption isotherms of this material were performed at pH 5 and 7. Taking into account the real application of this novel material in real water, the experiments were performed at pH 7, achieving an adsorption capacity higher than 4.9 mgPO4-P/gNC. Moreover, Freundlich, Langmuir, and a combination of them fit the experimental data and were used for interpreting the influence of pH on the sorption and the adsorption mechanism for this novel material. Furthermore, regeneration and reusability of the NC were tested, obtaining 97.5% recovery of phosphate for the first cycle, and at least seven cycles of adsorption-desorption were carried out with more than 40% of recovery. Thus, this work described a novel magnetic nanoadsorbent with properties for phosphate recovery in wastewater. PMID:26849360

  1. Novel magnetite nanoparticle based on BODIPY as fluorescent hybrid material for Ag(I) detection in aqueous medium.

    PubMed

    Kursunlu, Ahmed Nuri; Ozmen, Mustafa; Guler, Ersin

    2016-06-01

    This manuscript describes a highly selective and ultra-sensitive detection of Ag(I) in aqueous solution using amine coated magnetite nanoparticles modified boron-dipyrromethene by spectrofluorometer. Fe3O4 nanoparticles were synthesized by co-precipitation of Fe(2+)and Fe(3+)in an ammonia solution. Amine modified Fe3O4 was prepared by using (3-aminopropyl)triethoxysilane as silanization agent. The covalent binding of boron-dipyrromethene to amine modified Fe3O4 was confirmed by means of Fourier Transform infrared spectroscopy, transmission electron microscopy, dynamic light scattering, UV-vis and fluorimeter measurements and obtained nanoparticle-boron dipyrromethene structure. The binding abilities of nanoparticle-boron dipyrromethene towards different metal ions have been investigated by some spectroscopic methods as UV-vis, fluorescence spectroscopy, Job plot, etc. and the novel surface displayed high selectivity and sensitivity for Ag(I) among all tested metals. PMID:27130108

  2. Influence of aqueous environment on agglomeration and dissolution of thiol-functionalised mesoporous silica-coated magnetite nanoparticles.

    PubMed

    Hakami, Othman; Zhang, Yue; Banks, Charles J

    2015-03-01

    The purpose of the present research work is to investigate the stability and dissolution of magnetite (Fe3O4) nanoparticles (NPs) and thiol-functionalised mesoporous silica-coated magnetite NPs (TF-SCMNPs). The state of NPs in an aqueous environment was investigated under different pH conditions. Changes in the NPs' mean diameter due to aggregation were measured over a specific time. The effects of contact time and pH on the dissolution of NPs were also investigated. In order to avoid possible aggregation, Fe3O4 NPs were coated with silica and functionalised further with thiol organic groups. These methods imparted excellent stability to magnetite NPs in an aqueous medium over a wide range of pH values with reasonable hydrodynamic size. The organic group bound magnetite NPs allowed these particles to circulate over a long time in the aqueous system, and particle aggregation and sedimentation did not occur. The trend of decreasing zeta potential was observed after grafting thiol onto the surface of the SCMNPs. The results also revealed that silica exhibited a noteworthy efficient in eliminating the pH dependence and enhancing the NP stability of SCMNPs and SH-SCMNPs in aqueous medium. On the other hand, the dissolution of Fe3O4 NPs was found to be detrimental at pH 2.0 and 4.0 or had a long contact time. PMID:24898295

  3. The intrinsic antimicrobial activity of citric acid-coated manganese ferrite nanoparticles is enhanced after conjugation with the antifungal peptide Cm-p5.

    PubMed

    Lopez-Abarrategui, Carlos; Figueroa-Espi, Viviana; Lugo-Alvarez, Maria B; Pereira, Caroline D; Garay, Hilda; Barbosa, João Arg; Falcão, Rosana; Jiménez-Hernández, Linnavel; Estévez-Hernández, Osvaldo; Reguera, Edilso; Franco, Octavio L; Dias, Simoni C; Otero-Gonzalez, Anselmo J

    2016-01-01

    Diseases caused by bacterial and fungal pathogens are among the major health problems in the world. Newer antimicrobial therapies based on novel molecules urgently need to be developed, and this includes the antimicrobial peptides. In spite of the potential of antimicrobial peptides, very few of them were able to be successfully developed into therapeutics. The major problems they present are molecule stability, toxicity in host cells, and production costs. A novel strategy to overcome these obstacles is conjugation to nanomaterial preparations. The antimicrobial activity of different types of nanoparticles has been previously demonstrated. Specifically, magnetic nanoparticles have been widely studied in biomedicine due to their physicochemical properties. The citric acid-modified manganese ferrite nanoparticles used in this study were characterized by high-resolution transmission electron microscopy, which confirmed the formation of nanocrystals of approximately 5 nm diameter. These nanoparticles were able to inhibit Candida albicans growth in vitro. The minimal inhibitory concentration was 250 µg/mL. However, the nanoparticles were not capable of inhibiting Gram-negative bacteria (Escherichia coli) or Gram-positive bacteria (Staphylococcus aureus). Finally, an antifungal peptide (Cm-p5) from the sea animal Cenchritis muricatus (Gastropoda: Littorinidae) was conjugated to the modified manganese ferrite nanoparticles. The antifungal activity of the conjugated nanoparticles was higher than their bulk counterparts, showing a minimal inhibitory concentration of 100 µg/mL. This conjugate proved to be nontoxic to a macrophage cell line at concentrations that showed antimicrobial activity. PMID:27563243

  4. The intrinsic antimicrobial activity of citric acid-coated manganese ferrite nanoparticles is enhanced after conjugation with the antifungal peptide Cm-p5

    PubMed Central

    Lopez-Abarrategui, Carlos; Figueroa-Espi, Viviana; Lugo-Alvarez, Maria B; Pereira, Caroline D; Garay, Hilda; Barbosa, João ARG; Falcão, Rosana; Jiménez-Hernández, Linnavel; Estévez-Hernández, Osvaldo; Reguera, Edilso; Franco, Octavio L; Dias, Simoni C; Otero-Gonzalez, Anselmo J

    2016-01-01

    Diseases caused by bacterial and fungal pathogens are among the major health problems in the world. Newer antimicrobial therapies based on novel molecules urgently need to be developed, and this includes the antimicrobial peptides. In spite of the potential of antimicrobial peptides, very few of them were able to be successfully developed into therapeutics. The major problems they present are molecule stability, toxicity in host cells, and production costs. A novel strategy to overcome these obstacles is conjugation to nanomaterial preparations. The antimicrobial activity of different types of nanoparticles has been previously demonstrated. Specifically, magnetic nanoparticles have been widely studied in biomedicine due to their physicochemical properties. The citric acid-modified manganese ferrite nanoparticles used in this study were characterized by high-resolution transmission electron microscopy, which confirmed the formation of nanocrystals of approximately 5 nm diameter. These nanoparticles were able to inhibit Candida albicans growth in vitro. The minimal inhibitory concentration was 250 µg/mL. However, the nanoparticles were not capable of inhibiting Gram-negative bacteria (Escherichia coli) or Gram-positive bacteria (Staphylococcus aureus). Finally, an antifungal peptide (Cm-p5) from the sea animal Cenchritis muricatus (Gastropoda: Littorinidae) was conjugated to the modified manganese ferrite nanoparticles. The antifungal activity of the conjugated nanoparticles was higher than their bulk counterparts, showing a minimal inhibitory concentration of 100 µg/mL. This conjugate proved to be nontoxic to a macrophage cell line at concentrations that showed antimicrobial activity. PMID:27563243

  5. Quasi-Cubic Magnetite/Silica Core-Shell Nanoparticles as Enhanced MRI Contrast Agents for Cancer Imaging

    PubMed Central

    Cowell, Simon F.; Garg, Ashish; Eu, Peter; Bhargava, Suresh K.; Bansal, Vipul

    2011-01-01

    Development of magnetic resonance imaging (MRI) contrast agents that can be readily applied for imaging of biological tissues under clinical settings is a challenging task. This is predominantly due to the expectation of an ideal MR agent being able to be synthesized in large quantities, possessing longer shelf life, reasonable biocompatibility, tolerance against its aggregation in biological fluids, and high relaxivity, resulting in better contrast during biological imaging. Although a repertoire of reports address various aforementioned issues, the previously reported results are far from optimal, which necessitates further efforts in this area. In this study, we demonstrate facile large-scale synthesis of sub-100 nm quasi-cubic magnetite and magnetite/silica core-shell (Mag@SiO2) nanoparticles and their applicability as a biocompatible T2 contrast agent for MRI of biological tissues. Our study suggests that silica-coated magnetite nanoparticles reported in this study can potentially act as improved MR contrast agents by addressing a number of aforementioned issues, including longer shelf life and stability in biological fluids. Additionally, our in vitro and in vivo studies clearly demonstrate the importance of silica coating towards improved applicability of T2 contrast agents for cancer imaging. PMID:21747962

  6. Particle size and magnetic properties dependence on growth temperature for rapid mixed co-precipitated magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Fang, Mei; Ström, Valter; Olsson, Richard T.; Belova, Lyubov; Rao, K. V.

    2012-04-01

    Magnetite nanoparticles have been prepared by co-precipitation using a custom-designed jet mixer to achieve rapid mixing (RM) of reactants in a timescale of milliseconds. The quick and stable nucleation obtained allows control of the particle size and size distribution via a more defined growth process. Nanoparticles of different sizes were prepared by controlling the processing temperature in the first few seconds post-mixing. The average size of the nanoparticles investigated using a Tecnai transmission electron microscope is found to increase with the temperature from 3.8 nm at 1 ± 1 °C to 10.9 nm for particles grown at 95 ± 1 °C. The temperature dependence of the size distribution follows the same trend and is explained in terms of Ostwald ripening of the magnetite nanoparticles during the co-precipitation of Fe2+ and Fe3+. The magnetic properties were studied by monitoring the blocking temperature via both DC and AC techniques. Strikingly, the obtained RM particles maintain the high magnetization (as high as ˜88 A m2 kg-1 at 500 kA m-1) while the coercivity is as low as ˜12 A m-1 with the expected temperature dependence. Besides, by adding a drop of tetramethylammonium hydroxide, aqueous ferrofluids with long term stability are obtained, suggesting their suitability for applications in ferrofluid technology and biomedicine.

  7. Anisotropy of Bullet-Shaped Magnetite Nanoparticles in the Magnetotactic Bacteria Desulfovibrio magneticus sp. Strain RS-1

    PubMed Central

    Chariaou, Michalis; Rahn-Lee, Lilah; Kind, Jessica; García-Rubio, Inés; Komeili, Arash; Gehring, Andreas U.

    2015-01-01

    Magnetotactic bacteria (MTB) build magnetic nanoparticles in chain configuration to generate a permanent dipole in their cells as a tool to sense the Earth’s magnetic field for navigation toward favorable habitats. The majority of known MTB align their nanoparticles along the magnetic easy axes so that the directions of the uniaxial symmetry and of the magnetocrystalline anisotropy coincide. Desulfovibrio magneticus sp. strain RS-1 forms bullet-shaped magnetite nanoparticles aligned along their (100) magnetocrystalline hard axis, a configuration energetically unfavorable for formation of strong dipoles. We used ferromagnetic resonance spectroscopy to quantitatively determine the magnetocrystalline and uniaxial anisotropy fields of the magnetic assemblies as indicators for a cellular dipole with stable direction in strain RS-1. Experimental and simulated ferromagnetic resonance spectral data indicate that the negative effect of the configuration is balanced by the bullet-shaped morphology of the nanoparticles, which generates a pronounced uniaxial anisotropy field in each magnetosome. The quantitative comparison with anisotropy fields of Magnetospirillum gryphiswaldense, a model MTB with equidimensional magnetite particles aligned along their (111) magnetic easy axes in well-organized chain assemblies, shows that the effectiveness of the dipole is similar to that in RS-1. From a physical perspective, this could be a reason for the persistency of bullet-shaped magnetosomes during the evolutionary development of magnetotaxis in MTB. PMID:25762338

  8. Particle size and magnetic properties dependence on growth temperature for rapid mixed co-precipitated magnetite nanoparticles.

    PubMed

    Fang, Mei; Ström, Valter; Olsson, Richard T; Belova, Lyubov; Rao, K V

    2012-04-13

    Magnetite nanoparticles have been prepared by co-precipitation using a custom-designed jet mixer to achieve rapid mixing (RM) of reactants in a timescale of milliseconds. The quick and stable nucleation obtained allows control of the particle size and size distribution via a more defined growth process. Nanoparticles of different sizes were prepared by controlling the processing temperature in the first few seconds post-mixing. The average size of the nanoparticles investigated using a Tecnai transmission electron microscope is found to increase with the temperature from 3.8 nm at 1 ± 1 °C to 10.9 nm for particles grown at 95 ± 1 °C. The temperature dependence of the size distribution follows the same trend and is explained in terms of Ostwald ripening of the magnetite nanoparticles during the co-precipitation of Fe(2+) and Fe(3+). The magnetic properties were studied by monitoring the blocking temperature via both DC and AC techniques. Strikingly, the obtained RM particles maintain the high magnetization (as high as ∼88 A m(2) kg(-1) at 500 kA m(-1)) while the coercivity is as low as ∼12 A m(-1) with the expected temperature dependence. Besides, by adding a drop of tetramethylammonium hydroxide, aqueous ferrofluids with long term stability are obtained, suggesting their suitability for applications in ferrofluid technology and biomedicine. PMID:22433909

  9. Multi-stage freezing of HEUR polymer networks with magnetite nanoparticles.

    PubMed

    Campanella, A; Holderer, O; Raftopoulos, K N; Papadakis, C M; Staropoli, M P; Appavou, M S; Müller-Buschbaum, P; Frielinghaus, H

    2016-04-01

    We observe a change in the segmental dynamics of hydrogels based on hydrophobically modified ethoxylated urethanes (HEUR) when hydrophobic magnetite nanoparticles (MNPs) are embedded in the hydrogels. The dynamics of the nanocomposite hydrogels is investigated using dielectric relaxation spectroscopy (DRS) and neutron spin echo (NSE) spectroscopy. The magnetic nanoparticles within the hydrophobic domains of the HEUR polymer network increase the size of these domains and their distance. The size increase leads to a dilution of the polymers close to the hydrophobic domain, allowing higher mobility of the smallest polymer blobs close to the "center". This is reflected in the decrease of the activation energy of the β-process detected in the DRS data. The increase in distance leads to an increase of the size of the largest hydrophilic polymer blobs. Therefore, the segmental dynamics of the largest blobs is slowed down. At short time scales, i.e. 10(-9) s < τ < 10(-3) s, the suppression of the segmental dynamics is reflected in the α-relaxation processes detected in the DRS data and in the decrease of the relaxation rate Γ of the segmental motion in the NSE data with increasing concentration of magnetic nanoparticles. The stepwise (multi-stage) freezing of the small blobs is only visible for the pure hydrogel at low temperatures. On the other hand, the glass transition temperature (Tg) decreases upon increasing the MNP loading, indicating an acceleration of the segmental dynamics at long time scales (τ∼ 100 s). Therefore, it would be possible to tune the Tg of the hydrogels by varying the MNP concentration. The contribution of the static inhomogeneities to the total scattering function Sst(q) is extracted from the NSE data, revealing a more ordered gel structure than the one giving rise to the total scattering function S(q), with a relaxed correlation length ξNSE = (43 ± 5) Å which is larger than the fluctuating correlation length from a static investigation

  10. Synthesis of lithium iron phosphate/carbon microspheres by using polyacrylic acid coated iron phosphate nanoparticles derived from iron(III) acrylate.

    PubMed

    Xu, Dongwei; He, Yan-Bing; Chu, Xiaodong; Ding, Zhaojun; Li, Baohua; He, Jianfu; Du, Hongda; Qin, Xianying; Kang, Feiyu

    2015-03-01

    Lithium iron phosphate/carbon (LiFePO4 /C) microspheres with high rate and cycling performance are synthesized from iron phosphate/polyacrylic acid (FePO4 /PAA) nanoparticles. Iron(III) acrylate is used as a precursor for both the iron and carbon sources. FePO4 nanoparticles are first produced by a coprecipitation reaction. The byproduct, acrylic acid ions, is polymerized in situ to form a uniform PAA layer on the surface of the FePO4 nanoparticles. The as-prepared LiFePO4 /C microspheres are composed of primary nanoparticles with sizes of 40-50 nm. The nanoparticles are fully coated with a thin, uniform carbon layer derived from the decomposition of the PAA layer. The uniform carbon-coating layer cooperates with interstitial and boundary carbon derived from sucrose successfully to construct an excellent interconnecting conductive network in the microspheres. As a result of the unique structure, the as-prepared LiFePO4 /C microspheres display both high electronic and ionic conductivities, which contribute to their high rate performance (162.9 mAh g(-1) at 0.1C and 126.1 mAh g(-1) at 5C) and excellent cycling stability (97.1% of capacity retention after 500 cycles at 5C/5C). PMID:25469674

  11. One pot synthesis of water-dispersible dehydroascorbic acid coated Fe3O4 nanoparticles under atmospheric air: blood cell compatibility and enhanced magnetic resonance imaging.

    PubMed

    Gupta, Hariom; Paul, P; Kumar, Naresh; Baxi, Seema; Das, Dipti P

    2014-09-15

    Water dispersible and biologically important molecule dehydroascorbic acid (DHA, capable to cross the blood brain barrier) coated Fe3O4 superparamagnetic nanoparticles having an average size of ∼6 nm were synthesized through one pot aqueous coprecipitation method under atmospheric air. An antioxidant ascorbic acid (AA) used in the synthesis oxidized itself to dehydroascorbic acid (DHA) to consume dissolved or available oxygen in reaction mixture which died away the oxidative impact of atmospheric air and formed DHA encapsulated the Fe3O4 nanoparticles which stabilized the Fe3O4 nanoparticles and significantly enhanced their colloidal solubility in water. Fe3O4 phase, superparamagnetic property, DHA coating and stable colloidal solubility in water were confirmed by means of XPS, VSM, IR and zeta potential analysis respectively. T1, T2 and T2(∗) weighted magnetic resonance imaging (MRI) and corresponding relaxivity (r1=0.416, r2=50.28 and r2(∗)=123.65 mM(-1) and r2/r1=120.86, r2(∗)r1=297.23) of colloidally dispersed DHA-coated nanoparticle water phantom revealed a strong contrast enhancement in T2 and T2(∗) weighted images. The compatibility of DHA-coated Fe3O4 nanoparticles toward human blood cells was examined by means of cell counting and cell morphological analysis with the use of optical microscope and scanning electron microscope imaging. PMID:24956575

  12. Phase stabilization of magnetite (Fe3O4) nanoparticles with B2O3 addition: A significant enhancement on the phase transition temperature

    NASA Astrophysics Data System (ADS)

    Topal, Uğur; Aksan, Mehmet Ali

    2016-05-01

    Magnetite nanoparticles (MNPs) are extensively investigated for biomedical applications, particularly as contrast agents for Magnetic Resonance Imaging and as drug delivery agent and heat mediators for cancer therapy. Tuning the magnetic properties of the magnetite nanoparticles with doping of foreign atoms has a crucial importance for determining the application areas of these materials and so attracts much interests. On the other hand the doping with foreign atoms requires high temperature annealing, and it causes a phase transition to the hematite phase above 400 °C. In this work the phase transition temperature from the magnetite to the hematite phase has been increased by 200 °C, which is the highest enhancement reported in literature. It was achieved by addition of the appropriate amounts of B2O3. Our experiments indicates that the 5.0 wt% of B2O3 addition stabilizes and keeps the existence of single phase magnetite up to 600 °C.

  13. Immobilization of Thiadiazole Derivatives on Magnetite Mesoporous Silica Shell Nanoparticles in Application to Heavy Metal Removal from Biological Samples

    SciTech Connect

    Emadi, Masoomeh; Shams, Esmaeil

    2010-12-02

    In this report magnetite was synthesized by a coprecipitation method, then coated with a layer of silica. Another layer of mesoporous silica was added by a sol-gel method, then 5-amino-1,3,4-thiadiazole-thiol (ATT) was immobilized onto the synthesized nanoparticles with a simple procedure. This was followed by a series of characterizations, including transmission electron microscopy (TEM), FT-IR spectrum, elemental analysis and XRD. Heavy metal uptake of the modified nanoparticles was examined by atomic absorption spectroscopy. For further investigation we chose Cu{sup 2+} as the preferred heavy metal to evaluate the amount of adsorption, as well as the kinetics and mechanism of adsorption. Finally, the capacity of our nanoparticles for the heavy metal removal from blood was shown. We found that the kinetic rate of Cu{sup 2+} adsorption was 0.05 g/mg/min, and the best binding model was the Freundlich isotherm.

  14. Structural and magnetic study of zinc-doped magnetite nanoparticles and ferrofluids for hyperthermia applications

    NASA Astrophysics Data System (ADS)

    Mendoza Zélis, P.; Pasquevich, G. A.; Stewart, S. J.; Fernández van Raap, M. B.; Aphesteguy, J.; Bruvera, I. J.; Laborde, C.; Pianciola, B.; Jacobo, S.; Sánchez, F. H.

    2013-03-01

    Cubic-like shaped ZnxFe3-xO4 particles with crystallite mean sizes D between 15 and 117 nm were obtained by co-precipitation. Particle size effects and preferential occupation of spinel tetrahedral site by Zn2+ ions led to noticeable changes of physical properties. D ⩾ 30 nm particles displayed nearly bulk properties, which were dominated by Zn concentration. For D ⩽ 30 nm, dominant magnetic relaxation effects were observed by Mössbauer spectroscopy, with the mean blocking size DB ˜ 13 to 15 nm. Saturation magnetization increased with x up to x ˜ 0.1-0.3 and decreased for larger x. Power absorbed by water and chitosan-based ferrofluids from a 260 kHz radio frequency field was measured as a function of x, field amplitude H0 and ferrofluid concentration. For H0 = 41 kA m-1 the maximum specific absorption rate was 367 W g-1 for D = 16 nm and x = 0.1. Absorption results are interpreted within the framework of the linear response theory for H0 ⩽ 41 kA m-1. A departure towards a saturation regime was observed for higher fields. Simulations based on a two-level description of nanoparticle magnetic moment relaxation qualitatively agree with these observations. The frequency factor of the susceptibility dissipative component, derived from experimental results, showed a sharp maximum at D ˜ 16 nm. This behaviour was satisfactorily described by simulations based on moment relaxation processes, which furthermore indicated a crossover from Néel to Brown mechanisms at D ˜ 18 nm. Hints for further improvement of magnetite particles as nanocalefactors for magnetic hyperthermia are discussed.

  15. Magneto-electro-responsive material based on magnetite nanoparticles/polyurethane composites.

    PubMed

    Petcharoen, Karat; Sirivat, Anuvat

    2016-04-01

    Multi-functional materials in actuator applications have been developed toward reversibility and sensitivity under various actuating fields. In this work, magneto-electro-responsive materials consisting of a polyurethane (PU) matrix and its composites embedded with magnetite nanoparticles (MNP) as a dispersed phase were fabricated to tailor the electromechanical properties and bending performance under electric, magnetic, and electromagnetic fields. Due to the superior characteristics of MNP over other magnetic materials, the composites fabricated with electronic polarization were highly responsive under electric field. The highest storage modulus sensitivity belonged to the 1.0% v/v MNP/PU composite which possessed the value of 3.46 at the electric field 2 kV mm(-1). Moreover, all of the PU composites behaved as an electrostrictive material in which the stress depended quadratically on the electric field. It was demonstrated that the PU composites also possessed very good recoverability, fast response (<15s) and large bending angle relative to that of pristine PU under applied electric field. Interestingly, the steady state storage modulus response was attained within the first electrical actuation cycle and the PU composite was a fully reversible material. In addition, it was shown that superparamagnetism was a common characteristic of all fabricated composites under magnetic field. The 3.0%v/v MNP/PU composite provided the largest bending distance up to 23.60mm, and 14.10mm under the magnetic field of 5000 G, and the electromagnetic field of 320 G, respectively. In summary, the MNP/PU composite material is a potential candidate to be used as a smart material under the influences of electric and/or magnetic fields over other existing dielectric materials. PMID:26838855

  16. Highly Efficient Arsenic Removal Using a Composite of Ultrafine Magnetite Nanoparticles Interlinked by Silane Coupling Agents

    PubMed Central

    Chang, Shu-Chi; Yu, Yu-Han; Li, Cheng-Hao; Wu, Chin-Ching; Lei, Hao-Yun

    2012-01-01

    Arsenic (As) contamination in groundwater is a great environmental health concern and is often the result of contact between groundwater and arsenic-containing rocks or sediments and from variation of pH and redox potentials in the subsurface. In the past decade, magnetite nanoparticles (MNPs) have been shown to have high adsorption activity towards As. Alerted by the reported cytotoxicity of 5–12 nm MNP, we studied the adsorption behavior of 1.15 nm MNP and a MNP composite (MNPC), MNPs interlinked by silane coupling agents. With an initial concentration of As at 25 mg L−1, MNPs exhibited high adsorption capacity for As(V) and As (III), 206.9 mg·g−1 and 168.6 mg·g−1 under anaerobic conditions, respectively, and 109.9 mg·g−1 and 108.6 mg·g−1 under aerobic conditions, respectively. Under aerobic conditions, MNPC achieved even higher adsorption capacity than MNP, 165.1 mg·g−1 on As(V) and 157.9 mg·g−1 on As(III). For As(V) at 50 mg L−1, MNPC achieved an adsorption capacity as high as 341.8 mg·g−1, the highest in the literature. A kinetic study indicated that this adsorption reaction can reach equilibrium within 15 min and the rate constant of As(V) is about 1.9 times higher than that of As(III). These results suggested that MNPC can serve as a highly effective adsorbent for fast removal of As. PMID:23202769

  17. Optimization of polymeric dispersant concentration for the dispersion-stability of magnetite nanoparticles in water solution.

    PubMed

    Song, Geun-Dong; Kim, Mun-Hwan; Maeng, Wan-Young

    2014-12-01

    Fouling of various Fe oxide particulates on heat transfer tubes in the coolant of the secondary system of a nuclear power plant has been known to reduce the heat transfer performance and degrade the integrity of system components. Thus, in order to mitigate such a fouling problem, an addition of polymeric dispersant has been proposed to remove the oxide partculates. In this paper, experimental studies was conducted for evaluating the effect of polymeric dispersants (PAA: Polyacrylic acid, PMA: Polymethacrylic acid, PAAMA: Polymaleic acid-co-acrylic acid) on the dispersion stability of magnetite nanoparticles (MNPs, Fe3O4) for the reduction of fouling and corrosion of carbon steel by the settling test, the transmittance, zeta-potential, and particle size measurements, and the electrochemical corrosion tests. It was observed that the critical concentration for maximizing the dispersionstability of MNPs was in the range of concentration ratio (dispersant/MNPs) of 0.1 to 0.01 and the dispersion-stability of MNPs was not improved when the dispersant concentration is above this critical value. This non-linearity above a critical dispersant concentration may be explained by the agglomerations between MNPs. While there is no significant increase of corrosion rate with an addition of up to 10 ppm PAA, the addition of 100 ppm PAA increases the growth rate of oxide layer rapidly and deteriorates the formation of protective oxide on carbon steel. It is thus reasonably stated that the optimization of polymeric dispersants variables and its impacts on the corrosion of structural materials is necessary for the best application at plants. PMID:25971094

  18. High temperature phase transformation studies in magnetite nanoparticles doped with Co2+ ion

    NASA Astrophysics Data System (ADS)

    Pati, S. S.; Gopinath, S.; Panneerselvam, G.; Antony, M. P.; Philip, John

    2012-09-01

    We investigate the effect of Co2+ ion doping in magnetite (Fe3O4) on its crystal structure, magnetic properties, and phase stability during air and vacuum annealing. The nanoparticles are prepared by co-precipitation method and the particles are characterized by XRD, small angle x-ray scattering (SAXS), themogravimetric and differential scanning calorimetry (DSC), and vibrating sample magnetometer. The SAXS analysis on the doped samples show the most probable size, shape, and the polydispersity of particles, synthesized with different fractions (0-0.6) of Co2+ ion doping remains almost the same. On increasing cobalt content ferrimagnetic to the antiferromagnetic hematite (α-Fe2O3) phase transformation temperature is found to increase dramatically. For 0.1 fraction of Co2+ metal ion doping, an enhancement of 100 °C in the γ-Fe2O3 to α-Fe2O3 phase transition temperature is observed in the air annealed samples, whereas magnetic nature remains stable up to 1000 °C in vacuum annealed samples. On increasing the cobalt fractions beyond 0.2, air annealed samples show no change in the phase transition temperature. The observed enhancement in the phase transition temperature is attributed to the increased activation energy for phase transformation in presence of Co2+. Further, the DSC results corroborate the finding of an increase in the maghemite to hematite phase transition temperature with increase in cobalt fraction (x). The decrease in enthalpy from 89.86 to 17.62 J g-1 with an increase in cobalt content indicates that the degree of conversion of maghemite to hematite decreases with the cobalt content, which is in good agreement with the Rietveld analysis. The decrease in the Ms value in air annealed sample is attributed to the re-distribution of cations in the tetrahedral and octahedral sites, as the Fe3+A-Fe3+B super-exchange interaction is different from the Co2+A-Fe3+B interaction. These results suggest that a very small percentage of Co2+ metal ion doping can

  19. Docetaxel loaded oleic acid-coated hydroxyapatite nanoparticles enhance the docetaxel-induced apoptosis through activation of caspase-2 in androgen independent prostate cancer cells.

    PubMed

    Luo, Yun; Ling, You; Guo, Wusheng; Pang, Jun; Liu, Weipeng; Fang, Youqiang; Wen, Xinqiao; Wei, Kun; Gao, Xin

    2010-10-15

    Docetaxel (Dtxl) remains the preferred choice of improving the survival of patients with hormone refractory prostate cancer (HRPC), but many patients suffer from modest drug response and significant toxicity. In the present study, we investigated the efficiency of novel Dtxl loaded-[1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-carboxy(polyethylene glycol)]2000 (DSPE-PEG-COOH) stabilized-oleic acid (OA) coated hydroxyapatite (HA) nanoparticles (Dtxl-NPs) and gained insights into the molecular mechanism of the apoptosis induced by these novel Dtxl-loaded nanoparticles. The drug encapsulation efficiency of Dtxl was 83.6% and the sustained drug release was observed over 30days. The Dtxl-NPs exhibited significantly more cytotoxicity in both prostate cancer cell lines (PC3 and DU145) compared with Dtxl in vitro and increased the Dtxl-induced apoptosis in the PC3 cells. Cell cycle analysis showed that the PC3 cells treated with Dtxl-NPs exhibited significant arrest in the G2-M phase but a higher sub-G(0)/G(1) population when compared with Dtxl. The enhanced apoptosis induced by Dtxl-NPs in the PC3 cells was associated with the changes in mitochondrial membrane potential (MMP) and seemed to involve the activation of caspase-2. The kinetic studies of caspases demonstrated an early activation of caspase-2 in Dtxl-NPs-induced apoptosis in PC3 cells, which differs from Dtxl-induced apoptosis. The inhibition of caspase-2 activation by small interfering RNA (siRNA) knockdown resulted in the significant inhibition of Dtxl-NPs-induced disruption of MMP and Dtxl-NPs-induced apoptosis, indicating that the activation of caspase-2 was the critical event before the mitochondrial depolarization in the PC3 cells. Our findings showed that nanoparticles, more than simple drug carriers, may play an active role in mediating the biological effects. PMID:20655966

  20. High-Temperature Magnetism as a Probe for Structural and Compositional Uniformity in Ligand-Capped Magnetite Nanoparticles

    PubMed Central

    2015-01-01

    To investigate magnetostructural relationships in colloidal magnetite (Fe3O4) nanoparticles (NPs) at high temperature (300–900 K), we measured the temperature dependence of magnetization (M) of oleate-capped magnetite NPs ca. 20 nm in size. Magnetometry revealed an unusual irreversible high-temperature dependence of M for these NPs, with dip and loop features observed during heating–cooling cycles. Detailed characterizations of as-synthesized and annealed Fe3O4 NPs as well as reference ligand-free Fe3O4 NPs indicate that both types of features in M(T) are related to thermal decomposition of the capping ligands. The ligand decomposition upon the initial heating induces a reduction of Fe3+ to Fe2+ and the associated dip in M, leading to more structurally and compositionally uniform magnetite NPs. Having lost the protective ligands, the NPs continually sinter during subsequent heating cycles, resulting in divergent M curves featuring loops. The increase in M with sintering proceeds not only through elimination of a magnetically dead layer on the particle surface, as a result of a decrease in specific surface area with increasing size, but also through an uncommonly invoked effect resulting from a significant change in Fe3+/Fe2+ ratio with heat treatment. The interpretation of irreversible features in M(T) indicates that reversible M(T) behavior, conversely, can be expected only for ligand-free, structurally and compositionally uniform magnetite NPs, suggesting a general applicability of high-temperature M(T) measurements as an analytical method for probing the structure and composition of magnetic nanomaterials. PMID:25506407

  1. Fine tuning of magnetite nanoparticle size distribution using dissymmetric potential pulses in the presence of biocompatible surfactants and the electrochemical characterization of the nanoparticles.

    PubMed

    Rodríguez-López, A; Cruz-Rivera, J J; Elías-Alfaro, C G; Betancourt, I; Ruiz-Silva, H; Antaño-López, R

    2015-01-01

    The effects of varying the surfactant concentration and the anodic pulse potential on the properties and electrochemical behaviors of magnetite nanoparticles were investigated. The nanoparticles were synthesized with an electrochemical method based on applying dissymmetric potential pulses, which offers the advantage that can be used to tune the particle size distribution very precisely in the range of 10 to 50 nm. Under the conditions studied, the surfactant concentration directly affects the size distribution, with higher concentrations producing narrower distributions. Linear voltammetry was used to characterize the electrochemical behavior of the synthesized nanoparticles in both the anodic and cathodic regions, which are attributed to the oxidation of Fe(2+) and the reduction of Fe(3+); these species are part of the spinel structure of magnetite. Electrochemical impedance spectroscopy data indicated that the reduction and oxidation reactions of the nanoparticles are not controlled by the mass transport step, but by the charge transfer step. The sample with the highest saturation magnetization was that synthesized in the presence of polyethylene glycol. PMID:25492019

  2. Preparation and characterization of anion exchange resin decorated with magnetite nanoparticles for removal of p-toluic acid from aqueous solution

    NASA Astrophysics Data System (ADS)

    Davarpanah, Morteza; Ahmadpour, Ali; Rohani Bastami, Tahereh

    2015-02-01

    Polystyrene resin was covalently functionalized with diethanolamine and then decorated with magnetite nanoparticles by a novel and simple co-precipitation method using iron(II) sulfate as precursor. The products were characterized by Fourier transform infrared spectroscopy, elemental analysis, X-ray diffraction, Mössbauer spectroscopy, field-emission scanning electron microscopy and vibrating sample magnetometer. Adsorption of p-toluic acid (p-TA) onto magnetite-decorated polystyrene (MAG-PS) was studied and compared with that of diethanolamine-functionalized polystyrene and a commercial anion exchange resin. Results showed that the magnetite nanoparticles with an average size of 20.4 nm were successfully formed on the surface of polystyrene resin, and MAG-PS was exhibited high affinity for the removal of p-TA.

  3. The role of magnetite nanoparticles in the reduction of nitrate in groundwater by zero-valent iron.

    PubMed

    Cho, Dong-Wan; Song, Hocheol; Schwartz, Franklin W; Kim, Bokseong; Jeon, Byong-Hun

    2015-04-01

    Magnetite nanoparticles were used as an additive material in a zero-valent iron (Fe0) reaction to reduce nitrate in groundwater and its effects on nitrate removal were investigated. The addition of nano-sized magnetite (NMT) to Fe0 reactor markedly increased nitrate reduction, with the rate proportionally increasing with NMT loading. Field emission scanning electron microscopy analysis revealed that NMT aggregates were evenly distributed and attached on the Fe0 surface due to their magnetic properties. The rate enhancement effect of NMT is presumed to arise from its role as a corrosion promoter for Fe0 corrosion as well as an electron mediator that facilitated electron transport from Fe0 to adsorbed nitrate. Nitrate reduction by Fe0 in the presence of NMT proceeded much faster in groundwater (GW) than in de-ionized water. The enhanced reduction of nitrate in GW was attributed to the adsorption or formation of surface complex by the cationic components in GW, i.e., Ca2+ and Mg2+, in the Fe0-H2O interface that promoted electrostatic attraction of nitrate to the reaction sites. Moreover, the addition of NMT imparted superior longevity to Fe0, enabling completion of four nitrate reduction cycles, which otherwise would have been inactivated during the first cycle without an addition of NMT. The results demonstrate the potential applicability of a Fe0/NMT system in the treatment of nitrate-contaminated GW. PMID:25665757

  4. Definitive identification of magnetite nanoparticles in the abdomen of the honeybee Apis mellifera

    NASA Astrophysics Data System (ADS)

    Desoil, M.; Gillis, P.; Gossuin, Y.; Pankhurst, Q. A.; Hautot, D.

    2005-01-01

    The biogenic magnetic properties of the honeybee Apis mellifera were investigated with a view to understanding the bee's physiological response to magnetic fields. The magnetisations of bee abdomens on one hand, and heads and thoraxes on the other hand, were measured separately as functions of temperature and field. Both the antiferromagnetic responses of the ferrihydrite cores of the iron storage protein ferritin, and the ferrimagnetic responses of nanoscale magnetite (Fe3O4) particles, were observed. Relatively large magnetite particles (ca. 30 nm or more), capable of retaining a remanent magnetisation at room temperature, were found in the abdomens, but were absent in the heads and thoraxes. In both samples, more than 98% of the iron atoms were due to ferritin.

  5. Partial slip effect in flow of magnetite-Fe3O4 nanoparticles between rotating stretchable disks

    NASA Astrophysics Data System (ADS)

    Hayat, Tasawar; Qayyum, Sumaira; Imtiaz, Maria; Alzahrani, Faris; Alsaedi, Ahmed

    2016-09-01

    This paper addresses the flow of magnetic nanofluid (ferrofluid) between two parallel rotating stretchable disks with different rotating and stretching velocities. Water based fluid comprising magnetite-Fe3O4 nanoparticles is addressed. Velocity slip and temperature jump at solid-fluid interface are also taken into account. Appropriate transformations reduce the nonlinear partial differential system to ordinary differential system. Convergent series solutions are obtained. Effects of various pertinent parameters on the velocity and temperature profiles are shown and evaluated. Computations for skin friction coefficient and Nusselt number are presented and examined for the influence of involved parameters. It is noted that tangential velocity of fluid decreases for larger velocity slip parameter. Fluid temperature also reduces for increasing value of thermal slip parameter. Surface drag force and heat transfer rate at lower disk are enhanced when magnetic field strength is increased.

  6. Grafting of Poly(methyl methacrylate) Brushes from Magnetite Nanoparticles Using a Phosphonic Acid Based Initiator by Ambient Temperature Atom Transfer Radical Polymerization (ATATRP)

    PubMed Central

    2008-01-01

    Poly(methyl methacrylate) in the brush form is grown from the surface of magnetite nanoparticles by ambient temperature atom transfer radical polymerization (ATATRP) using a phosphonic acid based initiator. The surface initiator was prepared by the reaction of ethylene glycol with 2-bromoisobutyrl bromide, followed by the reaction with phosphorus oxychloride and hydrolysis. This initiator is anchored to magnetite nanoparticles via physisorption. The ATATRP of methyl methacrylate was carried out in the presence of CuBr/PMDETA complex, without a sacrificial initiator, and the grafting density is found to be as high as 0.90 molecules/nm2. The organic–inorganic hybrid material thus prepared shows exceptional stability in organic solvents unlike unfunctionalized magnetite nanoparticles which tend to flocculate. The polymer brushes of various number average molecular weights were prepared and the molecular weight was determined using size exclusion chromatography, after degrafting the polymer from the magnetite core. Thermogravimetric analysis, X-ray photoelectron spectra and diffused reflection FT-IR were used to confirm the grafting reaction.

  7. Neuronal adhesion, proliferation and differentiation of embryonic stem cells on hybrid scaffolds made of xanthan and magnetite nanoparticles.

    PubMed

    Glaser, Talita; Bueno, Vânia B; Cornejo, Daniel R; Petri, Denise F S; Ulrich, Henning

    2015-08-01

    Hybrid scaffolds made of xanthan and magnetite nanoparticles (XCA/mag) were prepared by dipping xanthan membranes (XCA) into dispersions of magnetic nanoparticles for different periods of time. The resulting hybrid scaffolds presented magnetization values ranging from 0.25 emu g(-1) to 1.80 emu g(-1) at 70 kOe and corresponding iron contents ranging from 0.25% to 2.3%, respectively. They were applied as matrices for in vitro embryoid body adhesion and neuronal differentiation of embryonic stem cells; for comparison, neat XCA and commercial plastic plates were also used. Adhesion rates were more pronounced when cells were seeded on XCA/mag than on neat XCA or plastic dishes; however, proliferation levels were independent from those of the scaffold type. Embryonic stem cells showed similar differentiation rates on XCA/mag scaffolds with magnetization of 0.25 and 0.60 emu g(-1), but did not survive on scaffolds with 1.80 emu g(-1). Differentiation rates, expressed as the number of neurons obtained on the chosen scaffolds, were the largest on neat XCA, which has a high density of negative charge, and were smallest on the commercial plastic dishes. The local magnetic field inherent of magnetite particles present on the surface of XCA/mag facilitates synapse formation, because synaptophysin expression and electrical transmission were increased when compared to the other scaffolds used. We conclude that XCA/mag and XCA hydrogels are scaffolds with distinguishable performance for adhesion and differentiation of ESCs into neurons. PMID:26154495

  8. Magnetite Fe3O4 nanoparticles synthesis by wet chemical reduction and their characterization

    NASA Astrophysics Data System (ADS)

    Chaki, S. H.; Malek, Tasmira J.; Chaudhary, M. D.; Tailor, J. P.; Deshpande, M. P.

    2015-09-01

    The authors report the synthesis of Fe3O4 nanoparticles by wet chemical reduction technique at ambient temperature and its characterization. Ferric chloride hexa-hydrate (FeCl3 · 6H2O) and sodium boro-hydrate (NaBH4) were used for synthesis of Fe3O4 nanoparticles at ambient temperature. The elemental composition of the synthesized Fe3O4 nanoparticles was determined by energy dispersive analysis of x-rays technique. The x-ray diffraction (XRD) technique was used for structural characterization of the nanoparticles. The crystallite size of the nanoparticles was determined using XRD data employing Scherrer’s formula and Hall-Williamson’s plot. Surface morphology of as-synthesized Fe3O4 nanoparticles was studied by scanning electron microscopy. High resolution transmission electron microscopy analysis of the as-synthesized Fe3O4 nanoparticles showed narrow range of particles size distribution. The optical absorption of the synthesized Fe3O4 nanoparticles was studied by UV-vis-NIR spectroscopy. The as-synthesized nanoparticles were analyzed by Fourier transform infrared spectroscopy technique for absorption band study in the infrared region. The magnetic properties of the as-synthesized Fe3O4 nanoparticles were evaluated by vibrating sample magnetometer technique. The thermal stability of the as-synthesized Fe3O4 nanoparticles was studied by thermogravimetric technique. The obtained results are elaborated and discussed in details in this paper.

  9. Magnetic properties of jet-printer inks containing dispersed magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Tiberto, Paola; Barrera, Gabriele; Celegato, Federica; Coïsson, Marco; Chiolerio, Alessandro; Martino, Paola; Pandolfi, Paolo; Allia, Paolo

    2013-04-01

    Two ferrofluid inks for jet-printing, containing magnetite NPs of slightly different average radius (sample A: 6 nm; sample B: 8 nm) were prepared by adding a dispersion of magnetite nanopowders in n-hexane to an insulating ink. Isothermal magnetization loops of inks were measured by means of a vibrating sample magnetometer in the temperature interval 5-300 K up to 70 kOe. The inks were then ejected at room temperature on standard paper by means of either a thermal ink jet head (TIJ; sample A) or a piezoelectric ink jet head (PIJ; sample B). Magnetic properties of prints on paper (FC/ZFC curves, isothermal magnetic loops and related hysteretic properties) were measured between 10 and 300 K using an alternating gradient force magnetometer up to 20 kOe. The inks display a different magnetic behavior with respect to both prints. In particular, the dispersed NPs are characterized by an effective radius (and ensuing magnetic interaction) larger than expected on the basis of the properties of the starting powders. Instead, the NP radii in both prints are closer to the starting values. The printed magnetic films show an almost perfect superparamagnetic (SP) response around room temperature; however, at temperatures lower than 100 K the SP scaling is not observed and both samples behave as interacting superparamagnetic (ISP) materials. The evolution from the SP to the ISP regime is marked by a steady increase in the hysteretic properties of both samples. Particular attention will be paid to the study of magnetic interactions occurring among NPs. The effect of the ejection process on the degree of aggregation of magnetite NPs will be here studied.

  10. Acute Phase Pulmonary Responses to a Single Intratracheal Spray Instillation of Magnetite (Fe3O4) Nanoparticles in Fischer 344 Rats

    PubMed Central

    Tada, Yukie; Yano, Norio; Takahashi, Hiroshi; Yuzawa, Katsuhiro; Ando, Hiroshi; Kubo, Yoshikazu; Nagasawa, Akemichi; Ogata, Akio; Nakae, Dai

    2012-01-01

    Iron nanomaterials are of considerable interest for application to nanotechnology-related fields including environmental catalysis, biomedical imaging, drug delivery and hyperthermia, because of their superparamagnetic characteristics and high catalytic abilities. However, information about potential risks of iron nanomaterials is limited. The present study assessed pulmonary responses to a single intratracheal spray instillation of triiron tetraoxide nanoparticles (magnetite) in rats. Ten-week-old male and female Fischer 344 rats (n=5/group) were exposed to a single intratracheal spray instillation of 0 (vehicle), 5.0, 15.0 or 45.0 mg/kg body weight (BW) of magnetite. After 14 days, the rats were sacrificed, and biological consequences were investigated. The lung weights of the 15.0 and 45.0 mg/kg BW male and female groups were significantly higher than those of the control groups. The lungs of treated rats showed enlargement and black patches originating from the color of magnetite. The typical histopathological changes in the lungs of the treated rats included infiltration of macrophages phagocytosing magnetite, inflammatory cell infiltration, granuloma formation and an increase of goblet cells in the bronchial epithelium. The results clearly show that instilled magnetite causes foreign body inflammatory and granulating lesions in the lung. These pulmonary responses occur in a dose-dependent manner in association with the increase in lung weight. PMID:23345925

  11. Acute phase pulmonary responses to a single intratracheal spray instillation of magnetite (fe(3)o(4)) nanoparticles in Fischer 344 rats.

    PubMed

    Tada, Yukie; Yano, Norio; Takahashi, Hiroshi; Yuzawa, Katsuhiro; Ando, Hiroshi; Kubo, Yoshikazu; Nagasawa, Akemichi; Ogata, Akio; Nakae, Dai

    2012-12-01

    Iron nanomaterials are of considerable interest for application to nanotechnology-related fields including environmental catalysis, biomedical imaging, drug delivery and hyperthermia, because of their superparamagnetic characteristics and high catalytic abilities. However, information about potential risks of iron nanomaterials is limited. The present study assessed pulmonary responses to a single intratracheal spray instillation of triiron tetraoxide nanoparticles (magnetite) in rats. Ten-week-old male and female Fischer 344 rats (n=5/group) were exposed to a single intratracheal spray instillation of 0 (vehicle), 5.0, 15.0 or 45.0 mg/kg body weight (BW) of magnetite. After 14 days, the rats were sacrificed, and biological consequences were investigated. The lung weights of the 15.0 and 45.0 mg/kg BW male and female groups were significantly higher than those of the control groups. The lungs of treated rats showed enlargement and black patches originating from the color of magnetite. The typical histopathological changes in the lungs of the treated rats included infiltration of macrophages phagocytosing magnetite, inflammatory cell infiltration, granuloma formation and an increase of goblet cells in the bronchial epithelium. The results clearly show that instilled magnetite causes foreign body inflammatory and granulating lesions in the lung. These pulmonary responses occur in a dose-dependent manner in association with the increase in lung weight. PMID:23345925

  12. Frequency-dependent magnetic susceptibility of magnetite and cobalt ferrite nanoparticles embedded in PAA hydrogel.

    PubMed

    van Berkum, Susanne; Dee, Joris T; Philipse, Albert P; Erné, Ben H

    2013-01-01

    Chemically responsive hydrogels with embedded magnetic nanoparticles are of interest for biosensors that magnetically detect chemical changes. A crucial point is the irreversible linkage of nanoparticles to the hydrogel network, preventing loss of nanoparticles upon repeated swelling and shrinking of the gel. Here, acrylic acid monomers are adsorbed onto ferrite nanoparticles, which subsequently participate in polymerization during synthesis of poly(acrylic acid)-based hydrogels (PAA). To demonstrate the fixation of the nanoparticles to the polymer, our original approach is to measure low-field AC magnetic susceptibility spectra in the 0.1 Hz to 1 MHz range. In the hydrogel, the magnetization dynamics of small iron oxide nanoparticles are comparable to those of the particles dispersed in a liquid, due to fast Néel relaxation inside the particles; this renders the ferrogel useful for chemical sensing at frequencies of several kHz. However, ferrogels holding thermally blocked iron oxide or cobalt ferrite nanoparticles show significant decrease of the magnetic susceptibility resulting from a frozen magnetic structure. This confirms that the nanoparticles are unable to rotate thermally inside the hydrogel, in agreement with their irreversible fixation to the polymer network. PMID:23673482

  13. Frequency-Dependent Magnetic Susceptibility of Magnetite and Cobalt Ferrite Nanoparticles Embedded in PAA Hydrogel

    PubMed Central

    van Berkum, Susanne; Dee, Joris T.; Philipse, Albert P.; Erné, Ben H.

    2013-01-01

    Chemically responsive hydrogels with embedded magnetic nanoparticles are of interest for biosensors that magnetically detect chemical changes. A crucial point is the irreversible linkage of nanoparticles to the hydrogel network, preventing loss of nanoparticles upon repeated swelling and shrinking of the gel. Here, acrylic acid monomers are adsorbed onto ferrite nanoparticles, which subsequently participate in polymerization during synthesis of poly(acrylic acid)-based hydrogels (PAA). To demonstrate the fixation of the nanoparticles to the polymer, our original approach is to measure low-field AC magnetic susceptibility spectra in the 0.1 Hz to 1 MHz range. In the hydrogel, the magnetization dynamics of small iron oxide nanoparticles are comparable to those of the particles dispersed in a liquid, due to fast Néel relaxation inside the particles; this renders the ferrogel useful for chemical sensing at frequencies of several kHz. However, ferrogels holding thermally blocked iron oxide or cobalt ferrite nanoparticles show significant decrease of the magnetic susceptibility resulting from a frozen magnetic structure. This confirms that the nanoparticles are unable to rotate thermally inside the hydrogel, in agreement with their irreversible fixation to the polymer network. PMID:23673482

  14. Scale-up of the production of highly reactive biogenic magnetite nanoparticles using Geobacter sulfurreducens.

    PubMed

    Byrne, J M; Muhamadali, H; Coker, V S; Cooper, J; Lloyd, J R

    2015-06-01

    Although there are numerous examples of large-scale commercial microbial synthesis routes for organic bioproducts, few studies have addressed the obvious potential for microbial systems to produce inorganic functional biomaterials at scale. Here we address this by focusing on the production of nanoscale biomagnetite particles by the Fe(III)-reducing bacterium Geobacter sulfurreducens, which was scaled up successfully from laboratory- to pilot plant-scale production, while maintaining the surface reactivity and magnetic properties which make this material well suited to commercial exploitation. At the largest scale tested, the bacterium was grown in a 50 l bioreactor, harvested and then inoculated into a buffer solution containing Fe(III)-oxyhydroxide and an electron donor and mediator, which promoted the formation of magnetite in under 24 h. This procedure was capable of producing up to 120 g of biomagnetite. The particle size distribution was maintained between 10 and 15 nm during scale-up of this second step from 10 ml to 10 l, with conserved magnetic properties and surface reactivity; the latter demonstrated by the reduction of Cr(VI). The process presented provides an environmentally benign route to magnetite production and serves as an alternative to harsher synthetic techniques, with the clear potential to be used to produce kilogram to tonne quantities. PMID:25972437

  15. Scale-up of the production of highly reactive biogenic magnetite nanoparticles using Geobacter sulfurreducens

    PubMed Central

    Byrne, J. M.; Muhamadali, H.; Coker, V. S.; Cooper, J.; Lloyd, J. R.

    2015-01-01

    Although there are numerous examples of large-scale commercial microbial synthesis routes for organic bioproducts, few studies have addressed the obvious potential for microbial systems to produce inorganic functional biomaterials at scale. Here we address this by focusing on the production of nanoscale biomagnetite particles by the Fe(III)-reducing bacterium Geobacter sulfurreducens, which was scaled up successfully from laboratory- to pilot plant-scale production, while maintaining the surface reactivity and magnetic properties which make this material well suited to commercial exploitation. At the largest scale tested, the bacterium was grown in a 50 l bioreactor, harvested and then inoculated into a buffer solution containing Fe(III)-oxyhydroxide and an electron donor and mediator, which promoted the formation of magnetite in under 24 h. This procedure was capable of producing up to 120 g of biomagnetite. The particle size distribution was maintained between 10 and 15 nm during scale-up of this second step from 10 ml to 10 l, with conserved magnetic properties and surface reactivity; the latter demonstrated by the reduction of Cr(VI). The process presented provides an environmentally benign route to magnetite production and serves as an alternative to harsher synthetic techniques, with the clear potential to be used to produce kilogram to tonne quantities. PMID:25972437

  16. Preparation of well-dispersed gold/magnetite nanoparticles embedded on cellulose nanocrystals for efficient immobilization of papain enzyme.

    PubMed

    Mahmoud, Khaled A; Lam, Edmond; Hrapovic, Sabahudin; Luong, John H T

    2013-06-12

    A nanocomposite consisting of magnetite nanoparticles (Fe3O4NPs) and Au nanoparticles (AuNPs) embedded on cellulose nanocrystals (CNCs) was used as a magnetic support for the covalent conjugation of papain and facilitated recovery of this immobilized enzyme. Fe3O4NPs (10-20 nm in diameter) and AuNPs (3-7 nm in diameter) were stable and well-dispersed on the CNC surface. Energy-dispersive spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used to evaluate the surface composition and structure of CNC/Fe3O4NPs/AuNPs. The nanocomposite was successfully used for the immobilization and separation of papain from the reaction mixture. The optimal enzyme loading was 186 mg protein/g CNC/Fe3O4NPs/AuNPs, significantly higher than the value reported in the literature. The activity of immobilized papain was studied by electrochemical detection of its specific binding to the Thc-Fca-Gly-Gly-Tyr-Arg inhibitory sequence bound to an Au electrode. The immobilized enzyme retained 95% of its initial activity after 35 days of storage at 4 °C, compared to 41% for its free form counterpart. PMID:23676842

  17. Time dependent magnetically induced variations in optical transmission of magnetite nanoparticle aqueous suspension

    NASA Astrophysics Data System (ADS)

    Malynych, Serhiy; Moroz, Iryna

    2012-02-01

    We observe time dependent variations in the light intensity transmitted through an aqueous suspension of Fe3O4 nanoparticles caused by applied DC magnetic field. Two types of variations can be distinguished. Fast response takes less than 1ms while slow variations occur at the time interval fromseconds to hundreds of minutes. Possible mechanisms of these variations are discussed. Formation of chain-like structures consisted from iron oxide nanoparticles is responsible for the slow variations. It is also accompanied by a diffraction pattern when the magnetic field is orthogonal to the light beam. Fast variations are due to particle rotation and reorientation of the magnetic moment inside a nanoparticle.

  18. Enzyme-functionalized gold-coated magnetite nanoparticles as novel hybrid nanomaterials: synthesis, purification and control of enzyme function by low-frequency magnetic field.

    PubMed

    Majouga, Alexander; Sokolsky-Papkov, Marina; Kuznetsov, Artem; Lebedev, Dmitry; Efremova, Maria; Beloglazkina, Elena; Rudakovskaya, Polina; Veselov, Maxim; Zyk, Nikolay; Golovin, Yuri; Klyachko, Natalia; Kabanov, Alexander

    2015-01-01

    The possibility of remotely inducing a defined effect on NPs by means of electromagnetic radiation appears attractive. From a practical point of view, this effect opens horizons for remote control of drug release systems, as well as modulation of biochemical functions in cells. Gold-coated magnetite nanoparticles are perfect candidates for such application. Herein, we have successfully synthesized core-shell NPs having magnetite cores and gold shells modified with various sulphur containing ligands and developed a new, simple and robust procedure for the purification of the resulting nanoparticles. The carboxylic groups displayed at the surface of the NPs were utilized for NP conjugation with a model enzyme (ChT). In the present study, we report the effect of the low-frequency AC magnetic field on the catalytic activity of the immobilized ChT. We show that the enzyme activity decreases upon exposure of the NPs to the field. PMID:25460600

  19. Anisotropy of the magnetoviscous effect in a ferrofluid with weakly interacting magnetite nanoparticles.

    PubMed

    Linke, J M; Odenbach, S

    2015-05-01

    The anisotropy of the magnetoviscous effect of a ferrofluid has been studied in a specially designed slit die viscometer, which allows three distinct orientations of the magnetic field with respect to the fluid flow. The corresponding Miesowicz viscosity coefficients were determined in dependence of the shear rate and the magnetic field intensity to gain a comprehensive magnetorheological characterization of the fluid. The particles in the fluid have a mean diameter of 13 nm corresponding to an interaction parameter of λ ≈ 1.3 for magnetite. Thus, the fluid can be expected to show a transition from non-interacting individual particles to microstructures with chain-like associated particles when the magnetic field intensity is increased and the shear rate is decreased. The observed field and shear dependent anisotropy of the magnetoviscous effect is explained coherently in terms of these microstructural changes in the fluid. PMID:25837303

  20. Anisotropy of the magnetoviscous effect in a ferrofluid with weakly interacting magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Linke, J. M.; Odenbach, S.

    2015-05-01

    The anisotropy of the magnetoviscous effect of a ferrofluid has been studied in a specially designed slit die viscometer, which allows three distinct orientations of the magnetic field with respect to the fluid flow. The corresponding Miesowicz viscosity coefficients were determined in dependence of the shear rate and the magnetic field intensity to gain a comprehensive magnetorheological characterization of the fluid. The particles in the fluid have a mean diameter of 13 nm corresponding to an interaction parameter of λ ≈ 1.3 for magnetite. Thus, the fluid can be expected to show a transition from non-interacting individual particles to microstructures with chain-like associated particles when the magnetic field intensity is increased and the shear rate is decreased. The observed field and shear dependent anisotropy of the magnetoviscous effect is explained coherently in terms of these microstructural changes in the fluid.

  1. Preparation and characterization of 6-mercaptopurine-coated magnetite nanoparticles as a drug delivery system

    PubMed Central

    Dorniani, Dena; Hussein, Mohd Zobir bin; Kura, Aminu Umar; Fakurazi, Sharida; Shaari, Abdul Halim; Ahmad, Zalinah

    2013-01-01

    Background Iron oxide nanoparticles are of considerable interest because of their use in magnetic recording tape, ferrofluid, magnetic resonance imaging, drug delivery, and treatment of cancer. The specific morphology of nanoparticles confers an ability to load, carry, and release different types of drugs. Methods and results We synthesized superparamagnetic nanoparticles containing pure iron oxide with a cubic inverse spinal structure. Fourier transform infrared spectra confirmed that these Fe3O4 nanoparticles could be successfully coated with active drug, and thermogravimetric and differential thermogravimetric analyses showed that the thermal stability of iron oxide nanoparticles coated with chitosan and 6-mercaptopurine (FCMP) was markedly enhanced. The synthesized Fe3O4 nanoparticles and the FCMP nanocomposite were generally spherical, with an average diameter of 9 nm and 19 nm, respectively. The release of 6-mercaptopurine from the FCMP nanocomposite was found to be sustained and governed by pseudo-second order kinetics. In order to improve drug loading and release behavior, we prepared a novel nanocomposite (FCMP-D), ie, Fe3O4 nanoparticles containing the same amounts of chitosan and 6-mercaptopurine but using a different solvent for the drug. The results for FCMP-D did not demonstrate “burst release” and the maximum percentage release of 6-mercaptopurine from the FCMP-D nanocomposite reached about 97.7% and 55.4% within approximately 2,500 and 6,300 minutes when exposed to pH 4.8 and pH 7.4 solutions, respectively. By MTT assay, the FCMP nanocomposite was shown not to be toxic to a normal mouse fibroblast cell line. Conclusion Iron oxide coated with chitosan containing 6-mercaptopurine prepared using a coprecipitation method has the potential to be used as a controlled-release formulation. These nanoparticles may serve as an alternative drug delivery system for the treatment of cancer, with the added advantage of sparing healthy surrounding cells and

  2. Synthesis and functionalization of magnetite nanoparticles with different amino-functional alkoxysilanes

    NASA Astrophysics Data System (ADS)

    Bini, Rafael A.; Marques, Rodrigo Fernando C.; Santos, Francisco J.; Chaker, Juliano A.; Jafelicci, Miguel

    2012-02-01

    Superparamagnetic iron oxide (SPIO) nanoparticles show great promise for many biotechnological applications. This paper addresses the synthesis and characterization of SPIO nanoparticles grafted with three different alkoxysilanes: 3-aminopropyl-triethoxysilane (APTES), 3-aminopropyl-ethyl-diethoxysilane (APDES) and 3-aminopropyl-diethy-ethoxysilane (APES). SPIO nanoparticles with an average particle diameter of 10 nm were prepared by chemical sonoprecipitation. As confirmed by Fourier transform infrared (FTIR) spectroscopy, silylation of these nanoparticles occurs through a two-step process. Decreasing the number of alkoxide groups reduced the concentration of free amino groups on the SPIO surface ([SPIO-NH2]-APTES>APDES>APES). This phenomenon results from steric contributions and the formation of H-bonded amines provided by the ethyl groups present in the APDES and APES molecules. A simulation of SPIO nanoparticles in a saline physiologic solution shows that the ethyl groups impart larger steric stability onto the ferrofluids, which reduces aggregation. The magnetization (M) versus magnetic field (H) curves show that the synthesized iron oxide nanoparticles display superparamagnetic behavior. The zero-field cooling (ZFC) and field cooling (FC) curves show that the changes in the blocking temperature depend on the alkoxysilane-functionalized particle surface.

  3. Synthetic and biogenic magnetite nanoparticles for tracking of stem cells and dendritic cells

    NASA Astrophysics Data System (ADS)

    Schwarz, Sebastian; Fernandes, Fabiana; Sanroman, Laura; Hodenius, Michael; Lang, Claus; Himmelreich, Uwe; Schmitz-Rode, Thomas; Schueler, Dirk; Hoehn, Mathias; Zenke, Martin; Hieronymus, Thomas

    2009-05-01

    Accurate delivery of cells to target organs is critical for success of cell-based therapies with stem cells or immune cells such as antigen-presenting dendritic cells (DC). Labeling with contrast agents before implantation provides a powerful means for monitoring cellular migration using magnetic resonance imaging (MRI). In this study, we investigated the uptake of fully synthesized or bacterial magnetic nanoparticles (MNPs) into hematopoietic Flt3 + stem cells and DC from mouse bone marrow. We show that (i) uptake of both synthetic and biogenic nanoparticles into cells endow magnetic activity and (ii) low numbers of MNP-loaded cells are readily detected by MRI.

  4. Facile integration of multiple magnetite nanoparticles for theranostics combining efficient MRI and thermal therapy

    NASA Astrophysics Data System (ADS)

    Huang, Guoming; Zhu, Xianglong; Li, Hui; Wang, Lirong; Chi, Xiaoqin; Chen, Jiahe; Wang, Xiaomin; Chen, Zhong; Gao, Jinhao

    2015-01-01

    Multifunctional nanostructures with both diagnostic and therapeutic capabilities have attracted considerable attention in biomedical research because they can offer great advantages in disease management and prognosis. In this work, a facile way to transfer the hydrophobic iron oxide (IO) nanoparticles into aqueous media by employing carboxylic graphene oxide (GO-COOH) as the transferring agent has been reported. In this one-step process, IO nanoparticles adhere to GO-COOH and form water-dispersible clusters via hydrophobic interactions between the hydrophobic ligands of IO nanoparticles and the basal plane of GO-COOH. The multiple IO nanoparticles on GO-COOH sheets (IO/GO-COOH) present a significant increase in T2 contrast enhancement. Moreover, the IO/GO-COOH nanoclusters also display a high photothermal conversion efficiency and can effectively inhibit tumor growth through the photothermal effects. It is envisioned that such IO/GO-COOH nanocomposites combining efficient MRI and photothermal therapy hold great promise in theranostic applications.Multifunctional nanostructures with both diagnostic and therapeutic capabilities have attracted considerable attention in biomedical research because they can offer great advantages in disease management and prognosis. In this work, a facile way to transfer the hydrophobic iron oxide (IO) nanoparticles into aqueous media by employing carboxylic graphene oxide (GO-COOH) as the transferring agent has been reported. In this one-step process, IO nanoparticles adhere to GO-COOH and form water-dispersible clusters via hydrophobic interactions between the hydrophobic ligands of IO nanoparticles and the basal plane of GO-COOH. The multiple IO nanoparticles on GO-COOH sheets (IO/GO-COOH) present a significant increase in T2 contrast enhancement. Moreover, the IO/GO-COOH nanoclusters also display a high photothermal conversion efficiency and can effectively inhibit tumor growth through the photothermal effects. It is envisioned

  5. The Complexes of Bisphosphonate and Magnetite Nanoparticles to Remove Uranyl Ions from Aqueous Phase

    SciTech Connect

    Wang, L.; Yang, Z.; Gao, J.; Xu, K.; Gu, H.; Xu, B.; Zhang, B.; Zhang, X.

    2007-03-20

    Using tetraethyl-3-amino-propane-1,1-bisphosphonate (BP) as the functional molecule, we functionalized Fe3O4 magnetic nanoparticles via dopamine (DA) linkage to create a system with an Fe3O4-DA-BP nanostructure, which possesses high specificity for removing uranyl ions from water or blood. This work demonstrates that magnetic nanoparticles, combined with specific receptor-ligand interactions, promise a sensitive and rapid platform for the detection, recovery, and decorporation of radioactive metal toxins from biological environment.

  6. Oleate Coated Magnetic Cores Based on Magnetite, Zn Ferrite and Co Ferrite Nanoparticles - Preparation, Physical Characterization and Biological Impact on Helianthus Annuus Photosynthesis

    SciTech Connect

    Ursache-Oprisan, Manuela; Foca-nici, Ecaterina; Cirlescu, Aurelian; Caltun, Ovidiu; Creanga, Dorina

    2010-12-02

    Sodium oleate was used as coating shell for magnetite, Zn ferrite and Co ferrite powders to stabilize them in the form of aqueous magnetic suspensions. The physical characterization was carried out by applying X-ray diffraction and magnetization measurements. Both crystallite size and magnetic core diameter ranged between 7 and 11 nm. The influence of magnetic nanoparticle suspensions (corresponding to magnetic nanoparticle levels of 10{sup -14}-10{sup -15}/cm{sup 3}) on sunflower seedlings was studied considering the changes in the photosynthesis pigment levels. Similar responses were obtained for magnetite and cobalt ferrite nanoparticle treatment consisting in the apparent inhibition of chlorophyll biosynthesis while for zinc ferrite nanoparticles some concentrations seemed to have stimulatory effects on the chlorophylls as well as on the carotene levels. But the chlorophyll ratio was diminished in the case of all three types of magnetic nanoparticles meaning their slight negative effect on the light harvesting complex II (LHC II) from the chloroplast membranes and consequently on the photosynthesis efficiency.

  7. Facile integration of multiple magnetite nanoparticles for theranostics combining efficient MRI and thermal therapy.

    PubMed

    Huang, Guoming; Zhu, Xianglong; Li, Hui; Wang, Lirong; Chi, Xiaoqin; Chen, Jiahe; Wang, Xiaomin; Chen, Zhong; Gao, Jinhao

    2015-02-14

    Multifunctional nanostructures with both diagnostic and therapeutic capabilities have attracted considerable attention in biomedical research because they can offer great advantages in disease management and prognosis. In this work, a facile way to transfer the hydrophobic iron oxide (IO) nanoparticles into aqueous media by employing carboxylic graphene oxide (GO-COOH) as the transferring agent has been reported. In this one-step process, IO nanoparticles adhere to GO-COOH and form water-dispersible clusters via hydrophobic interactions between the hydrophobic ligands of IO nanoparticles and the basal plane of GO-COOH. The multiple IO nanoparticles on GO-COOH sheets (IO/GO-COOH) present a significant increase in T2 contrast enhancement. Moreover, the IO/GO-COOH nanoclusters also display a high photothermal conversion efficiency and can effectively inhibit tumor growth through the photothermal effects. It is envisioned that such IO/GO-COOH nanocomposites combining efficient MRI and photothermal therapy hold great promise in theranostic applications. PMID:25581879

  8. Mercury Removal From Aqueous Solutions With Chitosan-Coated Magnetite Nanoparticles Optimized Using the Box-Behnken Design

    PubMed Central

    Rahbar, Nadereh; Jahangiri, Alireza; Boumi, Shahin; Khodayar, Mohammad Javad

    2014-01-01

    Background: Nowadays, removal of heavy metals from the environment is an important problem due to their toxicity. Objectives: In this study, a modified method was used to synthesize chitosan-coated magnetite nanoparticles (CCMN) to be used as a low cost and nontoxic adsorbent. CCMN was then employed to remove Hg2+ from water solutions. Materials and Methods: To remove the highest percentage of mercury ions, the Box-Behnken model of response surface methodology (RSM) was applied to simultaneously optimize all parameters affecting the adsorption process. Studied parameters of the process were pH (5-8), initial metal concentration (2-8 mg/L), and the amount of damped adsorbent (0.25-0.75 g). A second-order mathematical model was developed using regression analysis of experimental data obtained from 15 batch runs. Results: The optimal conditions predicted by the model were pH = 5, initial concentration of mercury ions = 6.2 mg/L, and the amount of damped adsorbent = 0.67 g. Confirmatory testing was performed and the maximum percentage of Hg2+ removed was found to be 99.91%. Kinetic studies of the adsorption process specified the efficiency of the pseudo second-order kinetic model. The adsorption isotherm was well-fitted to both the Langmuir and Freundlich models. Conclusions: CCMN as an excellent adsorbent could remove the mercury ions from water solutions at low and moderate concentrations, which is the usual amount found in environment. PMID:24872943

  9. Enhanced Cellular Uptake of Silica-Coated Magnetite Nanoparticles Compared with PEG-Coated Ones in Stem Cells.

    PubMed

    Lee, Dong Heon; Kang, Myunggoo; Lee, Hong Jai; Kim, Jeong Ah; Choi, Yun-Kyong; Cho, Hyunjin; Park, Jung-Keug; Park, Tai Hyun; Jung, Hyun

    2015-08-01

    Monodispersed magnetite (Fe3O4) nanoparticles (NPs) were prepared through the thermal decomposition method. The obtained NPs were surface modified with silica (SiO2) and polyethylene glycol (PEG), to enhance their stability in aqueous environment and their cellular uptake efficiency for biomedical applications. The NPs were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), Fourier transform infrared (FT-IR) spectroscopy, and dynamic light scattering (DLS). The cytotoxicity of these NPs on bone marrow mesenchymal stem cells (BM-MSCs) was measured by MTT assay (cell viability test) at various concentrations (2, 5, 12.5, 25, and 50 µg/mL). The cells remained more than 90% viable at concentrations as high as 50 µg/mL. To compare the cellular uptake efficiency, these NPs were treated in BM-MSCs and the Fe concentration within the cells was measured by inductively coupled plasma-atomic emission spectrometry (ICP-AES) analysis. The uptake process displayed a time- and dose-dependency. The uptake amount of SiO2-coated Fe3O4 (Fe3O4@SiO2) NPs was about 10 times higher than that of the PEG-coated ones (Fe3O4@PEG). PMID:26369110

  10. Effect of protein corona magnetite nanoparticles derived from bread in vitro digestion on Caco-2 cells morphology and uptake.

    PubMed

    Di Silvio, Desirè; Rigby, Neil; Bajka, Balazs; Mackie, Alan; Baldelli Bombelli, Francesca

    2016-06-01

    Nanoparticles (NPs) in biological fluids immediately interact with proteins forming a biomolecular corona (PC) that imparts their biological identity. While several studies on the formation of the PC in human plasma have been reported, the PC of orally administrated NPs has been less investigated, mostly in the presence of a food matrix. In fact, food matrixes when digested are subject of several dynamic changes that will certainly affect the PC formed on the NPs. The lack of studies on this topic is clearly related to the difficulty in isolating representative PC NPs from such a complex environment. In this work magnetite NPs were added to in vitro simulated digestion simultaneously with bread and PC NPs were isolated after gastric and duodenal phases by sucrose gradient ultracentrifugation (UC). The PC NPs were characterized in terms of size and protein composition. Translocation studies were then performed on Caco-2 monolayers in a serum free environment and cell morphology was characterized by confocal microscopy. PC NPs isolated from gastric and duodenal phases were different in size, surface charge and protein corona composition. NP cellular uptake was enhanced by the digestive PC inducing morphology changes in the cell monolayer. Overall, in this work we were able to isolate PC NPs from digested fluids in the presence of a food matrix and study their biological response on Caco-2 cells. PMID:26520468

  11. Impact of Biohybrid Magnetite Nanoparticles and Moroccan Propolis on Adherence of Methicillin Resistant Strains of Staphylococcus aureus.

    PubMed

    El-Guendouz, Soukaina; Aazza, Smail; Lyoussi, Badiaa; Bankova, Vassya; Lourenço, João P; Costa, Ana M Rosa; Mariano, José F; Miguel, Maria G; Faleiro, Maria L

    2016-01-01

    Biofilm bacteria are more resistant to antibiotics than planktonic cells. Propolis possesses antimicrobial activity. Generally, nanoparticles containing heavy metals possess antimicrobial and antibiofilm properties. In this study, the ability of adherence of Methicillin Resistant Strains of Staphylococcus aureus (MRSA) to catheters treated with magnetite nanoparticles (MNPs), produced by three methods and functionalized with oleic acid and a hydro-alcoholic extract of propolis from Morocco, was evaluated. The chemical composition of propolis was established by gas chromatography mass spectrometry (GC-MS), and the fabricated nanostructures characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Mossbauer spectroscopy and Fourrier transform infrared spectroscopy (FTIR). The capacity for impairing biofilm formation was dependent on the strain, as well as on the mode of production of MNPs. The co-precipitation method of MNPs fabrication using Fe(3+) and Na₂SO₃ solution and functionalized with oleic acid and propolis was the most effective in the impairment of adherence of all MRSA strains to catheters (p < 0.001). The adherence of the strain MRSA16 was also significantly lower (p < 0.001) when the catheters were treated with the hybrid MNPs with oleic acid produced by a hydrothermal method. The anti-MRSA observed can be attributed to the presence of benzyl caffeate, pinocembrin, galangin, and isocupressic acid in propolis extract, along with MNPs. However, for MRSA16, the impairment of its adherence on catheters may only be attributed to the hybrid MNPs with oleic acid, since very small amount, if any at all of propolis compounds were added to the MNPs. PMID:27618006

  12. Magnetic magnetite (Fe3O4) nanoparticle synthesis and applications for lead (Pb2+) and chromium (Cr6+) removal from water.

    PubMed

    Rajput, Shalini; Pittman, Charles U; Mohan, Dinesh

    2016-04-15

    Magnetic magnetite (Fe3O4) nanoparticles synthesized by chemical co-precipitation were characterized using XRD, TEM, SEM-EDX, FT-IR, ED-XRF, PPMS, point of zero charge (pHpzc) and surface area measurements. As-prepared Fe3O4 nanoparticles were successful for aqueous Cr(6+) and Pb(2+) removal. Batch adsorption experiments systematically investigated the influence of pH, temperature, contact time and adsorbate/adsorbent concentration on Cr(6+) and Pb(2+) adsorption. Maximum Cr(6+) and Pb(2+) removal occurred at pH 2.0 and 5.0, respectively. Sorption data fit pseudo-second order kinetics, indicating a chemical adsorption. The Freundlich, Langmuir, Redlich-Peterson, Toth, Radke and Sips adsorption isotherm models were applied to describe equilibrium data. The Sips and Langmuir models best described Cr(6+) and Pb(2+) adsorption on magnetite nanoparticles, respectively. The maximum Langmuir adsorption capacities were 34.87 (Cr(6+)) and 53.11 (Pb(2+))mg/g at 45°C, respectively. Fe3O4 nanoparticles are promising potential adsorbents and exhibited remarkable reusability for metal ions removal in water and wastewater treatment. PMID:26859095

  13. Fabrication of smart magnetite/reduced graphene oxide composite nanoparticles and their magnetic stimuli-response.

    PubMed

    Hong, Cheng Hai; Kim, Min Wook; Zhang, Wen Ling; Moon, Il Jae; Choi, Hyoung Jin

    2016-11-01

    Novel Fe3O4/reduced graphene oxide (RGO) composite nanoparticles were synthesized and confirmed by FT-IR spectra as good candidates for magnetic stimuli-responsive magnetorheological (MR) materials. The morphology of Fe3O4/RGO was observed by both scanning and transmission electron microscopy and their sedimentation stability improved due to a decreased density of the synthesized composites. The MR performance of the Fe3O4/RGO-based fluid was investigated with a rotational rheometer, and the Cho-Choi-Jhon model of the rheological equation of state was adopted to explain their performances for the entire shear rate region. PMID:27475706

  14. Long-term Pulmonary Responses to Quadweekly Intermittent Intratracheal Spray Instillations of Magnetite (Fe3O4) Nanoparticles for 52 Weeks in Fischer 344 Rats

    PubMed Central

    Tada, Yukie; Yano, Norio; Takahashi, Hiroshi; Yuzawa, Katsuhiro; Ando, Hiroshi; Kubo, Yoshikazu; Nagasawa, Akemichi; Inomata, Akiko; Ogata, Akio; Nakae, Dai

    2013-01-01

    Information about potential risks of iron nanomaterials is still limited, while a wide variety of applications are expected. We recently reported acute phase responses of male and female Fischer 344 rats after a single intratracheal spray instillation of Fe3O4 nanoparticles (magnetite), clearly showing dose-dependent pulmonary inflammatory changes (Tada et al., J Toxicol Pathol 25, 233–239, 2012). The present study assessed long-term responses of male and female Fischer 344 rats to multiple administrations of magnetite. Ten-week-old male and female Fischer 344 rats (n=20/group) were exposed to a total of 13 quadweekly intermittent intratracheal spray instillations of magnetite during the experimental period of 52 weeks, at doses of 0, 0.2 (low), 1.0 (medium) and 5.0 (high-dose) mg/kg body weight per administration. Absolute and relative lung weights of the high-dose group were significantly higher than those of the control group. Macroscopically, slight enlargement and scattered black patches were recognized in the lungs and the lung-associated lymph nodes of the high-dose group. Histopathologically, infiltration of macrophages phagocytosing magnetite (all dose groups) and of chronic inflammatory cells (medium- and high-dose males and high-dose females), alveolar bronchiolization and granuloma (high-dose group) were observed. In addition, alveolar hyperplasias were observed in some rats of the high-dose group, and cytoplasmic overexpression of β-catenin protein was immunohistochemically found in such lesions. The present results clearly show that instilled magnetite causes chronic inflammatory responses in the lung. These responses occur in a dose-dependent manner without apparent differences among sexes PMID:24526812

  15. Monodisperse magnetite nanoparticle tracers for in vivo magnetic particle imaging.

    PubMed

    Khandhar, Amit P; Ferguson, R Matthew; Arami, Hamed; Krishnan, Kannan M

    2013-05-01

    Magnetic Particle Imaging (MPI) is a new biomedical imaging modality that produces real-time, high-resolution tomographic images of superparamagnetic iron oxide (SPIO) nanoparticle tracer distributions. In this study, we synthesized monodisperse tracers for enhanced MPI performance and investigated both, their blood clearance time using a 25 kHz magnetic particle spectrometer (MPS), and biodistribution using a combination of quantitative T2-weighted MRI and tissue histology. In vitro and in vivo MPI performance of our magnetic nanoparticle tracers (MNTs), subject to biological constraints, were compared to commercially available SPIOs (Resovist). Monodisperse MNTs showed a 2-fold greater signal per unit mass, and 20% better spatial resolution. In vitro evaluation of tracers showed that MPI performance of our MNTs is preserved in blood, serum-rich cell-culture medium and gel; thus independent of changes in hydrodynamic volume and fluid viscosity - a critical prerequisite for in vivo MPI. In a rodent model, our MNTs circulated for 15 min - 3× longer than Resovist - and supported our in vitro evaluation that MPI signal is preserved in the physiological environment. Furthermore, MRI and histology analysis showed that MNTs distribute in the reticuloendothelial system (RES) in a manner similar to clinically approved SPIO agents. MNTs demonstrating long-circulation times and optimized MPI performance show potential as angiography tracers and blood-pool agents for the emerging MPI imaging modality. PMID:23434348

  16. Controlling the optimum dose of AMPTS functionalized-magnetite nanoparticles for hyperthermia cancer therapy

    NASA Astrophysics Data System (ADS)

    Arum, Yosefine; Song, Youngjin; Oh, Junghwan

    2011-12-01

    Magnetic hyperthermia has been used for many years to treat a variety of malignant tumors. One of the problems in magnetic hyperthermia is the choice of the correct particle concentration to achieve a defined temperature increase in the tumor tissue. In this study, we evaluated magnetic heat distribution induced by Fe3O4-APTMS magnetic nanoparticles in agar tissue phantom when it subjected to the AC magnetic filed. Using the correct nanoparticle dosage and considering their specific loss power, it is possible to estimate the efficiency of this therapeutic method. The experimental data were compared with a computer-based model, which were created using COMSOL Multiphysics to simulate the heat dissipation within the tissue for typical configurations of the tumor position as well as particle distribution within the tumor. Heating the cancer cells up to 50°C for 10 min was sufficient for complete cell killing and the heat dose of 19.9 W/gtissue is required for 5-mm tumor. Cell viability assay showed that MNPs exhibited no significant cytotoxicity against HeLa cells. Additionally, it was observed that the FITC-labeled Fe3O4-APTMS MNPs presented high cell biocompatibility and cellular uptake for efficient endocytosis.

  17. Conjugating Methotrexate to magnetite (Fe3O4) nanoparticles via trichloro-s-triazine†‡

    PubMed Central

    Young, Kaylie L.; Xu, Chenjie; Xie, Jin

    2009-01-01

    Monodisperse Fe3O4 nanoparticles (NPs) originally synthesized with a hydrophobic oleylamine capping ligand were made water soluble and conjugated to the anticancer drug Methotrexate (MTX) using a new chemistry based on the readily available linker trichloro-s-triazine (TsT). This new linker is much more versatile than those that currently exist for attaching biomolecules to magnetic NPs. The MTX-conjugated NPs were found to be stable under physiological conditions for over 72 hours and MTX was shown to maintain its anticancer activity after conjugation to the NP surface. Through cell viability studies and intracellular uptake studies, MTX-conjugated NPs were shown to have targeting specificity for a tumor cell line (9L rat glioma) over a healthy cell line (Cultured Pulmonary Artery Endothelial). Additionally the MTX-conjugated NPs were visualized inside 9L cells using fluorescence microscopy to help elucidate their path within a cell after internalization. PMID:19915686

  18. Improved triplet state parameters for indium octacarboxy phthalocyanines when conjugated to quantum dots and magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Tshangana, Charmaine; Nyokong, Tebello

    2015-06-01

    Fe3O4 magnetic nanoparticles (MNPs) and glutathione (GSH) capped CdSe@ZnS quantum dots (QDs) were separately coordinated to indium octacarboxy phthalocyanine (InPc(COOH)8) to form ClInPc(COOH)8-MNPs and ClInPc(COOH)8-GSH-CdSe@ZnS, respectively. The photophysical parameters (triplet state and fluorescence quantum yields and lifetimes) were determined for the conjugates. The triplet quantum yields increased from ΦT = 0.49 for InPc(COOH)8 alone to ΦT = 0.61 and 0.56 for InPc(COOH)8 in the conjugates: ClInPc(COOH)8-MNPs and ClInPc(COOH)8-GSH-CdSe@ZnS, respectively. The lifetimes also became longer for the conjugates compared to Pc alone.

  19. Synthesis and characterization of magnetite nanoparticles encapsulated in a bovine hemoglobin microgel

    NASA Astrophysics Data System (ADS)

    Mody, Puja J.

    This study shows the successful synthesis and characterization of a novel material that is composed of iron oxide particles within a protein gel. During the synthesis, bovine hemoglobin surrounds the forming Fe 3O4 nanoparticles, resulting in a biocompatible hydrogel, which has the potential to be used as a targeted drug delivery vehicle and as an MRI contrast agent. The structure, size, and thermal stability of these hydrogel complexes were analyzed using a range of techniques. Powder x-ray diffraction and infrared spectroscopy indicated the presence of Fe3O 4 and hemoglobin without significant interactions between particles in the solid state. Microscopy analysis determined the average size of these microgel complexes to be 4-9 mum2 in area (˜2-3 mum in diameter), and DSC analysis indicated that none of the microgels exhibited a denaturing or unfolding transition below 54°C regardless of the iron: hemoglobin ratio. Initial testing has been performed on the ability of these materials to act as magnetically activated drug delivery vehicles. Other pertinent tests (for magnetic properties and MRI applicability) are currently proceeding at external labs.

  20. Protein Corona Formation on Magnetite Nanoparticles: Effects of Culture Medium Composition, and Its Consequences on Superparamagnetic Nanoparticle Cytotoxicity.

    PubMed

    Mbeh, D A; Javanbakht, T; Tabet, L; Merhi, Y; Maghni, K; Sacher, E; Yahia, L H

    2015-05-01

    The physicochemical properties and potential cytotoxicity of nanoparticles (NPs) are significantly influenced by their inter- action with proteins, which results in corona formation. Here, we have determined whether corona formation, resulting from interactions between superparamagnetic iron oxide nanoparticles (SPIONs) and different cell culture media, may have consequences for driving NP toxic effects. To address this issue, complementary methods were used. The deter- mination of the hydrodynamic size distribution by ζ (zeta) potential measurement indicated that SPIONs were negatively charged under all conditions but that the actual charge was differed with the cell culture medium used. In vitro protein adsorption studies were carried out using the Bradford protein assay and Fourier transform infrared spectroscopy (FTIR). The Bradford assay revealed that the concentration of unadsorbed proteins and other biomolecules decreased when the SPION concentration increased. FTIR showed that the proteins were, indeed, adsorbed onto the NP surface. This was followed by matrix-assisted laser desorption/ionization time-of-flight secondary ion mass spectrometry (MALDI TOF-SIMS), to identify the adsorbed proteins. Ultimately, three different cell viability assays led to the conclusion that the SPIONs were not toxic for all the concentrations used here. In summary, we found that corona formation on the SPIONs depends on the composition of the culture media but has no consequence for nanotoxicity. We have shown that the application of complementary methods has provided novel insights into SPION/protein interactions. PMID:26349395

  1. Synthesis and characterization of dextran coated magnetite nanoparticles for diagnostics and therapy

    PubMed Central

    Khalkhali, Maryam; Sadighian, Somayeh; Rostamizadeh, Kobra; Khoeini, Farhad; Naghibi, Mehran; Bayat, Nahid; Habibizadeh, Mina; Hamidi, Mehrdad

    2015-01-01

    Introduction: Expansion of efficacious theranostic systems is of pivotal significance for medicine and human healthcare. Magnetic nanoparticles (MNPs) are known as drug delivery system and magnetic resonance imaging (MRI) contrast agent. MNPs as drug carriers have attracted significant attention because of the delivery of drugs loaded onto MNPs to solid tumors, maintaining them in the target site by an external electromagnetic field, and subsequently releasing drugs in a controlled manner. On the other hand, it is believed that MNPs possess high potential as MRI contrast agents. The aim of this work was to payload curcumin into dextran coated MNPs and investigate their potential as theranostic systems for controlled drug delivery and MRI imaging. Methods: MNPs were synthesized as a core and coated with dextran as polymeric shell to provide steric stabilization. Curcumin as anticancer drug was selected to be loaded into NPs. To characterize the synthesized NPs, various techniques (e.g., DLS, FESEM, FT-IR, XRD, and VSM) were utilized. In vitro drug release of curcumin was evaluated at 37˚C at the pH value of 5.4 and 7.4.The feasibility of employment of dextran coated MNPs as MRI contrast agents were also studied. Results: Formulations prepared from dextran coated MNPs showed high loading (13%) and encapsulation efficiency (95%). In vitro release study performed in the phosphate-buffered saline (PBS, pH= 7.4, 5.4) revealed that the dextran coated MNPs possess sustained release behavior at least for 4 days with the high extent of drug release in acidic media. Vibrating sample magnetometer (VSM) analysis proved the superparamagnetic properties of the dextran coated MNPs with relatively high-magnetization value indicating that they were sufficiently sensitive to external magnetic fields as magnetic drug carriers. Furthermore, dextran coated MNPs exhibited high potential as T2 contrast agents for MRI. Conclusion: Based on our findings, we propose the dextran coated MNPs

  2. Magnetite nanoparticles coated with β-cyclodextrin functionalized-ionic liquid: Synthesis and its preliminary investigation as a new sensing material

    NASA Astrophysics Data System (ADS)

    Sinniah, Subathra; Mohamad, Sharifah; Manan, Ninie S. A.

    2015-12-01

    In this study, a novel surface of modified magnetite nanoparticles Fe3O4 was coated with β-cyclodextrin-funclionalized ionic liquid (Fe3O4-β-CD-IL) via the co-precipitation method in alkaline salt medium. β-Cyclodextrin-functionalized-ionic liquid has been effectively coated onto the surface of Fe3O4 magnetite nanoparticles. The instruments used to investigate the architecture are: Fourier Transform Infrared Spectroscopy, X-ray Powder Diffraction, Electron Microscope-Energy Dispersive X-Ray Spectrometry, Transmission Electron Microscope, Field Emission Scanning Electron Microscope, Vibrating Sample Magnetometer and Brunauer-Emmett-Teller isotherm. A Vibration Sample Magnetometer analysis verified that the Fe3O4-β-CD-IL attained excellent magnetic properties. The analysis of High Resolution Transmission Electron Microscope shows that the Fe3O4-β-CD-IL produced monodisperse particles with minimal aggregation. Moreover, electrochemical studies have revealed that this new material showed outstanding ability to recognize Bisphenol A with lower electrochemical potential at 0.5 V than other comparative materials, as well as a higher detection current. Thus, this material has promising potential as a new electrode material in sensor applications.

  3. Immobilized molybdenum-thiosemicarbazide Schiff base complex on the surface of magnetite nanoparticles as a new nanocatalyst for the epoxidation of olefins

    NASA Astrophysics Data System (ADS)

    Mohammadikish, M.; Masteri-Farahani, M.; Mahdavi, S.

    2014-03-01

    In this work, a new magnetically recoverable nanocatalyst was developed by immobilization of thiosemicarbazide ligand on the surface of silica coated magnetite nanoparticles (SCMNPs) through Schiff base condensation and followed complexation with MoO2(acac)2. Characterization of the prepared nanocatalyst was performed with different physicochemical methods such as Fourier transform infrared (FT-IR) and atomic absorption spectroscopies, X-ray diffraction (XRD), vibrating sample magnetometry (VSM), thermogravimetric analysis (TGA), field-emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). The prepared catalyst catalyzed the epoxidation of olefins and allyl alcohols with tert-butyl hydroperoxide (TBHP) and cumene hydroperoxide (CHP) quantitatively with excellent selectivity toward the corresponding epoxides under mild reaction conditions.

  4. Adsorption and kinetic studies of seven different organic dyes onto magnetite nanoparticles loaded tea waste and removal of them from wastewater samples.

    PubMed

    Madrakian, Tayyebeh; Afkhami, Abbas; Ahmadi, Mazaher

    2012-12-01

    Adsorption of seven different organic dyes from aqueous solutions onto magnetite nanoparticles loaded tea waste (MNLTW) was studied. MNLTW was prepared via a simple method and was fully characterized. The properties of this magnetic adsorbent were characterized by scanning electron microscopy and X-ray diffraction. Adsorption characteristics of the MNLTW adsorbent was examined using Janus green, methylene blue, thionine, crystal violet, Congo red, neutral red and reactive blue 19 as adsorbates. Dyes adsorption process was thoroughly studied from both kinetic and equilibrium points of view for all adsorbents. The experimental isotherm data were analyzed using Langmuir, Freundlich, Sips, Redlich-Peterson, Brouers-Sotolongo and Temkin isotherms. The results from Langmuir isotherm indicated that the capacity of MNLTW for the adsorption of cationic dyes was higher than that for anionic dyes. The adsorption kinetics was tested for the pseudo-first order and pseudo-second order kinetic models at different experimental conditions. PMID:23058993

  5. Adsorption and kinetic studies of seven different organic dyes onto magnetite nanoparticles loaded tea waste and removal of them from wastewater samples

    NASA Astrophysics Data System (ADS)

    Madrakian, Tayyebeh; Afkhami, Abbas; Ahmadi, Mazaher

    2012-12-01

    Adsorption of seven different organic dyes from aqueous solutions onto magnetite nanoparticles loaded tea waste (MNLTW) was studied. MNLTW was prepared via a simple method and was fully characterized. The properties of this magnetic adsorbent were characterized by scanning electron microscopy and X-ray diffraction. Adsorption characteristics of the MNLTW adsorbent was examined using Janus green, methylene blue, thionine, crystal violet, Congo red, neutral red and reactive blue 19 as adsorbates. Dyes adsorption process was thoroughly studied from both kinetic and equilibrium points of view for all adsorbents. The experimental isotherm data were analyzed using Langmuir, Freundlich, Sips, Redlich-Peterson, Brouers-Sotolongo and Temkin isotherms. The results from Langmuir isotherm indicated that the capacity of MNLTW for the adsorption of cationic dyes was higher than that for anionic dyes. The adsorption kinetics was tested for the pseudo-first order and pseudo-second order kinetic models at different experimental conditions.

  6. o-Vanillin functionalized mesoporous silica - coated magnetite nanoparticles for efficient removal of Pb(II) from water

    NASA Astrophysics Data System (ADS)

    Culita, Daniela C.; Simonescu, Claudia Maria; Patescu, Rodica-Elena; Dragne, Mioara; Stanica, Nicolae; Oprea, Ovidiu

    2016-06-01

    o-Vanillin functionalized mesoporous silica - coated magnetite (Fe3O4@MCM-41-N-oVan) was synthesized and fully characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, N2 adsorption-desorption technique and magnetic measurements. The capacity of Fe3O4@MCM-41-N-oVan to adsorb Pb(II) from aqueous solutions was evaluated in comparison with raw mesoporous silica - coated magnetite (Fe3O4@MCM-41) and amino - modified mesoporous silica coated magnetite (Fe3O4@MCM-41-NH2). The effect of adsorption process parameters such us pH, contact time, initial Pb(II) concentration was also investigated. The adsorption data were successfully fitted with the Langmuir model, exhibiting a maximum adsorption capacity of 155.71 mg/g at pH=4.4 and T=298 K. The results revealed that the adsorption rate was very high at the beginning of the adsorption process, 80-90% of the total amount of Pb(II) being removed within the first 60 min, depending on the initial concentration. The results of the present work suggest that Fe3O4@MCM-41-N-oVan is a suitable candidate for the separation of Pb(II) from contaminated water.

  7. Single step synthesis of amine-functionalized mesoporous magnetite nanoparticles and their application for copper ions removal from aqueous solution.

    PubMed

    Gao, Jining; He, Yingjuan; Zhao, Xianying; Ran, Xinze; Wu, Yonghui; Su, Yongping; Dai, Jianwu

    2016-11-01

    Amine-functionalized mesoporous superparamagnetic Fe3O4 nanoparticles with an average size of 70nm have been synthesized using a single step solvothermal method by the introduction of triethylenetetramine (TETA), a chelating agent recommended for the removal of excess copper in patients with Wilson's disease. The synthesized nanoparticles were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, nitrogen adsorption/desorption isotherm, vibrating sample magnetometer (VSM), and Fourier transform infrared spectroscopy (FTIR). It is confirmed that the magnetic nanoparticles have been functionalized with TETA during the synthetic process, and the concentration of TETA is crucial for the formation of monodisperse mesoporous nanoparticles. The obtained single-crystal magnetic nanoparticles have a high magnetization, which enhances their response to external magnetic field and therefore should greatly facilitate the manipulation of the particles in practical uses. Reaction parameters affecting the formation of mesoporous structure were explored, and a possible formation mechanism involving templated aggregation and recrystallization processes was proposed. The capacity of the synthesized amine-functionalized Fe3O4 nanoparticles toward Cu(II) removal from aqueous solution was investigated. The adsorption rate of Cu(II) on amine-functionalized Fe3O4 nanoparticles followed a pseudo-second order kinetic model. The results of this study demonstrated that the amine-functionalized mesoporous superparamagnetic Fe3O4 nanoparticles could be used as an efficient adsorbent in water treatment and would also find potential application for Cu(II) removal in vivo. PMID:27475709

  8. Superparamagnetic iron oxide polyacrylic acid coated γ-Fe{sub 2}O{sub 3} nanoparticles do not affect kidney function but cause acute effect on the cardiovascular function in healthy mice

    SciTech Connect

    Iversen, Nina K.; Frische, Sebastian; Thomsen, Karen; Laustsen, Christoffer; Pedersen, Michael; Hansen, Pernille B.L.; Bie, Peter; Fresnais, Jérome; Berret, Jean-Francois; Baatrup, Erik; Wang, Tobias

    2013-01-15

    This study describes the distribution of intravenously injected polyacrylic acid (PAA) coated γ-Fe{sub 2}O{sub 3} NPs (10 mg kg{sup −1}) at the organ, cellular and subcellular levels in healthy BALB/cJ mice and in parallel addresses the effects of NP injection on kidney function, blood pressure and vascular contractility. Magnetic resonance imaging (MRI) and transmission electron microscopy (TEM) showed accumulation of NPs in the liver within 1 h after intravenous infusion, accommodated by intracellular uptake in endothelial and Kupffer cells with subsequent intracellular uptake in renal cells, particularly the cytoplasm of the proximal tubule, in podocytes and mesangial cells. The renofunctional effects of NPs were evaluated by arterial acid–base status and measurements of glomerular filtration rate (GFR) after instrumentation with chronically indwelling catheters. Arterial pH was 7.46 ± 0.02 and 7.41 ± 0.02 in mice 0.5 h after injections of saline or NP, and did not change over the next 12 h. In addition, the injections of NP did not affect arterial PCO{sub 2} or [HCO{sub 3}{sup −}] either. Twenty-four and 96 h after NP injections, the GFR averaged 0.35 ± 0.04 and 0.35 ± 0.01 ml min{sup −1} g{sup −1}, respectively, values which were statistically comparable with controls (0.29 ± 0.02 and 0.33 ± 0.1 ml{sup –1} min{sup –1} 25 g{sup –1}). Mean arterial blood pressure (MAP) decreased 12–24 h after NP injections (111.1 ± 11.5 vs 123.0 ± 6.1 min{sup −1}) associated with a decreased contractility of small mesenteric arteries revealed by myography to characterize endothelial function. In conclusion, our study demonstrates that accumulation of superparamagnetic iron oxide nanoparticles does not affect kidney function in healthy mice but temporarily decreases blood pressure. -- Highlights: ► PAA coated γ-Fe{sub 2}O{sub 3} nanoparticles were injected intravenously into healthy mice. ► We examine the distribution and physiological effects of

  9. Magnetic/NIR-responsive drug carrier, multicolor cell imaging, and enhanced photothermal therapy of gold capped magnetite-fluorescent carbon hybrid nanoparticles.

    PubMed

    Wang, Hui; Cao, Guixin; Gai, Zheng; Hong, Kunlun; Banerjee, Probal; Zhou, Shuiqin

    2015-05-01

    This paper reports a type of multifunctional hybrid nanoparticle (NP) composed of gold nanocrystals coated on and/or embedded in a magnetite-fluorescent porous carbon core-shell NP template (Fe3O4@PC-CDs-Au) for biomedical applications, including magnetic/NIR-responsive drug release, multicolor cell imaging, and enhanced photothermal therapy. The synthesis of the Fe3O4@PC-CDs-Au NPs firstly involves the preparation of core-shell template NPs with magnetite nanocrystals clustered in the cores and fluorescent carbon dots (CDs) embedded in a porous carbon shell, followed by an in situ reduction of silver ions (Ag(+)) loaded in the porous carbon shell and a subsequent replacement of Ag NPs with Au NPs through a galvanic replacement reaction using HAuCl4 as a precursor. The Fe3O4@PC-CDs-Au NPs can enter the intracellular region and light up mouse melanoma B16F10 cells in multicolor mode. The porous carbon shell, anchored with hydrophilic hydroxyl/carboxyl groups, endows the Fe3O4@PC-CDs-Au NPs with excellent stability in the aqueous phase and a high loading capacity (719 mg g(-1)) for the anti-cancer drug doxorubicin (DOX). The superparamagnetic Fe3O4@PC-CDs-Au NPs with a saturation magnetization of 23.26 emu g(-1) produce localized heat under an alternating magnetic field, which triggers the release of the loaded drug. The combined photothermal effects of the Au nanocrystals and the CDs on/in the carbon shell can not only regulate the release rate of the loaded drug, but also efficiently kill tumor cells under NIR irradiation. Benefitting from their excellent optical properties, their magnetic field and NIR light-responsive drug release capabilities and their enhanced photothermal effect, such nanostructured Fe3O4@PC-CDs-Au hybrid NPs are very promising for simultaneous imaging diagnostics and high efficacy therapy. PMID:25854197

  10. Characterization of different magnetite cobalt nanoparticles in hydrocarbon-based magnetic fluids by means of static and dynamic magnetization measurements

    NASA Astrophysics Data System (ADS)

    Ayala-Valenzuela, Oscar; Fannin, Paul C.; Betancourt-Galindo, Rebeca; Rodríguez-Fernández, Oliverio; Matutes-Aquino, José

    2007-04-01

    Magnetic nanoparticles with different compositions (Co xFe 3-xO 4, 0⩽ x⩽0.1) were synthesized from metal salts using a coprecipitation technique to produce magnetic fluids following a peptization technique. The liquid carrier was the hydrocarbon Isopar M and the surfactant was oleic acid. The colloidal-sized ferrimagnetic nanoparticles produced were found to be superparamagnetic. Measurements of the complex magnetic susceptibility were carried out to evaluate the resonant frequency fres, the anisotropy constant K, and anisotropy field HA. fres was found to be a linear function of the cobalt content of the magnetic nanoparticles over the range of cobalt content studied.

  11. Mechanism of in situ surface polymerization of gallic acid in an environmental-inspired preparation of carboxylated core-shell magnetite nanoparticles.

    PubMed

    Tóth, Ildikó Y; Szekeres, Márta; Turcu, Rodica; Sáringer, Szilárd; Illés, Erzsébet; Nesztor, Dániel; Tombácz, Etelka

    2014-12-30

    Magnetite nanoparticles (MNPs) with biocompatible coatings are good candidates for MRI (magnetic resonance imaging) contrasting, magnetic hyperthermia treatments, and drug delivery systems. The spontaneous surface induced polymerization of dissolved organic matter on environmental mineral particles inspired us to prepare carboxylated core-shell MNPs by using a ubiquitous polyphenolic precursor. Through the adsorption and in situ surface polymerization of gallic acid (GA), a polygallate (PGA) coating is formed on the nanoparticles (PGA@MNP) with possible antioxidant capacity. The present work explores the mechanism of polymerization with the help of potentiometric acid-base titration, dynamic light scattering (for particle size and zeta potential determination), UV-vis (UV-visible light spectroscopy), FTIR-ATR (Fourier-transformed infrared spectroscopy by attenuated total reflection), and XPS (X-ray photoelectron spectroscopy) techniques. We observed the formation of ester and ether linkages between gallate monomers both in solution and in the adsorbed state. Higher polymers were formed in the course of several weeks both on the surface of nanoparticles and in the dispersion medium. The ratio of the absorbances of PGA supernatants at 400 and 600 nm (i.e., the E4/E6 ratio commonly used to characterize the degree of polymerization of humic materials) was determined to be 4.3, similar to that of humic acids. Combined XPS, dynamic light scattering, and FTIR-ATR results revealed that, prior to polymerization, the GA monomers became oxidized to poly(carboxylic acid)s due to ring opening while Fe(3+) ions reduced to Fe(2+). Our published results on the colloidal and chemical stability of PGA@MNPs are referenced thoroughly in the present work. Detailed studies on biocompatibility, antioxidant property, and biomedical applicability of the particles will be published. PMID:25517214

  12. Effective extraction and simultaneous determination of Sudan dyes from tomato sauce and chili-containing foods using magnetite/reduced graphene oxide nanoparticles coupled with high-performance liquid chromatography.

    PubMed

    Zhang, Ming-Yue; Wang, Man-Man; Hao, Yu-Lan; Shi, Xin-Ran; Wang, Xue-Sheng

    2016-05-01

    A simple, effective, and robust magnetic solid-phase extraction method was developed using magnetite/reduced graphene oxide nanoparticles as the adsorbent for the simultaneous determination of Sudan dyes (I, II, III, and IV) in foodstuffs. The magnetite/reduced graphene oxide nanoparticles were characterized by X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry. The extraction parameters including extraction time, elution solution, and elution time and volume were investigated in detail. Such magnetite/reduced graphene oxide nanoparticles based magnetic solid-phase extraction in combination with high-performance liquid chromatography and variable wavelength detection gave the detection limits of 3-6 μg/kg for Sudan I-IV in chili sauce, tomato sauce, chili powder, and chili flake samples. The recoveries were 79.6-108% at three spiked levels with the intra- and inter-day relative standard deviations of 1.2-8.6 and 4.5-9.6%, respectively. The feasibility was further performed by a comparison with commercial alumina-N. This method is suitable for the routine analysis of Sudan dyes due to its sensitivity, simplicity, and low cost. PMID:26970251

  13. Simple and Rapid Synthesis of Magnetite/Hydroxyapatite Composites for Hyperthermia Treatments via a Mechanochemical Route

    PubMed Central

    Iwasaki, Tomohiro; Nakatsuka, Ryo; Murase, Kenya; Takata, Hiroshige; Nakamura, Hideya; Watano, Satoru

    2013-01-01

    This paper presents a simple method for the rapid synthesis of magnetite/hydroxyapatite composite particles. In this method, superparamagnetic magnetite nanoparticles are first synthesized by coprecipitation using ferrous chloride and ferric chloride. Immediately following the synthesis, carbonate-substituted (B-type) hydroxyapatite particles are mechanochemically synthesized by wet milling dicalcium phosphate dihydrate and calcium carbonate in a dispersed suspension of magnetite nanoparticles, during which the magnetite nanoparticles are incorporated into the hydroxyapatite matrix. We observed that the resultant magnetite/hydroxyapatite composites possessed a homogeneous dispersion of magnetite nanoparticles, characterized by an absence of large aggregates. When this material was subjected to an alternating magnetic field, the heat generated increased with increasing magnetite concentration. For a magnetite concentration of 30 mass%, a temperature increase greater than 20 K was achieved in less than 50 s. These results suggest that our composites exhibit good hyperthermia properties and are promising candidates for hyperthermia treatments. PMID:23629669

  14. Ultrasound mediation for one-pot sonosynthesis and deposition of magnetite nanoparticles on cotton/polyester fabric as a novel magnetic, photocatalytic, sonocatalytic, antibacterial and antifungal textile.

    PubMed

    Rastgoo, Madine; Montazer, Majid; Malek, Reza M A; Harifi, Tina; Mahmoudi Rad, Mahnaz

    2016-07-01

    A magnetic cotton/polyester fabric with photocatalytic, sonocatalytic, antibacterial and antifungal activities was successfully prepared through in-situ sonosynthesis method under ultrasound irradiation. The process involved the oxidation of Fe(2+) to Fe(3+) via hydroxyl radicals generated through bubbles collapse in ultrasonic bath. The treated samples were analyzed by X-ray diffraction, field emission scanning electron microscopy, energy dispersive X-ray spectroscopy and vibrating sample magnetometry. Photocatalytic and sonocatalytic activities of magnetite treated fabrics were also evaluated toward Reactive Blue 2 decoloration under sunlight and ultrasound irradiation. Central composite design based on response surface methodology was applied to study the influence of iron precursor, pH and surfactant concentration to obtain appropriate amount for the best magnetism. Findings suggested the potential of one-pot sonochemical method to synthesize and fabricate Fe3O4 nanoparticles on cotton/polyester fabric possessing appropriate saturation magnetization, 95% antibacterial efficiency against Staphylococcus aureus and 99% antifungal effect against Candida albicans, 87% and 70% dye photocatalytic and sonocatalytic decoloration along with enhanced mechanical properties using only one iron rich precursor at low temperature. PMID:26964948

  15. Salicylic acid functionalized silica-coated magnetite nanoparticles for solid phase extraction and preconcentration of some heavy metal ions from various real samples

    PubMed Central

    2011-01-01

    A method for the preconcentration of trace heavy metal ions in environmental samples has been reported. The presented method is based on the sorption of Cu(II), Cd(II), Ni(II) and Cr(III) ions with salicylic acid as respective chelate on silica-coated magnetite nanoparticles. Prepared adsorbent was characterized by XRD, SEM, BET and FT-IR measurements. The metals content of the sorbed complexes are eluted using 4.0 mL of 1.0 mol L-1 nitric acid. The influences of the analytical parameters including pH, amount of solid phase and condition of eluting solution, the effects of matrix ions on the retention of the analytes were examined. The accuracy and precision of suggested method were tested by analyzing of certified reference materials. The detection limits (3Sb/m, N = 8) for Cu(II), Cd(II), Ni(II) and Cr(III) ions are 0.22, 0.11, 0.27 and 0.15 μg L-1, respectively, and the maximum preconcentration factor is 200. The method was successfully applied to the evaluation of these trace and toxic metals in various waters, foods and other samples. PMID:21762480

  16. Two novel calixarene functionalized iron oxide magnetite nanoparticles as a platform for magnetic separation in the liquid-liquid/solid-liquid extraction of oxyanions.

    PubMed

    Sayin, Serkan; Ozcan, Fatih; Yilmaz, Mustafa

    2013-05-01

    This article focuses on the syntheses of 25,27-bis[3-(N-ethylsulfonic acid)aminopropxy]-26,28-dihydroxy-5,11,17,23-tetra-tert-butyl-calix[4]arene (3) and 25,27-bis[3-(N-ethyl-dihydrogen phosphate)aminopropxy]-26,28-dihydroxy-5,11,17,23-tetra-tert-butyl-calix[4]arene (4) as well as their immobilization onto [3-(2,3-epoxypropoxy)-propyl]-trimethoxysilane-modified Fe3O4 magnetite nanoparticles, and the extraction abilities of four new extractants which were characterized by a combination of FTIR, (1)H NMR, elemental analyses, transmission electron microscopy (TEM) and thermogravimetric analyses (TGA) involving electrostatic and hydrogen bonding interactions between the calixarene and oxide anions such as arsenate and dichromate anions. The extraction results indicate that these new calixarene derivatives having high extraction capabilities would be used as effective extractants for the removal of the dichromate/arsenate ions from water. PMID:23498279

  17. Enhanced selectivity and capacity of clinoptilolite for Cd2+ removal from aqueous solutions by incorporation of magnetite nanoparticles and surface modification with cysteine.

    PubMed

    Sharifi, Masumeh; Baghdadi, Majid

    2016-01-01

    In this study, magnetic zeolite (MZ) nanocomposite modified with cysteine was developed in order to enhance selectivity and capacity of clinoptilolite for cadmium ion. The prepared MZ nanocomposite is containing clinoptilolite and magnetite nanoparticles with weight ratio of 3:1. The synthesized nanocomposite was characterized by transmission electron microscopy, X-ray diffraction and vibrating sample magnetometer. Surface modification was confirmed by Fourier transform infrared spectrometer. Experiments were carried out to find the optimum conditions for modification of clinoptilolite and to investigate the effective parameters (pH, adsorbent dosage, contact time, and temperature) on the adsorption of Cd(2+) ion by modified clinoptilolite. The results showed enhanced selectivity of modified MZ in the presence of other naturally occurring cations (Na(+), K(+), Ca(2+) and Mg(2+)) and ammonium. Kinetic and equilibrium data were well fitted by a pseudo second-order and Langmuir model, respectively, with high correlation coefficients. The maximum adsorption capacities of the modified and non-modified clinoptilolite were found to be 20.0 mg/g and 5.2 mg/g, respectively. Thermodynamic parameters revealed that the adsorption process is spontaneous and endothermic under studied conditions. PMID:27148732

  18. Magnetic/NIR-responsive drug carrier, multicolor cell imaging, and enhanced photothermal therapy of gold capped magnetite-fluorescent carbon hybrid nanoparticles

    DOE PAGESBeta

    Wang, Hui; Cao, Guixin; Gai, Zheng; Hong, Kunlun; Banerjee, Probal; Zhou, Shuiqin

    2015-03-25

    In our paper reports a type of multifunctional hybrid nanoparticle (NP) composed of gold nanocrystals coated on and/or embedded in a magnetite-fluorescent porous carbon core-shell NP template (Fe3O4@PC-CDs-Au) for biomedical applications, including magnetic/NIR-responsive drug release, multicolor cell imaging, and enhanced photothermal therapy. The synthesis of the Fe3O4@PC-CDs-Au NPs firstly involves the preparation of core-shell template NPs with magnetite nanocrystals clustered in the cores and fluorescent carbon dots (CDs) embedded in a porous carbon shell, followed by an in situ reduction of silver ions (Ag+) loaded in the porous carbon shell and a subsequent replacement of Ag NPs with Au NPsmore » through a galvanic replacement reaction using HAuCl4 as a precursor. Moreover, the Fe3O4@PC-CDsAu NPs can enter the intracellular region and light up mouse melanoma B16F10 cells in multicolor mode. The porous carbon shell, anchored with hydrophilic hydroxyl/carboxyl groups, endows the Fe3O4@PC-CDs-Au NPs with excellent stability in the aqueous phase and a high loading capacity (719 mg g-1) for the anti-cancer drug doxorubicin (DOX). The superparamagnetic Fe3O4@PC-CDs-Au NPs with a saturation magnetization of 23.26 emu g-1 produce localized heat under an alternating magnetic field, which triggers the release of the loaded drug. The combined photothermal effects of the Au nanocrystals and the CDs on/in the carbon shell can not only regulate the release rate of the loaded drug, but also efficiently kill tumor cells under NIR irradiation. Finally, in benefitting from their excellent optical properties, their magnetic field and NIR light-responsive drug release capabilities and their enhanced photothermal effect, such nanostructured Fe3O4@PC-CDs-Au hybrid NPs are very promising for simultaneous imaging diagnostics and high efficacy therapy.« less

  19. Magnetic/NIR-responsive drug carrier, multicolor cell imaging, and enhanced photothermal therapy of gold capped magnetite-fluorescent carbon hybrid nanoparticles

    SciTech Connect

    Wang, Hui; Cao, Guixin; Gai, Zheng; Hong, Kunlun; Banerjee, Probal; Zhou, Shuiqin

    2015-03-25

    In our paper reports a type of multifunctional hybrid nanoparticle (NP) composed of gold nanocrystals coated on and/or embedded in a magnetite-fluorescent porous carbon core-shell NP template (Fe3O4@PC-CDs-Au) for biomedical applications, including magnetic/NIR-responsive drug release, multicolor cell imaging, and enhanced photothermal therapy. The synthesis of the Fe3O4@PC-CDs-Au NPs firstly involves the preparation of core-shell template NPs with magnetite nanocrystals clustered in the cores and fluorescent carbon dots (CDs) embedded in a porous carbon shell, followed by an in situ reduction of silver ions (Ag+) loaded in the porous carbon shell and a subsequent replacement of Ag NPs with Au NPs through a galvanic replacement reaction using HAuCl4 as a precursor. Moreover, the Fe3O4@PC-CDsAu NPs can enter the intracellular region and light up mouse melanoma B16F10 cells in multicolor mode. The porous carbon shell, anchored with hydrophilic hydroxyl/carboxyl groups, endows the Fe3O4@PC-CDs-Au NPs with excellent stability in the aqueous phase and a high loading capacity (719 mg g-1) for the anti-cancer drug doxorubicin (DOX). The superparamagnetic Fe3O4@PC-CDs-Au NPs with a saturation magnetization of 23.26 emu g-1 produce localized heat under an alternating magnetic field, which triggers the release of the loaded drug. The combined photothermal effects of the Au nanocrystals and the CDs on/in the carbon shell can not only regulate the release rate of the loaded drug, but also efficiently kill tumor cells under NIR irradiation. Finally, in benefitting from their excellent optical properties, their magnetic field and NIR light-responsive drug release capabilities and their enhanced photothermal effect, such nanostructured Fe3O4@PC-CDs-Au hybrid NPs are very promising for simultaneous imaging

  20. Oleic acid coated magnetic nano-particles: Synthesis and characterizations

    SciTech Connect

    Panda, Biswajit Goyal, P. S.

    2015-06-24

    Magnetic nano particles of Fe{sub 3}O{sub 4} coated with oleic acid were synthesized using wet chemical route, which involved co-precipitation of Fe{sup 2+} and Fe{sup 3+} ions. The nano particles were characterized using XRD, TEM, FTIR, TGA and VSM. X-ray diffraction studies showed that nano particles consist of single phase Fe{sub 3}O{sub 4} having inverse spinel structure. The particle size obtained from width of Bragg peak is about 12.6 nm. TEM analysis showed that sizes of nano particles are in range of 6 to 17 nm with a dominant population at 12 - 14 nm. FTIR and TGA analysis showed that -COOH group of oleic acid is bound to the surface of Fe{sub 3}O{sub 4} particles and one has to heat the sample to 278° C to remove the attached molecule from the surface. Further it was seen that Fe{sub 3}O{sub 4} particles exhibit super paramagnetism with a magnetization of about 53 emu/ gm.

  1. Magnetic/NIR-responsive drug carrier, multicolor cell imaging, and enhanced photothermal therapy of gold capped magnetite-fluorescent carbon hybrid nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, Hui; Cao, Guixin; Gai, Zheng; Hong, Kunlun; Banerjee, Probal; Zhou, Shuiqin

    2015-04-01

    This paper reports a type of multifunctional hybrid nanoparticle (NP) composed of gold nanocrystals coated on and/or embedded in a magnetite-fluorescent porous carbon core-shell NP template (Fe3O4@PC-CDs-Au) for biomedical applications, including magnetic/NIR-responsive drug release, multicolor cell imaging, and enhanced photothermal therapy. The synthesis of the Fe3O4@PC-CDs-Au NPs firstly involves the preparation of core-shell template NPs with magnetite nanocrystals clustered in the cores and fluorescent carbon dots (CDs) embedded in a porous carbon shell, followed by an in situ reduction of silver ions (Ag+) loaded in the porous carbon shell and a subsequent replacement of Ag NPs with Au NPs through a galvanic replacement reaction using HAuCl4 as a precursor. The Fe3O4@PC-CDs-Au NPs can enter the intracellular region and light up mouse melanoma B16F10 cells in multicolor mode. The porous carbon shell, anchored with hydrophilic hydroxyl/carboxyl groups, endows the Fe3O4@PC-CDs-Au NPs with excellent stability in the aqueous phase and a high loading capacity (719 mg g-1) for the anti-cancer drug doxorubicin (DOX). The superparamagnetic Fe3O4@PC-CDs-Au NPs with a saturation magnetization of 23.26 emu g-1 produce localized heat under an alternating magnetic field, which triggers the release of the loaded drug. The combined photothermal effects of the Au nanocrystals and the CDs on/in the carbon shell can not only regulate the release rate of the loaded drug, but also efficiently kill tumor cells under NIR irradiation. Benefitting from their excellent optical properties, their magnetic field and NIR light-responsive drug release capabilities and their enhanced photothermal effect, such nanostructured Fe3O4@PC-CDs-Au hybrid NPs are very promising for simultaneous imaging diagnostics and high efficacy therapy.This paper reports a type of multifunctional hybrid nanoparticle (NP) composed of gold nanocrystals coated on and/or embedded in a magnetite-fluorescent porous

  2. Nanosized Fe3O4 an efficient PCR yield enhancer-Comparative study with Au, Ag nanoparticles.

    PubMed

    Kambli, Priyanka; Kelkar-Mane, Varsha

    2016-05-01

    Nanomaterials-assisted PCR is a promising field of nanobiotechnology that amalgamates nanomaterials into the conventional PCR system to achieve better amplification of desired product. With literature documenting the variable effects of these nanomaterials on the PCR yield and amplification; it was thought worthwhile to compare the PCR enhancing efficiency of three transition metal nanoparticles in form of stable colloidal suspensions at varying concentrations.The nanoparticles(NPs) of silver, gold and magnetite were chemically synthesized by reducing their respective salts and characterized using UV-vis spectroscopy. Their morphology was assessed using nanoparticle tracking system and AFM. The effect of these nanofluids on amplification of 800 bp prokaryotic DNA template with 30% GC content was studied using conventional thermal cycler. The reaction kinetics for all the three nanofluids yielded a Gaussian curve of amplification with varying concentrations. The ammonium salt of oleic acid coated magnetite (Fe3O4) nanoparticles at a concentration of 0.72 × 10(-2)nM and average size of 33 nm demonstrated highest amplification efficiency of 190% as compared to the citrate stabilized AgNP-25 nm (45%) and AuNP-15.19 nm (134%) using a conventional PCR system. The major reasons that allow Fe3O4 NPs outperform the other 2 transition metal NP's seem to be attributed to its heat conduction property as well as effective adsorption of PCR components onto the ammonium salt of oleic acid coated magnetite nanofluids. The data from our study offers valuable information for the application of ferrofluids as economically, efficient and effective alternative for nanomaterial-assisted PCR yield enhancers. PMID:26896662

  3. Magnetite and its production

    SciTech Connect

    Koebbe, E.R.

    1993-12-31

    The supply of high quality magnetite for the cleaning of coal using dense medium cyclones and vessels is of concern to all coal preparation operations. This paper describes the production of high purity magnetite (Fe{sub 3}O{sub 4}) from a domestic underground mining operation in Missouri, Pea Ridge Iron Ore Company. Emphasis will be placed on the mining and processing of the magnetite ore into the various magnetite products required by coal preparation plants.

  4. Magnetic solid phase extraction based on magnetite/reduced graphene oxide nanoparticles for determination of trace isocarbophos residues in different matrices.

    PubMed

    Yan, Shan; Qi, Ting-Ting; Chen, De-Wen; Li, Zhao; Li, Xiu-Juan; Pan, Si-Yi

    2014-06-20

    A simple one-step solvothermal method was applied for the preparation of magnetite/reduced graphene oxide (MRGO), and the synthetic nanocomposites with a magnetic particle size of ∼8nm were used as an adsorbent for magnetic solid phase extraction of isocarbophos (ICP) in different sample matrices prior to gas chromatography (GC) detection. The identity of the nanomaterial was confirmed using Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy and transmission electron microscopy. It was shown that Fe3O4 nanoparticles with a uniform size were homogeneously anchored on RGO nanosheets. Increased oxidation degrees of graphite oxide, big particle sizes and large loading amounts of Fe3O4 on the surface of RGO led to a decrease of adsorption capacity of MRGO to ICP. The adsorption behavior of this adsorbent was better fitted by the pseudo-second-order kinetic model. Several parameters affecting the extraction efficiency were investigated and optimized, including adsorbent dosage, extraction time, ionic strength and desorption conditions. And then, a rapid and effective method based on MRGO combined with GC was developed for the determination of ICP in aqueous samples. A linear range from 0.05 to 50ngmL(-1) was obtained with a high correlation coefficient (R(2)) of 0.9995, and the limit of detection was found to be 0.0044ngmL(-1). This method was successfully applied to the analysis of ICP in five kinds of samples, including apple, rice, lake water, cowpea and cabbage. The recoveries in different sample matrices were in the range from 81.00% to 108.51% with relative standard deviations less than 9.72%. It can be concluded that the proposed analytical method is highly-efficient, sensitive, precise, accurate and practicable. PMID:24800969

  5. Influence of magnetite stoichiometry on U(VI) reduction.

    PubMed

    Latta, Drew E; Gorski, Christopher A; Boyanov, Maxim I; O'Loughlin, Edward J; Kemner, Kenneth M; Scherer, Michelle M

    2012-01-17

    Hexavalent uranium (U(VI)) can be reduced enzymatically by various microbes and abiotically by Fe(2+)-bearing minerals, including magnetite, of interest because of its formation from Fe(3+) (oxy)hydroxides via dissimilatory iron reduction. Magnetite is also a corrosion product of iron metal in suboxic and anoxic conditions and is likely to form during corrosion of steel waste containers holding uranium-containing spent nuclear fuel. Previous work indicated discrepancies in the extent of U(VI) reduction by magnetite. Here, we demonstrate that the stoichiometry (the bulk Fe(2+)/Fe(3+) ratio, x) of magnetite can, in part, explain the observed discrepancies. In our studies, magnetite stoichiometry significantly influenced the extent of U(VI) reduction by magnetite. Stoichiometric and partially oxidized magnetites with x ≥ 0.38 reduced U(VI) to U(IV) in UO(2) (uraninite) nanoparticles, whereas with more oxidized magnetites (x < 0.38) and maghemite (x = 0), sorbed U(VI) was the dominant phase observed. Furthermore, as with our chemically synthesized magnetites (x ≥ 0.38), nanoparticulate UO(2) was formed from reduction of U(VI) in a heat-killed suspension of biogenic magnetite (x = 0.43). X-ray absorption and Mössbauer spectroscopy results indicate that reduction of U(VI) to U(IV) is coupled to oxidation of Fe(2+) in magnetite. The addition of aqueous Fe(2+) to suspensions of oxidized magnetite resulted in reduction of U(VI) to UO(2), consistent with our previous finding that Fe(2+) taken up from solution increased the magnetite stoichiometry. Our results suggest that magnetite stoichiometry and the ability of aqueous Fe(2+) to recharge magnetite are important factors in reduction of U(VI) in the subsurface. PMID:22148359

  6. A simple and fast method based on mixed hemimicelles coated magnetite nanoparticles for simultaneous extraction of acidic and basic pollutants.

    PubMed

    Asgharinezhad, Ali Akbar; Ebrahimzadeh, Homeira

    2016-01-01

    One of the considerable and disputable areas in analytical chemistry is a single-step simultaneous extraction of acidic and basic pollutants. In this research, a simple and fast coextraction of acidic and basic pollutants (with different polarities) with the aid of magnetic dispersive micro-solid phase extraction based on mixed hemimicelles assembly was introduced for the first time. Cetyltrimethylammonium bromide (CTAB)-coated Fe3O4 nanoparticles as an efficient sorbent was successfully applied to adsorb 4-nitrophenol and 4-chlorophenol as two acidic and chlorinated aromatic amines as basic model compounds. Using a central composite design methodology combined with desirability function approach, the optimal experimental conditions were evaluated. The opted conditions were pH = 10; concentration of CTAB = 0.86 mmol L(-1); sorbent amount = 55.5 mg; sorption time = 11.0 min; no salt addition to the sample, type, and volume of the eluent = 120 μL methanol containing 5% acetic acid and 0.01 mol L(-1) HCl; and elution time = 1.0 min. Under the optimum conditions, detection limits and linear dynamic ranges were achieved in the range of 0.05-0.1 and 0.25-500 μg L(-1), respectively. The percent of extraction recoveries and relative standard deviations (n = 5) were in the range of 71.4-98.0 and 4.5-6.5, respectively. The performance of the optimized method was certified by coextraction of other acidic and basic compounds. Ultimately, the applicability of the method was successfully confirmed by the extraction and determination of the target analytes in various water samples, and satisfactory results were obtained. PMID:26507332

  7. Antibacterial Performance of Alginic Acid Coating on Polyethylene Film

    PubMed Central

    Karbassi, Elika; Asadinezhad, Ahmad; Lehocký, Marian; Humpolíček, Petr; Vesel, Alenka; Novák, Igor; Sáha, Petr

    2014-01-01

    Alginic acid coated polyethylene films were examined in terms of surface properties and bacteriostatic performance against two most representative bacterial strains, that is, Escherichia coli and Staphylococcus aureus. Microwave plasma treatment followed by brush formation in vapor state from three distinguished precursors (allylalcohol, allylamine, hydroxyethyl methacrylate) was carried out to deposit alginic acid on the substrate. Surface analyses via various techniques established that alginic acid was immobilized onto the surface where grafting (brush) chemistry influenced the amount of alginic acid coated. Moreover, alginic acid was found to be capable of bacterial growth inhibition which itself was significantly affected by the brush type. The polyanionic character of alginic acid as a carbohydrate polymer was assumed to play the pivotal role in antibacterial activity. The cell wall composition of two bacterial strains along with the substrates physicochemical properties accounted for different levels of bacteriostatic performance. PMID:25196604

  8. Synthesis and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy.

    PubMed

    Ivashchenko, Olena; Lewandowski, Mikołaj; Peplińska, Barbara; Jarek, Marcin; Nowaczyk, Grzegorz; Wiesner, Maciej; Załęski, Karol; Babutina, Tetyana; Warowicka, Alicja; Jurga, Stefan

    2015-10-01

    The article is devoted to preparation and characterization of magnetite/silver/antibiotic nanocomposites for targeted antimicrobial therapy. Magnetite nanopowder was produced by thermochemical technique; silver was deposited on the magnetite nanoparticles in the form of silver clusters. Magnetite/silver nanocomposite was investigated by XRD, SEM, TEM, AFM, XPS, EDX techniques. Adsorptivity of magnetite/silver nanocomposite towards seven antibiotics from five different groups was investigated. It was shown that rifampicin, doxycycline, ceftriaxone, cefotaxime and doxycycline may be attached by physical adsorption to magnetite/silver nanocomposite. Electrostatic surfaces of antibiotics were modeled and possible mechanism of antibiotic attachment is considered in this article. Raman spectra of magnetite, magnetite/silver and magnetite/silver/antibiotic were collected. It was found that it is difficult to detect the bands related to antibiotics in the magnetite/silver/antibiotic nanocomposite spectra due to their overlap by the broad carbon bands of magnetite nanopowder. Magnetic measurements revealed that magnetic saturation of the magnetite/silver/antibiotic nanocomposites decreased on 6-19 % in comparison with initial magnetite nanopowder. Pilot study of antimicrobial properties of the magnetite/silver/antibiotic nanocomposites were performed towards Bacillus pumilus. PMID:26117765

  9. Deterioration of polyamino acid-coated alginate microcapsules in vivo.

    PubMed

    van Raamsdonk, J M; Cornelius, R M; Brash, J L; Chang, P L

    2002-01-01

    The implantation of immuno-isolated recombinant cell lines secreting a therapeutic protein in alginate microcapsules presents an alternative approach to gene therapy. Its clinical efficacy has recently been demonstrated in treating several genetic diseases in murine models. However, its application to humans will depend on the long-term structural stability of the microcapsules. Based on previous implantations in canines, it appears that survival of alginate-poly-L-lysine-alginate microcapsules in such large animals is short-lived. This article reports on the biological factors that may have contributed to the degradation of these microcapsules after implantation in dogs. Alginate microcapsules coated with poly-L-lysine or poly-L-arginine were implanted in subcutaneous or intraperitoneal sites. The retrieved microcapsules showed a loss of mechanical stability, as measured by resistance to osmotic stress. The polyamino acid coats were rendered fragile and easily lost, particularly when poly-L-lysine was used for coating and the intraperitoneal site was used for implantation. Various plasma proteins were associated with the retrieved microcapsules and identified with western blotting to include Factor XI, Factor XII, prekallikrein, HMWK, fibrinogen, plasminogen, ATIII, transferrin, alpha-1-antitrypsin, fibronectin, IgG, alpha-2-macroglobulin, vitronectin, prothrombin, apolipoprotein A1, and particularly albumin, a major Ca-transporting plasma protein. Complement proteins (C3, Factor B, Factor H, Factor I) and C3 activation fragments were detected. Release of the amino acids from the microcapsule polyamino acid coats was observed after incubation with plasma. indicating the occurrence of proteolytic degradation. Hence, the loss of long-term stability of the polyamino acid-coated alginate microcapsules is associated with activation of the complement system, degradation of the polyamino acid coating, and destabilization of the alginate core matrix, probably through loss

  10. Mesoporous silica magnetite nanocomposite synthesized by using a neutral surfactant

    NASA Astrophysics Data System (ADS)

    Souza, K. C.; Salazar-Alvarez, G.; Ardisson, J. D.; Macedo, W. A. A.; Sousa, E. M. B.

    2008-05-01

    Magnetite nanoparticles coated by mesoporous silica were synthesized by an alternative chemical route using a neutral surfactant and without the application of any functionalization method. The magnetite (Fe3O4) nanoparticles were prepared by precipitation from aqueous media, and then coated with mesoporous silica by using nonionic block copolymer surfactants as the structure-directing agents. The mesoporous SiO2-coated Fe3O4 samples were characterized by x-ray diffraction, Fourier-transform infrared spectroscopy, N2 adsorption-desorption isotherms, transmission electron microscopy, 57Fe Mössbauer spectroscopy, and vibrating sample magnetometry. Our results revealed that the magnetite nanoparticles are completely coated by well-ordered mesoporous silica with free pores and stable (~8 nm thick) pore walls, and that the structural and magnetic properties of the Fe3O4 nanoparticles are preserved in the applied synthesis route.

  11. Fabrication of chitosan-magnetite nanocomposite strip for chromium removal

    NASA Astrophysics Data System (ADS)

    Sureshkumar, Vaishnavi; Kiruba Daniel, S. C. G.; Ruckmani, K.; Sivakumar, M.

    2016-02-01

    Environmental pollution caused by heavy metals is a serious threat. In the present work, removal of chromium was carried out using chitosan-magnetite nanocomposite strip. Magnetite nanoparticles (Fe3O4) were synthesized using chemical co-precipitation method at 80 °C. The nanoparticles were characterized using UV-visible spectroscopy, fourier transform infrared spectroscopy, X-ray diffraction spectrometer, atomic force microscope, dynamic light scattering and vibrating sample magnetometer, which confirm the size, shape, crystalline nature and magnetic behaviour of nanoparticles. Atomic force microscope revealed that the particle size was 15-30 nm and spherical in shape. The magnetite nanoparticles were mixed with chitosan solution to form hybrid nanocomposite. Chitosan strip was casted with and without nanoparticle. The affinity of hybrid nanocomposite for chromium was studied using K2Cr2O7 (potassium dichromate) solution as the heavy metal solution containing Cr(VI) ions. Adsorption tests were carried out using chitosan strip and hybrid nanocomposite strip at different time intervals. Amount of chromium adsorbed by chitosan strip and chitosan-magnetite nanocomposite strip from aqueous solution was evaluated using UV-visible spectroscopy. The results confirm that the heavy metal removal efficiency of chitosan-magnetite nanocomposite strip is 92.33 %, which is higher when compared to chitosan strip, which is 29.39 %.

  12. Experimental Deformation of Magnetite

    NASA Astrophysics Data System (ADS)

    Till, J. L.; Rybacki, E.; Morales, L. F. G.

    2015-12-01

    Magnetite is an important iron ore mineral and the most prominent Fe-oxide phase in the Earth's crust. The systematic occurrence of magnetite in zones of intense deformation in oceanic core complexes suggests that it may play a role in strain localization in some silicate rocks. We performed a series of high-temperature deformation experiments on synthetic magnetite aggregates and natural single crystals to characterize the rheological behavior of magnetite. As starting material, we used fine-grained magnetite powder that was hot isostatically pressed at 1100°C for several hours, resulting in polycrystalline material with a mean grain size of around 40 μm and containing 3-5% porosity. Samples were deformed to 15-20% axial strain under constant load (approximating constant stress) conditions in a Paterson-type gas apparatus for triaxial deformation at temperatures between 900 and 1100°C and 300 MPa confining pressure. The aggregates exhibit typical power-law creep behavior. At high stresses, samples deformed by dislocation creep exhibit stress exponents close to 3, revealing a transition to near-Newtonian creep with stress exponents around 1.3 at lower stresses. Natural magnetite single crystals deformed at 1 atm pressure and temperatures between 950°C and 1150 °C also exhibit stress exponents close to 3, but with lower flow stresses and a lower apparent activation energy than the aggregates. Such behavior may result from the different oxygen fugacity buffers used. Crystallographic-preferred orientations in all polycrystalline samples are very weak and corroborate numerical models of CPO development, suggesting that texture development in magnetite may be inherently slow compared with lower symmetry phases. Comparison of our results with experimental deformation data for various silicate minerals suggests that magnetite should be weaker than most silicates during ductile creep in dry igneous rocks.

  13. High-performance iron oxide nanoparticles for magnetic particle imaging - guided hyperthermia (hMPI)

    NASA Astrophysics Data System (ADS)

    Bauer, Lisa M.; Situ, Shu F.; Griswold, Mark A.; Samia, Anna Cristina S.

    2016-06-01

    through selective doping of magnetite nanoparticles with zinc. Moreover, we demonstrated focused magnetic hyperthermia heating by adapting the field gradient used in MPI. By saturating the iron oxide nanoparticles outside of a field free region (FFR) with an external static field, we can selectively heat a target region in our test sample. By comparing zinc-doped magnetite cubic nanoparticles with undoped spherical nanoparticles, we could show a 5-fold improvement in the specific absorption rate (SAR) in magnetic hyperthermia while providing good MPI signal, thereby demonstrating the potential for high-performance focused hyperthermia therapy through an MPI-guided approach (hMPI). Electronic supplementary information (ESI) available: Detailed IONP synthetic methods, description of magnetic particle relaxometer set-up, TEM of reference IONP (Senior Scientific PrecisionMRX™ 25 nm oleic acid-coated nanoparticles), concentration dependent PSF of all IONP samples, PSF and SAR of Zn-Sph and Zn-Cube mixture sample, upper right quadrant of field-dependent hysteresis curve labelled with static field strengths, and the magnetic hyperthermia temperature profiles with and without the presence of external magnetic fields. See DOI: 10.1039/c6nr01877g

  14. Synthesis, characterisation and application of silica-magnetite nanocomposites

    NASA Astrophysics Data System (ADS)

    Bruce, Ian J.; Taylor, James; Todd, Michael; Davies, Martin J.; Borioni, Enrico; Sangregorio, Claudio; Sen, Tapas

    2004-12-01

    Silica-magnetite composites were prepared for eventual applications in biomolecular separations (nucleic acids). Their production on large scale has been optimised and they have been extensively characterised in a physical and chemical context. They perform at least as well, if not better than a commercially available equivalent at adsorbing and eluting DNA. Several methods for the preparation of magnetite were compared in order to select one, which produced particles, possessing high magnetic susceptibility, low rate of sedimentation and good chemical stability. Of the main methods studied: (i) oxidative hydrolysis of iron(II) sulphate in alkaline media, (ii) alkaline hydrolysis of iron(II) and iron(III) chloride solutions, and (iii) precipitation from iron(II) and iron(III) chloride solutions by hydrolysis of urea, method (i) produced the 'best' magnetite particles. Silica-magnetite composites were prepared using the 'best' magnetite, and, for comparison, two methods for depositing silica were used to coat the silica onto magnetite nanoparticles, from silicic acid at pH 10 and by acid hydrolysis of tetraethoxysilane (TEOS) at 90 °C. The best method for yielding silica-magnetite composites that worked well in DNA adsorption and elution proved to be that involving silicic acid and this material could be made in 20 g batch sizes. Silica-magnetite composites from the two methods proved to have distinct and different physical and chemical properties. All magnetite and silica-magnetite samples were fully characterised for their relative chemical composition using Fourier-transform infrared, XRF and thermo-gravimetric analysis. Their physical characteristics were determined using scanning electron microscopy and N2 adsorption and Mossbauer spectroscopy was used to confirm the identity of the iron oxides produced. Selected samples were comparatively tested for their ability to adsorb, and subsequently elute, 2-deoxyguanosine-5-monophosphate (GMP) and its non

  15. Preparation of size-controlled magnetite nanoparticles with a graphene and polymeric ionic liquid coating for the quick, easy, cheap, effective, rugged and safe extraction of preservatives from vegetables.

    PubMed

    Chen, Yaling; Cao, Shurui; Zhang, Lei; Xi, Cunxian; Li, Xianliang; Chen, Zhiqiong; Wang, Guoming

    2016-05-27

    Size-controlled magnetite nanoparticles (Fe3O4) with 200-1000nm were synthesized by co-precipitation method. Then Fe3O4@SiO2@G@PIL was synthesized and used as modified QuEChERS adsorbent for the determination of preservatives in vegetables. The size of about 200nm of Fe3O4 in Fe3O4@SiO2@G@PIL was selected as optimum size to clean-up. It not only exerted the nanometer features of magnetic nanoparticles, but also displayed the large specific surface area of graphene (G) and the solvent effects of polymeric ionic liquids (PILs). Various experimental parameters have been investigated. Under the optimized conditions, a simple, rapid and effective method for the determination of 20 preservatives residues in vegetables was established by modified QuEChERS to gas chromatography/mass spectrometry (GC-MS) analysis. The good linearity with correlation coefficients (R(2)) of 0.9972-0.9999 was obtained over the range of 0.02-2.00mg/L for 20 preservatives. The detection limits of the proposed method for 20 preservatives ranged from 0.82 to 6.64μg/kg. The adsorbent was successfully applied for extraction and determination of preservatives in vegetable samples, which thus was time-saving with keeping good clean-up performance. PMID:27109197

  16. Monodisperse magnetite (Fe3O4) nanoparticles modified with water soluble polymers for the diagnosis of breast cancer by MRI method

    NASA Astrophysics Data System (ADS)

    Rezayan, Ali Hossein; Mosavi, Majid; Kheirjou, Somayyeh; Amoabediny, Ghasem; Ardestani, Mehdi Shafiee; Mohammadnejad, Javad

    2016-12-01

    In this study, magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. To enhance the biocompatibility and colloidal stability of the synthesized nanoparticles, they were modified with carboxyl functionalized PEG via dopamine (DPA) linker. Both modified and unmodified Fe3O4 nanoparticles exhibited super paramagnetic behavior (particle size below 20 nm). The saturation magnetization (Ms) of PEGdiacid-modified Fe3O4 was 45 emu/g, which was less than the unmodified Fe3O4 nanoparticles (70 emu/g). This difference indicated that PEGdiacid polymer was immobilized on the surface of Fe3O4 nanoparticles successfully. To evaluate the efficiency of the resulting nanoparticles as contrast agents for magnetic resonance imaging (MRI), different concentration of MNPs and different value of echo time TE were investigated. The results showed that by increasing the concentration of the nanoparticles, transverse relaxation time (T2) decreased, which subsequently resulted in MR signal enhancement. T2-weighted MR images of the different concentration of MNPs in different value of echo time TE indicated that MR signal intensity increased with increase in TE value up to 66 and then remained constant. The cytotoxicity effect of the modified and unmodified nanoparticles was evaluated in three different concentrations (12, 60 and 312 mg l-1) on MDA-MB-231 cancer cells for 24 and 48 h. In both tested time (24 and 48 h) for all three samples, the modified nanoparticles had long life time than unmodified nanoparticles. Cellular uptake of modified MNPs was 80% and reduced to 9% by the unmodified MNPs.

  17. Magnetite nano-islands on Graphene

    NASA Astrophysics Data System (ADS)

    Anderson, Nathaniel; Zhang, Qiang; Rosenberg, Richard; Vaknin, David

    X-ray magnetic circular dichroism (XMCD) of ex-situ iron nano-islands grown on graphene reveals that iron oxidation spontaneously leads to the formation of magnetite nano-particles - i.e, the formation of the inverse spinel Fe3O4. Fe islands have been grown with two different heights (20 and 75 MLs) on epitaxial graphene and we have determined their magnetic behavior both as function of temperature and applied external field. Our XAS and XMCD at an applied magnetic field of B = 5 T show that the thin film (20 MLs) is totally converted to magnetite whereas the thicker film (75 MLs) exhibits magnetite properties but also those of pure metal iron. For both samples, temperature dependence of the XMCD shows clear transitions at ~120 K consistent with the Verwey transition of bulk magnetite. XMCD at low temperatures shows a weak hysteresis and provide the average spin and angular-momentum moments, the dipolar term, and the total moment . In addition, manipulation and comparison of the XMCD data from both samples allows us to extract information about the pure iron nano-islands from the thicker sample. Ames Laboratory is supported by the U.S. DOE, BES, MSE Contract No. DE-AC02-07CH11358. APS is supported by U.S. DOE Contract No. DE-AC02-06CH11357.

  18. Bisphosphonate release profiles from magnetite microspheres.

    PubMed

    Miyazaki, Toshiki; Inoue, Tatsuya; Shirosaki, Yuki; Kawashita, Masakazu; Matsubara, Takao; Matsumine, Akihiko

    2014-10-01

    Hyperthermia has been suggested as a novel, minimally invasive cancer treatment method. After implantation of magnetic nano- or microparticles around a tumour through blood vessels, irradiation with alternating magnetic fields facilitates the efficient in situ hyperthermia even for deep-seated tumours. On the basis of this idea, if the microspheres are capable of delivering drugs, they could be promising multifunctional biomaterials effective for chemotherapy as well as hyperthermia. In the present study, magnetite microspheres were prepared by aggregation of the iron oxide colloid in water-in-oil (W/O) emulsion. The release behaviour of alendronate, a typical bisphosphonate, from the microspheres was examined in vitro as a model of the bone tumour prevention and treatment system. The alendronate was successfully incorporated onto the porous magnetite microspheres in vacuum conditions. The drug-loaded microspheres maintained their original spherical shapes even after shaking in ultrapure water for 3 days, suggesting that they have sufficient mechanical integrity for clinical use. It was attributed to high aggregation capability of the magnetite nanoparticles through van der Waals and weak magnetic attractions. The microspheres showed slow release of the alendronate in vitro, resulting from tight covalent or ionic interaction between the magnetite and the alendronate. The release rate was diffusion-controlled type and well controlled by the alendronate concentration in drug incorporation to the microspheres. PMID:24854985

  19. Magnetite reveals ambient field strength at low temperatures

    NASA Astrophysics Data System (ADS)

    Smirnov, Alexei V.; Tarduno, John A.

    Magnetite (Fe3O4) is the most important and oldest known magnetic mineral on Earth (Figure l). We have come a long way from the magnetite loadstone compasses of ancient China; magnetite and titanomagnetite have been established as the principal carriers of geologically important remanent magnetizations in rocks, the study of which led to the plate tectonic paradigm. We now recognize that magnetite plays an important role in the biosphere. Some organisms contain intra-cellular particles of Fe3O4 that they use for spatial orientation and navigation. When preserved in rocks, these particles—called "magnetofossils"— can provide important insight into the origin and development of life here, and perhaps, on other planets [e.g., Thomas-Keprta et al., 2000]. Magnetite is now used in the medical field and in nanotechnology research. Nanoparticles of magnetite are used as a contrasting agent in magnetic resonance imaging and are being developed to deliver site-specific drugs for the treatment of cancer [Alexiou et al., 2000]. Such applications add to a long list of industrial uses of magnetite that range from magnetic ink to magnetic recording media.

  20. Wet-chemical green synthesis of L-lysine amino acid stabilized biocompatible iron-oxide magnetic nanoparticles.

    PubMed

    Krishna, Rahul; Titus, Elby; Krishna, Rohit; Bardhan, Neelkanth; Bahadur, Dhirendra; Gracio, José

    2012-08-01

    In this paper, we report a novel method for the synthesis of L-Lysine (lys) amino acid coated maghemite (gamma-Fe2O3) magnetic nanoparticles (MNPs). The facile and cost effective method permitted preparation of the high-quality superparamagnetic gamma-Fe2O3 MNPs with hydrophilic and biocompatible nature. For this work, first we synthesized magnetite phase Fe3O4/lys by wet chemical method and oxidized to y-Fe2O3 in controlled oxidizing environment, as evidenced by XRD and VSM magnetometry. The crystallite size and magnetization of gamma-Fe2O3/lys MNPs was found to be 14.5 nm, 40.6 emu/gm respectively. The surface functionalization by L-lysine amino acid and metal-ligand bonding was also confirmed by FTIR spectroscopy. The hydrodynamic diameter, colloidal stability and surface charge on MNPs were characterized by DLS and zeta potential analyser. PMID:22962801

  1. Advancing Sustainable Catalysis with Magnetite Surface Modification and Synthetic Applications

    EPA Science Inventory

    This article surveys the recent developments in the synthesis, surface modification, and synthetic applications of magnetitenanoparticles. The emergence of iron(II,III) oxide (triiron tetraoxide or magnetite; Fe3O4, or FeO•Fe2O3) nanoparticles as a sustainable support in het...

  2. Multiple ordering in magnetite.

    NASA Technical Reports Server (NTRS)

    Cullen, J. R.; Callen, E. R.

    1973-01-01

    Results of a self-consistent band calculation of the ground-state energy and charge orderings based on a tight-binding scheme in magnetite are presented. They show that below a critical (about 2.2) value of the ratio of interatomic Coulomb energy to bandwidth the lowest energy state has no order. Between this critical value and 2.5, the preferred state is multiply ordered.

  3. Fourier transform infrared and Raman spectroscopy studies on magnetite/Ag/antibiotic nanocomposites

    NASA Astrophysics Data System (ADS)

    Ivashchenko, Olena; Jurga-Stopa, Justyna; Coy, Emerson; Peplinska, Barbara; Pietralik, Zuzanna; Jurga, Stefan

    2016-02-01

    This article presents a study on the detection of antibiotics in magnetite/Ag/antibiotic nanocomposites using Fourier transform infrared (FTIR) and Raman spectroscopy. Antibiotics with different spectra of antimicrobial activities, including rifampicin, doxycycline, cefotaxime, and ceftriaxone, were studied. Mechanical mixtures of antibiotics and magnetite/Ag nanocomposites, as well as antibiotics and magnetite nanopowder, were investigated in order to identify the origin of FTIR bands. FTIR spectroscopy was found to be an appropriate technique for this task. The spectra of the magnetite/Ag/antibiotic nanocomposites exhibited very weak (for doxycycline, cefotaxime, and ceftriaxone) or even no (for rifampicin) antibiotic bands. This FTIR "invisibility" of antibiotics is ascribed to their adsorbed state. FTIR and Raman measurements show altered Csbnd O, Cdbnd O, and Csbnd S bonds, indicating adsorption of the antibiotic molecules on the magnetite/Ag nanocomposite structure. In addition, a potential mechanism through which antibiotic molecules interact with magnetite/Ag nanoparticle surfaces is proposed.

  4. Magnetite induces oxidative stress and apoptosis in lung epithelial cells.

    PubMed

    Ramesh, Vani; Ravichandran, Prabakaran; Copeland, Clinton L; Gopikrishnan, Ramya; Biradar, Santhoshkumar; Goornavar, Virupaxi; Ramesh, Govindarajan T; Hall, Joseph C

    2012-04-01

    There is an ongoing concern regarding the biocompatibility of nanoparticles with sizes less than 100 nm as compared to larger particles of the same nominal substance. In this study, we investigated the toxic properties of magnetite stabilized with polyacrylate sodium. The magnetite was characterized by X-ray powder diffraction analysis, and the mean particle diameter was calculated using the Scherrer formula and was found to be 9.3 nm. In this study, we treated lung epithelial cells with different concentrations of magnetite and investigated their effects on oxidative stress and cell proliferation. Our data showed an inhibition of cell proliferation in magnetite-treated cells with a significant dose-dependent activation and induction of reactive oxygen species. Also, we observed a depletion of antioxidants, glutathione, and superoxide dismutase, respectively, as compared with control cells. In addition, apoptotic-related protease/enzyme such as caspase-3 and -8 activities, were increased in a dose-dependent manner with corresponding increased levels of DNA fragmentation in magnetite-treated cells compared to than control cells. Together, the present study reveals that magnetite exposure induces oxidative stress and depletes antioxidant levels in the cells to stimulate apoptotic pathway for cell death. PMID:22147200

  5. Application of the Z-scan technique to determine the optical Kerr coefficient and two-photon absorption coefficient of magnetite nanoparticles colloidal suspension

    NASA Astrophysics Data System (ADS)

    Vivacqua, Marco; Espinosa, Daniel; Martins Figueiredo Neto, Antônio

    2012-06-01

    We investigate the occurrence of the optical Kerr effect and two-photon absorption when an oil-based magnetic Fe3O4 nanoparticles colloidal suspension is illuminated with high intensity femtosecond laser pulses. The frequency of the pulses is controlled and the Z-scan technique is employed in our measurements of the nonlinear optical Kerr coefficient (n2) and two-photon absorption coefficient (β). From these values it was possible to calculate the real and imaginary parts of the third-order susceptibility. We observed that increasing the pulse frequency, additional physical processes take place, increasing artificially the absolute values of n2 and β. The experimental conditions are discussed to assure the obtention of reliable values of these nonlinear optical parameters, which may be useful in all-optical switching and optical power limiting applications.

  6. Extraction of quinolones from milk samples using bentonite/magnetite nanoparticles before determination by high-performance liquid chromatography with fluorimetric detection.

    PubMed

    Jin, Tao; Wu, Hao; Gao, Nannan; Chen, Xiaodan; Lai, Huajie; Zheng, Jinfeng; Du, Liming

    2016-02-01

    In this work, bentonite magnetic nanoparticles synthesized by a typical coprecipitation method were used as the adsorbent for the magnetic solid-phase extraction of six quinolones (ciprofloxacin, difloxacin, enrofloxacin, norfloxacin, sarafloxacin, and lomefloxacin) from milk samples followed by high-performance liquid chromatography with fluorimetric detection. Under the optimized conditions, the linear quantitation range for the six quinolones was 0.3-200 ng/mL, and the correlation coefficients of the calibration curves ranged from 0.9994 to 0.9999. The detection limit of the method was 0.1 ng/mL. Recoveries of quinolones from pure and low-fat spiked milk samples varied from 80.4 to 92.7% and from 81.3 to 93.5%, respectively. These results demonstrated that the proposed method for the determination of six quinolones in milk samples was rapid, reliable, and efficient. PMID:26576704

  7. Porphyrin-magnetite nanoconjugates for biological imaging

    PubMed Central

    2011-01-01

    Background The use of silica coated magnetic nanoparticles as contrast agents has resulted in the production of highly stable, non-toxic solutions that can be manipulated via an external magnetic field. As a result, the interaction of these nanocomposites with cells is of vital importance in understanding their behaviour and biocompatibility. Here we report the preparation, characterisation and potential application of new "two-in-one" magnetic fluorescent nanocomposites composed of silica-coated magnetite nanoparticles covalently linked to a porphyrin moiety. Method The experiments were performed by administering porphyrin functionalised silica-coated magnetite nanoparticles to THP-1 cells, a human acute monocytic leukaemia cell line. Cells were cultured in RPMI 1640 medium with 25 mM HEPES supplemented with heat-inactivated foetal bovine serum (FBS). Results We have synthesised, characterised and analysed in vitro, a new multimodal (magnetic and fluorescent) porphyrin magnetic nanoparticle composite (PMNC). Initial co-incubation experiments performed with THP-1 macrophage cells were promising; however the PMNC photobleached under confocal microscopy study. β-mercaptoethanol (β-ME) was employed to counteract this problem and resulted not only in enhanced fluorescence emission, but also allowed for elongated imaging and increased exposure times of the PMNC in a cellular environment. Conclusion Our experiments have demonstrated that β-ME visibly enhances the emission intensity. No deleterious effects to the cells were witnessed upon co-incubation with β-ME alone and no increases in background fluorescence were recorded. These results should present an interest for further development of in vitro biological imaging techniques. PMID:21477294

  8. Synthesis and magnetic characterization of magnetite obtained by monowavelength visible light irradiation

    SciTech Connect

    Lin, Yulong; Wei, Yu; Sun, Yuhan; Wang, Jing

    2012-03-15

    Highlights: Black-Right-Pointing-Pointer Magnetite was synthesized under monowavelength LED irradiation at room temperature. Black-Right-Pointing-Pointer Different wavelength irradiations led to distinctive characteristics of magnetite. Black-Right-Pointing-Pointer Particle sizes of magnetite were controlled by different irradiation wavelengths. Black-Right-Pointing-Pointer Wavelength affects the magnetic characteristics of magnetite. -- Abstract: Magnetite (Fe{sub 3}O{sub 4}) nanoparticles were controllably synthesized by aerial oxidation Fe{sup II}EDTA solution under different monowavelength light-emitting diode (LED) lamps irradiation at room temperature. The results of the X-ray diffraction (XRD) spectra show the formation of magnetite nanoparticle further confirmed by Fourier transform infrared spectroscope (FTIR) and the difference in crystallinity of as-prepared samples. Fe{sub 3}O{sub 4} particles are nearly spherical in shape based on transmission electron microscopy (TEM). Average crystallite sizes of magnetite can be controlled by different irradiation light wavelengths from XRD and TEM: 50.1, 41.2, and 20.3 nm for red, green, and blue light irradiation, respectively. The magnetic properties of Fe{sub 3}O{sub 4} samples were investigated. Saturation magnetization values of magnetic nanoparticles were 70.1 (sample M-625), 65.3 (sample M-525), and 58.2 (sample M-460) emu/g, respectively.

  9. Release Behavior and Toxicity Profiles towards Leukemia (WEHI-3B) Cell Lines of 6-Mercaptopurine-PEG-Coated Magnetite Nanoparticles Delivery System

    PubMed Central

    Kura, Aminu Umar; Hussein-Al-Ali, Samer Hasan; Hussein, Mohd Zobir bin; Fakurazi, Sharida; Shaari, Abdul Halim; Ahmad, Zalinah

    2014-01-01

    The coating of an active drug, 6-mercaptopurine, into the iron oxide nanoparticles-polyethylene glycol (FNPs-PEG) in order to form a new nanocomposite, FPEGMP-2, was accomplished using coprecipitation technique. The resulting nanosized with a narrow size distribution magnetic polymeric particles show the superparamagnetic properties with 38.6 emu/g saturation magnetization at room temperature. Fourier transform infrared spectroscopy and the thermal analysis study supported the formation of the nanocomposite and the enhancement of thermal stability in the resulting nanocomposite comparing with its counterpart in free state. The loading of 6-mercaptopurine (MP) in the FPEGMP-2 nanocomposite was estimated to be about 5.6% and the kinetic experimental data properly correlated with the pseudo-second order model. Also, the release of MP from the FPEGMP-2 nanocomposite shows the sustained release manner which is remarkably lower in phosphate buffered solution at pH 7.4 than pH 4.8, due to different release mechanism. The maximum percentage release of MP from the nanocomposite reached about 60% and 97% within about 92 and 74 hours when exposed to pH 7.4 and 4.8, respectively. PMID:24895684

  10. Biotemplated magnetic nanoparticle arrays.

    PubMed

    Galloway, Johanna M; Bramble, Jonathan P; Rawlings, Andrea E; Burnell, Gavin; Evans, Stephen D; Staniland, Sarah S

    2012-01-23

    Immobilized biomineralizing protein Mms6 templates the formation of uniform magnetite nanoparticles in situ when selectively patterned onto a surface. Magnetic force microscopy shows that the stable magnetite particles maintain their magnetic orientation at room temperature, and may be exchange coupled. This precision-mixed biomimetic/soft-lithography methodology offers great potential for the future of nanodevice fabrication. PMID:22052737

  11. Synthesis, Characterization and In Vitro Study of Biocompatible Cinnamaldehyde Functionalized Magnetite Nanoparticles (CPGF Nps) For Hyperthermia and Drug Delivery Applications in Breast Cancer

    PubMed Central

    Wani, Kirtee D.; Kadu, Brijesh S.; Mansara, Prakash; Gupta, Preeti; Deore, Avinash V.; Chikate, Rajeev C.; Poddar, Pankaj; Dhole, Sanjay D.; Kaul-Ghanekar, Ruchika

    2014-01-01

    Cinnamaldehyde, the bioactive component of the spice cinnamon, and its derivatives have been shown to possess anti-cancer activity against various cancer cell lines. However, its hydrophobic nature invites attention for efficient drug delivery systems that would enhance the bioavailability of cinnamaldehyde without affecting its bioactivity. Here, we report the synthesis of stable aqueous suspension of cinnamaldehyde tagged Fe3O4 nanoparticles capped with glycine and pluronic polymer (CPGF NPs) for their potential application in drug delivery and hyperthermia in breast cancer. The monodispersed superparamagnetic NPs had an average particulate size of ∼20 nm. TGA data revealed the drug payload of ∼18%. Compared to the free cinnamaldehyde, CPGF NPs reduced the viability of breast cancer cell lines, MCF7 and MDAMB231, at lower doses of cinnamaldehyde suggesting its increased bioavailability and in turn its therapeutic efficacy in the cells. Interestingly, the NPs were non-toxic to the non-cancerous HEK293 and MCF10A cell lines compared to the free cinnamaldehyde. The novelty of CPGF nanoparticulate system was that it could induce cytotoxicity in both ER/PR positive/Her2 negative (MCF7) and ER/PR negative/Her2 negative (MDAMB231) breast cancer cells, the latter being insensitive to most of the chemotherapeutic drugs. The NPs decreased the growth of the breast cancer cells in a dose-dependent manner and altered their migration through reduction in MMP-2 expression. CPGF NPs also decreased the expression of VEGF, an important oncomarker of tumor angiogenesis. They induced apoptosis in breast cancer cells through loss of mitochondrial membrane potential and activation of caspase-3. Interestingly, upon exposure to the radiofrequency waves, the NPs heated up to 41.6°C within 1 min, suggesting their promise as a magnetic hyperthermia agent. All these findings indicate that CPGF NPs prove to be potential nano-chemotherapeutic agents in breast cancer. PMID:25268975

  12. In vitro cytotoxicity of superparamagnetic iron oxide nanoparticles on neuronal and glial cells. Evaluation of nanoparticle interference with viability tests.

    PubMed

    Costa, Carla; Brandão, Fátima; Bessa, Maria João; Costa, Solange; Valdiglesias, Vanessa; Kiliç, Gözde; Fernández-Bertólez, Natalia; Quaresma, Pedro; Pereira, Eulália; Pásaro, Eduardo; Laffon, Blanca; Teixeira, João Paulo

    2016-03-01

    Superparamagnetic iron oxide nanoparticles (ION) have attracted great interest for use in several biomedical fields. In general, they are considered biocompatible, but little is known of their effects on the human nervous system. The main objective of this work was to evaluate the cytotoxicity of two ION (magnetite), coated with silica and oleic acid, previously determining the possible interference of the ION with the methodological procedures to assure the reliability of the results obtained. Human neuroblastoma SHSY5Y and glioblastoma A172 cells were exposed to different concentrations of ION (5-300 µg ml(-1)), prepared in complete and serum-free cell culture medium for three exposure times (3, 6 and 24 h). Cytotoxicity was evaluated by means of the MTT, neutral red uptake and alamar blue assays. Characterization of the main physical-chemical properties of the ION tested was also performed. Results demonstrated that both ION could significantly alter absorbance readings. To reduce these interferences, protocols were modified by introducing additional washing steps and cell-free systems. Significant decreases in cell viability were observed for both cell lines in specific conditions by all assays. In general, oleic acid-coated ION were less cytotoxic than silica-coated ION; besides, a serum-protective effect was observed for both ION studied and cell lines. These results contribute to increase the knowledge of the potential harmful effects of ION on the human nervous system. Understanding these effects is essential to establish satisfactory regulatory policies on the safe use of magnetite nanoparticles in biomedical applications. PMID:26212026

  13. Preparation of magnetite aqueous dispersion for magnetic fluid hyperthermia

    NASA Astrophysics Data System (ADS)

    Kikuchi, Teppei; Kasuya, Ryo; Endo, Shota; Nakamura, Akira; Takai, Toshiyuki; Metzler-Nolte, Nils; Tohji, Kazuyuki; Balachandran, Jeyadevan

    2011-05-01

    An aqueous magnetic suspension was prepared by dispersing amphiphilic co-polymer-coated monodispersed magnetite nanoparticles synthesized through thermal decomposition of iron acetylacetonate (Fe(acac) 3) in a mixture of oleic acid and oleylamine. The average diameter of narrow-size-distributed magnetite nanoparticles varied between 5 and 12 nm depending on the experimental parameters such as reaction temperature, metal salt concentration and oleic acid/oleylamine ratio. Though the as-synthesized particles were coated with oleate and were dispersible in organic solvent, their surfaces were modified using amphiphilic co-polymers composed of poly(maleic anhydride-alt-1-octadecene) and polyethylene glycol-methyl ether and made dispersible in water. Infrared spectra of the sample indicated the existence of -COOH groups on the surface for further conjugation with biomolecules for targeted cancer therapy.

  14. Design of stable polyether-magnetite complexes in aqueous media: effects of the anchor group, molecular weight, and chain density.

    PubMed

    Miles, William C; Huffstetler, Philip P; Goff, Jonathan D; Chen, Alfred Y; Riffle, J S; Davis, Richey M

    2011-05-01

    The colloidal stability of polymer-stabilized nanoparticles is critical for therapeutic use. However, phosphates in physiological media can induce polymer desorption and consequently flocculation. Colloidal characteristics of PEO-magnetite nanoparticles with different anchors for attaching PEO to magnetite were examined in PBS. The effects of the number of anchors, PEO molecular weight, and chain density were examined. It was observed that ammonium phosphonates anchored PEO to magnetite effectively in phosphate-containing solutions because of interactions between the phosphonates and magnetite. Additionally, a method to estimate the magnetite surface coverage was developed and was found to be critical to the prediction of colloidal stability. This is key to understanding how functionalized surfaces interact with their environment. PMID:21476527

  15. Fabrication of novel multihollow superparamagnetic magnetite/polystyrene nanocomposite microspheres via water-in-oil-in-water double emulsions.

    PubMed

    Yang, Song; Liu, Huarong; Zhang, Zhicheng

    2008-09-16

    We herein present a novel and simple synthetic strategy for fabricating multihollow superparamagnetic magnetite/polystyrene nanocomposite microspheres via water-in-oil-in-water double emulsions. Amphipathic magnetite nanoparticles surface-modified with oleic acid act as an oil-soluble emulsifier and sodium dodecyl sulfate acts as a water-soluble surfactant in the system. The final products were thoroughly characterized by X-ray powder diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and field-emission scanning electron microscopy, which showed the formation of multihollow magnetite/polystyrene nanocomposite microspheres. Preliminary results of magnetic properties of multihollow magnetite/polystyrene microspheres were reported. The effect of the content of amphipathic magnetite nanoparticles on the morphology of nanocomposite microspheres was studied. Furthermore, the mechanism of formation of multihollow magnetic nanocomposite microspheres was also discussed. PMID:18715023

  16. Functional biocompatible magnetite-cellulose nanocomposite fibrous networks: Characterization by fourier transformed infrared spectroscopy, X-ray powder diffraction and field emission scanning electron microscopy analysis

    NASA Astrophysics Data System (ADS)

    Habibi, Neda

    2015-02-01

    The preparation and characterization of functional biocompatible magnetite-cellulose nano-composite fibrous material is described. Magnetite-cellulose nano-composite was prepared by a combination of the solution-based formation of magnetic nano-particles and subsequent coating with amino celluloses. Characterization was accomplished using X-ray powder diffraction (XRD), fourier transformed infrared (FTIR) and field emission scanning electron microscopy (FESEM) analysis. The peaks of Fe3O4 in the XRD pattern of nanocomposite confirm existence of the nanoparticles in the amino cellulose matrix. Magnetite-cellulose particles exhibit an average diameter of roughly 33 nm as demonstrated by field emission scanning electron microscopy. Magnetite nanoparticles were irregular spheres dispersed in the cellulose matrix. The vibration corresponding to the Nsbnd CH3 functional group about 2850 cm-1 is assigned in the FTIR spectra. Functionalized magnetite-cellulose nano-composite polymers have a potential range of application as targeted drug delivery system in biomedical field.

  17. Magnetic microbes: Bacterial magnetite biomineralization

    SciTech Connect

    Prozorov, Tanya

    2015-09-14

    Magnetotactic bacteria are a diverse group of prokaryotes with the ability to orient and migrate along the magnetic field lines in search for a preferred oxygen concentration in chemically stratified water columns and sediments. These microorganisms produce magnetosomes, the intracellular nanometer-sized magnetic crystals surrounded by a phospholipid bilayer membrane, typically organized in chains. Magnetosomes have nearly perfect crystal structures with narrow size distribution and species-specific morphologies, leading to well-defined magnetic properties. As a result, the magnetite biomineralization in these organisms is of fundamental interest to diverse disciplines, from biotechnology to astrobiology. As a result, this article highlights recent advances in the understanding of the bacterial magnetite biomineralization.

  18. Structure-function studies of the magnetite-biomineralizing magnetosome-associated protein MamC.

    PubMed

    Nudelman, Hila; Valverde-Tercedor, Carmen; Kolusheva, Sofiya; Perez Gonzalez, Teresa; Widdrat, Marc; Grimberg, Noam; Levi, Hilla; Nelkenbaum, Or; Davidov, Geula; Faivre, Damien; Jimenez-Lopez, Concepcion; Zarivach, Raz

    2016-06-01

    Magnetotactic bacteria are Gram-negative bacteria that navigate along geomagnetic fields using the magnetosome, an organelle that consists of a membrane-enveloped magnetic nanoparticle. Magnetite formation and its properties are controlled by a specific set of proteins. MamC is a small magnetosome-membrane protein that is known to be active in iron biomineralization but its mechanism has yet to be clarified. Here, we studied the relationship between the MamC magnetite-interaction loop (MIL) structure and its magnetite interaction using an inert biomineralization protein-MamC chimera. Our determined structure shows an alpha-helical fold for MamC-MIL with highly charged surfaces. Additionally, the MamC-MIL induces the formation of larger magnetite crystals compared to protein-free and inert biomineralization protein control experiments. We suggest that the connection between the MamC-MIL structure and the protein's charged surfaces is crucial for magnetite binding and thus for the size control of the magnetite nanoparticles. PMID:26970040

  19. Mechanisms of ciprofloxacin removal by nano-sized magnetite.

    PubMed

    Rakshit, Sudipta; Sarkar, Dibyendu; Elzinga, Evert J; Punamiya, Pravin; Datta, Rupali

    2013-02-15

    An understanding of the interaction mechanisms of antibiotics with environmentally relevant sorbents is important to determine the environmental fate of antibiotics and to develop wastewater treatment strategies. Magnetite (Fe(3)O(4)(s)) is ubiquitous in the environment and occurs as a secondary corrosion product of iron nanoparticles that are commonly used as a remediation material. In this study, we aimed to assess the sorption mechanisms of ciprofloxacin (CIP), an important class of fluoroquinolone antibiotics, with magnetite nanoparticles using a combination of wet chemical and in situ ATR-FTIR spectroscopic measurements. Ciprofloxacin sorption was characterized as a function of pH (3.4-8.0), CIP concentration (1-500 μM), ionic strength (0.5, 0.1, and 0.01 M NaCl), and competing anion such as phosphate (0.1mM) to cover a broad range of environmentally relevant geochemical conditions. Results indicated a bell-shaped sorption envelop where sorption of CIP on nano-Fe(3)O(4)(s) increased from 45% to 80% at pH 3.44-5.97; beyond that sorption gradually decreased to a value of 25% at pH 8.39. Phosphate had negligible effect on CIP sorption. In situ ATR-FTIR results indicated inner-sphere coordination of CIP at the magnetite surface mediated by carboxylic acid groups. Results suggest that nano-Fe(3)O(4)(s) has the potential to remove CIP from wastewater effectively. PMID:23313895

  20. Development and characterization of fatty acid-coated microgels within microfluidic systems

    NASA Astrophysics Data System (ADS)

    Kraft, Mary L.

    2003-10-01

    Fatty acid-coated hydrogel microstructures (mugels) were prepared within microfluidic devices and their properties were investigated. A photopolymerization technique was used to position pH-sensitive mugels within microchannels, and lipophilic acid chlorides were covalently grafted to these objects with an in situ process. The resulting hydrophobic coatings served as selectively permeable barriers that enabled pH-sensitive mugels to remain contracted while bathed by buffered solutions that caused expansion in unmodified samples. Modified mugels were capable of swelling once the fatty acid coating was physically disrupted. Barrier permeability was also chemically induced with buffered detergent solutions, triggering complete hydrogel expansion through an asymmetric process. The influence of the fatty acid chain length on the ion gradient stability in the absence of perturbing additives was investigated. In contrast to solid-supported self-assembled monolayers (SAMs), the ion gradient stability of the modified mugels did not increase with increasing chain length, suggesting the structure of the fatty acid coating was inherently different from that of a SAM. The structure of the fatty acid-modified mugels was elucidated through the characterization of comparable hydrogel substrates. Imaging the microstructures with scanning electron microscopy revealed a rough and irregular hydrogel surface, which indicated structural assessment would be challenging since many surface characterization techniques require smooth substrates to acquire depth profiles. The presence of the fatty acid coating was confirmed through investigation of an analogous model system with X-ray photoelectron spectroscopy and secondary ion mass spectrometry. Laser scanning confocal microscopy and the use of a lipophilic fluorescent dye indicated the coating was confined to the periphery of the mugel. Transmission electron microscopy imaging of modified nonionic hydrogels revealed the mugel matrix was

  1. Dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay: a quantitative method for oxidative stress assessment of nanoparticle-treated cells.

    PubMed

    Aranda, A; Sequedo, L; Tolosa, L; Quintas, G; Burello, E; Castell, J V; Gombau, L

    2013-03-01

    No consensus exists on how to address possible toxicity of nanomaterials as they interfere with most in vitro screening tests based on colorimetric and fluorimetric probes such as the dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay for detection of oxidative species. In the present research, nanomaterial interaction with DCFH-DA was studied in relation to its nature and/or assay conditions (cell-based and time exposure) by incubating Rhodamine (Rhd)-labeled 25nm and 50nm silica (SiO2), naked and oleic acid coated magnetite, (Fe3O4) and maghemite (Fe2O3) iron oxide, titanium dioxide (TiO2) and poly(ethylene oxide)-poly(lactide/glycolide) acid (PLGA-PEO) nanoparticles (NPs) with metabolically active rat hepatocytes for 4 and 24-h periods. Data indicated that nanoparticle uptake correlated with quenching of dye fluorescence emission. In spite of their masking effect, the oxidative potential of NPs could be detected at a limited threshold concentration when exposed for periods of time longer than those frequently used for this test. However, changes in the experimental conditions did not systematically result in free radical formation for all nanomaterials tested. Overall data indicate that despite the quenching effect of nanoparticles on DCFH-DA assay, it can be considered as a useful tool for quantitative measurement of NPs-induced oxidative stress by minor modifications of standardized protocols. PMID:23357416

  2. Carboxymethyldextran/magnetite hybrid microspheres designed for hyperthermia.

    PubMed

    Miyazaki, Toshiki; Anan, Shota; Ishida, Eiichi; Kawashita, Masakazu

    2013-05-01

    Recently, organic-inorganic hybrids composed of derivatives of dextran, a polysaccharide, and magnetite nanoparticles have attracted much attention as novel thermoseeds. If they can be fabricated into microspheres of size 20-30 μm, they are expected to show not only hyperthermia effects but also embolization effects in human liver and kidney cancers. In this study, we examined the fabrication of carboxymethyldextran/magnetite microspheres using a water/oil emulsion as the reaction medium. Improvement of the chemical stability of the microcapsules by coating with silica using a sol-gel process was also investigated. The obtained hollow microspheres contained particles of size 20-30 μm. Silica coating using an appropriate catalyst for hydrolysis and polycondensation of alkoxysilanes was found to be effective for preventing dissolution and collapse in simulated body environments. PMID:23371771

  3. Bioelectric and Morphological Response of Liquid-Covered Human Airway Epithelial Calu-3 Cell Monolayer to Periodic Deposition of Colloidal 3-Mercaptopropionic-Acid Coated CdSe-CdS/ZnS Core-Multishell Quantum Dots

    PubMed Central

    Turdalieva, Aizat; Solandt, Johan; Shambetova, Nestan; Xu, Hao; Blom, Hans; Brismar, Hjalmar; Zelenina, Marina; Fu, Ying

    2016-01-01

    Lung epithelial cells are extensively exposed to nanoparticles present in the modern urban environment. Nanoparticles, including colloidal quantum dots (QDs), are also considered to be potentially useful carriers for the delivery of drugs into the body. It is therefore important to understand the ways of distribution and the effects of the various types of nanoparticles in the lung epithelium. We use a model system of liquid-covered human airway epithelial Calu-3 cell cultures to study the immediate and long-term effects of repeated deposition of colloidal 3-mercaptopropionic-acid coated CdSe-CdS/ZnS core-multishell QDs on the lung epithelial cell surface. By live confocal microscope imaging and by QD fluorescence measurements we show that the QD permeation through the mature epithelial monolayers is very limited. At the time of QD deposition, the transepithelial electrical resistance (TEER) of the epithelial monolayers transiently decreased, with the decrement being proportional to the QD dose. Repeated QD deposition, once every six days for two months, lead to accumulation of only small amounts of the QDs in the cell monolayer. However, it did not induce any noticeable changes in the long-term TEER and the molecular morphology of the cells. The colloidal 3-mercaptopropionic-acid coated CdSe-CdS/ZnS core-multishell QDs could therefore be potentially used for the delivery of drugs intended for the surface of the lung epithelia during limited treatment periods. PMID:26913754

  4. Bioelectric and Morphological Response of Liquid-Covered Human Airway Epithelial Calu-3 Cell Monolayer to Periodic Deposition of Colloidal 3-Mercaptopropionic-Acid Coated CdSe-CdS/ZnS Core-Multishell Quantum Dots.

    PubMed

    Turdalieva, Aizat; Solandt, Johan; Shambetova, Nestan; Xu, Hao; Blom, Hans; Brismar, Hjalmar; Zelenina, Marina; Fu, Ying

    2016-01-01

    Lung epithelial cells are extensively exposed to nanoparticles present in the modern urban environment. Nanoparticles, including colloidal quantum dots (QDs), are also considered to be potentially useful carriers for the delivery of drugs into the body. It is therefore important to understand the ways of distribution and the effects of the various types of nanoparticles in the lung epithelium. We use a model system of liquid-covered human airway epithelial Calu-3 cell cultures to study the immediate and long-term effects of repeated deposition of colloidal 3-mercaptopropionic-acid coated CdSe-CdS/ZnS core-multishell QDs on the lung epithelial cell surface. By live confocal microscope imaging and by QD fluorescence measurements we show that the QD permeation through the mature epithelial monolayers is very limited. At the time of QD deposition, the transepithelial electrical resistance (TEER) of the epithelial monolayers transiently decreased, with the decrement being proportional to the QD dose. Repeated QD deposition, once every six days for two months, lead to accumulation of only small amounts of the QDs in the cell monolayer. However, it did not induce any noticeable changes in the long-term TEER and the molecular morphology of the cells. The colloidal 3-mercaptopropionic-acid coated CdSe-CdS/ZnS core-multishell QDs could therefore be potentially used for the delivery of drugs intended for the surface of the lung epithelia during limited treatment periods. PMID:26913754

  5. Arsenic(III) and arsenic(V) speciation during transformation of lepidocrocite to magnetite.

    PubMed

    Wang, Yuheng; Morin, Guillaume; Ona-Nguema, Georges; Brown, Gordon E

    2014-12-16

    Bioreduction of As(V) and As-bearing iron oxides is considered to be one of the key processes leading to arsenic pollution in groundwaters in South and Southeast Asia. Recent laboratory studies with simple aqueous media showed that secondary Fe(II)-bearing phases (e.g., magnetite and green rust), which commonly precipitate during bioreduction of iron oxides, captured arsenic species. The aim of the present study was to follow arsenic speciation during the abiotic Fe(II)-induced transformation of As(III)- and As(V)-doped lepidocrocite to magnetite, and to evaluate the influence of arsenic on the transformation kinetics and pathway. We found green rust formation is an intermediate phase in the transformation. Both As(III) and As(V) slowed the transformation, with the effect being greater for As(III) than for As(V). Prior to the formation of magnetite, As(III) adsorbed on both lepidocrocite and green rust, whereas As(V) associated exclusively with green rust, When magnetite precipitated, As(III) formed surface complexes on magnetite nanoparticles and As(V) is thought to have been incorporated into the magnetite structure. These processes dramatically lowered the availability of As in the anoxic systems studied. These results provide insights into the behavior of arsenic during magnetite precipitation in reducing environments. We also found that As(V) removal from solution was higher than As(III) removal following magnetite formation, which suggests that conversion of As(III) to As(V) is preferred when using As-magnetite precipitation to treat As-contaminated groundwaters. PMID:25425339

  6. Remanence in authigenic magnetite: Testing the hydrocarbon-magnetite hypothesis

    SciTech Connect

    Elmore, R.D.; Crawford, L. )

    1990-04-10

    Paleomagnetic, rock magnetic, petrographic, and geochemical studies of hydrocarbon-saturated speleothems in southern Oklahoma indicate there is a relation between hydrocarbons and a chemical magnetization that resides in magnetite. The speleothems, which are composed of light and dark calcite bands, occur in caves of karst origin in the Ordovician Kindblade Formation. Vertebrate fossils interbedded with the deposits indicate they are Permian in age. The dark bands contain primary hydrocarbon-filled fluid inclusions. The dark calcites possess over an order of magnitude stronger natural remanent magnetization than the lighter bands which do not yield stable decay during demagnetization. Alternating field (AF) and thermal demagnetization of specimens of the dark bands reveal a Permian direction of magnetization (declination = 160, inclination = 3, k = 17, {alpha}95 = 5, n = 56). The results of rock magnetic experiments, and the fact that most maximum unblocking temperatures are below 580 C, suggest that the dominant component resides in magnetite. In some specimens stable decay to 640 C suggests the presence of a weak component residing in hematite. The presence of authigenic magnetite spheres in magnetic extracts of the dark calcites supports a chemical origin for the magnetization. Shallow burial depths probably eliminate the possibility of a thermoviscous magnetization. The occurrence of primary hydrocarbons seeped into the caves during precipitation of the speleothems and were trapped in the calcite crystals. The relationship between intensity of magnetization and hydrocarbon abundance leads the authors to propose that chemical conditions created by the hydrocarbons caused precipitation of authigenic magnetite and acquisition of the associated chemical remanence.

  7. In Vitro characterization of low modulus linoleic acid coated strontium-substituted hydroxyapatite containing PMMA bone cement.

    PubMed

    Lam, W M; Pan, H B; Fong, M K; Cheung, W S; Wong, K L; Li, Z Y; Luk, K D K; Chan, W K; Wong, C T; Yang, C; Lu, W W

    2011-01-01

    Poly (methyl methacrylate) (PMMA) bone cement is widely used in vertebral body augmentation procedures such as vertebroplasty and balloon kyphoplasty. Filling high modulus PMMA increases the modulus of filled verterbra, increasing the risk of fracture in the adjacent vertebra. On the other hand, in porous PMMA bone cements, wear particle generation and deterioration of mechanical performance are the major drawbacks. This study adopts a new approach by utilizing linoleic acid coated strontium substituted hydroxyapatite nanoparticle (Sr-5 HA) and linoleic acid as plasticizer reducing bone cement's modulus with minimal impact on its strength. We determined the compressive strength (UCS) and modulus (Ec), hydrophobicity, injectability, in vitro bioactivity and biocompatibility of this bone cement at different filler and linoleic acid loading. At 20 wt % Sr5-HA incorporation, UCS and Ec were reduced from 63 ± 2 MPa, 2142 ± 129 MPa to 58 ± 2 MPa, 1785 ± 64 MPa, respectively. UCS and Ec were further reduced to 49 ± 2 MPa and 774 ± 70 MPa respectively when 15 v/v of linoleic acid was incorporated. After 7 days of incubation, pre-osteoblast cells (MC3T3-E1) attached on 20 wt % Sr5-HA and 20 wt % Sr5-HA with 15 v/v of linoleic acid group were higher (3.73 ± 0.01 x 10⁴, 2.27 ± 0.02 x 10⁴) than their PMMA counterpart (1.83 ± 0.04 x 10⁴). Incorporation of Sr5-HA with linoleic acid in monomer phase is more effective in reducing the bone cement's stiffness than Sr5-HA alone. Combination of low stiffness and high mechanical strength gives the novel bone cement the potential for use in vertebroplasty cement applications. PMID:21053263

  8. Synthesis of nanoparticle CT contrast agents: in vitro and in vivo studies

    NASA Astrophysics Data System (ADS)

    Kim, Sung June; Xu, Wenlong; Wasi Ahmad, Md; Baeck, Jong Su; Chang, Yongmin; Bae, Ji Eun; Chae, Kwon Seok; Kim, Tae Jeong; Park, Ji Ae; Lee, Gang Ho

    2015-10-01

    Water-soluble and biocompatible D-glucuronic acid coated Na2WO4 and BaCO3 nanoparticles were synthesized for the first time to be used as x-ray computed tomography (CT) contrast agents. Their average particle diameters were 3.2 ± 0.1 and 2.8 ± 0.1 nm for D-glucuronic acid coated Na2WO4 and BaCO3 nanoparticles, respectively. All the nanoparticles exhibited a strong x-ray attenuation. In vivo CT images were obtained after intravenous injection of an aqueous sample suspension of D-glucuronic acid coated Na2WO4 nanoparticles, and positive contrast enhancements in the kidney were clearly shown. These findings indicate that the nanoparticles reported in this study may be promising CT contrast agents.

  9. Magnetic microbes: Bacterial magnetite biomineralization

    DOE PAGESBeta

    Prozorov, Tanya

    2015-09-14

    Magnetotactic bacteria are a diverse group of prokaryotes with the ability to orient and migrate along the magnetic field lines in search for a preferred oxygen concentration in chemically stratified water columns and sediments. These microorganisms produce magnetosomes, the intracellular nanometer-sized magnetic crystals surrounded by a phospholipid bilayer membrane, typically organized in chains. Magnetosomes have nearly perfect crystal structures with narrow size distribution and species-specific morphologies, leading to well-defined magnetic properties. As a result, the magnetite biomineralization in these organisms is of fundamental interest to diverse disciplines, from biotechnology to astrobiology. As a result, this article highlights recent advances inmore » the understanding of the bacterial magnetite biomineralization.« less

  10. Dissolution and reduction of magnetite by bacteria

    NASA Technical Reports Server (NTRS)

    Kostka, J. E.; Nealson, K. H.

    1995-01-01

    Magnetite (Fe3O4) is an iron oxide of mixed oxidation state [Fe(II), Fe(III)] that contributes largely to geomagnetism and plays a significant role in diagenesis in marine and freshwater sediments. Magnetic data are the primary evidence for ocean floor spreading and accurate interpretation of the sedimentary magnetic record depends on an understanding of the conditions under which magnetite is stable. Though chemical reduction of magnetite by dissolved sulfide is well known, biological reduction has not been considered likely based upon thermodynamic considerations. This study shows that marine and freshwater strains of the bacterium Shewanella putrefaciens are capable of the rapid dissolution and reduction of magnetite, converting millimolar amounts to soluble Fe(II)in a few days at room temperature. Conditions under which magnetite reduction is optimal (pH 5-6, 22-37 degrees C) are consistent with an enzymatic process and not with simple chemical reduction. Magnetite reduction requires viable cells and cell contact, and it appears to be coupled to electron transport and growth. In a minimal medium with formate or lactate as the electron donor, more than 10 times the amount of magnetite was reduced over no carbon controls. These data suggest that magnetite reduction is coupled to carbon metabolism in S. putrefaciens. Bacterial reduction rates of magnetite are of the same order of magnitude as those estimated for reduction by sulfide. If such remobilization of magnetite occurs in nature, it could have a major impact on sediment magnetism and diagenesis.

  11. Dissolution and reduction of magnetite by bacteria.

    PubMed

    Kostka, J E; Nealson, K H

    1995-10-01

    Magnetite (Fe3O4) is an iron oxide of mixed oxidation state [Fe(II), Fe(III)] that contributes largely to geomagnetism and plays a significant role in diagenesis in marine and freshwater sediments. Magnetic data are the primary evidence for ocean floor spreading and accurate interpretation of the sedimentary magnetic record depends on an understanding of the conditions under which magnetite is stable. Though chemical reduction of magnetite by dissolved sulfide is well known, biological reduction has not been considered likely based upon thermodynamic considerations. This study shows that marine and freshwater strains of the bacterium Shewanella putrefaciens are capable of the rapid dissolution and reduction of magnetite, converting millimolar amounts to soluble Fe(II)in a few days at room temperature. Conditions under which magnetite reduction is optimal (pH 5-6, 22-37 degrees C) are consistent with an enzymatic process and not with simple chemical reduction. Magnetite reduction requires viable cells and cell contact, and it appears to be coupled to electron transport and growth. In a minimal medium with formate or lactate as the electron donor, more than 10 times the amount of magnetite was reduced over no carbon controls. These data suggest that magnetite reduction is coupled to carbon metabolism in S. putrefaciens. Bacterial reduction rates of magnetite are of the same order of magnitude as those estimated for reduction by sulfide. If such remobilization of magnetite occurs in nature, it could have a major impact on sediment magnetism and diagenesis. PMID:11539843

  12. Trace elements in magnetite as petrogenetic indicators

    NASA Astrophysics Data System (ADS)

    Dare, Sarah A. S.; Barnes, Sarah-Jane; Beaudoin, Georges; Méric, Julien; Boutroy, Emilie; Potvin-Doucet, Christophe

    2014-10-01

    We have characterized the distribution of 25 trace elements in magnetite (Mg, Al, Si, P, Ca, Sc, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ga, Ge, Y, Zr, Nb, Mo, Sn, Hf, Ta, W, and Pb), using laser ablation ICP-MS and electron microprobe, from a variety of magmatic and hydrothermal ore-forming environments and compared them with data from the literature. We propose a new multielement diagram, normalized to bulk continental crust, designed to emphasize the partitioning behavior of trace elements between magnetite, the melt/fluid, and co-crystallizing phases. The normalized pattern of magnetite reflects the composition of the melt/fluid, which in both magmatic and hydrothermal systems varies with temperature. Thus, it is possible to distinguish magnetite formed at different degrees of crystal fractionation in both silicate and sulfide melts. The crystallization of ilmenite or sulfide before magnetite is recorded as a marked depletion in Ti or Cu, respectively. The chemical signature of hydrothermal magnetite is distinct being depleted in elements that are relatively immobile during alteration and commonly enriched in elements that are highly incompatible into magnetite (e.g., Si and Ca). Magnetite formed from low-temperature fluids has the lowest overall abundance of trace elements due to their lower solubility. Chemical zonation of magnetite is rare but occurs in some hydrothermal deposits where laser mapping reveals oscillatory zoning, which records the changing conditions and composition of the fluid during magnetite growth. This new way of plotting all 25 trace elements on 1 diagram, normalized to bulk continental crust and elements in order of compatibility into magnetite, provides a tool to help understand the processes that control partitioning of a full suit of trace elements in magnetite and aid discrimination of magnetite formed in different environments. It has applications in both petrogenetic and provenance studies, such as in the exploration of ore deposits and in

  13. Magnetite fractionation of "chalcophile" elements

    NASA Astrophysics Data System (ADS)

    Mavrogenes, J. A.; Jenner, F. E.; Arculus, R. J.

    2008-12-01

    Submarine-quenched glasses provide the clearest record of magmatic evolution available, especially with respect to potentially volatile elements and compounds. A comprehensive suite of arc- and backarc glasses recovered during several research voyages in the SW Pacific are being analysed by a number of research teams in an effort to document genesis and fractionation processes involved in the evolution of subduction- related magma systems. As part of these studies, a suite of basalt to dacite composition glasses recovered from the arc-like Pacmanus Site in the Manus Backarc Basin have been examined in detail. Sun et al. (2004) found trends of increasing enrichments of Re, Cu, and Au with SiO2 in the range from 50 to 60 wt% SiO2. From this stage of magmatic evolution, marked depletions in all these elements are observed in glasses of higher SiO2 contents. The reasons for this trend have been unclear, although a mechanism involving the cessation of olivine and initiation of magnetite saturation was proposed by Sun et al. Our analysis of a larger suite of glasses from the Manus Basin has now confirmed these trends, and found the same behaviour for Zn and Mn. Similarly, analysis of a suite of basalt to dacite glasses recovered from the arc-like Valu Fa Ridge in the Lau Backarc Basin has produced trends for these elements very similar to those of the Pacmanus location. LA-ICP-MS analysis of microphenocrysts in these glasses has shown that magnetite is highly enriched in Re relative to the coexisting melt (Kd up to 7.8 for Re). Magnetite/melt partition coefficients for Re, Mn and Yb can be used to precisely model the liquid line of descent during magnetite (plus clinopyroxene and plagioclase) fractionation using Re vs. Mn/Yb. The variation of Pt abundances with SiO2 for both these suites contrasts with other nominally chalcophile trace elements in showing rapid early depletion from the most Mg-rich basalt through to more SiO2-rich compositions, with no maximum at 60 wt

  14. Drug permeation and cellular interaction of amino acid-coated drug combination powders for pulmonary delivery.

    PubMed

    Vartiainen, Ville; Bimbo, Luis M; Hirvonen, Jouni; Kauppinen, Esko I; Raula, Janne

    2016-05-17

    The effect of three amino acid coatings (L-leucine, L-valine and L-phenylalanine) on particle integrity, aerosolization properties, cellular interaction, cytocompatibility, and drug permeation properties of drug combination powder particles (beclomethasone dipropionate and salbutamol sulphate) for dry powder inhalation (DPI) was investigated. Particles with crystalline L-leucine coating resulted in intact separated particles, with crystalline L-valine coating in slightly sintered particles and with amorphous L-phenylalanine coating in strongly fused particles. The permeation of beclomethasone dipropionate across a Calu-3 differentiated cell monolayer was increased when compared with its physical mixture. Drug crystal formation was also observed on the Calu-3 cell monolayer. The L-leucine coated particles were further investigated for cytocompatibility in three human pulmonary (Calu-3, A549 and BEAS-2B) and one human macrophage (THP-1) cell lines, where they showed excellent tolerability. The l-leucine coated particles were also examined for their ability to elicit reactive oxygen species in pulmonary BEAS-2B and macrophage THP-1 cell lines. The study showed the influence of the amino acid coatings for particle formation and performance and their feasibility for combination therapy for pulmonary delivery. PMID:27034001

  15. Biogenic Magnetite in Martian Meteorite ALH84001

    NASA Technical Reports Server (NTRS)

    Thomas-Keprta, K. L.; Bazylinski, Dennis; Wentworth, Susan J.; McKay, David S.; Kirschvink, Joseph L.; Clemett, SImon J.; Bell, Mary Sue; Golden, D. C.; Gibson, Everett K., Jr.

    1999-01-01

    Fine-grained magnetite (Fe3O4) in martian meteorite ALH84001, generally less than 200 nm in size, is located primarily in the rims that surround the carbonate globules. There are two populations of ALH84001 magnetites, which are likely formed at low temperature by inorganic and biogenic processes. Nearly 27% of ALH84001 magnetite particles, also called elongated prisms, have characteristics which make them uniquely identifiable as biological precipitates. Additional information is contained in the original extended abstract.

  16. Magnetite as a prokaryotic biomarker: A review

    NASA Astrophysics Data System (ADS)

    Jimenez-Lopez, Concepcion; Romanek, Christopher S.; Bazylinski, Dennis A.

    2010-06-01

    Over the years, nanometer-sized magnetite (Fe3O4) crystals have been recovered from many modern and ancient environments including sediments and soils and even meteorites. In some cases these crystals have been used as "magnetofossils" for evidence of the past presence of specific microbes. Magnetite nanocrystals can be formed by a number of different biological and inorganic mechanisms resulting in crystals with different physical and magnetic characteristics. Prokaryotes (bacteria) biomineralize magnetite through two methods that differ mechanistically, including: biologically induced mineralization (BIM) and biologically controlled mineralization (BCM). Magnetite nanocrystals produced by BIM are known to be synthesized by the dissimilatory iron-reducing bacteria, are deposited external to the cell, and generally are physically indistinguishable from magnetite particles formed inorganically. BCM magnetites, in contrast, are synthesized by the magnetotactic bacteria and some higher organisms and are precipitated intracellularly as membrane-bounded structures called magnetosomes. These magnetites appear to have unique crystal morphologies and a narrow size range leading to their original use as magnetofossils. Because of the discovery of nanometer-sized crystals of magnetite in the Martian meteorite ALH84001, the use of these criteria for the determination of whether magnetite crystals could constitute a prokaryotic biomarker was questioned. Thus, there is currently great debate over what criteria to use in the determination of whether specific magnetite crystals are biogenic or not. In the last decade, additional criteria have been established (e.g., the Magnetite Assay for Biogenicity), and new tools and technologies have been developed to determine the origin of specific types of magnetite crystals.

  17. Properties of intracellular magnetite crystals produced by Desulfovibrio magneticus strain RS-1

    NASA Astrophysics Data System (ADS)

    Pósfai, Mihály; Moskowitz, Bruce M.; Arató, Balázs; Schüler, Dirk; Flies, Christine; Bazylinski, Dennis A.; Frankel, Richard B.

    2006-09-01

    Desulfovibrio magneticus strain RS-1 is an anaerobic sulfate-reducing bacterium. Cells form intracellular nanocrystals of magnetite but are only weakly magnetotactic. In order to understand the unusual magnetic response of this strain, we studied magnetite crystals within cells grown with fumarate and sulfate. Many cells grown under either condition did not form magnetic crystals while others contained only 1 to 18 small (˜ 40 nm) magnetite-containing magnetosomes. Bulk magnetic measurements of whole cells showed a superparamagnetic-like behavior, indicating that many of the magnetite crystals are too small to have a permanent magnetic moment at ambient temperature. The temperature of the Verwey transition is lower (˜ 86 K) than of magnetite from other magnetotactic strains, likely indicating partial oxidation of magnetite into maghemite. As a result of the small size and small number of magnetite magnetosomes, the magnetic moments of most cells grown anaerobically with fumarate or sulfate are insufficient for magnetotaxis. In addition to intracellular magnetite, in some cultures another iron oxide, hematite, formed on the surfaces of cells. The hematite grains are embedded in an extracellular polymeric material, indicating that the crystals likely resulted from a biologically-induced mineralization process. Although the hematite particles appear to consist of aggregations of many small (5 to 10 nm) grains, the grains have a consensus orientation and thus the whole particle diffracts as a single crystal. The aligned arrangement of nanoparticles within larger clusters may reflect either a templated nucleation of hematite crystallites in an extracellular organic matrix, or result from a self-assembling process during the crystallization of hematite from ferric gels or ferrihydrite.

  18. Novel protocol for the solid-state synthesis of magnetite for medical practices

    NASA Astrophysics Data System (ADS)

    Paiva, D. L.; Andrade, A. L.; Pereira, M. C.; Fabris, J. D.; Domingues, R. Z.; Alvarenga, M. E.

    2015-06-01

    It is reported a novel approach to prepare nanoparticles of magnetite (Fe3O4) by heating a mixture of synthetic commercial maghemite ( γFe2O3) with sucrose. This solid-state reaction leads to the chemical reduction of part of the Fe3+ of the precursor oxide to render Fe2+ and Fe3+ in octahedral and Fe3+ in tetrahedral sites of the Fe-O coordination framework. Powder X-ray diffraction patterns, FTIR and 298 K Mössbauer spectra confirm the conversion of maghemite into magnetite. Based on these results, the optimal sucrose:maghemite rate was found to be 4.

  19. Magnetite decorated activated carbon composites for water purification

    NASA Astrophysics Data System (ADS)

    Barala, Sunil Kumar; Arora, Manju; Saini, Parveen

    2013-06-01

    Activated carbon decorated with magnetite (ACMG) nanoparticles composites have been prepared by facile method via impregnation of AC with stable dispersion of superparamagnetic MG nanoparticles followed by drying. These composites exhibit both magnetic and porosity behavior which can be easily optimized by controlling the weight ratio of two phases. The structural, magnetic, thermal and morphological properties of these as synthesized ACMG samples were characterized by powder XRD, FTIR, VSM and SEM techniques. The ACMG powder has been used for water purification having methylene blue (MB) dye as an impurity. The nanoporosity of these composites allow rapid adsorption of MB and their magnetic behavior helps in single step separation of MB adsorbed ACMG particles by the application of external magnetic field.

  20. Generation of drugs coated iron nanoparticles through high energy ball milling

    NASA Astrophysics Data System (ADS)

    Radhika Devi, A.; Chelvane, J. A.; Prabhakar, P. K.; Padma Priya, P. V.; Doble, Mukesh; Murty, B. S.

    2014-03-01

    The iron nanoparticles coated with oleic acid and drugs such as folic acid/Amoxicillin were synthesized by high energy ball milling and characterized by X-ray diffraction, Transmission electron microscope, zeta potential, dynamic light scattering, Fourier Transform Infra red (FT-IR) measurements, and thermo gravimetric analysis (TGA). FT-IR and TGA measurements show good adsorption of drugs on oleic acid coated nanoparticles. Magnetic measurements indicate that saturation magnetization is larger for amoxicillin coated particles compared to folic acid coated particles. The biocompatibility of the magnetic nanoparticles prepared was evaluated by in vitro cytotoxicity assay using L929 cells as model cells.

  1. Generation of drugs coated iron nanoparticles through high energy ball milling

    SciTech Connect

    Radhika Devi, A.; Murty, B. S.; Chelvane, J. A.; Prabhakar, P. K.; Padma Priya, P. V.; Doble, Mukesh

    2014-03-28

    The iron nanoparticles coated with oleic acid and drugs such as folic acid/Amoxicillin were synthesized by high energy ball milling and characterized by X-ray diffraction, Transmission electron microscope, zeta potential, dynamic light scattering, Fourier Transform Infra red (FT-IR) measurements, and thermo gravimetric analysis (TGA). FT-IR and TGA measurements show good adsorption of drugs on oleic acid coated nanoparticles. Magnetic measurements indicate that saturation magnetization is larger for amoxicillin coated particles compared to folic acid coated particles. The biocompatibility of the magnetic nanoparticles prepared was evaluated by in vitro cytotoxicity assay using L929 cells as model cells.

  2. Moessbauer Characterization of Magnetite/Polyaniline Magnetic Nanocomposite

    SciTech Connect

    Rodriguez, Anselmo F. R.; Faria, Fernando S. E. D. V.; Lopez, Jorge L.; Mesquita, Antonio G. G.; Coaquira, Jose A. H.; Oliveira, Aderbal C.; Morais, Paulo C.; Azevedo, Ricardo B.; Araujo, Ana C. V. de; Alves, Severino Jr.; Azevedo, Walter M. de

    2010-12-02

    Aniline surface coated Fe{sub 3}O{sub 4} nanoparticles have been successfully synthesized by UV irradiation varying the time and the acid media (HCl, HNO{sub 3}, or H{sub 2}SO{sub 4}). The synthesized material represents a promising platform for application in nerve regeneration. XRD patterns are consistent with the crystalline structure of magnetite. Nevertheless, for UV irradiation times longer than 2 h, extra XRD lines reveal the presence of goethite. The mean crystallite size of uncoated particles is estimated to be 25.4 nm, meanwhile that size is reduced to 19.9 nm for the UV irradiated sample in HCl medium for 4 h. Moessbauer spectra of uncoated nanoparticles reveal the occurrence of thermal relaxation at room temperature, while the 77 K-Moessbauer spectrum suggests the occurrence of electron localization effects similar to that expected in bulk magnetite. The Mossbauer spectra of UV irradiated sample in HCl medium during 4 h, confirms the presence of the goethite phase. For this sample, the thermal relaxation is more evident, since the room temperature spectrum shows larger spectral area for the nonmagnetic component due to the smaller crystallite size. Meanwhile, the 77 K-Moessbauer spectrum suggests the absence of the electron localization effect above 77 K.

  3. Enzymatic polymerization of natural anacardic acid and antibiofouling effects of polyanacardic acid coatings.

    PubMed

    Chelikani, Rahul; Kim, Yong Hwan; Yoon, Do-Young; Kim, Dong-Shik

    2009-05-01

    Anacardic acid, separated from cashew nut shell liquid, is well known for its strong antibiotic and antioxidant activities. Recent findings indicate that phenolic compounds from plant sources have an effect on Gram-negative bacteria biofilm formation. In this work, a polyphenolic coating was prepared from anacardic acid using enzymatic synthesis and tested for its effects on biofilm formation of both Gram-negative and Gram-positive bacteria. Natural anacardic acid was enzymatically polymerized using soybean peroxidase. Hydrogen peroxide and phenothiazine-10-propionic acid were used as an oxidizing agent and redox mediator, respectively. Nuclear magnetic resonance and Fourier transform infrared (FTIR) analyses showed the formation of oxyphenylene and phenylene units through the phenol rings. No linkage through the alkyl chain was observed, which proved a high chemo-selectivity of the enzyme. Aqueous solvents turned out to play an important role in the polymer production yield and molecular weight. With 2-propanol, the highest production yield (61%) of polymer (molecular weight = 3,900) was observed, and with methanol, higher-molecular-weight polymers (5,000) were produced with lower production yields (43%). The resulting polyanacardic acid was cross-linked on a solid surface to form a permanent natural polymer coating. The FTIR analysis indicates that the cross-linking between the polymers took place through the unsaturated alkyl side chains. The polyanacardic acid coating was then tested for its antibiofouling effect against Gram-negative and Gram-positive bacteria and compared with the antibiofouling effects of polycardanol coatings reported in the literature. The polyanacardic acid coating showed more reduction in biofilm formation on its surface than polycardanol coatings in the case of Gram-positive bacteria, while in the case of Gram-negative bacteria, it showed a similar reduction in biofilm formation as polycardanol. PMID:18592408

  4. Magnetite Particle Size Distribution and Pellet Oxidation

    NASA Astrophysics Data System (ADS)

    Cho, Hyeon Jeong; Tang, Ming; Pistorius, Petrus Christiaan

    2014-08-01

    Oxidation of magnetite pellets is commonly performed to prepare strong pellets for ironmaking. This article presents a contribution to quantitative understanding of fundamental pellet oxidation kinetics, based on measured oxidation kinetics of magnetite particles and pellets. The commonly observed "plateau" oxidation behavior is confirmed to be consistent with the effect of very large differences in magnetite particle sizes in the concentrate from which pellets are produced. The magnetite particles range in size from less than a micron to several tens of a microns; changing the size distribution by inert sintering of pellets decreases both the plateau level of oxidation and the specific surface area, in ways that are compatible with an assumed Rosin-Rammler magnetite particle size distribution.

  5. Magnetite-Amyloid-β deteriorates activity and functional organization in an in vitro model for Alzheimer’s disease

    PubMed Central

    Teller, Sara; Tahirbegi, Islam Bogachan; Mir, Mònica; Samitier, Josep; Soriano, Jordi

    2015-01-01

    The understanding of the key mechanisms behind human brain deterioration in Alzheimer’ disease (AD) is a highly active field of research. The most widespread hypothesis considers a cascade of events initiated by amyloid-β peptide fibrils that ultimately lead to the formation of the lethal amyloid plaques. Recent studies have shown that other agents, in particular magnetite, can also play a pivotal role. To shed light on the action of magnetite and amyloid-β in the deterioration of neuronal circuits, we investigated their capacity to alter spontaneous activity patterns in cultured neuronal networks. Using a versatile experimental platform that allows the parallel monitoring of several cultures, the activity in controls was compared with the one in cultures dosed with magnetite, amyloid-β and magnetite-amyloid-β complex. A prominent degradation in spontaneous activity was observed solely when amyloid-β and magnetite acted together. Our work suggests that magnetite nanoparticles have a more prominent role in AD than previously thought, and may bring new insights in the understanding of the damaging action of magnetite-amyloid-β complex. Our experimental system also offers new interesting perspectives to explore key biochemical players in neurological disorders through a controlled, model system manner. PMID:26608215

  6. Magnetite-Amyloid-β deteriorates activity and functional organization in an in vitro model for Alzheimer’s disease

    NASA Astrophysics Data System (ADS)

    Teller, Sara; Tahirbegi, Islam Bogachan; Mir, Mònica; Samitier, Josep; Soriano, Jordi

    2015-11-01

    The understanding of the key mechanisms behind human brain deterioration in Alzheimer’ disease (AD) is a highly active field of research. The most widespread hypothesis considers a cascade of events initiated by amyloid-β peptide fibrils that ultimately lead to the formation of the lethal amyloid plaques. Recent studies have shown that other agents, in particular magnetite, can also play a pivotal role. To shed light on the action of magnetite and amyloid-β in the deterioration of neuronal circuits, we investigated their capacity to alter spontaneous activity patterns in cultured neuronal networks. Using a versatile experimental platform that allows the parallel monitoring of several cultures, the activity in controls was compared with the one in cultures dosed with magnetite, amyloid-β and magnetite-amyloid-β complex. A prominent degradation in spontaneous activity was observed solely when amyloid-β and magnetite acted together. Our work suggests that magnetite nanoparticles have a more prominent role in AD than previously thought, and may bring new insights in the understanding of the damaging action of magnetite-amyloid-β complex. Our experimental system also offers new interesting perspectives to explore key biochemical players in neurological disorders through a controlled, model system manner.

  7. Vortex magnetic structure in framboidal magnetite reveals existence of water droplets in an ancient asteroid

    NASA Astrophysics Data System (ADS)

    Kimura, Yuki; Sato, Takeshi; Nakamura, Norihiro; Nozawa, Jun; Nakamura, Tomoki; Tsukamoto, Katsuo; Yamamoto, Kazuo

    2013-10-01

    The majority of water has vanished from modern meteorites, yet there remain signatures of water on ancient asteroids. How and when water disappeared from the asteroids is important, because the final fluid-concentrated chemical species played critical roles in the early evolution of organics and in the final minerals in meteorites. Here we show evidence of vestigial traces of water based on a nanometre-scale palaeomagnetic method, applying electron holography to the framboids in the Tagish Lake meteorite. The framboids are colloidal crystals composed of three-dimensionally ordered magnetite nanoparticles and therefore are only able to form against the repulsive force induced by the surface charge of the magnetite as a water droplet parches in microgravity. We demonstrate that the magnetites have a flux closure vortex structure, a unique magnetic configuration in nature that permits the formation of colloidal crystals just before exhaustion of water from a local system within a hydrous asteroid.

  8. Controls on soluble Pu concentrations in PuO2/magnetite suspensions.

    PubMed

    Felmy, Andrew R; Moore, Dean A; Pearce, Carolyn I; Conradson, Steven D; Qafoku, Odeta; Buck, Edgar C; Rosso, Kevin M; Ilton, Eugene S

    2012-11-01

    Time-dependent reduction of PuO(2)(am) was studied over a range of pH values in the presence of aqueous Fe(II) and magnetite (Fe(3)O(4)) nanoparticles. At early time frames (up to 56 days) very little aqueous Pu was mobilized from PuO(2)(am), even though measured pH and redox potentials, coupled to equilibrium thermodynamic modeling, indicated the potential for significant reduction of PuO(2)(am) to relatively soluble Pu(III). Introduction of Eu(III) or Nd(III) to the suspensions as competitive cations to displace possible sorbed Pu(III) resulted in the release of significant concentrations of aqueous Pu. However, the similarity of aqueous Pu concentrations that resulted from the introduction of Eu(III)/Nd(III) to suspensions with and without magnetite indicated that the Pu was solubilized from PuO(2)(am), not from magnetite. PMID:23016948

  9. Vortex magnetic structure in framboidal magnetite reveals existence of water droplets in an ancient asteroid.

    PubMed

    Kimura, Yuki; Sato, Takeshi; Nakamura, Norihiro; Nozawa, Jun; Nakamura, Tomoki; Tsukamoto, Katsuo; Yamamoto, Kazuo

    2013-01-01

    The majority of water has vanished from modern meteorites, yet there remain signatures of water on ancient asteroids. How and when water disappeared from the asteroids is important, because the final fluid-concentrated chemical species played critical roles in the early evolution of organics and in the final minerals in meteorites. Here we show evidence of vestigial traces of water based on a nanometre-scale palaeomagnetic method, applying electron holography to the framboids in the Tagish Lake meteorite. The framboids are colloidal crystals composed of three-dimensionally ordered magnetite nanoparticles and therefore are only able to form against the repulsive force induced by the surface charge of the magnetite as a water droplet parches in microgravity. We demonstrate that the magnetites have a flux closure vortex structure, a unique magnetic configuration in nature that permits the formation of colloidal crystals just before exhaustion of water from a local system within a hydrous asteroid. PMID:24149376

  10. In-situ precipitation of ultra-stable nano-magnetite slurry

    NASA Astrophysics Data System (ADS)

    Ramimoghadam, Donya; Bagheri, Samira; Hamid, Sharifah Bee Abd

    2015-04-01

    In this contribution, we prepared water-based magnetic fluids of iron oxide nanoparticles using an in-situ precipitation method. The effect of dodecanoic acid addition as a surfactant on the physico-chemical and magnetic properties of iron oxide nanoparticles was investigated as well. The quantity of the surfactant was varied between 3 and 5 g. Raman spectroscopy and X-ray diffraction (XRD) were utilized to confirm the presence of spinel phase magnetites (Fe3O4). Dynamic light scattering (DLS) and transmission electron microscopy (TEM) were used to characterize the resulting magnetic nanoparticles' size and morphology. The results showed polydispersed hexagonal nanoparticles (average diameter of ca. 70 nm) as a result of the protocol. Moreover, the pH-dependent stability of the samples confirms that magnetite nanofluids were highly stable in the wide range of pH, from 4-12. The optimal amount of dodecanoic acid to produce ultra-stable nano-magnetite slurry with the highest saturation magnetization of 8.6 emu g-1 was determined to be 4.5 g.

  11. Brain glutathione redox system significance for the control of silica-coated magnetite nanoparticles with or without mercury co-exposures mediated oxidative stress in European eel (Anguilla anguilla L.).

    PubMed

    Anjum, Naser A; Srikanth, Koigoora; Mohmood, Iram; Sayeed, Iqbal; Trindade, Tito; Duarte, Armando C; Pereira, Eduarda; Ahmad, Iqbal

    2014-06-01

    This in vitro study investigates the impact of silica-coated magnetite particles (Fe3O4@SiO2/SiDTC, hereafter called IONP; 2.5 mg L(-1)) and its interference with co-exposure to persistent contaminant (mercury, Hg; 50 μg L(-1)) during 0, 2, 4, 8, 16, 24, 48, and 72 h on European eel (Anguilla anguilla) brain and evaluates the significance of the glutathione (GSH) redox system in this context. The extent of damage (membrane lipid peroxidation, measured as thiobarbituric acid reactive substances, TBARS; protein oxidation, measured as reactive carbonyls, RCs) decreased with increasing period of exposure to IONP or IONP + Hg which was accompanied with differential responses of glutathione redox system major components (glutathione reductase, GR; glutathione peroxidase, GPX; total GSH, TGSH). The occurrence of antagonism between IONP and Hg impacts was evident at late hour (72 h), where significantly decreased TBARS and RC levels and GR and glutathione sulfo-transferase (GST) activity imply the positive effect of IONP + Hg concomitant exposure against Hg-accrued negative impacts [vs. early (2 h) hour of exposure]. A period of exposure-dependent IONP alone and IONP + Hg joint exposure-accrued impact was perceptible. Additionally, increased susceptibility of the GSH redox system to increased period of exposure to Hg was depicted, where insufficiency of elevated GR for the maintenance of TGSH required for membrane lipid and cellular protein protection was displayed. Overall, a fine-tuning among brain glutathione redox system components was revealed controlling IONP + Hg interactive impacts successfully. PMID:24627197

  12. Magnetorheological behavior of magnetite covered clay particles in aqueous suspensions

    NASA Astrophysics Data System (ADS)

    Galindo-Gonzalez, C.; Lopez-Lopez, M. T.; Duran, J. D. G.

    2012-08-01

    Montmorillonite clay particles coated with magnetite nanoparticles suspended in aqueous media behave as magnetorheological fluids with enhanced stability as compared to conventional ones. In this work, the study of the magnetorheological behavior of these suspensions of magnetite-clay composite particles has been carried out. For this purpose, both steady and dynamic rheological measurements were carried out in the absence and in the presence of external magnetic fields. In the first kind of experiments, the rheograms of the suspensions (shear stress versus shear rate plot) are analyzed as a function of the strength of the magnetic field applied. In the second one, oscillatory stresses are applied to the system, and the storage modulus is studied as a function of the external magnetic field. In the absence of magnetic field, the suspensions develop a weak yield stress due to the aggregation of the magnetite covered clay particles. In the presence of magnetic field, the yield stress is strongly dependent on the magnetic field strength inside the samples, demonstrating that the suspensions experience a magnetorheological effect, moderate when the magnetic field strength is weak and stronger for values of magnetic field higher than 150-200 kA/m. Actually, the most intriguing result is the change of the trend in the dependence of the yield stress with the field. This dependence is approximately linear with the field for strength values smaller than 150-200 kA/m. On the other hand, for higher values, the yield stress increases with magnetic field following a power law with exponent 4.5.The results are interpreted by means of a model that relates the structure of the particles in the suspensions to the magnetic field applied and using the interaction energy between particles calculated by the extended DLVO theory to include magnetic interaction.

  13. Magnetically recyclable magnetite-ceria (Nanocat-Fe-Ce) nanocatalysts - applications in multicomponent reactions under benign conditions

    EPA Science Inventory

    A novel magnetite nanoparticle-supported ceria catalyst (Nanocat-Fe-Ce) has been successfully prepared by simple impregnation method and was well characterized by XRD, SIMS, FEG-SEM-EDS, and TEM. The exact nature of Nanocat-Fe-Ce was confirmed by X-ray photoelectron spectroscopy ...

  14. Removal of Aromatic Pollutant Surrogate from Water by Recyclable Magnetite-Activated Carbon Nanocomposite: An Experiment for General Chemistry

    ERIC Educational Resources Information Center

    Furlan, Ping Y.; Melcer, Michael E.

    2014-01-01

    A general chemistry laboratory experiment using readily available chemicals is described to introduce college students to an exciting class of nanocomposite materials. In a one-step room temperature synthetic process, magnetite nanoparticles are embedded onto activated carbon matrix. The resultant nanocomposite has been shown to combine the…

  15. Biogenic Magnetite in Martian Meteorite ALH84001

    NASA Technical Reports Server (NTRS)

    Thomas-Keprta, Kathie L.; Bazylinski, Dennis; Wentworth, Susan J.; McKay, David S.; Kirschvink, Joseph L.; Clemett, Simon J.; Bell, Mary Sue; Golden, D. C.

    1999-01-01

    Fine-grained magnetite (Fe3O4) in martian meteorite ALH84001, generally less than 200 microns in size, is located primarily in the rims that surround the carbonate globules. There are two populations of ALH84001 magnets, which are likely formed at low temperature by inorganic and biogenic processes. Nearly 27/o of ALH84001 magnetite particles. also called elongated prisms, have characteristics which make them uniquely identifiable as biological precipitates.

  16. The Verwey structure of a natural magnetite.

    PubMed

    Perversi, G; Cumby, J; Pachoud, E; Wright, J P; Attfield, J P

    2016-04-01

    A remarkably complex electronic order of Fe(2+)/Fe(3+) charges, Fe(2+) orbital states, and weakly metal-metal bonded Fe3 units known as trimerons, was recently discovered in stoichiometric magnetite (Fe3O4) below the 125 K Verwey transition. Here, the low temperature crystal structure of a natural magnetite from a mineral sample has been determined using the same microcrystal synchrotron X-ray diffraction method. Structure refinement demonstrates that the natural sample has the same complex electronic order as pure synthetic magnetite, with only minor reductions of orbital and trimeron distortions. Chemical analysis shows that the natural sample contains dopants such as Al, Si, Mg and Mn at comparable concentrations to extraterrestrial magnetites, for example, as reported in the Tagish Lake meteorite. Much extraterrestrial magnetite exists at temperatures below the Verwey transition and hence our study demonstrates that the low temperature phase of magnetite represents the most complex long-range electronic order known to occur naturally. PMID:26908195

  17. Magnetite biomineralization induced by Shewanella oneidensis

    NASA Astrophysics Data System (ADS)

    Perez-Gonzalez, Teresa; Jimenez-Lopez, Concepcion; Neal, Andrew L.; Rull-Perez, Fernando; Rodriguez-Navarro, Alejandro; Fernandez-Vivas, Antonia; Iañez-Pareja, Enrique

    2010-02-01

    Shewanella oneidensis is a dissimilatory iron reducing bacterium capable of inducing the extracellular precipitation of magnetite. This precipitation requires a combination of passive and active mechanisms. Precipitation occurs as a consequence of active production of Fe 2+(aq) when bacteria utilize ferrihydrite as a terminal electron acceptor, and the pH rise probably due to the bacterial metabolism of amino acids. As for passive mechanisms, the localized concentration of Fe 2+(aq) and Fe 3+(aq) at the net negatively charged cell wall, cell structures and/or cell debris induces a local rise of supersaturation of the system with respect to magnetite, triggering the precipitation of such a phase. These biologically induced magnetites are morphologically identical to those formed inorganically in free-drift experiments (closed system; 25 °C, 1 atm total pressure), both from aqueous solutions containing Fe(ClO 4) 2, FeCl 3, NaHCO 3, NaCO 3 and NaOH, and also from sterile culture medium added with FeCl 2. However, organic material becomes incorporated in substantial amounts into the crystal structure of S. oneidensis-induced magnetites, modifying such a structure compared to that of inorganic magnetites. This structural change and the presence of organic matter are detected by Raman and FT-IR spectroscopic analyses and may be used as a biomarker to recognize the biogenic origin of natural magnetites.

  18. Thermal Analysis of Acicular Shaped Magnetite

    NASA Technical Reports Server (NTRS)

    Lauer, H. V., Jr.; Ming, D. W.; Golden, D. C.

    2003-01-01

    We are in the process of developing a database on the thermal properties of well-characterized Martian analog materials in support of future Mars surface missions. The database contains the thermal behaviors of these analog materials under reduced and Earth ambient pressures. Magnetite in planetary materials has received considerable attention in recent years since the identification of fine grain single-domain magnetite in Martian meteorite ALH84001 and their possible link to past life on Mars (i.e., possible biominerals of magnetotactic bacteria). Because of its possible importance to Mars science, we report here the thermal properties of magnetite particles with acicular morphology, i.e., needle-shaped magnetite. Acicular shaped magnetite can be commercially produced from goethite (FeOOH) as the starting material via a H2 reduction process. However, instead of using this process or procedure, we report here on the thermal characterization of acicular magnetite formed under reducing conditions from well-characterized needle-shaped goethite at low temperature in controlled CO-CO2 1-bar atmosphere gas mixing furnaces.

  19. Ice formation on nitric acid-coated dust particles: Laboratory and modeling studies

    NASA Astrophysics Data System (ADS)

    Kulkarni, Gourihar; Zhang, Kai; Zhao, Chun; Nandasiri, Manjula; Shutthanandan, Vaithiyalingam; Liu, Xiaohong; Fast, Jerome; Berg, Larry

    2015-08-01

    Changes in the ice nucleation characteristics of atmospherically relevant mineral dust particles caused by a coating of nitric acid are not well understood. Further, the atmospheric implications of dust coatings on ice-cloud properties under different assumptions of primary ice nucleation mechanisms are unknown. We investigated the ice nucleation ability of Arizona Test Dust, illite, K-feldspar, and quartz as a function of temperature (-25°C to -30°C) and relative humidity with respect to water (75% to 110%). The particles (bare or nitric acid coated) were size selected at 250 nm, and the fraction of particles nucleating ice at various temperature and saturation conditions was determined. All of the dust species nucleated ice at subsaturated conditions, although the coated particles (except quartz) showed a reduction in their ice nucleation ability relative to bare particles. However, at supersaturated conditions, bare and coated particles had nearly equivalent ice nucleation characteristics. The results of a single-column model showed that simulated ice crystal number concentrations are mostly dependent upon the coated particle fraction, primary ice nucleation mechanisms, and competition among ice nucleation mechanisms to nucleate ice. In general, coatings were observed to modify ice-cloud properties, and the complexity of ice-cloud and mixed-phase-cloud evolution when different primary ice nucleation mechanisms compete for fixed water vapor budgets was supported.

  20. Reproducible Crystallite Size of Mono-Dispersed and Scalable Biologically Produced Metal-Substituted Nanometer-Sized Magnetites

    NASA Astrophysics Data System (ADS)

    Moon, J.; Rawn, C.; Rondinone, A.; Love, L.; Roh, Y.; Lauf, R.; Phelps, T.

    2008-12-01

    producing 13-90 nm magnetite or doped magnetites at a fraction of the cost of traditional chemical synthesis. While there are numerous approaches for the synthesis of nanoparticles, bacterial fermentation of magnetite or metal-substituted magnetite may represent a disruptive manufacturing technology with respect to yield, reproducibility and scalability.

  1. Structural characterization of copolymer embedded magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Nedelcu, G. G.; Nastro, A.; Filippelli, L.; Cazacu, M.; Iacob, M.; Rossi, C. Oliviero; Popa, A.; Toloman, D.; Dobromir, M.; Iacomi, F.

    2015-10-01

    Small magnetic nanoparticles (Fe3O4) were synthesized by co-precipitation and coated by emulsion polymerization with poly(methyl methacrylate-co-acrylic acid) (PMMA-co-AAc) to create surface functional groups that can attach drug molecules and other biomolecules. The coated and uncoated magnetite nanoparticles were stored for two years in normal closed ships and than characterized by Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, vibrating sample magnetometry, and electron paramagnetic resonance spectroscopy. The solid phase transformation of magnetite to maghemite, as well as an increase in particle size were evidenced for the uncoated nanoparticles. The coated nanoparticles preserved their magnetite structure and magnetic properties. The influences of monomers and surfactant layers on interactions between the magnetic nanoparticles evidenced that the thickness of the polymer has a significant effect on magnetic properties.

  2. Anisotropy of Silicate-Hosted Magnetite Inclusions

    NASA Astrophysics Data System (ADS)

    Scott, G. R.; Feinberg, J. M.; Renne, P. R.

    2004-12-01

    Anisotropy of magnetic properties is a hallmark of silicate crystals with oriented iron-oxide inclusions. Strongly magnetic magnetite-bearing silicates (10-1 A m-1) are common components of gabbros and layered intrusions, contributing to local and regional magnetic anomalies. Additionally, these iron-oxide silicates hold the promise of being exceptional paleomagnetic recorders owing to their features of: physical/chemical isolation from altering fluids, chemical equilibrium with their silicate host, and long relaxation times (enhanced coercivity). However, anisotropy of remanence must be understood before these advantageous features can be utilized. Measurements of single crystals of clinopyroxene and plagioclase (10-4 g) show anisotropy in direction and intensity that directly reflect the crystallography of the silicate host. The host controls both the crystallographic orientation of the magnetite (magnetocrystalline anisotropy) and the elongation direction of the magnetite inclusion (shape anisotropy). We have found another source of anisotropy that involves an internal exsolution of ulvöspinel within titanomagnetite inclusions. This also reflects a host control as this second exsolution occurs along the magnetite \\{100\\}. This fixed wall shape anisotropy creates an array of interacting single domain magnetite parallelepipeds, parallel to \\{100\\}. Each of these anisotropies contributes to enhanced coercivity of remanence, which significantly exceeds the IRM saturation magnetization for magnetite (300 mT). The anisotropy of IRM (aIRM@ 1.1 T) of magnetite-bearing clinopyroxene and plagioclase shows clustering of directions, reflecting the mixture of variables that include: inclusion elongation direction and abundance, orientation of magnetite easy axes relative to the applied field, inclusion aspect ratio and diameter, and pre-existing magnetic domain structure. For pyroxene (monoclinic) with two arrays of needle-shaped magnetite inclusions, the aIRM is

  3. Biofunctionalized magnetic hydrogel nanospheres of magnetite and κ-carrageenan

    NASA Astrophysics Data System (ADS)

    Daniel-da-Silva, Ana L.; Fateixa, Sara; Guiomar, António J.; Costa, Benilde F. O.; Silva, Nuno J. O.; Trindade, Tito; Goodfellow, Brian J.; Gil, Ana M.

    2009-09-01

    Magnetic hydrogel κ-carrageenan nanospheres were successfully prepared via water-in-oil (w/o) microemulsions combined with thermally induced gelation of the polysaccharide. The size of the nanospheres (an average diameter (∅) of about 50 and 75 nm) was modulated by varying the concentration of surfactant. The nanospheres contained superparamagnetic magnetite nanoparticles (∅8 nm), previously prepared by co-precipitation within the biopolymer. Carboxyl groups, at a concentration of about 4 mmol g-1, were successfully grafted at the surface of these magnetic nanospheres via carboxymethylation of the κ-carrageenan. The carboxylated nanospheres were shown to be thermo-sensitive in the 37-45 °C temperature range, indicating their potential as thermally controlled delivery systems for drugs and/or magnetic particles at physiological temperatures. Finally, preliminary results have been obtained for IgG antibody conjugation of the carboxylated nanospheres and the potential of these systems for bio-applications is discussed.

  4. The chemistry of hydrothermal magnetite: a review

    USGS Publications Warehouse

    Nadoll, Patrick; Angerer, Thomas; Mauk, Jeffrey L.; French, David; Walshe, John

    2014-01-01

    Magnetite (Fe3O4) is a well-recognized petrogenetic indicator and is a common accessory mineral in many ore deposits and their host rocks. Recent years have seen an increased interest in the use of hydrothermal magnetite for provenance studies and as a pathfinder for mineral exploration. A number of studies have investigated how specific formation conditions are reflected in the composition of the respective magnetite. Two fundamental questions underlie these efforts — (i) How can the composition of igneous and, more importantly, hydrothermal magnetite be used to discriminate mineralized areas from barren host rocks, and (ii) how can this assist exploration geologists to target ore deposits at greater and greater distances from the main mineralization? Similar to igneous magnetite, the most important factors that govern compositional variations in hydrothermal magnetite are (A) temperature, (B) fluid composition — element availability, (C) oxygen and sulfur fugacity, (D) silicate and sulfide activity, (E) host rock buffering, (F) re-equilibration processes, and (G) intrinsic crystallographic controls such as ionic radius and charge balance. We discuss how specific formation conditions are reflected in the composition of magnetite and review studies that investigate the chemistry of hydrothermal and igneous magnetite from various mineral deposits and their host rocks. Furthermore, we discuss the redox-related alteration of magnetite (martitization and mushketovitization) and mineral inclusions in magnetite and their effect on chemical analyses. Our database includes published and previously unpublished magnetite minor and trace element data for magnetite from (1) banded iron formations (BIF) and related high-grade iron ore deposits in Western Australia, India, and Brazil, (2) Ag–Pb–Zn veins of the Coeur d'Alene district, United States, (3) porphyry Cu–(Au)–(Mo) deposits and associated (4) calcic and magnesian skarn deposits in the southwestern United

  5. Size control of in vitro synthesized magnetite crystals by the MamC protein of Magnetococcus marinus strain MC-1.

    PubMed

    Valverde-Tercedor, C; Montalbán-López, M; Perez-Gonzalez, T; Sanchez-Quesada, M S; Prozorov, T; Pineda-Molina, E; Fernandez-Vivas, M A; Rodriguez-Navarro, A B; Trubitsyn, D; Bazylinski, Dennis A; Jimenez-Lopez, C

    2015-06-01

    Magnetotactic bacteria are a diverse group of prokaryotes that share the unique ability of biomineralizing magnetosomes, which are intracellular, membrane-bounded crystals of either magnetite (Fe3O4) or greigite (Fe3S4). Magnetosome biomineralization is mediated by a number of specific proteins, many of which are localized in the magnetosome membrane, and thus is under strict genetic control. Several studies have partially elucidated the effects of a number of these magnetosome-associated proteins in the control of the size of magnetosome magnetite crystals. However, the effect of MamC, one of the most abundant proteins in the magnetosome membrane, remains unclear. In this present study, magnetite nanoparticles were synthesized inorganically in free-drift experiments at 25 °C in the presence of different concentrations of the iron-binding recombinant proteins MamC and MamCnts (MamC without its first transmembrane segment) from the marine, magnetotactic bacterium Magnetococcus marinus strain MC-1 and three commercial proteins [α-lactalbumin (α-Lac), myoglobin (Myo), and lysozyme (Lyz)]. While no effect was observed on the size of magnetite crystals formed in the presence of the commercial proteins, biomimetic synthesis in the presence of MamC and MamCnts at concentrations of 10-60 μg/mL resulted in the production of larger and more well-developed magnetite crystals (~30-40 nm) compared to those of the control (~20-30 nm; magnetite crystals grown protein-free). Our results demonstrate that MamC plays an important role in the control of the size of magnetite crystals and could be utilized in biomimetic synthesis of magnetite nanocrystals. PMID:25874532

  6. Novel magnetite-silica nanocomposite (Fe3O4-SBA-15) particles for DNA binding and gene delivery aided by a magnet array.

    PubMed

    Yiu, Humphrey H P; McBain, Stuart C; Lethbridge, Zoe A D; Lees, Martin R; Palona, Iryna; Olariu, Cristina I; Dobson, Jon

    2011-04-01

    Novel magnetite-silica nanocomposite particles were prepared using SBA-15 nanoporous silica as template. Magnetite nanoparticles were impregnated into the nanopore array of the silica template through thermal decomposition of iron(III) acetylacetonate, Fe(AcAc)3 at 200 degrees C. These composite particles were characterized using TEM, XRD and SQUID magnetometry. The TEM images showed that the size of composite particles was around 500 nm and the particles retained the nanoporous array of SBA-15. The formation of magnetite nanoparticles was confirmed by the powder XRD study. These composite particles also exhibited ferrimagnetic properties. By coating with short chain polyethyleneimine (PEI), these particles are capable of binding DNA molecules for gene delivery and transfection. With an external magnetic field, the transfection efficiency was shown to have an increase of around 15%. The results indicated that these composite nanoparticles may be further developed as a new tool for nanomagnetic gene transfection. PMID:21776740

  7. Cobalt ferrite nanoparticles with improved aqueous colloidal stability and electrophoretic mobility

    NASA Astrophysics Data System (ADS)

    Munjal, Sandeep; Khare, Neeraj

    2016-04-01

    We have synthesized CoFe2O4 (CFO) nanoparticles of size ˜ 12.2 nm by hydrothermal synthesis method. To control the size of these CFO nanoparticles, oleic acid was used as a surfactant. The inverse spinel phase of the synthesized nanoparticles was confirmed by X-ray diffraction method. As synthesized oleic acid coated CFO (OA@CFO) nanoparticles has very less electrophoretic mobility in the water and are not water dispersible. These OA@CFO nanoparticles were successfully turned into water soluble phase with a better colloidal aqueous stability, through a chemical treatment using citric acid. The modified citric acid coated CFO (CA@CFO) nanoparticles were dispersible in water and form a stable aqueous solution with high electrophoretic mobility.

  8. Hygroscopic growth and droplet activation of soot particles: uncoated, succinic or sulfuric acid coated

    NASA Astrophysics Data System (ADS)

    Henning, S.; Ziese, M.; Kiselev, A.; Saathoff, H.; Möhler, O.; Mentel, T. F.; Buchholz, A.; Spindler, C.; Michaud, V.; Monier, M.; Sellegri, K.; Stratmann, F.

    2011-10-01

    The hygroscopic growth and droplet activation of uncoated soot particles and such coated with succinic acid and sulfuric acid were investigated during the IN-11 campaign at the Aerosol Interaction and Dynamics in the Atmosphere (AIDA) facility. A GFG-1000 soot generator applying nitrogen, respectively argon as carrier gas and a miniCAST soot generator were utilized to generate soot particles. Different organic carbon (OC) to black carbon (BC) ratios were adjusted for the CAST-soot by varying the fuel to air ratio. The hygroscopic growth was investigated by means of the mobile Leipzig Aerosol Cloud Interaction Simulator (LACIS-mobile) and two different Hygroscopicity Tandem Differential Mobility Analyzers (HTDMA, VHTDMA). Two Cloud Condensation Nucleus Counter (CCNC) were applied to measure the activation of the particles. For the untreated soot particles neither hygroscopic growth nor activation was observed, with exception of a partial activation of GFG-soot generated with argon as carrier gas. Coatings of succinic acid lead to a detectable hygroscopic growth of GFG-soot and enhanced the activated fraction of GFG- (carrier gas: argon) and CAST-soot, whereas no hygroscopic growth of the coated CAST-soot was found. Sulfuric acid coatings lead to an OC-content dependent hygroscopic growth of CAST-soot. Such a dependence was not observed for activation measurements. Coating with sulfuric acid decreased the amount of Polycyclic Aromatic Hydrocarbons (PAH), which were detected by AMS-measurements in the CAST-soot, and increased the amount of substances with lower molecular weight than the initial PAHs. We assume, that these reaction products increased the hygroscopicity of the coated particles in addition to the coating substance itself.

  9. Hygroscopic growth and droplet activation of soot particles: uncoated, succinic or sulfuric acid coated

    NASA Astrophysics Data System (ADS)

    Henning, S.; Ziese, M.; Kiselev, A.; Saathoff, H.; Möhler, O.; Mentel, T. F.; Buchholz, A.; Spindler, C.; Michaud, V.; Monier, M.; Sellegri, K.; Stratmann, F.

    2012-05-01

    The hygroscopic growth and droplet activation of uncoated soot particles and such coated with succinic acid and sulfuric acid were investigated during the IN-11 campaign at the Aerosol Interaction and Dynamics in the Atmosphere (AIDA) facility. A GFG-1000 soot generator applying either nitrogen or argon as carrier gas and a miniCAST soot generator were utilized to generate soot particles. Different organic carbon (OC) to black carbon (BC) ratios were adjusted for the CAST-soot by varying the fuel to air ratio. The hygroscopic growth was investigated by means of the mobile Leipzig Aerosol Cloud Interaction Simulator (LACIS-mobile) and two different Hygroscopicity Tandem Differential Mobility Analyzers (HTDMA, VHTDMA). Two Cloud Condensation Nucleus Counter (CCNC) were applied to measure the activation of the particles. For the untreated soot particles neither hygroscopic growth nor activation was observed at a supersaturation of 1%, with exception of a partial activation of GFG-soot generated with argon as carrier gas. Coatings of succinic acid lead to a detectable hygroscopic growth of GFG-soot and enhanced the activated fraction of GFG- (carrier gas: argon) and CAST-soot, whereas no hygroscopic growth of the coated CAST-soot was found. Sulfuric acid coatings led to an OC-content dependent hygroscopic growth of CAST-soot. Such a dependence was not observed for activation measurements. Coating with sulfuric acid decreased the amount of Polycyclic Aromatic Hydrocarbons (PAH), which were detected by AMS-measurements in the CAST-soot, and increased the amount of substances with lower molecular weight than the initial PAHs. We assume that these reaction products increased the hygroscopicity of the coated particles in addition to the coating substance itself.

  10. Ice formation on nitric acid coated dust particles: Laboratory and modeling studies

    SciTech Connect

    Kulkarni, Gourihar R.; Zhang, Kai; Zhao, Chun; Nandasiri, Manjula I.; Shutthanandan, V.; Liu, Xiaohong; Fast, Jerome D.; Berg, Larry K.

    2015-08-16

    Changes in the ice nucleation characteristics of atmospherically relevant mineral dust particles due to nitric acid coating are not well understood. Further, the atmospheric implications of dust coating on ice-cloud properties under different assumptions of primary ice nucleation mechanisms are unknown. We investigated ice nucleation ability of Arizona test dust, illite, K-feldspar and quartz as a function of temperature (-25 to -30°C) and relative humidity with respect to water (75 to 110%). Particles were size selected at 250 nm and transported (bare or coated) to the ice nucleation chamber to determine the fraction of particles nucleating ice at various temperature and water saturation conditions. All dust nucleated ice at water-subsaturated conditions, but the coated particles showed a reduction in their ice nucleation ability compared to bare particles. However, at water-supersaturated conditions, we observed that bare and coated particles had nearly similar ice nucleation characteristics. X-ray diffraction patterns indicated that structural properties of bare dust particles modified after acid treatment. We found that lattice parameters were slightly different, but crystallite sizes of the coated particles were reduced compared to bare particles. Next, single-column model results show that simulated ice crystal number concentrations mostly depends upon fraction of particles that are coated, primary ice nucleation mechanisms, and the competition between ice nucleation mechanisms to nucleate ice. In general, we observed that coating modify the ice-cloud properties and the picture of ice and mixed-phase cloud evolution is complex when different primary ice nucleation mechanisms are competing for fixed water vapor mass.

  11. nanoparticles

    NASA Astrophysics Data System (ADS)

    Andreu-Cabedo, Patricia; Mondragon, Rosa; Hernandez, Leonor; Martinez-Cuenca, Raul; Cabedo, Luis; Julia, J. Enrique

    2014-10-01

    Thermal energy storage (TES) is extremely important in concentrated solar power (CSP) plants since it represents the main difference and advantage of CSP plants with respect to other renewable energy sources such as wind, photovoltaic, etc. CSP represents a low-carbon emission renewable source of energy, and TES allows CSP plants to have energy availability and dispatchability using available industrial technologies. Molten salts are used in CSP plants as a TES material because of their high operational temperature and stability of up to 500°C. Their main drawbacks are their relative poor thermal properties and energy storage density. A simple cost-effective way to improve thermal properties of fluids is to dope them with nanoparticles, thus obtaining the so-called salt-based nanofluids. In this work, solar salt used in CSP plants (60% NaNO3 + 40% KNO3) was doped with silica nanoparticles at different solid mass concentrations (from 0.5% to 2%). Specific heat was measured by means of differential scanning calorimetry (DSC). A maximum increase of 25.03% was found at an optimal concentration of 1 wt.% of nanoparticles. The size distribution of nanoparticle clusters present in the salt at each concentration was evaluated by means of scanning electron microscopy (SEM) and image processing, as well as by means of dynamic light scattering (DLS). The cluster size and the specific surface available depended on the solid content, and a relationship between the specific heat increment and the available particle surface area was obtained. It was proved that the mechanism involved in the specific heat increment is based on a surface phenomenon. Stability of samples was tested for several thermal cycles and thermogravimetric analysis at high temperature was carried out, the samples being stable.

  12. Electrical conductivity of magnetite-bearing serpentinite during shear deformation

    NASA Astrophysics Data System (ADS)

    Kawano, Seiya; Yoshino, Takashi; Katayama, Ikuo

    2012-10-01

    Electrical conductivity of serpentinite with various amounts of magnetite was measured during shear deformation at high pressure and temperatures (P = 1.0 GPa, T = 750 K) corresponding to mantle wedge conditions to evaluate the contribution of aligned magnetite to the bulk conductivity of serpentinite. Under hydrostatic conditions, the sample conductivity considerably increases when the magnetite volume fraction exceeds 25% in volume, suggesting the presence of the percolation threshold for magnetite interconnection. During shear deformation, the conductivity for the samples with less than 25 vol.% magnetite increased by an order of magnitude or higher with increasing shear strain up to 9, which is likely a result of the clustering or realignment of magnetite grains in the serpentinites. However, activation enthalpy was nearly constant before and after deformation experiments, suggesting that shear deformation is unlikely to enhance establishment of interconnection of magnetite. Consequently, more than 25 vol.% magnetite is needed to establish connectivity of magnetite in serpentinite. On the other hand, the conductivity of serpentinite with low volume fraction of magnetite (5%), which is typical concentration of natural serpentinites, is almost similar to that of magnetite-free serpentinites. The present results show that the interconnection of magnetite in serpentinites by shear deformation is not expected as an origin of the high conductivity anomaly occasionally observed at the slab interface in the mantle wedge. The origin of high conductivity, therefore, indicates the presence of aqueous fluid with high salinity rather than the magnetite interconnection.

  13. Pond sediment magnetite grains show a distinctive microbial community.

    PubMed

    Song, H-K; Sonkaria, S; Khare, V; Dong, K; Lee, H-T; Ahn, S-H; Kim, H-K; Kang, H-J; Lee, S-H; Jung, S P; Adams, J M

    2015-07-01

    Formation of magnetite in anaerobic sediments is thought to be enhanced by the activities of iron-reducing bacteria. Geobacter has been implicated as playing a major role, as in culture its cells are often associated with extracellular magnetite grains. We studied the bacterial community associated with magnetite grains in sediment of a freshwater pond in South Korea. Magnetite was isolated from the sediment using a magnet. The magnetite-depleted fraction of sediment was also taken for comparison. DNA was extracted from each set of samples, followed by PCR for 16S bacterial ribosomal RNA (rRNA) gene and HiSeq sequencing. The bacterial communities of the magnetite-enriched and magnetite-depleted fractions were significantly different. The enrichment of three abundant operational taxonomic units (OTUs) suggests that they may either be dependent upon the magnetite grain environment or may be playing a role in magnetite formation. The most abundant OTU in magnetite-enriched fractions was Geobacter, bolstering the case that this genus is important in magnetite formation in natural systems. Other major OTUs strongly associated with the magnetite-enriched fraction, rather than the magnetite-depleted fraction, include a Sulfuricella and a novel member of the Betaproteobacteria. The existence of distinct bacterial communities associated with particular mineral grain types may also be an example of niche separation and coexistence in sediments and soils, which cannot usually be detected due to difficulties in separating and concentrating minerals. PMID:25592636

  14. Size dependent microbial oxidation and reduction of magnetite nano- and micro-particles.

    PubMed

    Byrne, James M; van der Laan, Gerrit; Figueroa, Adriana I; Qafoku, Odeta; Wang, Chongmin; Pearce, Carolyn I; Jackson, Michael; Feinberg, Joshua; Rosso, Kevin M; Kappler, Andreas

    2016-01-01

    The ability for magnetite to act as a recyclable electron donor and acceptor for Fe-metabolizing bacteria has recently been shown. However, it remains poorly understood whether microbe-mineral interfacial electron transfer processes are limited by the redox capacity of the magnetite surface or that of whole particles. Here we examine this issue for the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducing bacteria Geobacter sulfurreducens, comparing magnetite nanoparticles (d ≈ 12 nm) against microparticles (d ≈ 100-200 nm). By integrating surface-sensitive and bulk-sensitive measurement techniques we observed a particle surface that was enriched in Fe(II) with respect to a more oxidized core. This enables microbial Fe(II) oxidation to occur relatively easily at the surface of the mineral suggesting that the electron transfer is dependent upon particle size. However, microbial Fe(III) reduction proceeds via conduction of electrons into the particle interior, i.e. it can be considered as more of a bulk electron transfer process that is independent of particle size. The finding has potential implications on the ability of magnetite to be used for long range electron transport in soils and sediments. PMID:27492680

  15. Size dependent microbial oxidation and reduction of magnetite nano- and micro-particles

    PubMed Central

    Byrne, James M.; van der Laan, Gerrit; Figueroa, Adriana I.; Qafoku, Odeta; Wang, Chongmin; Pearce, Carolyn I.; Jackson, Michael; Feinberg, Joshua; Rosso, Kevin M.; Kappler, Andreas

    2016-01-01

    The ability for magnetite to act as a recyclable electron donor and acceptor for Fe-metabolizing bacteria has recently been shown. However, it remains poorly understood whether microbe-mineral interfacial electron transfer processes are limited by the redox capacity of the magnetite surface or that of whole particles. Here we examine this issue for the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducing bacteria Geobacter sulfurreducens, comparing magnetite nanoparticles (d ≈ 12 nm) against microparticles (d ≈ 100–200 nm). By integrating surface-sensitive and bulk-sensitive measurement techniques we observed a particle surface that was enriched in Fe(II) with respect to a more oxidized core. This enables microbial Fe(II) oxidation to occur relatively easily at the surface of the mineral suggesting that the electron transfer is dependent upon particle size. However, microbial Fe(III) reduction proceeds via conduction of electrons into the particle interior, i.e. it can be considered as more of a bulk electron transfer process that is independent of particle size. The finding has potential implications on the ability of magnetite to be used for long range electron transport in soils and sediments. PMID:27492680

  16. Size dependent microbial oxidation and reduction of magnetite nano- and micro-particles

    NASA Astrophysics Data System (ADS)

    Byrne, James M.; van der Laan, Gerrit; Figueroa, Adriana I.; Qafoku, Odeta; Wang, Chongmin; Pearce, Carolyn I.; Jackson, Michael; Feinberg, Joshua; Rosso, Kevin M.; Kappler, Andreas

    2016-08-01

    The ability for magnetite to act as a recyclable electron donor and acceptor for Fe-metabolizing bacteria has recently been shown. However, it remains poorly understood whether microbe-mineral interfacial electron transfer processes are limited by the redox capacity of the magnetite surface or that of whole particles. Here we examine this issue for the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducing bacteria Geobacter sulfurreducens, comparing magnetite nanoparticles (d ≈ 12 nm) against microparticles (d ≈ 100–200 nm). By integrating surface-sensitive and bulk-sensitive measurement techniques we observed a particle surface that was enriched in Fe(II) with respect to a more oxidized core. This enables microbial Fe(II) oxidation to occur relatively easily at the surface of the mineral suggesting that the electron transfer is dependent upon particle size. However, microbial Fe(III) reduction proceeds via conduction of electrons into the particle interior, i.e. it can be considered as more of a bulk electron transfer process that is independent of particle size. The finding has potential implications on the ability of magnetite to be used for long range electron transport in soils and sediments.

  17. Uranium (VI) recovery from aqueous medium using novel floating macroporous alginate-agarose-magnetite cryobeads.

    PubMed

    Tripathi, Anuj; Melo, Jose Savio; D'Souza, Stanislaus Francis

    2013-02-15

    This study presents a novel development of a floating polymeric-magnetite cryobead for the recovery of hexavalent uranium from the aqueous sub-surfaces. The alginate-agarose-magnetite cryobeads were synthesized by the process of cryotropic-gelation at subzero-temperature. The physico-chemical properties of cryobeads showed high surface area and high interconnected porosity (≈ 90%). Low density of these cryobeads explains their floating property in the aqueous medium. The rheological analysis of cryobeads showed its stability and increased stiffness after uranium adsorption. The presence of magnetite nanoparticles in the porous cryobeads facilitates the recovery of these beads by applying an external magnetic field. Maximum uranium adsorption (97 ± 2%) was observed in the pH range of 4.5-5.5. The thermodynamic parameters suggest passive endothermic adsorption behaviour. HCl was found to be an efficient eluent for the uranium desorption. Five repeated cycles for the desorption of uranium from biosorbent showed 69 ± 3% of uranium recovery. These results suggest stability of these novel floating magnetite-cryobeads under environmental conditions with potential for the recovery of uranium from contaminated aqueous subsurfaces. PMID:23280054

  18. Evaluating the cytotoxicity of palladium/magnetite nano-catalysts intended for wastewater treatment.

    PubMed

    Hildebrand, Heike; Kühnel, Dana; Potthoff, Annegret; Mackenzie, Katrin; Springer, Armin; Schirmer, Kristin

    2010-01-01

    Palladium/magnetite nanoparticulate catalysts were developed for efficient elimination of halogenated organic pollutants from contaminated wastewater. Particle recovery from treated water can be ensured via magnetic separation. However, in worst-case scenarios, this catalyst removal step might fail, leading to particle release into the environment. Therefore, a toxicological study was conducted to investigate the impact of both pure magnetite and palladium/magnetite nanoparticle exposure upon human skin (HaCaT) and human colon (CaCo-2) cell lines and a cell line from rainbow trout gills (RTgill-W1). To quantify cell viability after particle exposure, three endpoints were examined for all tested cell lines. Additionally, the formation of reactive oxygen species was studied for the human cells. The results showed only minor effects of the particles on the tested cell systems and support the assumption that palladium/magnetite nano-catalysts can be implemented for a new wastewater treatment technology in which advantageous catalyst properties outweigh the risks. PMID:19783337

  19. Oxidation of pyrite in coal to magnetite

    USGS Publications Warehouse

    Thorpe, A.N.; Senftle, F.E.; Alexander, C.C.; Dulong, F.T.

    1984-01-01

    When bituminous coal is heated in an inert atmosphere (He) containing small amounts of oxygen at 393-455 ??C, pyrite (FeS2) in coal is partially converted to magnetite (Fe304). The maximum amount of Fe304 formed during the time of heating corresponds to 5-20% of the total pyrite present, depending on the coal sample. The magnetite forms as an outer crust on the pyrite grains. The fact that the magnetic properties of the pyrite grains are substantially increased by the magnetite crust suggests that pyrite can be separated from coal by use of a low magnetic field. In a laboratory test, 75% removal is obtained by means of a 500 Oe magnet on three samples, and 60% on a fourth sample. ?? 1984.

  20. Scaffold of Asymmetric Organic Compounds - Magnetite Plaquettes

    NASA Technical Reports Server (NTRS)

    Chan, Q. H. S.; Zolensky, M. E.; Martinez, J.

    2015-01-01

    Life on Earth shows preference towards the set of organics with particular spatial configurations, this 'selectivity' is a crucial criterion for life. With only rare exceptions, life prefers the left- (L-) form over the right- (D-) form of amino acids, resulting in an L-enantiomeric excess (L-ee). Recent studies have shown Lee for alpha-methyl amino acids in some chondrites. Since these amino acids have limited terrestrial occurrence, the origin of their stereoselectivity is nonbiological, and it seems appropriate to conclude that chiral asymmetry, the molecular characteristic that is common to all terrestrial life form, has an abiotic origin. A possible abiotic mechanism that can produce chiral asymmetry in meteoritic amino acids is their formation with the presence of asymmetric catalysts, as mineral crystallization can produce spatially asymmetric structures. Magnetite is shown to be an effective catalyst for the formation of amino acids that are commonly found in chondrites. Magnetite 'plaquettes' (or 'platelets'), first described by Jedwab, show an interesting morphology of barrel-shaped stacks of magnetite disks with an apparent dislocation-induced spiral growth that seem to be connected at the center. A recent study by Singh et al. has shown that magnetites can self-assemble into helical superstructures. Such molecular asymmetry could be inherited by adsorbed organic molecules. In order to understand the distribution of 'spiral' magnetites in different meteorite classes, as well as to investigate their apparent spiral configurations and possible correlation to molecular asymmetry, we observed polished sections of carbonaceous chondrites (CC) using scanning electron microscope (SEM) imaging. The sections were also studied by electron backscattered diffraction (EBSD) in order to reconstruct the crystal orientation along the stack of magnetite disks.

  1. Rock magnetism linked to human brain magnetite

    NASA Astrophysics Data System (ADS)

    Kirschvink, Joseph L.

    Magnetite has a long and distinguished career as one of the most important minerals in geophysics, as it is responsible for most of the remanent magnetization in marine sediments and the oceanic crust. It may come as a surprise to discover that it also ranks as the third or fourth most diverse mineral product formed biochemically by living organisms, and forms naturally in a variety of human tissues [Kirschvink et al., 1992].Magnetite was discovered in teeth of the Polyplacophora mollusks over 30 years ago, in magnetotactic bacteria nearly 20 years ago, in honey bees and homing pigeons nearly 15 years ago, but only recently in human tissue.

  2. Origin of magnetite and pyrrhotite in carbonaceous chondrites

    NASA Technical Reports Server (NTRS)

    Herndon, J. M.; Rowe, M. W.; Larson, E. E.; Watson, D. E.

    1975-01-01

    It is proposed that a substantial fraction of the magnetite, at least, resulted from the oxidation of troilite. Pyrrhotite is expected as a direct consequence of magnetite formation through this reaction. During thermomagnetic experiments on troilite, magnetite formation was observed at temperatures as low as 373 K, provided that the oxygen fugacity was held in the magnetite stability field, and that the troilite was sufficiently finely divided.

  3. The cadmium–mercaptoacetic acid complex contributes to the genotoxicity of mercaptoacetic acid-coated CdSe-core quantum dots

    PubMed Central

    Tang, Weikun; Fan, Junpeng; He, Yide; Huang, Bihai; Liu, Huihui; Pang, Daiwen; Xie, Zhixiong

    2012-01-01

    Quantum dots (QDs) have many potential clinical and biological applications because of their advantages over traditional fluorescent dyes. However, the genotoxicity potential of QDs still remains unclear. In this paper, a plasmid-based system was designed to explore the genotoxic mechanism of QDs by detecting changes in DNA configuration and biological activities. The direct chemicobiological interactions between DNA and mercaptoacetic acid-coated CdSecore QDs (MAA–QDs) were investigated. After incubation with different concentrations of MAA–QDs (0.043, 0.13, 0.4, 1.2, and 3.6 μmol/L) in the dark, the DNA conversion of the covalently closed circular (CCC) DNA to the open circular (OC) DNA was significantly enhanced (from 13.9% ± 2.2% to 59.9% ± 12.8%) while the residual transformation activity of plasmid DNA was greatly decreased (from 80.7% ± 12.8% to 13.6% ± 0.8%), which indicated that the damages to the DNA structure and biological activities induced by MAA–QDs were concentration-dependent. The electrospray ionization mass spectrometry data suggested that the observed genotoxicity might be correlated with the cadmium–mercaptoacetic acid complex (Cd–MAA) that is formed in the solution of MAA–QDs. Circular dichroism spectroscopy and transformation assay results indicated that the Cd–MAA complex might interact with DNA through the groove-binding mode and prefer binding to DNA fragments with high adenine and thymine content. Furthermore, the plasmid transformation assay could be used as an effective method to evaluate the genotoxicities of nanoparticles. PMID:22679373

  4. The cadmium-mercaptoacetic acid complex contributes to the genotoxicity of mercaptoacetic acid-coated CdSe-core quantum dots.

    PubMed

    Tang, Weikun; Fan, Junpeng; He, Yide; Huang, Bihai; Liu, Huihui; Pang, Daiwen; Xie, Zhixiong

    2012-01-01

    Quantum dots (QDs) have many potential clinical and biological applications because of their advantages over traditional fluorescent dyes. However, the genotoxicity potential of QDs still remains unclear. In this paper, a plasmid-based system was designed to explore the genotoxic mechanism of QDs by detecting changes in DNA configuration and biological activities. The direct chemicobiological interactions between DNA and mercaptoacetic acid-coated CdSecore QDs (MAA-QDs) were investigated. After incubation with different concentrations of MAA-QDs (0.043, 0.13, 0.4, 1.2, and 3.6 μmol/L) in the dark, the DNA conversion of the covalently closed circular (CCC) DNA to the open circular (OC) DNA was significantly enhanced (from 13.9% ± 2.2% to 59.9% ± 12.8%) while the residual transformation activity of plasmid DNA was greatly decreased (from 80.7% ± 12.8% to 13.6% ± 0.8%), which indicated that the damages to the DNA structure and biological activities induced by MAA-QDs were concentration-dependent. The electrospray ionization mass spectrometry data suggested that the observed genotoxicity might be correlated with the cadmium-mercaptoacetic acid complex (Cd-MAA) that is formed in the solution of MAA-QDs. Circular dichroism spectroscopy and transformation assay results indicated that the Cd-MAA complex might interact with DNA through the groove-binding mode and prefer binding to DNA fragments with high adenine and thymine content. Furthermore, the plasmid transformation assay could be used as an effective method to evaluate the genotoxicities of nanoparticles. PMID:22679373

  5. Magnetite/CdTe magnetic-fluorescent composite nanosystem for magnetic separation and bio-imaging

    NASA Astrophysics Data System (ADS)

    Kale, Anup; Kale, Sonia; Yadav, Prasad; Gholap, Haribhau; Pasricha, Renu; Jog, J. P.; Lefez, Benoit; Hannoyer, Béatrice; Shastry, Padma; Ogale, Satishchandra

    2011-06-01

    A new synthesis protocol is described to obtain a CdTe decorated magnetite bifunctional nanosystem via dodecylamine (DDA) as cross linker. High resolution transmission electron microscopy (HRTEM), energy-dispersive x-ray spectroscopy (EDAX), vibrating sample magnetometry (VSM), Fourier transform infrared spectroscopy (FTIR), diffuse reflectance spectroscopy (DRS) and fluorescence microscopy are used to characterize the constitution, size, composition and physical properties of these superparamagnetic-fluorescent nanoparticles. These CdTe decorated magnetite nanoparticles were then functionalized with anti-epidermal growth factor receptor (EGFR) antibody to specifically target cells expressing this receptor. The EGFR is a transmembrane glycoprotein and is expressed on tumor cells from different tissue origins including human leukemic cell line Molt-4 cells. The magnetite-CdTe composite nanosystem is shown to perform excellently for specific selection, magnetic separation and fluorescent detection of EGFR positive Molt-4 cells from a mixed population. Flow cytometry and confocal laser scanning microscopy results show that this composite nanosystem has great potential in antibody functionalized magnetic separation and imaging of cells using cell surface receptor antibody.

  6. Application of silica magnetite nanocomposites to the isolation of ultrapure plasmid DNA from bacterial cells

    NASA Astrophysics Data System (ADS)

    Chiang, Chen-Li; Sung, Ching-Shan; Chen, Chuh-Yean

    2006-10-01

    The aim of this study was to develop a simple and rapid method for purification of ultrapure plasmid DNA with high yields from bacterial cultures. Nanosized superparamagnetic nanoparticles (Fe 3O 4) were prepared by chemical precipitation method using Fe 2+, Fe 3+ salt, and ammonium hydroxide under a nitrogen atmosphere. Silica-magnetite nanocomposites were prepared by the method of acid hydrolysis of tetraethoxysilane (TEOS) to coat the silica onto magnetite nanoparticles. DNA was adsorbed to the support under high salt conditions, and recovered directly in water for immediate downstream application, without the need for precipitation. We demonstrated that a useful plasmid, pRSETB-EGFP, encoding for the green fluorescent protein with T7 promoter, could be amplified in Escherichia coli of DE3 strain. Up to approximately 43 μg of high-purity ( A260/ A280 ratio=1.75) plasmid DNA was isolated from 3 ml of an overnight bacterial culture. The eluted plasmid DNA was used directly for restriction enzyme digestion, bacterial cell transformation and polymerase chain reaction (PCR) amplification with success. The protocol, starting from the preparation of bacterial lysate and ending with purified plasmid takes less than 8 min. The silica-magnetite nanocomposites deliver significant time-savings, overall higher yields, lower RNA contamination, and better PCR amplification compared to commercial available silica-based and other methods.

  7. Redox cycling of Fe(II) and Fe(III) in magnetite by Fe-metabolizing bacteria.

    PubMed

    Byrne, James M; Klueglein, Nicole; Pearce, Carolyn; Rosso, Kevin M; Appel, Erwin; Kappler, Andreas

    2015-03-27

    Microorganisms are a primary control on the redox-induced cycling of iron in the environment. Despite the ability of bacteria to grow using both Fe(II) and Fe(III) bound in solid-phase iron minerals, it is currently unknown whether changing environmental conditions enable the sharing of electrons in mixed-valent iron oxides between bacteria with different metabolisms. We show through magnetic and spectroscopic measurements that the phototrophic Fe(II)-oxidizing bacterium Rhodopseudomonas palustris TIE-1 oxidizes magnetite (Fe3O4) nanoparticles using light energy. This process is reversible in co-cultures by the anaerobic Fe(III)-reducing bacterium Geobacter sulfurreducens. These results demonstrate that Fe ions bound in the highly crystalline mineral magnetite are bioavailable as electron sinks and electron sources under varying environmental conditions, effectively rendering magnetite a naturally occurring battery. PMID:25814583

  8. Magnetite biomineralization and ancient life on Mars.

    PubMed

    Frankel, R B; Buseck, P R

    2000-04-01

    Certain chemical and mineral features of the Martian meteorite ALH84001 were reported in 1996 to be probable evidence of ancient life on Mars. In spite of new observations and interpretations, the question of ancient life on Mars remains unresolved. Putative biogenic, nanometer magnetite has now become a leading focus in the debate. PMID:10742183

  9. Originof magnetite in martian meteorite ALH84001

    NASA Astrophysics Data System (ADS)

    Scott, E.; Fuller, M.

    2003-04-01

    The magnetization of ALH84001 is predominantly carried by single domain magnetite, which is found in association with carbonate. The magnetite is found in topotactic relationship with the carbonate in regions of iron rich carbonate, whereas in magnesium richer areas periclase is found. The magnetite formed from the carbonate by thermal decomposition of siderite at elevated temperature in a major impact event at about 4.0 Gyr. Chromite is also present in large amounts, but it is predominantly paramagnetic at room temperature with a Neel point close to 100^oK. Carbonate with associated magnetite is also found in the martian meteorite Nakhla. Experiments and theory show that siderite is a major product of percolation and evaporation of brines generated under pressures of more than 0.1bar of carbon dioxide. This is the preferred explanation for the carbonate in nakhla, as well as in ALH84001. Thermal decomposition of siderite may result from deep burial, magmatic heat sources, or as in the case of ALH84001, impact heating.

  10. Charge ordering and ferroelectricity in magnetite

    NASA Astrophysics Data System (ADS)

    Khomskii, Daniel

    2007-03-01

    Magnetite Fe3O4 is one of the most fascinating material in solid state physics. Besides being the first magnetic material known to the mankind, it is also the first example of an insulator-metal transition in transition metal oxides -- the famous Verwey transition [1]. One usually connects this transition with the charge ordering of Fe^2+ and Fe^3+. However the detailed pattern of CO in Fe3O4 is still a matter of debate. Another aspect, which is not so widely known and which did not yet receive sufficient attention, is that below TV, besides being completely spin polarised, magnetite apparently is also ferroelectric (FE) [2]. Thus it seems that magnetite, besides being the first magnetic material and the first transition metal oxide with an insulator-metal transition, is also the first multiferroic material. Using the idea of a coexistence of site-centred and bond-centred charge ordering [3], I suggest a novel type of ordering in magnetite which explains the observed FE in Fe3O4 and which agrees with the structural data. [1] Verwey E.J.W., Nature 144, 327 (1939) [2] Rado G.T. and Ferrari J.M., Phys.Rev.B 12, 5166 (1975); Kato K. and Iida S., J.Phys.Soc.Japan 50, 2844 (1981) [3] Efremov D.V., van den Brink J. and Khomskii D.I., Nature Mater. 3, 853 (2004)

  11. Magnetite in Black Sea Turtles (Chelonia agassizi)

    NASA Astrophysics Data System (ADS)

    Fuentes, A.; Urrutia-Fucugauchi, J.; Garduño, V.; Sanchez, J.; Rizzi, A.

    2004-12-01

    Previous studies have reported experimental evidence for magnetoreception in marine turtles. In order to increase our knowledge about magnetoreception and biogenic mineralization, we have isolated magnetite particles from the brain of specimens of black sea turtles Chelonia agassizi. Our samples come from natural deceased organisms collected the reserve area of Colola Maruata in southern Mexico. The occurrence of magnetite particles in brain tissue of black sea turtles offers the opportunity for further studies to investigate possible function of ferrimagnetic material, its mineralogical composition, grain size, texture and its location and structural arrangement within the host tissue. After sample preparation and microscopic examination, we localized and identified the ultrafine unidimensional particles of magnetite by scanning electron microscope (SEM). Particles present grain sizes between 10.0 to 40.0Mm. Our study provides, for the first time, evidence for biogenic formation of this material in the black sea turtles. The ultrafine particles are apparently superparamagnetic. Preliminary results from rock magnetic measurements are also reported and correlated to the SEM observations. The black turtle story on the Michoacan coast is an example of formerly abundant resource which was utilized as a subsistence level by Nahuatl indigenous group for centuries, but which is collapsing because of intensive illegal commercial exploitation. The most important nesting and breeding grounds for the black sea turtle on any mainland shore are the eastern Pacific coastal areas of Maruata and Colola, in Michoacan. These beaches are characterized by important amounts of magnetic mineral (magnetites and titanomagnetites) mixed in their sediments.

  12. The metal-insulator transition in magnetite.

    NASA Technical Reports Server (NTRS)

    Cullen, J. R.; Callen, E.

    1972-01-01

    We describe an electronic model for the low temperature transition in magnetite, in which the average number of electrons on a site is non-integral. The solution of the one-dimensional problem is reviewed, and the connection of the model with the Verwey ordering is discussed. Some of the implication of the three dimensional problem are discussed.

  13. Arsenic entrapment by nanocrystals of Al-magnetite: The role of Al in crystal growth and As retention.

    PubMed

    Freitas, Erico T F; Stroppa, Daniel G; Montoro, Luciano A; de Mello, Jaime W V; Gasparon, Massimo; Ciminelli, Virginia S T

    2016-09-01

    The nature of As-Al-Fe co-precipitates aged for 120 days are investigated in detail by High Resolution Transmission Electron Microscopy (HRTEM), Scanning TEM (STEM), electron diffraction, Energy Dispersive X-Ray Spectroscopy (EDS), Electron Energy-Loss Spectroscopy (EELS), and Energy Filtered Transmission Electron Microscopy (EFTEM). The Al present in magnetite is shown to favour As incorporation (up to 1.10 wt%) relative to Al-free magnetite and Al-goethite, but As uptake by Al-magnetite decreases with increasing Al substitution (3.53-11.37 mol% Al). Arsenic-bearing magnetite and goethite mesocrystals (MCs) are formed by oriented aggregation (OA) of primary nanoparticles (NPs). Well-crystalline magnetite likely formed by Otswald ripening was predominant in the Al-free system. The As content in Al-goethite MCs (having approximately 13% substituted Al) was close to the EDS detection limit (0.1 wt% As), but was below detection in Al-goethites with 23.00-32.19 mol% Al. Our results show for the first time the capacity of Al-magnetite to incorporate more As than Al-free magnetite, and the role of Al in favouring OA-based crystal growth under the experimental conditions, and therefore As retention in the formed MCs. The proposed mechanism of As incorporation involves adsorption of As onto the newly formed NPs. Arsenic is then trapped in the MCs as they grow by self-assembly OA upon attachment of the NPs. We conclude that Al may diffuse to the crystal faces with high surface energy to reduce the total energy of the system during the attachment events, thus favouring the oriented aggregation. PMID:27258899

  14. Transmission Electron Microscopy of Magnetite Plaquettes in Orgueil

    NASA Technical Reports Server (NTRS)

    Chan, Q. H. S.; Han, J.; Zolensky, M.

    2016-01-01

    Magnetite sometimes takes the form of a plaquette - barrel-shaped stack of magnetite disks - in carbonaceous chondrites (CC) that show evidence of aqueous alteration. The asymmetric nature of the plaquettes caused Pizzarello and Groy to propose magnetite plaquettes as a naturally asymmetric mineral that can indroduce symmetry-breaking in organic molecules. Our previous synchrotron X-ray computed microtomography (SXRCT) and electron backscatter diffraction (EBSD) analyses of the magnetite plaquettes in fifteen CCs indicate that magnetite plaquettes are composed of nearly parallel discs, and the crystallographic orientations of the discs change around a rotational axis normal to the discs surfaces. In order to further investigate the nanostructures of magnetite plaquettes, we made two focused ion beam (FIB) sections of nine magnetite plaquettes from a thin section of CI Orgueil for transmission electron microscope (TEM) analysis. The X-ray spectrum imaging shows that the magnetite discs are purely iron oxide Fe3O4 (42.9 at% Fe and 57.1 at% O), which suggest that the plaquettes are of aqueous origin as it is difficult to form pure magnetite as a nebular condensate. The selected area electron diffraction (SAED) patterns acquired across the plaquettes show that the magnetite discs are single crystals. SEM and EBSD analyses suggest that the planar surfaces of the magnetite discs belong to the {100} planes of the cubic inverse spinel structure, which are supported by our TEM observations. Kerridge et al. suggested that the epitaxial relationship between magnetite plaquette and carbonate determines the magnetite face. However, according to our TEM observation, the association of magnetite with porous networks of phyllosilicate indicates that the epitaxial relationship with carbonate is not essential to the formation of magnetite plaquettes. It was difficult to determine the preferred rotational orientation of the plaquettes due to the symmetry of the cubic structure

  15. Uptake of Cs and Sr radionuclides within oleic acid coated nanomagnetite-hematite composite

    NASA Astrophysics Data System (ADS)

    Mukhopadhyay, J.; Sengupta, Pranesh; Sen, D.; Mazumdar, S.; Tyagi, A. K.

    2015-12-01

    Nano-sized magnetic composite sorbent material like nanomagnetite - nanohematite has been synthesized for uptake of cesium and strontium ions from low level environmental effluents in effective decontamination from waste water. Synthesis of material was based on co-precipitation route and in situ coating of oleic acid on magnetite-hematite nanocomposite. Magnetic properties were studied for both the uncoated as prepared and coated nanocomposite materials. The magnetization curves showed no hysteresis or remnant magnetization. Both the materials exhibited super-paramagnetism. Saturation magnetization of the coated nanocomposite was found to be 30 emu/g whereas for as prepared nanocomposite it was 64 emu/g. Detailed characterizations of the materials was carried out by X ray diffraction and Transmission electron microscopic techniques and the grain sizes were found to vary between 10 and 15 nm range. Sorption experiments on cesium and strontium were carried out by batch mode equilibrium study. The uptake studies were performed by Atomic Absorption Spectroscopy for cesium ions and inductively coupled Plasma - Atomic Emission Spectroscopy for strontium ions. Size distributions of the particle were measure through Small Angle X ray Scattering (SAXS) experiment. Shifting in weak repulsive potential facilitates enhanced sorption for more period of time in stable condition in comparison of uncoated nanocomposite which forms larger aggregates.

  16. Following iron speciation in the early stages of magnetite magnetosome biomineralization

    DOE PAGESBeta

    Firlar, Emre; Perez-Gonzalez, Teresa; Olszewska, Agata; Faivre, Damien; Prozorov, Tanya

    2016-02-26

    Understanding magnetosome magnetite biomineralization is of fundamental interest to devising the strategies for bioinspired synthesis of magnetic materials at the nanoscale. Thus, we investigated the early stages of magnetosome formation in this work and correlated the size and emergent crystallinity of magnetosome nanoparticles with the changes in chemical environment of iron and oxygen by utilizing advanced analytical electron microscopy techniques. We observed that magnetosomes in the early stages of biomineralization with the sizes of 5–10 nm were amorphous, with a majority of iron present as Fe3+, indicative of ferric hydroxide. The magnetosomes with intermediate sizes showed partially crystalline structure withmore » a majority of iron present as Fe3+ and trace amounts of Fe2+. The fully maturated magnetosomes were indexed to magnetite. Furthermore, our approach provides spatially resolved structural and chemical information of individual magnetosomes with different particle sizes, attributed to magnetosomes at different stages of biomineralization.« less

  17. Redox cycling of Fe(II) and Fe(III) in magnetite by Fe-metabolizing bacteria

    SciTech Connect

    Byrne, James; Klueglein, Nicole; Pearce, Carolyn I.; Rosso, Kevin M.; Appel, Erwin; Kappler, Andreas

    2015-03-26

    Despite the regular occurrence of both magnetite and iron-metabolizing bacteria in the same environments, it is currently unknown whether the iron(II) and iron(III) in magnetite can be cycled between different bacteria and whether or how magnetic properties are affected by this metabolic activity. We show through magnetic and spectroscopic measurements that the phototrophic Fe(II)-oxidizer Rhodopseudomonas palustris TIE-1 can oxidize solid-phase magnetite nanoparticles using light energy, leading to a decrease in the measured magnetic susceptibility (MS). This process likely occurs at the surface and is reversible in the dark by the Fe(III)-reducer Geobacter sulfurreducens resulting in an increase in MS. These results show that iron ions bound in highly crystalline mineral magnetite are bioavailable as electron stores and electron sinks under varying environmental conditions, making magnetite a potential “biogeobattery” during day/night cycles. These findings are relevant for environmental studies and reinforce the impact of microbial redox processes on the global iron cycle.

  18. Structural Modification and Self-Assembly of Nanoscale Magnetite Synthesised in the Presence of an Anionic Surfactant

    NASA Astrophysics Data System (ADS)

    Malik, S.; Hewitt, I. J.; Powell, A. K.

    2014-07-01

    The earliest reported medical use of magnetite powder for internal applications was in the 10th century A.D. by the Persian physician and philosopher Avicenna of Bokhara [1,2]. Today magnetic nanoparticles are used for magnetic resonance imaging (MRI) and are potential colloidal mediators for cancer magnetic hyperthermia [3]. Twenty years ago magnetite (Fe3O4) was found to be present in the human brain [4] and more recently it has been reported that nanoscale biogenic magnetite (origin and formation uncertain) is associated with neurodegenerative diseases such as Parkinson's, Huntington's and Alzheimer's [5]. Here we show that the synthesis of magnetite in the presence of the surfactant sodium dodecyl sulphate (SDS) gives rise to a variety of nanoscale morphologies, some of which look remarkably similar to magnetite found in organisms, suggesting that similar processes may be involved. Furthermore, these 1D materials with diameters of quantum confined size are of interest in the areas of biosensors [6] and biomedical imaging [7].

  19. Highly monodisperse low-magnetization magnetite nanocubes as simultaneous T1-T2 MRI contrast agents

    NASA Astrophysics Data System (ADS)

    Sharma, V. K.; Alipour, A.; Soran-Erdem, Z.; Aykut, Z. G.; Demir, H. V.

    2015-06-01

    We report the first study of highly monodisperse and crystalline iron oxide nanocubes with sub-nm controlled size distribution (9.7 +/- 0.5 nm in size) that achieve simultaneous contrast enhancement in both T1- and T2-weighted magnetic resonance imaging (MRI). Here, we confirmed the magnetite structure of iron oxide nanocubes by X-ray diffraction (XRD), selected area electron diffraction (SAED) pattern, optical absorption and Fourier transformed infrared (FT-IR) spectra. These magnetite nanocubes exhibit superparamagnetic and paramagnetic behavior simultaneously by virtue of their finely controlled shape and size. The magnetic measurements reveal that the magnetic moment values are favorably much lower because of the small size and cubic shape of the nanoparticles, which results in an enhanced spin canting effect. As a proof-of-concept demonstration, we showed their potential as dual contrast agents for both T1- and T2-weighted MRI via phantom studies, in vivo imaging and relaxivity measurements. Therefore, these low-magnetization magnetite nanocubes, while being non-toxic and bio-compatible, hold great promise as excellent dual-mode T1 and T2 contrast agents for MRI.We report the first study of highly monodisperse and crystalline iron oxide nanocubes with sub-nm controlled size distribution (9.7 +/- 0.5 nm in size) that achieve simultaneous contrast enhancement in both T1- and T2-weighted magnetic resonance imaging (MRI). Here, we confirmed the magnetite structure of iron oxide nanocubes by X-ray diffraction (XRD), selected area electron diffraction (SAED) pattern, optical absorption and Fourier transformed infrared (FT-IR) spectra. These magnetite nanocubes exhibit superparamagnetic and paramagnetic behavior simultaneously by virtue of their finely controlled shape and size. The magnetic measurements reveal that the magnetic moment values are favorably much lower because of the small size and cubic shape of the nanoparticles, which results in an enhanced spin

  20. Acid-coated Textiles (pH 5.5-6.5)--a New Therapeutic Strategy for Atopic Eczema?

    PubMed

    Jaeger, Teresa; Rothmaier, Markus; Zander, Holger; Ring, Johannes; Gutermuth, Jan; Anliker, Mark D

    2015-07-01

    Increased transepidermal water loss (TEWL) and decreased skin capacitance are characteristic features of the disturbed epidermal barrier in atopic eczema (AE). The "acid mantle", which is a slightly acidic film on the surface of the skin has led to the development of acidic emollients for skin care. In this context, the effect of citric acid-coated textiles on atopic skin has not been examined to date. A textile carrier composed of cellulose fibres was coated with a citric acid surface layer by esterification, ensuring a constant pH of 5.5-6.5. Twenty patients with AE or atopic diathesis were enrolled in the study. In a double-blind, half-side experiment, patients had to wear these textiles for 12 h a day for 14 days. On day 0 (baseline), 7 and 14, tolerability (erythema, pruritus, eczema, wearing comfort) and efficacy on skin barrier were assessed by TEWL skin hydration (corneometry/capacitance), pH and clinical scoring of eczema (SCORAD). Citric acid-coated textiles were well tolerated and improved eczema and objective parameters of skin physiology, including barrier function and a reduced skin surface pH, with potential lower pathogenic microbial colonisation. PMID:24953993

  1. Process of magnetite fabric development during granite deformation

    NASA Astrophysics Data System (ADS)

    Mamtani, Manish A.; Piazolo, Sandra; Greiling, Reinhard O.; Kontny, Agnes; Hrouda, František

    2011-08-01

    This study evaluates the fabric defined by magnetite grains in a syntectonically deformed granite and deciphers the processes that led to magnetite fabric development. Anisotropy of anhysteretic remanence magnetization (AARM) analysis is performed in samples taken from different parts of the granite to establish that the magnetite grains define a fabric. Along with microstructural studies, the AARM data help conclude that this fabric is on account of shape preferred orientation (SPO) of the magnetite grains. The intensity of magnetite fabric (degree of anisotropy of the AARM ellipsoid) is higher in the southern parts as compared to the north, which is inferred to indicate a strain gradient. Electron back scattered diffraction (EBSD) analyses of magnetite grains were performed to determine if there are intracrystalline deformation features that could have influenced magnetite shape and SPO, and thus AARM data. Detailed crystallographic orientation data coupled with orientation contrast imaging did not reveal any subgrains and/or significant variations in crystallographic orientations within magnetite grains. Instead, grains exhibit fractures and are in places associated with quartz pressure fringes. Hence, neither the SPO nor the variation in the magnetite fabric intensity in the granite can be attributed to intracrystalline deformation of magnetite by dislocation creep. It is concluded that the magnetite grains were rheologically rigid and there was relative movement between the magnetite and the matrix minerals (quartz, feldspar and biotite). These matrix minerals actually define the fabric attractor and the magnetite grains passively rotated to align with it. Thus it is demonstrated that the magnetite fabric in the granite stems from rigid body movement rather than dislocation creep.

  2. Crystal structures and magnetic properties of magnetite (Fe3O4)/Polyvinyl alcohol (PVA) ribbon

    NASA Astrophysics Data System (ADS)

    Ardiyanti, Harlina; Suharyadi, Edi; Kato, Takeshi; Iwata, Satoshi

    2016-04-01

    Ribbon of magnetite (Fe3O4)/Polyvinyl Alcohol (PVA) nanoparticles have been successfully fabricated with various concentration of PVA synthesized by co-precipitation method. Particle size of nanoparticles Fe3O4 sample and ribbon Fe3O4/PVA 25% sample is about 9.34 nm and 11.29 nm, respectively. The result of Vibrating Sample Magnetometer (VSM) showed that saturation magnetization value decreased from 76.99 emu/g to 15.01 emu/g and coercivity increased from 49.30 Oe to 158.35 Oe as increasing concentration of PVA. Atomic Force Microscopy (AFM) analysis showed that encapsulated PVA given decreasing agglomeration, controlled shape of nanoparticles Fe3O4 more spherical and dispersed. Surface roughness decreased with increasing concentration of PVA.

  3. Synthesis, characterization and studies on magneto-viscous properties of magnetite dispersed water based nanofluids

    NASA Astrophysics Data System (ADS)

    Paul, Gayatri; Kumar Das, Prasanta; Manna, Indranil

    2016-04-01

    Magnetic nanofluids, commonly known as ferrofluids, containing surfactant coated magnetite nanoparticles (having mean size ∼11 nm) uniformly dispersed in water are synthesized by chemical co-precipitation method. The rheological properties of magnetic nanofluid at different concentrations of nanoparticle loading have been investigated by varying different parameters including the magnetic field strength. Shear thinning is observed in the non-Newtonian magnetic nanofluids under the application of magnetic field. The observed increase in yield stress (calculated by fitting the Herschel and Bulkley model) with the applied magnetic field and concentration of dispersed nanoparticles confirm the formation of large aggregates that restrict or prohibit the flow characteristics of the otherwise Newtonian magnetic nanofluid. The hysteresis observed during the application and withdrawal of magnetic field suggests that the chain or column like structures fail to relax within the allowed measurement time interval.

  4. Reversed ageing of Fe3O4 nanoparticles by hydrogen plasma

    PubMed Central

    Schmitz-Antoniak, Carolin; Schmitz, Detlef; Warland, Anne; Svechkina, Nataliya; Salamon, Soma; Piamonteze, Cinthia; Wende, Heiko

    2016-01-01

    Magnetite (Fe3O4) nanoparticles suffer from severe ageing effects when exposed to air even when they are dispersed in a solvent limiting their applications. In this work, we show that this ageing can be fully reversed by a hydrogen plasma treatment. By x-ray absorption spectroscopy and its associated magnetic circular dichroism, the electronic structure and magnetic properties were studied before and after the plasma treatment and compared to results of freshly prepared magnetite nanoparticles. While aged magnetite nanoparticles exhibit a more γ-Fe2O3 like behaviour, the hydrogen plasma yields pure Fe3O4 nanoparticles. Monitoring the temperature dependence of the intra-atomic spin dipole contribution to the dichroic spectra gives evidence that the structural, electronic and magnetic properties of plasma treated magnetite nanoparticles can outperform the ones of the freshly prepared batch. PMID:26902789

  5. Synthesis and characterisation of biologically compatible TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Cheyne, Richard W.; Smith, Tim Ad; Trembleau, Laurent; McLaughlin, Abbie C.

    2011-06-01

    We describe for the first time the synthesis of biocompatible TiO2 nanoparticles containing a functional NH2 group which are easily dispersible in water. The synthesis of water dispersible TiO2 nanoparticles coated with mercaptosuccinic acid is also reported. We show that it is possible to exchange the stearic acid from pre-synthesised fatty acid-coated anatase 5-nm nanoparticles with a range of organic ligands with no change in the size or morphology. With further organic functionalisation, these nanoparticles could be used for medical imaging or to carry cytotoxic radionuclides for radioimmunotherapy where ultrasmall nanoparticles will be essential for rapid renal clearance.

  6. Development and characterization of magnetic iron oxide nanoparticles with a cisplatin-bearing polymer coating for targeted drug delivery

    PubMed Central

    Unterweger, Harald; Tietze, Rainer; Janko, Christina; Zaloga, Jan; Lyer, Stefan; Dürr, Stephan; Taccardi, Nicola; Goudouri, Ourania-Menti; Hoppe, Alexander; Eberbeck, Dietmar; Schubert, Dirk W; Boccaccini, Aldo R; Alexiou, Christoph

    2014-01-01

    A highly selective and efficient cancer therapy can be achieved using magnetically directed superparamagnetic iron oxide nanoparticles (SPIONs) bearing a sufficient amount of the therapeutic agent. In this project, SPIONs with a dextran and cisplatin-bearing hyaluronic acid coating were successfully synthesized as a novel cisplatin drug delivery system. Transmission electron microscopy images as well as X-ray diffraction analysis showed that the individual magnetite particles were around 4.5 nm in size and monocrystalline. The small crystallite sizes led to the superparamagnetic behavior of the particles, which was exemplified in their magnetization curves, acquired using superconducting quantum interference device measurements. Hyaluronic acid was bound to the initially dextran-coated SPIONs by esterification. The resulting amide bond linkage was verified using Fourier transform infrared spectroscopy. The additional polymer layer increased the vehicle size from 22 nm to 56 nm, with a hyaluronic acid to dextran to magnetite weight ratio of 51:29:20. A maximum payload of 330 μg cisplatin/mL nanoparticle suspension was achieved, thus the particle size was further increased to around 77 nm with a zeta potential of −45 mV. No signs of particle precipitation were observed over a period of at least 8 weeks. Analysis of drug-release kinetics using the dialysis tube method revealed that these were driven by inverse ligand substitution and diffusion through the polymer shell as well as enzymatic degradation of hyaluronic acid. The biological activity of the particles was investigated in a nonadherent Jurkat cell line using flow cytometry. Further, cell viability and proliferation was examined in an adherent PC-3 cell line using xCELLigence analysis. Both tests demonstrated that particles without cisplatin were biocompatible with these cells, whereas particles with the drug induced apoptosis in a dose-dependent manner, with secondary necrosis after prolonged incubation

  7. Intrinsic peroxidase-like activity of ferromagnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Gao, Lizeng; Zhuang, Jie; Nie, Leng; Zhang, Jinbin; Zhang, Yu; Gu, Ning; Wang, Taihong; Feng, Jing; Yang, Dongling; Perrett, Sarah; Yan, Xiyun

    2007-09-01

    Nanoparticles containing magnetic materials, such as magnetite (Fe3O4), are particularly useful for imaging and separation techniques. As these nanoparticles are generally considered to be biologically and chemically inert, they are typically coated with metal catalysts, antibodies or enzymes to increase their functionality as separation agents. Here, we report that magnetite nanoparticles in fact possess an intrinsic enzyme mimetic activity similar to that found in natural peroxidases, which are widely used to oxidize organic substrates in the treatment of wastewater or as detection tools. Based on this finding, we have developed a novel immunoassay in which antibody-modified magnetite nanoparticles provide three functions: capture, separation and detection. The stability, ease of production and versatility of these nanoparticles makes them a powerful tool for a wide range of potential applications in medicine, biotechnology and environmental chemistry.

  8. Fluorescence and magnetic properties of hydrogels containing Fe3O4 nanoparticles

    NASA Astrophysics Data System (ADS)

    Alveroğlu, E.; Sözeri, H.; Baykal, A.; Kurtan, U.; Şenel, M.

    2013-04-01

    In this study, Fe3O4 (magnetite) nanoparticles were synthesized by in situ in polyacrylamide (PAAm) gels. Structural and magnetic properties of magnetite nanoparticles were investigated by X-Ray diffractometry (XRD), transmission electron microscopy (TEM) and vibrating sample magnetometry (VSM) methods. Interaction of pyranine molecules with Fe3O4 nanoparticles was investigated by fluorescence spectroscopy measurements in which pyranine (POH) molecules were used as a flouroprobe. It was observed that magnetite nanoparticles have single domain structure with average grain size of 12 nm which was also supported by magnetization measurements. M-H hysteresis curves revealed the superparamagnetic nature of magnetite nanoparticles synthesized in PAAm gels. Fluorescence measurements depicted that there is an interaction between POH and magnetite nanoparticles which was deduced from the presence of two new peaks at 380 nm and 405 nm in emission spectrum. Besides, it was observed that POH molecules could not diffuse into the gel when it consists of magnetite nanoparticles which also make the gel more homogeneous. As swelling ratio increases from 1 to 13, magnetization of the gel does not change which reveals that magnetic nanoparticles do not diffuse out of the gel during water-intake. This feature makes the gel suitable for applications as waste water treatments.

  9. Spin reorientation transition of magnetite (001)

    NASA Astrophysics Data System (ADS)

    Martín-García, Laura; Mascaraque, Arantzazu; Pabón, Beatriz M.; Bliem, Roland; Parkinson, Gareth S.; Chen, Gong; Schmid, Andreas K.; de la Figuera, Juan

    2016-04-01

    We have imaged the rearrangement of the magnetic domains on magnetite (001) when crossing the spin reorientation transition and the Verwey transition with nanometer resolution. By means of spin-polarized low-energy electron microscopy we have monitored the change in the easy axes lowering the temperature through both transitions in remanence. The spin reorientation transition occurs in two steps: initial nucleation and growth of domains with a new surface magnetic orientation is followed by a smooth evolution.

  10. Initial Test Determination of Cosmogenic Nuclides in Magnetite

    NASA Astrophysics Data System (ADS)

    Matsumura, H.; Caffee, M. W.; Nagao, K.; Nishiizumi, K.

    2014-12-01

    Long-lived radionuclides, such as 10Be, 26Al, and 36Cl, are produced by cosmic rays in surficial materials on Earth, and used for determinations of cosmic-ray exposure ages and erosion rates. Quartz and limestone are routinely used as the target minerals for these geomorphological studies. Magnetite also contains target elements that produce abundant cosmogenic nuclides when exposed to the cosmic rays. Magnetite has several notable merits that enable the measurement of cosmogenic nuclides: (1) the target elements for production of cosmogenic nuclides in magnetite comprise the dominant mineral form of magnetite, Fe3O4; (2) magnetite can be easily isolated, using a magnet, after rock milling; (3) multiple cosmogenic nuclides are produced by exposure of magnetite to cosmic-ray secondaries; and (4) cosmogenic nuclides produced in the rock containing the magnetite, but not within the magnetite itself, can be separated using nitric acid and sodium hydroxide leaches. As part of this initial study, magnetite was separated from a basaltic sample collected from the Atacama Desert in Chili (2,995 m). Then Be, Al, Cl, Ca, and Mn were separated from ~2 g of the purified magnetite. We measured cosmogenic 10Be, 26Al, and 36Cl concentrations in the magnetite by accelerator mass spectrometry at PRIME Lab, Purdue University. Cosmogenic 3He and 21Ne concentrations of aliquot of the magnetite were measured by mass spectrometry at the University of Tokyo. We also measured the nuclide concentrations from magnetite collected from a mine at Ishpeming, Michigan as a blank. The 10Be and 36Cl concentrations as well as 3He concentration produce concordant cosmic ray exposure ages of ~0.4 Myr for the Atacama basalt. However, observed high 26Al and 21Ne concentrations attribute to those nuclides incorporation from silicate impurity.

  11. Magnetite biomineralization in the human brain.

    PubMed Central

    Kirschvink, J L; Kobayashi-Kirschvink, A; Woodford, B J

    1992-01-01

    Although the mineral magnetite (Fe3O4) is precipitated biochemically by bacteria, protists, and a variety of animals, it has not been documented previously in human tissue. Using an ultrasensitive superconducting magnetometer in a clean-lab environment, we have detected the presence of ferromagnetic material in a variety of tissues from the human brain. Magnetic particle extracts from solubilized brain tissues examined with high-resolution transmission electron microscopy, electron diffraction, and elemental analyses identify minerals in the magnetite-maghemite family, with many of the crystal morphologies and structures resembling strongly those precipitated by magnetotactic bacteria and fish. These magnetic and high-resolution transmission electron microscopy measurements imply the presence of a minimum of 5 million single-domain crystals per gram for most tissues in the brain and greater than 100 million crystals per gram for pia and dura. Magnetic property data indicate the crystals are in clumps of between 50 and 100 particles. Biogenic magnetite in the human brain may account for high-field saturation effects observed in the T1 and T2 values of magnetic resonance imaging and, perhaps, for a variety of biological effects of low-frequency magnetic fields. Images PMID:1502184

  12. Experimental Shock Decomposition of Siderite to Magnetite

    NASA Technical Reports Server (NTRS)

    Bell, M. S.; Golden, D. C.; Zolensky, M. E.

    2005-01-01

    The debate about fossil life on Mars includes the origin of magnetites of specific sizes and habits in the siderite-rich portions of the carbonate spheres in ALH 84001 [1,2]. Specifically [2] were able to demonstrate that inorganic synthesis of these compositionally zoned spheres from aqueous solutions of variable ion-concentrations is possible. They further demonstrated the formation of magnetite from siderite upon heating at 550 C under a Mars-like CO2-rich atmosphere according to 3FeCO3 = Fe3O4 + 2CO2 + CO [3] and they postulated that the carbonates in ALH 84001 were heated to these temperatures by some shock event. The average shock pressure for ALH 84001, substantially based on the refractive index of diaplectic feldspar glasses [3,4,5] is some 35-40 GPa and associated temperatures are some 300-400 C [4]. However, some of the feldspar is melted [5], requiring local deviations from this average as high as 45-50 GPa. Indeed, [5] observes the carbonates in ALH 84001 to be melted locally, requiring pressures in excess of 60 GPa and temperatures > 600 C. Combining these shock studies with the above inorganic synthesis of zoned carbonates it seems possible to produce the ALH 84001 magnetites by the shock-induced decomposition of siderite.

  13. Preparation and characterization of MR fluid consisting of magnetite particle coated with PMMA

    NASA Astrophysics Data System (ADS)

    Hong, M. K.; Park, B. J.; Choi, H. J.

    2009-02-01

    To improve physical characteristics of MR fluid, we synthesize magnetite nanoparticles (MNP) in shape of magnetic core- poly(methyl methacrylate) (PMMA) polymeric shell by atomic transfer radical polymerization. Prepared MNPs-PMMA which possesses a density lower than that of pure MNPs were characterized by FT-IR, XPS and TEM. Synthesized MNP-PMMA based MR fluid which was dispersed in non-magnetic medium lubricant oil (Yu-base 8) with 10 vol% was prepared. Rheological properties such as shear viscosity, shear stress and storage modulus were measured by both static and dynamic tests using a rotational rheometer with various external magnetic field strength applied.

  14. A double-coated magnetite-based magnetic fluid evaluation by cytometry and genetic tests

    NASA Astrophysics Data System (ADS)

    Freitas, M. L. L.; Silva, L. P.; Azevedo, R. B.; Garcia, V. A. P.; Lacava, L. M.; Grisólia, C. K.; Lucci, C. M.; Morais, P. C.; Da Silva, M. F.; Buske, N.; Curi, R.; Lacava, Z. G. M.

    2002-11-01

    Magnetite nanoparticles pre-coated with dodecanoic acid and ethoxylated alcohol (DE) were used to obtain a physiologically stable magnetic fluid (DE-MF) sample. Three different doses of DE-MF were intraperitoneally applied to mice. Blood and peritoneum cytometry and micronucleus test were performed for 1-21 days after injection to investigate the DE-MF toxicity. Changes in cell population, peritoneum inflammation, and potential DE-MF genotoxic action were all time and dose dependent. At the lowest dose (5×10 15 particles/kg), DE-MF seems to be useful as a drug precursor with both diagnostic and therapeutic values.

  15. Ionic Driven Embedment of Hyaluronic Acid Coated Liposomes in Polyelectrolyte Multilayer Films for Local Therapeutic Delivery

    NASA Astrophysics Data System (ADS)

    Hayward, Stephen L.; Francis, David M.; Sis, Matthew J.; Kidambi, Srivatsan

    2015-10-01

    The ability to control the spatial distribution and temporal release of a therapeutic remains a central challenge for biomedical research. Here, we report the development and optimization of a novel substrate mediated therapeutic delivery system comprising of hyaluronic acid covalently functionalized liposomes (HALNPs) embedded into polyelectrolyte multilayer (PEM) platform via ionic stabilization. The PEM platform was constructed from sequential deposition of Poly-L-Lysine (PLL) and Poly(Sodium styrene sulfonate) (SPS) “(PLL/SPS)4.5” followed by adsorption of anionic HALNPs. An adsorption affinity assay and saturation curve illustrated the preferential HALNP deposition density for precise therapeutic loading. (PLL/SPS)2.5 capping layer on top of the deposited HALNP monolayer further facilitated complete nanoparticle immobilization, cell adhesion, and provided nanoparticle confinement for controlled linear release profiles of the nanocarrier and encapsulated cargo. To our knowledge, this is the first study to demonstrate the successful embedment of a translatable lipid based nanocarrier into a substrate that allows for temporal and spatial release of both hydrophobic and hydrophilic drugs. Specifically, we have utilized our platform to deliver chemotherapeutic drug Doxorubicin from PEM confined HALNPs. Overall, we believe the development of our HALNP embedded PEM system is significant and will catalyze the usage of substrate mediated delivery platforms in biomedical applications.

  16. Ionic Driven Embedment of Hyaluronic Acid Coated Liposomes in Polyelectrolyte Multilayer Films for Local Therapeutic Delivery

    PubMed Central

    Hayward, Stephen L.; Francis, David M.; Sis, Matthew J.; Kidambi, Srivatsan

    2015-01-01

    The ability to control the spatial distribution and temporal release of a therapeutic remains a central challenge for biomedical research. Here, we report the development and optimization of a novel substrate mediated therapeutic delivery system comprising of hyaluronic acid covalently functionalized liposomes (HALNPs) embedded into polyelectrolyte multilayer (PEM) platform via ionic stabilization. The PEM platform was constructed from sequential deposition of Poly-L-Lysine (PLL) and Poly(Sodium styrene sulfonate) (SPS) “(PLL/SPS)4.5” followed by adsorption of anionic HALNPs. An adsorption affinity assay and saturation curve illustrated the preferential HALNP deposition density for precise therapeutic loading. (PLL/SPS)2.5 capping layer on top of the deposited HALNP monolayer further facilitated complete nanoparticle immobilization, cell adhesion, and provided nanoparticle confinement for controlled linear release profiles of the nanocarrier and encapsulated cargo. To our knowledge, this is the first study to demonstrate the successful embedment of a translatable lipid based nanocarrier into a substrate that allows for temporal and spatial release of both hydrophobic and hydrophilic drugs. Specifically, we have utilized our platform to deliver chemotherapeutic drug Doxorubicin from PEM confined HALNPs. Overall, we believe the development of our HALNP embedded PEM system is significant and will catalyze the usage of substrate mediated delivery platforms in biomedical applications. PMID:26423010

  17. On-wafer magnetic resonance of magnetite nanoparticles

    NASA Astrophysics Data System (ADS)

    Little, Charles A. E.; Russek, Stephen E.; Booth, James C.; Kabos, Pavel; Usselman, Robert J.

    2015-11-01

    Magnetic resonance measurements of ferumoxytol and TEMPO were made using an on-wafer transmission line technique with a vector network analyzer, allowing for broadband measurements of small sample volumes (4 nL) and small numbers of spins (1 nmol). On-wafer resonance measurements were compared with standard single-frequency cavity-based electron paramagnetic resonance (EPR) measurements using a new power conservation approach and the results show similar line shape. On-wafer magnetic resonance measurements using integrated microfluidics and microwave technology can significantly reduce the cost and sample volumes required for EPR spectral analysis and allow for integration of EPR with existing lab-on-a-chip processing and characterization techniques for point-of-care medical diagnostic applications.

  18. Study of the surface chemistry and morphology of single walled carbon nanotube-magnetite composites

    NASA Astrophysics Data System (ADS)

    Marquez-Linares, F.; Uwakweh, O. N. C.; Lopez, N.; Chavez, E.; Polanco, R.; Morant, C.; Sanz, J. M.; Elizalde, E.; Neira, C.; Nieto, S.; Roque-Malherbe, R.

    2011-03-01

    The study of the morphologies of the single walled carbon nanotube (SWCNT), magnetite nanoparticles (MNP), and the composite based on them was carried with combined X-ray diffraction (XRD), Raman spectroscopy (RS), scanning electron microscopy (SEM), field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM). These techniques together with thermogravimetric analyses (TGA) and diffuse reflectance infrared transform spectroscopy (DRIFTS) confirmed the production of pure single phases, and that the composite material consisted of MNP attached to the outer surface of the SWCNT. The Mössbauer spectroscopy (MS) research showed the presence of a large quantity of Lewis acid sites in the highly dispersed magnetite particles supported on the SWCNT outer surface. The DRIFTS carbon dioxide adsorption study of the composites revealed significant adsorption of carbon dioxide, fundamentally in the Lewis acid sites. Then, the Lewis acid sites were observed to be catalytically active. Further, the electron exchange between the Lewis acid sites and the basic or amphoteric adsorbed molecules could influence the magnetic properties of the magnetite. Consequently, together with this first ever use of MS in the study of Lewis acid sites, this investigation revealed the potential of the composites for catalytic and sensors applications.

  19. Controls on Soluble Pu Concentrations in PuO2/Magnetite Suspensions

    SciTech Connect

    Felmy, Andrew R.; Moore, Dean A.; Pearce, Carolyn I.; Conradson, Steven D.; Qafoku, Odeta; Buck, Edgar C.; Rosso, Kevin M.; Ilton, Eugene S.

    2012-11-06

    Time-dependent reduction of PuO2(am) was studied over a range of pH values in the presence of aqueous Fe(II) and magnetite (Fe3O4) nanoparticles. At early time frames (up to 56 days) very little aqueous Pu was mobilized from PuO2(am), even though measured pH and redox potentials, coupled to equilibrium thermodynamic modeling indicated the potential for significant reduction of PuO2(am) to relatively soluble Pu(III). Introduction of Eu(III) or Nd(III) to the suspensions as competitive cations to displace possible sorbed Pu(III) resulted in the release of significant concentrations of aqueous Pu. However, the similarity of aqueous Pu concentrations that resulted from the introduction of Eu(III)/Nd(III) to suspensions with and without magnetite indicated that the Pu was displaced from the PuO2(am), not from magnetite. The fact that soluble forms of Pu can be displaced from the surface of PuO2(am) represents a potential, but previously unidentified, source of Pu to aqueous solution or subsurface groundwaters.

  20. A spectroscopic study of uranium(VI) interaction with magnetite

    NASA Astrophysics Data System (ADS)

    Aamrani, S. El; Giménez, J.; Rovira, M.; Seco, F.; Grivé, M.; Bruno, J.; Duro, L.; de Pablo, J.

    2007-08-01

    The uranium sorbed onto commercial magnetite has been characterized by using two different spectroscopic techniques such as X-ray photoelectron spectroscopy (XPS), and extended X-ray absorption fine structure (EXAFS). Magnetite samples have been put in contact with uranium(VI) solutions in conditions in which a high uranium uptake is expected. After several days, the magnetite surface has been analysed by XPS and EXAFS. The XPS results obtained are not conclusive regarding the uranium oxidation state in the magnetite surface. On the other hand, the results obtained with the EXAFS technique show that the uranium-magnetite sample spectrum has characteristics from both the UO 2 and schoepite spectra, e.g. a relatively high coordination number of equatorial oxygens and two axial oxygens, respectively. These results would indicate that the uranium sorbed onto magnetite would be a mixture of uranium(IV) and uranium(VI).

  1. Imaging the intracellular degradation of biodegradable polymer nanoparticles

    PubMed Central

    Barthel, Anne-Kathrin; Dass, Martin; Dröge, Melanie; Cramer, Jens-Michael; Baumann, Daniela; Urban, Markus; Landfester, Katharina; Mailänder, Volker

    2014-01-01

    Summary In recent years, the development of smart drug delivery systems based on biodegradable polymeric nanoparticles has become of great interest. Drug-loaded nanoparticles can be introduced into the cell interior via endocytotic processes followed by the slow release of the drug due to degradation of the nanoparticle. In this work, poly(L-lactic acid) (PLLA) was chosen as the biodegradable polymer. Although common degradation of PLLA has been studied in various biological environments, intracellular degradation processes have been examined only to a very limited extent. PLLA nanoparticles with an average diameter of approximately 120 nm were decorated with magnetite nanocrystals and introduced into mesenchymal stem cells (MSCs). The release of the magnetite particles from the surface of the PLLA nanoparticles during the intracellular residence was monitored by transmission electron microscopy (TEM) over a period of 14 days. It was demonstrated by the release of the magnetite nanocrystals from the PLLA surface that the PLLA nanoparticles do in fact undergo degradation within the cell. Furthermore, even after 14 days of residence, the PLLA nanoparticles were found in the MSCs. Additionally, the ultrastructural TEM examinations yield insight into the long term intercellular fate of these nanoparticles. From the statistical analysis of ultrastructural details (e.g., number of detached magnetite crystals, and the number of nanoparticles in one endosome), we demonstrate the importance of TEM studies for such applications in addition to fluorescence studies (flow cytometry and confocal laser scanning microscopy). PMID:25383302

  2. Estimation of Sintering Kinetics of Magnetite Pellet Using Optical Dilatometer

    NASA Astrophysics Data System (ADS)

    Sandeep Kumar, T. K.; Viswanathan, Neelakantan Nurni; Ahmed, Hesham M.; Andersson, Charlotte; Björkman, B.

    2016-02-01

    During induration of magnetite pellets, oxidation of magnetite followed by sintering of the oxidized magnetite (hematite) is desirable. Sintering of magnetite which hampers the oxidation of magnetite is aimed to be kept as low as possible. In succession to our earlier study on sintering behavior of oxidized magnetite (hematite), this paper focusses on the sintering behavior of magnetite phase in isolation with an objective to estimate their kinetic parameters. The pellets prepared from the concentrate of LKAB's mine, which majorly contains (>95 pct) magnetite, are used for the sintering studies. Optical Dilatometer is used to capture the sintering behavior of the magnetite pellet and determine their isothermal kinetics by deducing the three parameters, namely—activation energy ( Q), pre-exponential factor ( K'), and time exponent ( n) with the help of power law and Arrhenius equation. It is interesting to find that the time exponent ( n) is decreasing with the increase in sintering temperature. It is also interesting to note that the activation energy for sintering of magnetite pellet shows no single value. From the present investigation, two activation energies—477 kJ/mole [1173 K to 1373 K (900 °C to 1100 °C)] and 148 kJ/mole [1373 K to 1623 K (1100 °C to 1350 °C)]—were deduced for sintering of magnetite, suggesting two different mechanisms operating at lower and other at higher temperatures. The estimated kinetic parameters were used to predict the non-isothermal sintering behavior of magnetite using the sintering kinetic model. Predicted results were validated using experimental data.

  3. Stearic acid coating on circulating fluidized bed combustion fly ashes and its effect on the mechanical performance of polymer composites

    NASA Astrophysics Data System (ADS)

    Yao, Nina; Zhang, Ping; Song, Lixian; Kang, Ming; Lu, Zhongyuan; Zheng, Rong

    2013-08-01

    The aim of this work was to test circulating fluidized bed combustion fly ashes (CFAs) for its potential to be utilized in polymer composites manufacturing to improve its toughness. CFAs was coated by stearic acid and used in the composite of polypropylene/ethylene vinyl acetate/high density polyethylene (PP/EVA/HDPE) by molding process method. The resulting coated and uncoated CFAs were fully characterized by particle size analyzer, contact angles, powder X-ray diffraction (XRD), thermogravimetric analysis/differential thermal analysis (TGA/DTA), Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The stearic acid coated onto the surface of CFAs particles in the physical and chemical ways, and the total clad ratio reached 2.05% by measuring TGA/DTA curve. The percentage of CFAs particles focused to a narrow range 2-4 μm and the median mean size was 3.2 μm more than uncoated CFAs. The properties of hydrophobic and dispersive of CFAs particles improved and original activity was reserved after stearic acid coating. The stearic acid was verified as a coupling agent by how much effect it had on the mechanical properties. It showed the elongation at break of PP/EVA/HDPE reinforced with 15 wt% coated CFAs (c-CFAs) was 80.20% and higher than that of the uncoated. The stearic acid treatment of CFAs is a very promising approach to improve the mechanical strength due to the incorporation of stearic acid on the CFAs surface, and hence, further enhances the potential for recycling CFAs as a suitable filler material in polymer composites.

  4. Magnetization and susceptibility of ion-irradiated granular magnetite films

    SciTech Connect

    Jiang, W.; McCloy, J. S.; Lea, A. S.; Sundararajan, J. A.; Yao, Q.; Qiang, Y.

    2011-04-01

    Porous granular films of magnetite (Fe{sub 3}O{sub 4}) with grains of {approx}3 nm in size were prepared using a state-of-the-art nanocluster deposition system. The films are initially superparamagnetic but become magnetized following Si{sup 2+} ion irradiation. A significant increase in the grain size and a dramatic change in the microstructure are observed. There are dipolar interactions between the nanoparticles in both the unirradiated and irradiated films. The in-phase alternating current magnetic susceptibility of the unirradiated film shows a blocking temperature of {approx}150 K, depending on frequency. A broadened Verwey transition for the irradiated film occurs at {approx}75 K, above which the susceptibility exhibits unusual behavior: a nearly linear decrease with decreasing temperature. There are irreversible domain rotations in the irradiated film during zero-field cooling and warming cycles between 10 and 300 K. The observed behavior of the irradiated granular films is quite distinct from that of metallic nanostructures after irradiation, and is due to the dramatic change in microstructures.

  5. Extended release of vitamins from magnetite loaded polyanionic polymeric beads.

    PubMed

    Sonmez, Maria; Verisan, Cristina; Voicu, Georgeta; Ficai, Denisa; Ficai, Anton; Oprea, Alexandra Elena; Vlad, Mihaela; Andronescu, Ecaterina

    2016-08-30

    Here we explore a novel approach of increasing the release duration of folic and ascorbic acid from magnetite entrapped into calcium-alginate beads. Synthesis and characterization of magnetite-vitamins complexes are reported. The magnetite-vitamins complexes were characterized by FT-IR, XRD, SEM, BET and DTA-TG. Also calcium-alginate magnetic beads were prepared by dripping a mixture of sodium alginate with magnetite-vitamins complexes into calcium chloride solution. Extended release profile of the two experimental models was evaluated and quantified by UV-vis. PMID:26626225

  6. One-step continuous synthesis of functionalized magnetite nanoflowers

    NASA Astrophysics Data System (ADS)

    Thomas, G.; Demoisson, F.; Chassagnon, R.; Popova, E.; Millot, N.

    2016-04-01

    For the first time, functionalized magnetite nanoparticles (Fe3O4 NPs) that form aggregates with a nanoflower morphology were synthesized using a rapid (11 s) one-step continuous hydrothermal process, which was recently modified, and their application as a T 2 magnetic resonance imaging (MRI) contrast agent was evaluated. The nanoparticles functionalized with 3,4-dihydroxy-L-phenylalanine (LDOPA) or 3,4-dihydroxyhydrocinnamic acid (DHCA) consisted of small crystallites of approximately 15 nm of diameter that assembled to form flower-shaped aggregate structures. The Fe3O4-LDOPA nanoflowers exhibited a high transverse relaxivity, r 2 of 418 ± 10 l mmolFe -1 s-1 at 3 T owing to magnetic dipolar interactions, which is twice as that of the commercial Feridex®/Endorem®. The prepared nanostructures were compared with bare Fe3O4 NPs and citrated Fe3O4 NPs. DHCA, LDOPA, and citric acid (CA) were found to have an anti-oxidizing effect and to influence the crystallite size and the lattice parameter of the NPs. DHCA and LDOPA increased the crystallite size, whereas CA decreased it. Surface modification increased the colloidal stability of NPs as compared to bare NPs. Nanoflower suspensions of Fe3O4-LDOPA NPs were found to be stable in the phosphate-buffered saline, saline medium, and minimal essential medium and formed aggregates of sizes smaller than 120 nm. All samples were found to be superparamagnetic in nature and the highest saturation magnetization was obtained for the Fe3O4-LDOPA samples. These NPs can bind to polymers such as PEG, and to fluorescent and chelating agents owing to the presence of free -NH2 or -COOH groups on the surface of NPs, allowing their use in dual imaging applications.

  7. One-step continuous synthesis of functionalized magnetite nanoflowers.

    PubMed

    Thomas, G; Demoisson, F; Chassagnon, R; Popova, E; Millot, N

    2016-04-01

    For the first time, functionalized magnetite nanoparticles (Fe3O4 NPs) that form aggregates with a nanoflower morphology were synthesized using a rapid (11 s) one-step continuous hydrothermal process, which was recently modified, and their application as a T 2 magnetic resonance imaging (MRI) contrast agent was evaluated. The nanoparticles functionalized with 3,4-dihydroxy-L-phenylalanine (LDOPA) or 3,4-dihydroxyhydrocinnamic acid (DHCA) consisted of small crystallites of approximately 15 nm of diameter that assembled to form flower-shaped aggregate structures. The Fe3O4-LDOPA nanoflowers exhibited a high transverse relaxivity, r 2 of 418 ± 10 l mmolFe (-1) s(-1) at 3 T owing to magnetic dipolar interactions, which is twice as that of the commercial Feridex®/Endorem®. The prepared nanostructures were compared with bare Fe3O4 NPs and citrated Fe3O4 NPs. DHCA, LDOPA, and citric acid (CA) were found to have an anti-oxidizing effect and to influence the crystallite size and the lattice parameter of the NPs. DHCA and LDOPA increased the crystallite size, whereas CA decreased it. Surface modification increased the colloidal stability of NPs as compared to bare NPs. Nanoflower suspensions of Fe3O4-LDOPA NPs were found to be stable in the phosphate-buffered saline, saline medium, and minimal essential medium and formed aggregates of sizes smaller than 120 nm. All samples were found to be superparamagnetic in nature and the highest saturation magnetization was obtained for the Fe3O4-LDOPA samples. These NPs can bind to polymers such as PEG, and to fluorescent and chelating agents owing to the presence of free -NH2 or -COOH groups on the surface of NPs, allowing their use in dual imaging applications. PMID:26900748

  8. Monitoring of the aging of magnetic nanoparticles using Mössbauer spectroscopy

    NASA Astrophysics Data System (ADS)

    Rümenapp, Christine; Wagner, Friedrich E.; Gleich, Bernhard

    2015-04-01

    Magnetic nanoparticles made of magnetite have the advantage to be biocompatible and to have a good saturation magnetisation. In this work we show that magnetite nanoparticles change their magnetic and chemical characteristics over time, depending on their storage conditions. To determine the oxidation state of the iron in the core of the nanoparticles Mössbauer spectroscopy was used at 4.2 K. This method is very accurate, especially in distinguishing maghemite and magnetite. The nanoparticles prepared by a co-precipitation method and peptized using acidic media had a core diameter of 5-7 nm. The aging process was monitored until the core was completely oxidised to maghemite and no further change occurred. The greatest change in the magnetite content of the particles was seen during the first 12 h after preparation. To preserve the good magnetic characteristics of magnetite nanoparticles a coating that prevents oxidation is therefore essential. Our results show that the point in time of the characterisation of small magnetic nanoparticles is crucial for the results. Even though magnetite nanoparticles have been formed nearly stoichiometrically, their chemical properties change over time.

  9. Study of the surface chemistry and morphology of single walled carbon nanotube-magnetite composites

    SciTech Connect

    Marquez-Linares, F.; Uwakweh, O.N.C.; Lopez, N.; Chavez, E.; Polanco, R.; Morant, C.; Sanz, J.M.; Elizalde, E.; Neira, C.; Nieto, S.; Roque-Malherbe, R.

    2011-03-15

    The study of the morphologies of the single walled carbon nanotube (SWCNT), magnetite nanoparticles (MNP), and the composite based on them was carried with combined X-ray diffraction (XRD), Raman spectroscopy (RS), scanning electron microscopy (SEM), field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM). These techniques together with thermogravimetric analyses (TGA) and diffuse reflectance infrared transform spectroscopy (DRIFTS) confirmed the production of pure single phases, and that the composite material consisted of MNP attached to the outer surface of the SWCNT. The Moessbauer spectroscopy (MS) research showed the presence of a large quantity of Lewis acid sites in the highly dispersed magnetite particles supported on the SWCNT outer surface. The DRIFTS carbon dioxide adsorption study of the composites revealed significant adsorption of carbon dioxide, fundamentally in the Lewis acid sites. Then, the Lewis acid sites were observed to be catalytically active. Further, the electron exchange between the Lewis acid sites and the basic or amphoteric adsorbed molecules could influence the magnetic properties of the magnetite. Consequently, together with this first ever use of MS in the study of Lewis acid sites, this investigation revealed the potential of the composites for catalytic and sensors applications. -- Graphical abstract: A large amount of Lewis acid sites were found in the highly dispersed magnetite which is supported on the SWCNT outer surface. Display Omitted Research highlights: {yields} The obtained materials were completely characterized with XRD, Raman and SEM-TEM. {yields} DRIFT, TGA and adsorption of the composites allowed understand the material formation. {yields} This is the first report of a study of Lewis sites by Moessbauer spectroscopy.

  10. Magnetite in Desert Varnish and Applications to Rock Varnish on Mars

    NASA Astrophysics Data System (ADS)

    Mancinelli, R. L.; Bishop, J. L.; de, S.

    2002-03-01

    Magnetite in desert varnish is characterized here using DTA, IR and SEM. The presence of magnetite in desert varnish is significant because of the oxidizing environment. This situation is similar to that of Mars where magnetite may also be present.

  11. Viscosity studies of water based magnetite nanofluids

    NASA Astrophysics Data System (ADS)

    Anu, K.; Hemalatha, J.

    2016-05-01

    Magnetite nanofluids of various concentrations have been synthesized through co-precipitation method. The structural and topographical studies made with the X-Ray Diffractometer and Atomic Force Microscope are presented in this paper. The density and viscosity studies for the ferrofluids of various concentrations have been made at room temperature. The experimental viscosities are compared with theoretical values obtained from Einstein, Batchelor and Wang models. An attempt to modify the Rosensweig model is made and the modified Rosensweig equation is reported. In addition, new empirical correlation is also proposed for predicting viscosity of ferrofluid at various concentrations.

  12. High yield, facile aqueous synthesis and characterization of C18 functionalized iron oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Nair, Kishore Kumar; Kaur, Ranjeet; Iqbal, Nusrat; Hasan, Abshar; Alam, Samsul; Raza, S. K.

    2015-04-01

    The present study shows the synthesis of magnetite nanoparticles by co-precipitation method in three steps. The steps involve the precipitation of Fe3O4 nanoparticles followed by layer by layer functionalization with silica and tetraethoxy(octadyl)silane (C18). The prepared magnetite nanoparticles were investigated by SEM, TEM, XRD, FTIR and VSM. It was suggested that the intermediate iron oxide nanoparticles were formed by the competing processes of oxidation and crystal growth after decomposition of ferrous and ferric salts. The first step synthesized nanoparticles were of around 16 ± 4 nm, second step silica coating of 18 ± 3 nm and the final step C18 were of 56 ± 6 nm. The tetraethylorthosilicate hydrolyzed to form silicic acid which further polymerizes and thereby forms a layer of silica over magnetite nanoparticles. FTIR peaks at 2854 and 2921 cm-1 confirm the layering of C18 on silica encapsulated nanoparticles which corresponds to ˜CH2 and ˜(CH2)17CH3 carbon chain symmetric extension. The thickness of silica coating and C18 are 1.9 ± 0.3 nm and 38.6 ± 2.5 nm as confirmed from TEM size distribution curve. The saturation magnetism of magnetite, silica coated and C18 nanoparticles are 77.46, 74.53 and 68.76 emu g-1 respectively. Thus, Fe3O4, silica and C18 encapsulated magnetite nanoparticles were superparamagnetic.

  13. Functionalization of polydopamine coated magnetic nanoparticles with biological entities

    NASA Astrophysics Data System (ADS)

    Mǎgeruşan, Lidia; Mrówczyński, Radosław; Turcu, Rodica

    2015-12-01

    New hybrid materials, obtained through introduction of cysteine, lysine and folic acid as biological entities into polydopamine-coated magnetite nanoparticles, are reported. The syntheses are straight forward and various methods were applied for structural and morphological characterization of the resulting nanoparticles. XPS proved a very powerful tool for surface chemical analysis and it evidences the functionalization of polydopamine coated magnetite nanoparticles. The superparamagnetic behavior and the high values of saturation magnetization recommend all products for further application where magnetism is important for targeting, separation, or heating by alternative magnetic fields.

  14. Investigation of electrically driven transition in magnetite nanostructures

    NASA Astrophysics Data System (ADS)

    Fursina, Alexandra

    Magnetite, Fe3O4, is a strongly electronically correlated system and thus exhibits remarkable electrical and magnetic properties, including the Verwey transition at TV 122 K, which has attracted much attention since its 1939 discovery. Fe3O 4 has recently revealed a new effect. By performing experiments at the nanoscale, we have discovered a novel electric-field driven transition (EFD) in magnetite below TV, from high- to low-resistance states driven by application of high bias. The EFD transition is detected both in Fe3O4 nanoparticles and thin films, is hysteretic in voltage under continuous biasing, and is not caused by self-heating. In this thesis we report on a thorough investigation of this new EFD transition. First, we unveil the origin of hysteresis observed in I-V curves. By applying voltage in a pulsed manner with controlled parameters, we unambiguously demonstrate that while the transition is field-driven, hysteresis results from Joule heating in the low-resistance state. A simple relaxation-time thermal model captures the essentials of the hysteresis mechanism. Second, by doing multilead (four-terminal) electrical measurements, we quantitatively separate the contributions of the Fe3O4 channel and each metal/electrode interface, and explore the contact effects upon testing devices incorporating various contact metals We demonstrate that on the onset of the transition, contact resistances at both source and drain electrodes and the resistance of Fe3O4 channel decrease abruptly. Finally, we measured the distribution of switching voltages, V sw, its evolution with temperature, and its dependence on out-of-plane magnetic field. Based on the experimental facts collected in this work we suggest the possible mechanism of EFD transition in Fe 3O4 as a charge gap closure by electric field. This is one of the first experimental observation of a theoretically predicted EFD transition in correlated insulators. These studies demonstrate that nanoscale, nonequilibrium

  15. Copper Ferrocyanide-Functionalized Magnetic Nanoparticles for the Selective Removal of Radioactive Cesium.

    PubMed

    Yang, Hee-Man; Lee, Kune-Woo; Seo, Bum-Kyoung; Moon, Jei-Kwon

    2015-02-01

    Copper ferrocyanide-functionalized magnetite nanoparticles (Cu-FC-MNPs) were successfully synthesized by immobilizing copper and ferrocyanide on the surfaces of [1-(2 amino-ethyl)-3-aminopropyl] trimethoxysilane-modified magnetite nanoparticles. Radioactive cesium (Cs) adsorption tests were conducted to investigate the effectiveness of the Cu-FC-MNPS toward the removal of radioactive Cs. The Cu-FC-MNPs showed excellent separation properties using an external magnet in an aqueous solution. PMID:26353716

  16. Preparation and rheological studies of uncoated and PVA-coated magnetite nanofluid

    NASA Astrophysics Data System (ADS)

    Khosroshahi, M. E.; Ghazanfari, L.

    2012-12-01

    Experimental studies of rheological behavior of uncoated magnetite nanoparticles (MNPs)U and polyvinyl alcohol (PVA) coated magnetite nanoparticles (MNPs)C were performed. A Co-precipitation technique under N2 gas was used to prevent undesirable critical oxidation of Fe2+. The results showed that smaller particles can be synthesized in both cases by decreasing the NaOH concentration which in our case this corresponded to 35 nm and 7 nm using 0.9 M NaOH at 750 rpm for (MNPs)U and (MNPs)C. The stable magnetic fluid contained well-dispersed Fe3O4/PVA nanocomposites which indicated fast magnetic response. The rheological measurement of magnetic fluid indicated an apparent viscosity range (0.1-1.2) pa s at constant shear rate of 20 s-1 with a minimum value in the case of (MNPs)U at 0 T and a maximum value for (MNPs)C at 0.5 T. Also, as the shear rate increased from 20 s-1 to 150 s-1 at constant magnetic field, the apparent viscosity also decreased correspondingly. The water-based ferrofluid exhibited the non-Newtonian behavior of shear thinning under magnetic field.

  17. Addition of a Magnetite Layer onto a Polysulfone Water Treatment Membrane to Enhance Virus Removal

    NASA Astrophysics Data System (ADS)

    Raciny, Isabel

    The applicability of low-pressure membranes systems in distributed (point of use) water treatment is hindered by, among other things, their inability to remove potentially harmful viruses and ions via size exclusion. According to the USEPA and the Safe Drinking Water Act, drinking water treatment processes must be designed for 4-log virus removal. Batch experiments using magnetite nanoparticle (nano-Fe3O4) suspensions and water filtration experiments with Polysulfone (PSf) membranes coated with nano-Fe3O 4 were conducted to assess the removal of a model virus (bacteriophage MS2). The membranes were coated via a simple filtration protocol. Unmodified membranes were a poor adsorbent for MS2 bacteriophage with less than 0.5-log removal, whereas membranes coated with magnetite nanoparticles exhibited a removal efficiency exceeding 99.99% (4-log). Thus, a cartridge of PSf membranes coated with nano-Fe3O4 particles could be used to remove viruses from water. Such membranes showed negligible iron leaching into the filtrate, thus obviating concern about colored water. Further research is needed to reduce the loss of water flux caused by coating.

  18. Hybrid materials: Magnetite-Polyethylenimine-Montmorillonite, as magnetic adsorbents for Cr(VI) water treatment.

    PubMed

    Larraza, Iñigo; López-Gónzalez, Mar; Corrales, Teresa; Marcelo, Gema

    2012-11-01

    Hybrid materials formed by the combination of a sodium rich Montmorillonite (MMT), with magnetite nanoparticles (40 nm, Fe(3)O(4) NPs) coated with Polyethylenimine polymer (PEI 800 g/mol or PEI 25000 g/mol) were prepared. The intercalation of the magnetite nanoparticles coated with PEI among MMT platelets was achieved by cationic exchange. The resulting materials presented a high degree of exfoliation of the MMT sheets and a good dispersion of Fe(3)O(4) NPs on both the surface and among the layers of MMT. The presence of amine groups in the PEI structure not only aids the exfoliation of the MMT layers, but also gives to the hybrid material the necessary functionality to interact with heavy metals. These hybrid materials were used as magnetic sorbent for the removal of hexavalent chromium from water. The effect that pH, Cr(VI) concentration, and adsorbent material composition have on the Cr(VI) removal efficiency was studied. A complete characterization of the materials was performed. The hybrid materials showed a slight dependence of the removal efficiency with the pH in a wide range (1-9). A maximum amount of adsorption capacity of 8.8 mg/g was determined by the Langmuir isotherm. Results show that these hybrid materials can be considered as potential magnetic adsorbent for the Cr(VI) removal from water in a wide range of pH. PMID:22841705

  19. Synthesis and investigating the magnetic properties of magnetite nanocrystallites for drug delivery

    NASA Astrophysics Data System (ADS)

    Ansar, Muhammad Zaka; Atiq, Shahid; Riaz, Saira; Naseem, Shahzad; Ramay, Shahid M.; Mahmood, Asif

    2015-07-01

    In recent years, use of magnetic nanoparticles in biomedical applications has increased tremendously. In particular, magnetite (Fe3O4) nanoparticles being highly biocompatible are rated very high due to their potential applications in biomedicines, for instance in anticancer drug delivery. In this work, the Fe3O4 nanoparticles have been synthesized using a novel sol-gel based autocombustion technique. The crystal structure of the Fe3O4 phase was confirmed by the data obtained from X-ray diffraction. Scherrer’s formula was employed to estimate the crystallite size of the Fe3O4 nanoparticles. The structural morphology, investigated by using a scanning electron microscopy (SEM), revealed well-dispersed and uniform sized grains in the sample prepared using enhanced fuel concentration. A vibrating sample magnetometer (VSM) was employed to investigate the magnetic characteristics of the samples which confirmed the superparamagnetic nature of the Fe3O4 samples, essentially required for cancer treatment. These nanoparticles could further be modified and functionalized by suitable polymers to achieve better biocompatibility before being injected into the diseased cells.

  20. Facile synthesis of magnetically separable reduced graphene oxide/magnetite/silver nanocomposites with enhanced catalytic activity.

    PubMed

    Ji, Zhenyuan; Shen, Xiaoping; Yue, Xiaoyang; Zhou, Hu; Yang, Juan; Wang, Yuqin; Ma, Lianbo; Chen, Kangmin

    2015-12-01

    In this study, the combination of magnetite (Fe3O4) with reduced graphene oxide (RGO) generates a new hybrid substrate for the dispersion of noble metal nanoparticles. Well-dispersed silver (Ag) nanoparticles loaded on the surface of Fe3O4 modified RGO are achieved by an efficient two-step approach. Through reducing Ag(+) ions, highly dispersed Ag nanoparticles are in-situ formed on the RGO/Fe3O4 substrate. It is found that the existence of Fe3O4 nanocrystals can significantly improve the dispersity and decrease the particle size of the in-situ formed Ag nanoparticles. Magnetic study reveals that the as-prepared RGO/Fe3O4/Ag ternary nanocomposites display room-temperature superparamagnetic behavior. The catalytic properties of the RGO/Fe3O4/Ag ternary nanocomposites were evaluated with the reduction of 4-nitrophenol into 4-aminophenol as a model reaction. The as-synthesized RGO/Fe3O4/Ag ternary catalysts exhibit excellent catalytic stability and much higher catalytic activity than the corresponding RGO/Ag catalyst. Moreover, the RGO/Fe3O4/Ag catalysts can be easily magnetically separated for reuse. This study further demonstrates that nanoparticles modified graphene can act as an effective hybrid substrate for the synthesis of multi-component and multifunctional graphene-based composites. PMID:26263498

  1. Targeted images of KB cells using folate-conjugated gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Rathinaraj, Pierson; Lee, Kyubae; Park, Soo-Young; Kang, Inn-Kyu

    2015-01-01

    Mercaptosuccinic acid-coated gold (GM) nanoparticles were prepared and characterized by transmission electron microscopy and dynamic light scattering. Folic acid (F) was then conjugated to the GM to preferentially target oral squamous cancer (KB) cells with folate receptors expressed on their membranes and facilitate the transit of the nanoparticles across the cell membrane. Finally, a fluorescence dye (Atto) was conjugated to the nanoparticles to visualize their internalization into KB cells. After culture of the cells in a medium containing GM and folate-conjugated GM (GF), the interaction of surface-modified gold nanoparticles with KB cells was studied.

  2. Targeted images of KB cells using folate-conjugated gold nanoparticles.

    PubMed

    Rathinaraj, Pierson; Lee, Kyubae; Park, Soo-Young; Kang, Inn-Kyu

    2015-01-01

    Mercaptosuccinic acid-coated gold (GM) nanoparticles were prepared and characterized by transmission electron microscopy and dynamic light scattering. Folic acid (F) was then conjugated to the GM to preferentially target oral squamous cancer (KB) cells with folate receptors expressed on their membranes and facilitate the transit of the nanoparticles across the cell membrane. Finally, a fluorescence dye (Atto) was conjugated to the nanoparticles to visualize their internalization into KB cells. After culture of the cells in a medium containing GM and folate-conjugated GM (GF), the interaction of surface-modified gold nanoparticles with KB cells was studied. PMID:25852305

  3. Magnetic process for removing heavy metals from water employing magnetites

    DOEpatents

    Prenger, F. Coyne; Hill, Dallas D.; Padilla, Dennis D.; Wingo, Robert M.; Worl, Laura A.; Johnson, Michael D.

    2003-07-22

    A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. The magnetite is mixed with the water such that at least a portion of, and preferably the majority of, the heavy metal in the water is bound to the magnetite. Once this occurs the magnetite and absorbed metal is removed from the water by application of a magnetic field. In most applications the process is achieved by flowing the water through a solid magnetized matrix, such as steel wool, such that the magnetite magnetically binds to the solid matrix. The magnetized matrix preferably has remnant magnetism, but may also be subject to an externally applied magnetic field. Once the magnetite and associated heavy metal is bound to the matrix, it can be removed and disposed of, such as by reverse water or air and water flow through the matrix. The magnetite may be formed in-situ by the addition of the necessary quantities of Fe(II) and Fe(III) ions, or pre-formed magnetite may be added, or a combination of seed and in-situ formation may be used. The invention also relates to an apparatus for performing the removal of heavy metals from water using the process outlined above.

  4. Magnetic process for removing heavy metals from water employing magnetites

    DOEpatents

    Prenger, F. Coyne; Hill, Dallas D.

    2006-12-26

    A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. The magnetite is mixed with the water such that at least a portion of, and preferably the majority of, the heavy metal in the water is bound to the magnetite. Once this occurs the magnetite and absorbed metal is removed from the water by application of a magnetic field. In most applications the process is achieved by flowing the water through a solid magnetized matrix, such as steel wool, such that the magnetite magnetically binds to the solid matrix. The magnetized matrix preferably has remnant magnetism, but may also be subject to an externally applied magnetic field. Once the magnetite and associated heavy metal is bound to the matrix, it can be removed and disposed of, such as by reverse water or air and water flow through the matrix. The magnetite may be formed in-situ by the addition of the necessary quantities of Fe(II) and Fe(III) ions, or pre-formed magnetite may be added, or a combination of seed and in-situ formation may be used. The invention also relates to an apparatus for performing the removal of heavy metals from water using the process outlined above.

  5. Effect of magnetite on GPR for detection of buried landmines

    NASA Astrophysics Data System (ADS)

    van Dam, Remke L.; Borchers, Brian; Hendrickx, Jan M. H.

    2006-05-01

    Ferrimagnetic minerals such as magnetite and maghaemite can affect ground-penetrating radar (GPR) signals. This may lead to false alarms and missed targets when surveying for the detection of buried landmines and unexploded ordnance (UXO). In most field situations ferrimagnetic mineral content is too low to affect GPR wave behavior. However, in soils and sedimentary material with magnetite-rich parent material large concentrations of magnetite can be found. This paper is a first systematic experimental effort to study the effects of large concentrations of magnetite for GPR detection of subsurface targets. We study the effects of (i) different homogeneous mixtures of magnetite and quartz sand and (ii) magnetite concentrated in layers (placer deposits), on the propagation behavior of GPR waves and reflection characteristics of steel and plastic balls. The balls are buried in homogeneous mixtures of magnetite and quartz sand and below a layer of pure magnetite. Important observations include that the simulated placer deposits did have a large effect on the detectability of balls below the placer deposits and that homogeneous mixtures had no significant effect.

  6. Biogeochemical role of magnetite in urban soils (Review of publications)

    NASA Astrophysics Data System (ADS)

    Vodyanitskii, Yu. N.

    2013-03-01

    The surface horizons of urban soils are enriched in technogenic magnetite Fe3O4 accumulated from emissions. Its content there reaches 3-4% and more, whereas it does not exceed 0.1% in the back-ground soils. In urban soils, large spherical magnetite particles of pseudo-single-domain and multidomain fabric predominate; the cavities in magnetic spherules decrease their chemical stability and increase their reactivity. Magnetite is most often destroyed in urban soils due to complexing; its destruction may be initiated by mineral salts entering the soil with deicing mixtures and by organic acids excreted by roots (e.g., by oxalic acid). The high solubility of magnetite with ammonium oxalate should be taken into account when using Tamm's reagent for the analysis of urban soils. Magnetite is a mineral carrier of some heavy metals. Therefore, its content (as determined from the magnetic susceptibility) serves as an indirect index of soil pollution. In addition, magnetite may affect many soil properties as a reducer and sorbent. It adsorbs phosphorus thus preventing the penetration of this nutrient into rivers and lakes. Magnetite also oxidizes Cl-containing aliphatic hydrocarbons and purifies the soil. Although magnetite enters urban soils as a pollutant, its influence on the soil properties cannot be unambiguously judged as only negative.

  7. MAGNETITE RECOVERY IN COAL WASHING BY HIGH GRADIENT MAGNETIC SEPARATION

    EPA Science Inventory

    The report describes a demonstration of the successful recovery of magnetite from mixtures of magnetite and coal, like those found in a coal-washing circuit, by High Gradient Magnetic Separation. The demonstration was part of a research program at Francis Bitter National Magnet L...

  8. The I-Xe Age of Orgueil Magnetite: New Results

    NASA Technical Reports Server (NTRS)

    Pravdivtseva, O. V.; Hohenberg, C. M.; Meshik, A. P.

    2003-01-01

    I-Xe ages of Murchison and Orgueil magnetites were reported to be the oldest [1] and interpreted as the condensation time of the solar nebula. More recent measurements, conducted on a highly magnetic separate from Orgueil (but not pure magnetite), gave much younger I-Xe ages [2]. We have since performed new studies on two pure separates of Orgueil magnetite, confirming the later closing time of the I-Xe system in this mineral phase. In the previous work of Lewis and Anders [1] special attention was paid to the purity of the analyzed material. It was shown, that the trapped Xe resided mostly in hydrated silicates and the radiogenic 129Xe in magnetite [3]. Therefore, Orgueil was finely ground and stirred with a saturated LiCl solution for 8 days at 60 C to remove the silicate-magnetite intergrowth. Although this procedure yields magnetic fractions that are at least 90% pure [1], it could potentially contaminate the magnetite with iodine and produce noncorrelated 128Xe and spurious I-Xe ages. To avoid this possibility, in our first work with Orgueil we deliberately omitted separation in LiCl solution. Instead, the meteorite was ground into a fine powder and the highly magnetic fraction was separated with a hand magnet and was confirmed to be largely magnetite [2]. The new work, reported here, was done in order to confirm our previous results and investigate the effects of the LiCl treatment on the I-Xe system in magnetite.

  9. Intermediate magnetite formation during dehydration of goethite

    NASA Astrophysics Data System (ADS)

    Özdemir, Özden; Dunlop, David J.

    2000-04-01

    The dehydration of goethite has been studied by low-temperature induced magnetization (LTIM) and X-ray diffraction on well-characterized acicular crystals. Fresh samples were heated in air to temperatures between 155°C and 610°C. Goethite and hematite were the magnetically dominant phases after all runs except 500°C and 610°C, for which only hematite was found. However, partially dehydrated goethites after the 238-402°C runs had broad peaks or inflections in the LTIM curves around 120 K, suggesting the formation of an intermediate spinel phase. These samples were next given a saturation remanence in a field of 2 T at 10 K and the remanence was measured continuously during zero-field warming to 300 K. There was a decrease in remanence at the Verwey transition (120 K), diagnostic of magnetite. The possible formation of a small amount of magnetite is of serious concern in studies of goethite-bearing sediments and rocks. Chemical remanent magnetization (CRM) of this strongly magnetic spinel phase could significantly modify the direction as well as the intensity of the original goethite CRM. As well, it would be a new source of paleomagnetic noise as far as primary remanence carried by other mineral phases is concerned.

  10. Gd-DTPA Adsorption on Chitosan/Magnetite Nanocomposites.

    PubMed

    Pylypchuk, Ie V; Kołodyńska, D; Kozioł, M; Gorbyk, P P

    2016-12-01

    The synthesis of the chitosan/magnetite nanocomposites is presented. Composites were prepared by co-precipitation of iron(II) and iron(III) salts by aqueous ammonia in the 0.1 % chitosan solution. It was shown that magnetite synthesis in the chitosan medium does not affect the magnetite crystal structure. The thermal analysis data showed 4.6 % of mass concentration of chitosan in the hybrid chitosan/magnetite composite. In the concentration range of initial Gd-DTPA solution up to 0.4 mmol/L, addition of chitosan to magnetite increases the adsorption capacity and affinity to Gd-DTPA complex. The Langmuir and Freundlich adsorption models were applied to describe adsorption processes. Nanocomposites were characterized by scanning electron microscopy (SEM), differential thermal analysis (DTA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and specific surface area determination (ASAP) methods. PMID:27030468

  11. Magnetite deformation mechanism maps for better prediction of strain partitioning

    NASA Astrophysics Data System (ADS)

    Till, J. L.; Moskowitz, Bruce

    2013-02-01

    Abstract A meta-analysis of existing experimental deformation data for <span class="hlt">magnetite</span> and other spinel-structured ferrites reveals that previously published flow laws are inadequate to describe the general deformation behavior of <span class="hlt">magnetite</span>. Using updated rate equations for oxygen diffusion in <span class="hlt">magnetite</span>, we present new flow laws that closely predict creep rates similar to those found in deformation experiments and that can be used to predict strain partitioning between cubic Fe oxides and other phases in the Earth's crust. New deformation mechanism maps for <span class="hlt">magnetite</span> have been constructed as functions of temperature and grain size. Using the revised creep parameters, estimates of strain partitioning between <span class="hlt">magnetite</span>, ilmenite, and plagioclase indicate that concentrated zones of Fe-Ti oxides in oceanic crust near slow-spreading ridges could accommodate significant amounts of strain at moderate temperatures and may contribute to aseismic creep along spreading-segment faults.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016NRL....11..168P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016NRL....11..168P"><span id="translatedtitle">Gd-DTPA Adsorption on Chitosan/<span class="hlt">Magnetite</span> Nanocomposites</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pylypchuk, Ie. V.; Kołodyńska, D.; Kozioł, M.; Gorbyk, P. P.</p> <p>2016-03-01</p> <p>The synthesis of the chitosan/<span class="hlt">magnetite</span> nanocomposites is presented. Composites were prepared by co-precipitation of iron(II) and iron(III) salts by aqueous ammonia in the 0.1 % chitosan solution. It was shown that <span class="hlt">magnetite</span> synthesis in the chitosan medium does not affect the <span class="hlt">magnetite</span> crystal structure. The thermal analysis data showed 4.6 % of mass concentration of chitosan in the hybrid chitosan/<span class="hlt">magnetite</span> composite. In the concentration range of initial Gd-DTPA solution up to 0.4 mmol/L, addition of chitosan to <span class="hlt">magnetite</span> increases the adsorption capacity and affinity to Gd-DTPA complex. The Langmuir and Freundlich adsorption models were applied to describe adsorption processes. Nanocomposites were characterized by scanning electron microscopy (SEM), differential thermal analysis (DTA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and specific surface area determination (ASAP) methods.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015IJAsB..14..547H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015IJAsB..14..547H"><span id="translatedtitle">Hexagonal plate-like <span class="hlt">magnetite</span> nanocrystals produced in komatiite-H2O-CO2 reaction system at 450°C</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hao, Xi-Luo; Li, Yi-Liang</p> <p>2015-10-01</p> <p>Batch experiments of komatiite-H2O-CO2 system with temperatures from 200 to 450°C were performed to simulate the interactions between the newly formed ultramafic crust and the proto-atmosphere on Earth before the formation of its earliest ocean. Particularly, <span class="hlt">magnetite</span> nanocrystals were observed in the experiment carried out at 450°C that are characterized by their hexagonal platelet-like morphology and porous structure. Exactly the same set of lattice fringes on the two opposite sides of one pore suggests post-crystallization erosion. The results demonstrate that <span class="hlt">magnetite</span> could be produced by the direct interactions between the ultramafic rocky crust and the atmosphere before the formation of the ocean on the Hadean Earth. These <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span> could serve as a catalyst in the synthesis of simple organic molecules during the organochemical evolution towards life.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://ntrs.nasa.gov/search.jsp?R=20040121339&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dmagnetite','NASA-TRS'); return false;" href="http://ntrs.nasa.gov/search.jsp?R=20040121339&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dmagnetite"><span id="translatedtitle">Origin of <span class="hlt">magnetite</span> in oxidized CV chondrites: in situ measurement of oxygen isotope compositions of Allende <span class="hlt">magnetite</span> and olivine</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Choi, B. G.; McKeegan, K. D.; Leshin, L. A.; Wasson, J. T.</p> <p>1997-01-01</p> <p><span class="hlt">Magnetite</span> in the oxidized CV chondrite Allende mainly occurs as spherical nodules in porphyritic-olivine (PO) chondrules, where it is associated with Ni-rich metal and/or sulfides. To help constrain the origin of the <span class="hlt">magnetite</span>, we measured oxygen isotopic compositions of <span class="hlt">magnetite</span> and coexisting olivine grains in PO chondrules of Allende by an in situ ion microprobe technique. Five <span class="hlt">magnetite</span> nodules form a relatively tight cluster in oxygen isotopic composition with delta 18O values from -4.8 to -7.1% and delta 17O values from -2.9 to -6.3%. Seven coexisting olivine grains have oxygen isotopic compositions from -0.9 to -6.3% in delta 18O and from -4.6 to -7.9% in delta 17O. The delta 17O values of the <span class="hlt">magnetite</span> and coexisting olivine do not overlap; they range from -0.4 to -2.6%, and from -4.0 to -5.7%, respectively. Thus, the <span class="hlt">magnetite</span> is not in isotopic equilibrium with the olivine in PO chondrules, implying that it formed after the chondrule formation. The delta 17O of the <span class="hlt">magnetite</span> is somewhat more negative than estimates for the ambient solar nebula gas. We infer that the <span class="hlt">magnetite</span> formed on the parent asteroid by oxidation of metal by H2O which had previously experienced minor O isotope exchange with fine-grained silicates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/27455762','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/27455762"><span id="translatedtitle">Copper Ferrocyanide-Functionalized Magnetic Adsorbents Using Polyethyleneimine Coated Fe3O4 <span class="hlt">Nanoparticles</span> for the Removal of Radioactive Cesium.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yang, Hee-Man; Hong, Sang Bum; Cho, Yong Suk; Lee, Kune-Woo; Seo, Bum-Kyoung; Moon, Jei-Kwon</p> <p>2016-03-01</p> <p>Copper ferrocyanide-functionalized magnetic nano-adsorbents were successfully synthesized by electrostatic coating of citric <span class="hlt">acid</span> <span class="hlt">coated</span> Fe3O4 <span class="hlt">nanoparticles</span> with polyethyleneimine, and immobilizing copper and ferrocyanide on the surfaces of polyethyleneimine-coated <span class="hlt">nanoparticles</span>. Radioactive cesium (Cs) adsorption tests were conducted to investigate the effectiveness of the copper ferrocyanide-functionalized magnetic nano-adsorbents toward the removal of radioactive Cs. PMID:27455762</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015MinDe..50..607D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015MinDe..50..607D"><span id="translatedtitle">Did the massive <span class="hlt">magnetite</span> "lava flows" of El Laco (Chile) form by magmatic or hydrothermal processes? New constraints from <span class="hlt">magnetite</span> composition by LA-ICP-MS</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dare, Sarah A. S.; Barnes, Sarah-Jane; Beaudoin, Georges</p> <p>2015-06-01</p> <p>The El Laco <span class="hlt">magnetite</span> deposits consist of more than 98 % <span class="hlt">magnetite</span> but show field textures remarkably similar to mafic lava flows. Therefore, it has long been suggested that they represent a rare example of an effusive Fe oxide liquid. Field and petrographic evidence, however, suggest that the <span class="hlt">magnetite</span> deposits represent replacement of andesite flows and that the textures are pseudomorphs. We determined the trace element content of <span class="hlt">magnetite</span> by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) from various settings at El Laco and compared them with <span class="hlt">magnetite</span> from both igneous and hydrothermal environments. This new technique allows us to place constraints on the conditions under which <span class="hlt">magnetite</span> in these supposed <span class="hlt">magnetite</span> "lava flows" formed. The trace element content of <span class="hlt">magnetite</span> from the massive <span class="hlt">magnetite</span> samples is different to any known magmatic <span class="hlt">magnetite</span>, including primary <span class="hlt">magnetite</span> phenocrysts from the unaltered andesite host rocks at El Laco. Instead, the El Laco <span class="hlt">magnetite</span> is most similar in composition to hydrothermal <span class="hlt">magnetite</span> from high-temperature environments (>500 °C), such as iron oxide-copper-gold (IOCG) and porphyry-Cu deposits. The <span class="hlt">magnetite</span> trace elements from massive <span class="hlt">magnetite</span> are characterised by (1) depletion in elements considered relatively immobile in hydrothermal fluids (e.g. Ti, Al, Cr, Zr, Hf and Sc); (2) enrichment in elements that are highly incompatible with magmatic <span class="hlt">magnetite</span> (rare earth elements (REE), Si, Ca, Na and P) and normally present in very low abundance in magmatic <span class="hlt">magnetite</span>; (3) high Ni/Cr ratios which are typical of <span class="hlt">magnetite</span> from hydrothermal environments; and (4) oscillatory zoning of Si, Ca, Mg, REE and most high field strength elements, and zoning truncations indicating dissolution, similar to that formed in hydrothermal Fe skarn deposits. In addition, secondary <span class="hlt">magnetite</span> in altered, brecciated host rock, forming disseminations and veins, has the same composition as <span class="hlt">magnetite</span> from the massive</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2016NatSR...624873P&link_type=ABSTRACT','NASAADS'); return false;" href="http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2016NatSR...624873P&link_type=ABSTRACT"><span id="translatedtitle">High-resolution analytical imaging and electron holography of <span class="hlt">magnetite</span> particles in amyloid cores of Alzheimer’s disease</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Plascencia-Villa, Germán; Ponce, Arturo; Collingwood, Joanna F.; Arellano-Jiménez, M. Josefina; Zhu, Xiongwei; Rogers, Jack T.; Betancourt, Israel; José-Yacamán, Miguel; Perry, George</p> <p>2016-04-01</p> <p>Abnormal accumulation of brain metals is a key feature of Alzheimer’s disease (AD). Formation of amyloid-β plaque cores (APC) is related to interactions with biometals, especially Fe, Cu and Zn, but their particular structural associations and roles remain unclear. Using an integrative set of advanced transmission electron microscopy (TEM) techniques, including spherical aberration-corrected scanning transmission electron microscopy (Cs-STEM), nano-beam electron diffraction, electron holography and analytical spectroscopy techniques (EDX and EELS), we demonstrate that Fe in APC is present as iron oxide (Fe3O4) <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span>. Here we show that Fe was accumulated primarily as nanostructured particles within APC, whereas Cu and Zn were distributed through the amyloid fibers. Remarkably, these highly organized crystalline <span class="hlt">magnetite</span> nanostructures directly bound into fibrillar Aβ showed characteristic superparamagnetic responses with saturated magnetization with circular contours, as observed for the first time by off-axis electron holography of nanometer scale particles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/17677066','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/17677066"><span id="translatedtitle">Dipolar structures in <span class="hlt">magnetite</span> ferrofluids studied with small-angle neutron scattering with and without applied magnetic field.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Klokkenburg, M; Erné, B H; Wiedenmann, A; Petukhov, A V; Philipse, A P</p> <p>2007-05-01</p> <p>Field-induced structure formation in a ferrofluid with well-defined <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span> with a permanent magnetic dipole moment was studied with small-angle neutron scattering (SANS) as a function of the magnetic interactions. The interactions were tuned by adjusting the size of the well-defined, single-magnetic-domain <span class="hlt">magnetite</span> (Fe3O4) particles and by applying an external magnetic field. For decreasing particle dipole moments, the data show a progressive distortion of the hexagonal symmetry, resulting from the formation of magnetic sheets. The SANS data show qualitative agreement with recent cryogenic transmission electron microscopy results obtained in 2D [Klokkenburg, Phys. Rev. Lett. 97, 185702 (2006)] on the same ferrofluids. PMID:17677066</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/27121137','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/27121137"><span id="translatedtitle">High-resolution analytical imaging and electron holography of <span class="hlt">magnetite</span> particles in amyloid cores of Alzheimer's disease.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Plascencia-Villa, Germán; Ponce, Arturo; Collingwood, Joanna F; Arellano-Jiménez, M Josefina; Zhu, Xiongwei; Rogers, Jack T; Betancourt, Israel; José-Yacamán, Miguel; Perry, George</p> <p>2016-01-01</p> <p>Abnormal accumulation of brain metals is a key feature of Alzheimer's disease (AD). Formation of amyloid-β plaque cores (APC) is related to interactions with biometals, especially Fe, Cu and Zn, but their particular structural associations and roles remain unclear. Using an integrative set of advanced transmission electron microscopy (TEM) techniques, including spherical aberration-corrected scanning transmission electron microscopy (Cs-STEM), nano-beam electron diffraction, electron holography and analytical spectroscopy techniques (EDX and EELS), we demonstrate that Fe in APC is present as iron oxide (Fe3O4) <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span>. Here we show that Fe was accumulated primarily as nanostructured particles within APC, whereas Cu and Zn were distributed through the amyloid fibers. Remarkably, these highly organized crystalline <span class="hlt">magnetite</span> nanostructures directly bound into fibrillar Aβ showed characteristic superparamagnetic responses with saturated magnetization with circular contours, as observed for the first time by off-axis electron holography of nanometer scale particles. PMID:27121137</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/biblio/21072431','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/biblio/21072431"><span id="translatedtitle">Dipolar structures in <span class="hlt">magnetite</span> ferrofluids studied with small-angle neutron scattering with and without applied magnetic field</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Klokkenburg, M.; Erne, B. H.; Petukhov, A. V.; Philipse, A. P.; Wiedenmann, A.</p> <p>2007-05-15</p> <p>Field-induced structure formation in a ferrofluid with well-defined <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span> with a permanent magnetic dipole moment was studied with small-angle neutron scattering (SANS) as a function of the magnetic interactions. The interactions were tuned by adjusting the size of the well-defined, single-magnetic-domain <span class="hlt">magnetite</span> (Fe{sub 3}O{sub 4}) particles and by applying an external magnetic field. For decreasing particle dipole moments, the data show a progressive distortion of the hexagonal symmetry, resulting from the formation of magnetic sheets. The SANS data show qualitative agreement with recent cryogenic transmission electron microscopy results obtained in 2D [Klokkenburg et al., Phys. Rev. Lett. 97, 185702 (2006)] on the same ferrofluids.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4848473','PMC'); return false;" href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4848473"><span id="translatedtitle">High-resolution analytical imaging and electron holography of <span class="hlt">magnetite</span> particles in amyloid cores of Alzheimer’s disease</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Plascencia-Villa, Germán; Ponce, Arturo; Collingwood, Joanna F.; Arellano-Jiménez, M. Josefina; Zhu, Xiongwei; Rogers, Jack T.; Betancourt, Israel; José-Yacamán, Miguel; Perry, George</p> <p>2016-01-01</p> <p>Abnormal accumulation of brain metals is a key feature of Alzheimer’s disease (AD). Formation of amyloid-β plaque cores (APC) is related to interactions with biometals, especially Fe, Cu and Zn, but their particular structural associations and roles remain unclear. Using an integrative set of advanced transmission electron microscopy (TEM) techniques, including spherical aberration-corrected scanning transmission electron microscopy (Cs-STEM), nano-beam electron diffraction, electron holography and analytical spectroscopy techniques (EDX and EELS), we demonstrate that Fe in APC is present as iron oxide (Fe3O4) <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span>. Here we show that Fe was accumulated primarily as nanostructured particles within APC, whereas Cu and Zn were distributed through the amyloid fibers. Remarkably, these highly organized crystalline <span class="hlt">magnetite</span> nanostructures directly bound into fibrillar Aβ showed characteristic superparamagnetic responses with saturated magnetization with circular contours, as observed for the first time by off-axis electron holography of nanometer scale particles. PMID:27121137</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/biblio/1170078','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/biblio/1170078"><span id="translatedtitle">Ice Nucleation of Bare and Sulfuric <span class="hlt">Acid-coated</span> Mineral Dust Particles and Implication for Cloud Properties</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Kulkarni, Gourihar R.; Sanders, Cassandra N.; Zhang, Kai; Liu, Xiaohong; Zhao, Chun</p> <p>2014-08-27</p> <p>Ice nucleation properties of different dust species coated with soluble material are not well understood. We determined the ice nucleation ability of bare and sulfuric <span class="hlt">acid</span> <span class="hlt">coated</span> mineral dust particles as a function of temperature (-25 to -35 deg C) and relative humidity with respect to water (RHw). Five different mineral dust species: Arizona test dust (ATD), illite, montmorillonite, quartz and kaolinite were dry dispersed and size-selected at 150 nm and exposed to sulfuric acid vapors in the coating apparatus. The condensed sulfuric acid soluble mass fraction per particle was estimated from the cloud condensation nuclei activated fraction measurements. The fraction of dust particles nucleating ice at various temperatures and RHw was determined using a compact ice chamber. In water-subsaturated conditions, compared to bare dust particles, we found that only coated ATD particles showed suppression of ice nucleation ability while other four dust species did not showed the effect of coating on the fraction of particles nucleating ice. The results suggest that interactions between the dust surface and sulfuric acid vapor are important, such that interactions may or may not modify the surface via chemical reactions with sulfuric acid. At water-supersaturated conditions we did not observed the effect of coating, i.e. the bare and coated dust particles had similar ice nucleation behavior.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2012SPIE.8232E..0XG&link_type=ABSTRACT','NASAADS'); return false;" href="http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2012SPIE.8232E..0XG&link_type=ABSTRACT"><span id="translatedtitle">Fighting cancer with magnetic <span class="hlt">nanoparticles</span> and immunotherapy</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gutiérrez, L.; Mejías, R.; Barber, D. F.; Veintemillas-Verdaguer, S.; Serna, C. J.; Lázaro, F. J.; Morales, M. P.</p> <p>2012-03-01</p> <p>IFN-γ-adsorbed DMSA-coated <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span> can be used as an efficient in vivo drug delivery system for tumor immunotherapy. Magnetic <span class="hlt">nanoparticles</span>, with adsorbed interferon-γ, were targeted to the tumor site by application of an external magnetic field. A relevant therapeutic dosage of interferon in the tumor was detected and led to a notable reduction in tumor size. In general, only 10% of the total injected <span class="hlt">nanoparticles</span> after multiple exposures were found in tissues by AC susceptibility measurements of the corresponding resected tissues. Magnetic <span class="hlt">nanoparticle</span> biodistribution is affected by the application of an external magnetic field.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1810097','PMC'); return false;" href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1810097"><span id="translatedtitle">Biogenic <span class="hlt">magnetite</span> in the nematode caenorhabditis elegans.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Cranfield, Charles G; Dawe, Adam; Karloukovski, Vassil; Dunin-Borkowski, Rafal E; de Pomerai, David; Dobson, Jon</p> <p>2004-01-01</p> <p>The nematode Caenorhabditis elegans is widely used as a model system in biological research. Recently, examination of the production of heat-shock proteins in this organism in response to mobile phone-type electromagnetic field exposure produced the most robust demonstration to date of a non-thermal, deleterious biological effect. Though these results appear to be a sound demonstration of non-thermal bioeffects, to our knowledge, no mechanism has been proposed to explain them. We show, apparently for the first time, that biogenic <span class="hlt">magnetite</span>, a ferrimagnetic iron oxide, is present in C. elegans. Its presence may have confounding effects on experiments involving electromagnetic fields as well as implications for the use of this nematode as a model system for iron biomineralization in multi-cellular organisms. PMID:15801597</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/11717421','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/11717421"><span id="translatedtitle"><span class="hlt">Magnetite</span> morphology and life on Mars.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Buseck, P R; Dunin-Borkowski, R E; Devouard, B; Frankel, R B; McCartney, M R; Midgley, P A; Pósfai, M; Weyland, M</p> <p>2001-11-20</p> <p>Nanocrystals of <span class="hlt">magnetite</span> (Fe(3)O(4)) in a meteorite from Mars provide the strongest, albeit controversial, evidence for the former presence of extraterrestrial life. The morphological and size resemblance of the crystals from meteorite ALH84001 to crystals formed by certain terrestrial bacteria has been used in support of the biological origin of the extraterrestrial minerals. By using tomographic and holographic methods in a transmission electron microscope, we show that the three-dimensional shapes of such nanocrystals can be defined, that the detailed morphologies of individual crystals from three bacterial strains differ, and that none uniquely match those reported from the Martian meteorite. In contrast to previous accounts, we argue that the existing crystallographic and morphological evidence is inadequate to support the inference of former life on Mars. PMID:11717421</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=61068','PMC'); return false;" href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=61068"><span id="translatedtitle"><span class="hlt">Magnetite</span> morphology and life on Mars</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Buseck, Peter R.; Dunin-Borkowski, Rafal E.; Devouard, Bertrand; Frankel, Richard B.; McCartney, Martha R.; Midgley, Paul A.; Pósfai, Mihály; Weyland, Matthew</p> <p>2001-01-01</p> <p>Nanocrystals of <span class="hlt">magnetite</span> (Fe3O4) in a meteorite from Mars provide the strongest, albeit controversial, evidence for the former presence of extraterrestrial life. The morphological and size resemblance of the crystals from meteorite ALH84001 to crystals formed by certain terrestrial bacteria has been used in support of the biological origin of the extraterrestrial minerals. By using tomographic and holographic methods in a transmission electron microscope, we show that the three-dimensional shapes of such nanocrystals can be defined, that the detailed morphologies of individual crystals from three bacterial strains differ, and that none uniquely match those reported from the Martian meteorite. In contrast to previous accounts, we argue that the existing crystallographic and morphological evidence is inadequate to support the inference of former life on Mars. PMID:11717421</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/18301753','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/18301753"><span id="translatedtitle">Bats use <span class="hlt">magnetite</span> to detect the earth's magnetic field.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Holland, Richard A; Kirschvink, Joseph L; Doak, Thomas G; Wikelski, Martin</p> <p>2008-01-01</p> <p>While the role of magnetic cues for compass orientation has been confirmed in numerous animals, the mechanism of detection is still debated. Two hypotheses have been proposed, one based on a light dependent mechanism, apparently used by birds and another based on a "compass organelle" containing the iron oxide particles <span class="hlt">magnetite</span> (Fe(3)O(4)). Bats have recently been shown to use magnetic cues for compass orientation but the method by which they detect the Earth's magnetic field remains unknown. Here we use the classic "Kalmijn-Blakemore" pulse re-magnetization experiment, whereby the polarity of cellular <span class="hlt">magnetite</span> is reversed. The results demonstrate that the big brown bat Eptesicus fuscus uses single domain <span class="hlt">magnetite</span> to detect the Earths magnetic field and the response indicates a polarity based receptor. Polarity detection is a prerequisite for the use of <span class="hlt">magnetite</span> as a compass and suggests that big brown bats use <span class="hlt">magnetite</span> to detect the magnetic field as a compass. Our results indicate the possibility that sensory cells in bats contain freely rotating <span class="hlt">magnetite</span> particles, which appears not to be the case in birds. It is crucial that the ultrastructure of the <span class="hlt">magnetite</span> containing magnetoreceptors is described for our understanding of magnetoreception in animals. PMID:18301753</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://pubs.er.usgs.gov/publication/70034302','USGSPUBS'); return false;" href="http://pubs.er.usgs.gov/publication/70034302"><span id="translatedtitle">LA-ICP-MS of <span class="hlt">magnetite</span>: Methods and reference materials</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Nadoll, P.; Koenig, A.E.</p> <p>2011-01-01</p> <p><span class="hlt">Magnetite</span> (Fe3O4) is a common accessory mineral in many geologic settings. Its variable geochemistry makes it a powerful petrogenetic indicator. Electron microprobe (EMPA) analyses are commonly used to examine major and minor element contents in <span class="hlt">magnetite</span>. Laser ablation ICP-MS (LA-ICP-MS) is applicable to trace element analyses of <span class="hlt">magnetite</span> but has not been widely employed to examine compositional variations. We tested the applicability of the NIST SRM 610, the USGS GSE-1G, and the NIST SRM 2782 reference materials (RMs) as external standards and developed a reliable method for LA-ICP-MS analysis of <span class="hlt">magnetite</span>. LA-ICP-MS analyses were carried out on well characterized <span class="hlt">magnetite</span> samples with a 193 nm, Excimer, ArF LA system. Although matrix-matched RMs are sometimes important for calibration and normalization of LA-ICP-MS data, we demonstrate that glass RMs can produce accurate results for LA-ICP-MS analyses of <span class="hlt">magnetite</span>. Cross-comparison between the NIST SRM 610 and USGS GSE-1G indicates good agreement for <span class="hlt">magnetite</span> minor and trace element data calibrated with either of these RMs. Many elements show a sufficiently good match between the LA-ICP-MS and the EMPA data; for example, Ti and V show a close to linear relationship with correlation coefficients, R2 of 0.79 and 0.85 respectively. ?? 2011 The Royal Society of Chemistry.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/biblio/22399249','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/biblio/22399249"><span id="translatedtitle">Direct observations of field-induced assemblies in <span class="hlt">magnetite</span> ferrofluids</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Mousavi, N. S. Susan; Khapli, Sachin D.; Kumar, Sunil</p> <p>2015-03-14</p> <p>Evolution of microstructures in <span class="hlt">magnetite</span>-based ferrofluids with weak dipolar moments (particle size ≤ 10 nm) is studied with an emphasis on examining the effects of particle concentration (ϕ) and magnetic field strength (H) on the structures. <span class="hlt">Nanoparticles</span> are dispersed in water at three different concentrations, ϕ = 0.15%, 0.48%, and 0.59% (w/v) [g/ml%] and exposed to uniform magnetic fields in the range of H = 0.05–0.42 T. Cryogenic transmission electron microscopy is employed to provide in-situ observations of the field-induced assemblies in such systems. As the magnetic field increases, the Brownian colloids are observed to form randomly distributed chains aligned in the field direction, followed by head-to-tail chain aggregation and then lateral aggregation of chains termed as zippering. By increasing the field in low concentration samples, the number of chains increases, though their length does not change dramatically. Increasing concentration increases the length of the linear particle assemblies in the presence of a fixed external magnetic field. Thickening of the chains due to zippering is observed at relatively high fields. Through a systematic variation of concentration and magnetic field strength, this study shows that both magnetic field strength and change in concentration can strongly influence formation of microstructures even in weak dipolar systems. Additionally, the results of two commonly used support films on electron microscopy grids, continuous carbon and holey carbon films, are compared. Holey carbon film allows us to create local regions of high concentrations that further assist the development of field-induced assemblies. The experimental observations provide a validation of the zippering effect and can be utilized in the development of models for thermophysical properties such as thermal conductivity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4359171','PMC'); return false;" href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4359171"><span id="translatedtitle">Direct observations of field-induced assemblies in <span class="hlt">magnetite</span> ferrofluids</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mousavi, N. S. Susan</p> <p>2015-01-01</p> <p>Evolution of microstructures in <span class="hlt">magnetite</span>-based ferrofluids with weak dipolar moments (particle size ≤ 10 nm) is studied with an emphasis on examining the effects of particle concentration (ϕ) and magnetic field strength (H) on the structures. <span class="hlt">Nanoparticles</span> are dispersed in water at three different concentrations, ϕ = 0.15%, 0.48%, and 0.59% (w/v) [g/ml%] and exposed to uniform magnetic fields in the range of H = 0.05–0.42 T. Cryogenic transmission electron microscopy is employed to provide in-situ observations of the field-induced assemblies in such systems. As the magnetic field increases, the Brownian colloids are observed to form randomly distributed chains aligned in the field direction, followed by head-to-tail chain aggregation and then lateral aggregation of chains termed as zippering. By increasing the field in low concentration samples, the number of chains increases, though their length does not change dramatically. Increasing concentration increases the length of the linear particle assemblies in the presence of a fixed external magnetic field. Thickening of the chains due to zippering is observed at relatively high fields. Through a systematic variation of concentration and magnetic field strength, this study shows that both magnetic field strength and change in concentration can strongly influence formation of microstructures even in weak dipolar systems. Additionally, the results of two commonly used support films on electron microscopy grids, continuous carbon and holey carbon films, are compared. Holey carbon film allows us to create local regions of high concentrations that further assist the development of field-induced assemblies. The experimental observations provide a validation of the zippering effect and can be utilized in the development of models for thermophysical properties such as thermal conductivity. PMID:25829566</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2015JAP...117j3907M&link_type=ABSTRACT','NASAADS'); return false;" href="http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2015JAP...117j3907M&link_type=ABSTRACT"><span id="translatedtitle">Direct observations of field-induced assemblies in <span class="hlt">magnetite</span> ferrofluids</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Mousavi, N. S. Susan; Khapli, Sachin D.; Kumar, Sunil</p> <p>2015-03-01</p> <p>Evolution of microstructures in <span class="hlt">magnetite</span>-based ferrofluids with weak dipolar moments (particle size ≤ 10 nm) is studied with an emphasis on examining the effects of particle concentration (ϕ) and magnetic field strength (H) on the structures. <span class="hlt">Nanoparticles</span> are dispersed in water at three different concentrations, ϕ = 0.15%, 0.48%, and 0.59% (w/v) [g/ml%] and exposed to uniform magnetic fields in the range of H = 0.05-0.42 T. Cryogenic transmission electron microscopy is employed to provide in-situ observations of the field-induced assemblies in such systems. As the magnetic field increases, the Brownian colloids are observed to form randomly distributed chains aligned in the field direction, followed by head-to-tail chain aggregation and then lateral aggregation of chains termed as zippering. By increasing the field in low concentration samples, the number of chains increases, though their length does not change dramatically. Increasing concentration increases the length of the linear particle assemblies in the presence of a fixed external magnetic field. Thickening of the chains due to zippering is observed at relatively high fields. Through a systematic variation of concentration and magnetic field strength, this study shows that both magnetic field strength and change in concentration can strongly influence formation of microstructures even in weak dipolar systems. Additionally, the results of two commonly used support films on electron microscopy grids, continuous carbon and holey carbon films, are compared. Holey carbon film allows us to create local regions of high concentrations that further assist the development of field-induced assemblies. The experimental observations provide a validation of the zippering effect and can be utilized in the development of models for thermophysical properties such as thermal conductivity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/25954980','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/25954980"><span id="translatedtitle">Combination of magnetic and enhanced mechanical properties for copolymer-grafted <span class="hlt">magnetite</span> composite thermoplastic elastomers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jiang, Feng; Zhang, Yaqiong; Wang, Zhongkai; Wang, Wentao; Xu, Zhaohua; Wang, Zhigang</p> <p>2015-05-20</p> <p>Composite thermoplastic elastomers (CTPEs) of magnetic copolymer-grafted <span class="hlt">nanoparticles</span> (<span class="hlt">magnetite</span>, Fe3O4) were synthesized and characterized to generate magnetic CTPEs, which combined the magnetic property of Fe3O4 <span class="hlt">nanoparticles</span> and the thermoplastic elasticity of the grafted amorphous polymer matrix. Fe3O4 <span class="hlt">nanoparticles</span> served as stiff, multiple physical cross-linking points homogeneously dispersed in the grafted poly(n-butyl acrylate-co-methyl methacrylate) rubbery matrix synthesized via the activators regenerated by electron transfer for atom transfer radical polymerization method (ARGET ATRP). The preparation technique for magnetic CTPEs opened a new route toward developing a wide spectrum of magnetic elastomeric materials with strongly enhanced macroscopic properties. Differential scanning calorimetry (DSC) was used to measure the glass transition temperatures, and thermogravimetric analysis (TGA) was used to examine thermal stabilities of these CTPEs. The magnetic property could be conveniently tuned by adjusting the content of Fe3O4 <span class="hlt">nanoparticles</span> in CTPEs. Compared to their linear copolymers, these magnetic CTPEs showed significant increases in tensile strength and elastic recovery. In situ small-angle X-ray scattering measurement was conducted to reveal the microstructural evolution of CTPEs during tensile deformation. PMID:25954980</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012APS..OSF.CA025P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012APS..OSF.CA025P"><span id="translatedtitle">Nonspecific targeting of iron oxide <span class="hlt">nanoparticles</span> to the liver, kidney and spleen: A novel approach to achieving specificity</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Palihawadana Arachchige, Maheshika; Flack, Amanda; Chen, Xuequn; Li, Jing; Oupicky, David; Cheng, Y.-C. Norman; Shen, Yimin; Jena, Bhanu; Lawes, Gavin</p> <p>2012-10-01</p> <p>Recently there has been significant interest in developing Fe3O4 <span class="hlt">nanoparticles</span> for biomedical applications including targeted drug delivery and magnetic resonance imaging. One of the major problems in applying these <span class="hlt">nanoparticles</span> clinically is to minimize the undesirable filtration of these materials by the mononuclear phagocyte system. Preliminary MRI and magnetization studies on hyaluronic <span class="hlt">acid</span> <span class="hlt">coated</span> <span class="hlt">nanoparticles</span> injected intravenously into mice confirm that the <span class="hlt">nanoparticles</span> accumulate in the liver, spleen, and kidneys. To identify whether this <span class="hlt">nanoparticle</span> accumulation are due to some certain specific proteins, we exposed hyaluronic <span class="hlt">acid</span> <span class="hlt">coated</span> <span class="hlt">nanoparticles</span> to proteins extracted from these organs, together with blood plasma proteins, then used gel electrophoresis together with mass spectroscopy to identify the proteins binding to the <span class="hlt">nanoparticles</span>. We find that the accumulation of <span class="hlt">nanoparticles</span> in these organs can be due to specific binding by a small number of proteins. By appropriately functionalizing the Fe3O4 <span class="hlt">nanoparticles</span>, possibly by blocking the binding sites of these specific proteins, we expect that the <span class="hlt">nanoparticles</span> uptake in the liver, spleen, and kidneys will be reduced, which, in turn, could increase the concentration of <span class="hlt">nanoparticles</span> at tumor sites.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/biblio/1006299','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/biblio/1006299"><span id="translatedtitle">Platinum Attachments on Iron Oxide <span class="hlt">Nanoparticle</span> Surfaces</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Palchoudhury, Soubantika; Xu, Yaolin; An, Wei; Turner, C. H.; Bao, Yuping</p> <p>2010-04-30</p> <p>Platinum <span class="hlt">nanoparticles</span> supported on metal oxide surfaces have shown great potential as heterogeneous catalysts to accelerate electrochemical processes, such as the oxygen reduction reaction in fuel cells. Recently, the use of magnetic supports has become a promising research topic for easy separation and recovery of catalysts using magnets, such as Pt <span class="hlt">nanoparticles</span> supported on iron oxide <span class="hlt">nanoparticles</span>. The attachment of Pt on iron oxide <span class="hlt">nanoparticles</span> is limited by the wetting ability of the Pt (metal) on ceramic surfaces. A study of Pt <span class="hlt">nanoparticle</span> attachment on iron oxide <span class="hlt">nanoparticle</span> surfaces in an organic solvent is reported, which addresses the factors that promote or inhibit such attachment. It was discovered that the Pt attachment strongly depends on the capping molecules of the iron oxide seeds and the reaction temperature. For example, the attachment of Pt <span class="hlt">nanoparticles</span> on oleic <span class="hlt">acid</span> <span class="hlt">coated</span> iron oxide <span class="hlt">nanoparticles</span> was very challenging, because of the strong binding between the carboxylic groups and iron oxide surfaces. In contrast, when <span class="hlt">nanoparticles</span> are coated with oleic acid/tri-n-octylphosphine oxide or oleic acid/oleylamine, a significant increase in Pt attachment was observed. Electronic structure calculations were then applied to estimate the binding energies between the capping molecules and iron ions, and the modeling results strongly support the experimental observations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007JMMM..313..236H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007JMMM..313..236H"><span id="translatedtitle">Comparison of <span class="hlt">magnetite</span> nanocrystal formed by biomineralization and chemosynthesis</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Han, Lei; Li, Shuangyan; Yang, Yong; Zhao, Fengmei; Huang, Jie; Chang, Jin</p> <p>2007-06-01</p> <p><span class="hlt">Magnetite</span> nanocrystal has been widely used in many fields. Recently, a new <span class="hlt">magnetite</span> nanocrystal, called magnetosome, has been found in magnetotactic bacteria. In this article, we compared properties of <span class="hlt">magnetites</span> prepared by co-precipitation with those of magnetosomes isolated from MSR-1 in detail, such as crystalline, morphology, crystal-size distributions, vitro cytotoxicity, and magnetic properties and quantified primary amino groups on the magnetosomes membrane surface by fluorescamine assay for the first time. From the results, it was clear that the magnetosomes might have potential in the biomedical applications in the future.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://ntrs.nasa.gov/search.jsp?R=19800064650&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dmagnetite','NASA-TRS'); return false;" href="http://ntrs.nasa.gov/search.jsp?R=19800064650&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dmagnetite"><span id="translatedtitle">The case against UV photostimulated oxidation of <span class="hlt">magnetite</span>. [on Mars</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Morris, R. V.; Lauer, H. V., Jr.</p> <p>1980-01-01</p> <p>The kinetics of <span class="hlt">magnetite</span> oxidation in O2-bearing atmospheres in the presence of electromagnetic radiation was studied. No perceptible oxidation of <span class="hlt">magnetite</span> by ultraviolet (UV) photostimulation occurred. These results do not corroborate previous conclusions by Huguenin (1973, 1974) as to the occurrence of this process. Therefore, although the possibility that the process actually occurs cannot be ruled out, it is concluded that there is not yet a basis in laboratory experiments for inferring that UV photostimulated oxidation of <span class="hlt">magnetite</span> occurs naturally on the surface of Mars.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://ntrs.nasa.gov/search.jsp?R=19810054012&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dmagnetite','NASA-TRS'); return false;" href="http://ntrs.nasa.gov/search.jsp?R=19810054012&hterms=magnetite&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dmagnetite"><span id="translatedtitle">Graphite-<span class="hlt">magnetite</span> aggregates in ordinary chondritic meteorites</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Scott, E. R. D.; Taylor, G. J.; Rubin, A. E.; Keil, K.; Okada, A.</p> <p>1981-01-01</p> <p>The graphite-<span class="hlt">magnetite</span> component has been found (1) as abundant isolated inclusions in eight ordinary-chondritic, regolith breccias; (2) as the sole matrix in a new kind of unequilibrated chondrite that forms clasts in these regolith breccias; and (3) together with a Huss matrix in six unequilibrated ordinary chondrites. It is suggested that the component was formed by low-temperature, gas-solid reactions before the accretion of the meteorite, and that the isolated inclusions of graphite-<span class="hlt">magnetite</span> in regolith breccias were derived from bodies composed of the new kind of chondrite that has graphite-<span class="hlt">magnetite</span> as its sole matrix.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1981Natur.291..544S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1981Natur.291..544S"><span id="translatedtitle">Graphite-<span class="hlt">magnetite</span> aggregates in ordinary chondritic meteorites</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Scott, E. R. D.; Taylor, G. J.; Rubin, A. E.; Okada, A.; Keil, K.</p> <p>1981-06-01</p> <p>The graphite-<span class="hlt">magnetite</span> component has been found (1) as abundant isolated inclusions in eight ordinary-chondritic, regolith breccias; (2) as the sole matrix in a new kind of unequilibrated chondrite that forms clasts in these regolith breccias; and (3) together with a Huss matrix in six unequilibrated ordinary chondrites. It is suggested that the component was formed by low-temperature, gas-solid reactions before the accretion of the meteorite, and that the isolated inclusions of graphite-<span class="hlt">magnetite</span> in regolith breccias were derived from bodies composed of the new kind of chondrite that has graphite-<span class="hlt">magnetite</span> as its sole matrix.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4232385','PMC'); return false;" href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4232385"><span id="translatedtitle">Protein Binding for Detection of Small Changes on <span class="hlt">Nanoparticle</span> Surface</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Zeng, Shang; Huang, Yu-ming M.; Chang, Chia-en A.; Zhong, Wenwan</p> <p>2014-01-01</p> <p>Protein adsorption on <span class="hlt">nanoparticles</span> is closely associated with the physicochemical properties of particles, in particular, their surface property. We synthesized two batches of polyacrylic <span class="hlt">acid-coated</span> <span class="hlt">nanoparticles</span> under almost identical conditions except for heating duration and found differences in the head-group structure of the polyacrylic acid. The structure change was confirmed by NMR and MS. The two batches of particles had varied binding affinities to a selected group of proteins. Computational work confirmed that the head group of the polymer on the surface of a <span class="hlt">nanoparticle</span> could directly interact with a protein, and small structural changes in the head group were sufficient to result in a significant difference in the free energy of binding. Our results demonstrate that protein adsorption is so sensitive to the surface property of particles that it can reveal even small variations in the structure of a <span class="hlt">nanoparticle</span> surface ligand, and should be useful for quick assessment of <span class="hlt">nanoparticle</span> properties. PMID:24482794</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2015JMMM..380..280A&link_type=ABSTRACT','NASAADS'); return false;" href="http://adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2015JMMM..380..280A&link_type=ABSTRACT"><span id="translatedtitle">Magnetic poly(D,L-lactide) <span class="hlt">nanoparticles</span> loaded with aliskiren: A promising tool for hypertension treatment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Antal, Iryna; Kubovcikova, Martina; Zavisova, Vlasta; Koneracka, Martina; Pechanova, Olga; Barta, Andrej; Cebova, Martina; Antal, Vitaliy; Diko, Pavel; Zduriencikova, Martina; Pudlak, Michal; Kopcansky, Peter</p> <p>2015-04-01</p> <p>In this study anti-hypertensive drug called aliskiren was encapsulated in magnetic poly(D,L-lactide) <span class="hlt">nanoparticles</span> by the modified nanoprecipitation method. The effect of <span class="hlt">magnetite</span> and drug concentrations on the size distribution and zeta potential of polymer <span class="hlt">nanoparticles</span> was investigated. The optimized loadings were as follows: theoretical <span class="hlt">magnetite</span> loading was 20 mg/100 mg polymer <span class="hlt">nanoparticles</span> and aliskiren was encapsulated in magnetic poly(D,L-lactide) <span class="hlt">nanoparticles</span> at theoretical loading 0.6 mg aliskiren/100 mg magnetic polymer <span class="hlt">nanoparticles</span>. The physicochemical characteristics of <span class="hlt">nanoparticles</span> were studied, with spherical shape of <span class="hlt">nanoparticles</span> sized between 58 and 227 nm being one of the observed results. Differential scanning calorimetry and infrared spectroscopy confirmed that aliskiren was successfully identified in the magnetic poly(D,L-lactide) <span class="hlt">nanoparticles</span>. The in vivo experiments indicated that encapsulated aliskiren decreased blood pressure of the studied male spontaneously hypertensive rat even more significantly than common administered drug.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013APS..MARC45005S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013APS..MARC45005S"><span id="translatedtitle">Biomimetic control over size, shape and aggregation in magnetic <span class="hlt">nanoparticles</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sommerdijk, Nico</p> <p>2013-03-01</p> <p><span class="hlt">Magnetite</span> (Fe3O4) is a widespread magnetic iron oxide encountered in both geological and biomineralizing systems, which also has many technological applications, e.g. in ferrofluids, inks, magnetic data storage materials and as contrast agents in magnetic resonance imaging. As its magnetic properties depend largely on the size and shape of the crystals, control over crystal morphology is an important aspect in the application of <span class="hlt">magnetite</span> <span class="hlt">nanoparticles</span>, both in biology and synthetic systems. Indeed, in nature organisms such as magnetotactic bacteria demonstrate a precise control over the <span class="hlt">magnetite</span> crystal morphology, resulting in uniform and monodisperse <span class="hlt">nanoparticles</span>. The <span class="hlt">magnetite</span> formation in these bacteria is believed to occur through the co-precipitation of Fe(II) and Fe(III) ions, which is also the most widely applied synthetic route in industry. Synthetic strategies to <span class="hlt">magnetite</span> with controlled size and shape exist, but involve high temperatures and rather harsh chemical conditions. However, synthesis via co-precipitation generally yields poor control over the morphology and therefore over the magnetic properties of the obtained crystals. Here we demonstrate that by tuning the reaction kinetics we can achieve biomimetic control over the size and shape of <span class="hlt">magnetite</span> crystals but also over their organization in solution as well as their magnetic properties. We employ amino acids-based polymers to direct the formation of <span class="hlt">magnetite</span> in aqueous media at room temperature via both the co-precipitation and the partial oxidation method. By using 2D and 3D (cryo)TEM it is shown that acidic amino acid monomers are most effective in affecting the <span class="hlt">magnetite</span> particle morphology. By changing the composition of the polymers we can tune the morphology, the dispersibility as well as the magnetic properties of these <span class="hlt">nanoparticles</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ncbi.nlm.nih.gov/pubmed/19187208','PUBMED'); return false;" href="http://www.ncbi.nlm.nih.gov/pubmed/19187208"><span id="translatedtitle">Manganese in biogenic <span class="hlt">magnetite</span> crystals from magnetotactic bacteria.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Keim, Carolina N; Lins, Ulysses; Farina, Marcos</p> <p>2009-03-01</p> <p>Magnetotactic bacteria produce either <span class="hlt">magnetite</span> (Fe(3)O(4)) or greigite (Fe(3)S(4)) crystals in cytoplasmic organelles called magnetosomes. Whereas greigite magnetosomes can contain up to 10 atom% copper, <span class="hlt">magnetite</span> produced by magnetotactic bacteria was considered chemically pure for a long time and this characteristic was used to distinguish between biogenic and abiogenic crystals. Recently, it was shown that magnetosomes containing cobalt could be produced by three strains of Magnetospirillum. Here we show that <span class="hlt">magnetite</span> crystals produced by uncultured magnetotactic bacteria can incorporate manganese up to 2.8 atom% of the total metal content (Fe+Mn) when manganese chloride is added to microcosms. Thus, chemical purity can no longer be taken as a strict prerequisite to consider <span class="hlt">magnetite</span> crystals to be of biogenic origin. PMID:19187208</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20150010433','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20150010433"><span id="translatedtitle"><span class="hlt">Magnetite</span> Plaquettes Provide an Extraterrestrial Source of Asymmetric Components</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Chan, Q. H. S.; Zolensky, M. E.; Martinez, J. E.</p> <p>2015-01-01</p> <p>Molecular selectivity is a crucial criterion for life. A possible abiotic mechanism that can produce chiral asymmetry in meteoritic amino acids is their formation with the presence of asymmetric catalysts. <span class="hlt">Magnetite</span> (Fe3O4), a common mineral in some carbonaceous chondrites (CCs), has been shown to be an effective catalyst for the formation of amino acids that are commonly found in these meteorites. <span class="hlt">Magnetite</span> sometimes takes the form of plaquettes that consist of barrel-shaped stacks of <span class="hlt">magnetite</span> disks that resemble a spiral. However, a widely accepted description of the internal morphology of this particular <span class="hlt">magnetite</span> form is still lacking, which is necessary in order to confirm or disprove the spiral configuration.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009GeCoA..73.6631T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009GeCoA..73.6631T"><span id="translatedtitle">Origins of <span class="hlt">magnetite</span> nanocrystals in Martian meteorite ALH84001</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Thomas-Keprta, K. L.; Clemett, S. J.; McKay, D. S.; Gibson, E. K.; Wentworth, S. J.</p> <p>2009-11-01</p> <p>The Martian meteorite ALH84001 preserves evidence of interaction with aqueous fluids while on Mars in the form of microscopic carbonate disks. These carbonate disks are believed to have precipitated 3.9 Ga ago at beginning of the Noachian epoch on Mars during which both the oldest extant Martian surfaces were formed, and perhaps the earliest global oceans. Intimately associated within and throughout these carbonate disks are nanocrystal <span class="hlt">magnetites</span> (Fe 3O 4) with unusual chemical and physical properties, whose origins have become the source of considerable debate. One group of hypotheses argues that these <span class="hlt">magnetites</span> are the product of partial thermal decomposition of the host carbonate. Alternatively, the origins of <span class="hlt">magnetite</span> and carbonate may be unrelated; that is, from the perspective of the carbonate the <span class="hlt">magnetite</span> is allochthonous. For example, the <span class="hlt">magnetites</span> might have already been present in the aqueous fluids from which the carbonates were believed to have been deposited. We have sought to resolve between these hypotheses through the detailed characterization of the compositional and structural relationships of the carbonate disks and associated <span class="hlt">magnetites</span> with the orthopyroxene matrix in which they are embedded. Extensive use of focused ion beam milling techniques has been utilized for sample preparation. We then compared our observations with those from experimental thermal decomposition studies of sideritic carbonates under a range of plausible geological heating scenarios. We conclude that the vast majority of the nanocrystal <span class="hlt">magnetites</span> present in the carbonate disks could not have formed by any of the currently proposed thermal decomposition scenarios. Instead, we find there is considerable evidence in support of an alternative allochthonous origin for the <span class="hlt">magnetite</span> unrelated to any shock or thermal processing of the carbonates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AGUFMGP33E..04F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AGUFMGP33E..04F"><span id="translatedtitle">Synthetic clay-<span class="hlt">magnetite</span> aggregates designed for controlled deposition experiments</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Feinberg, J. M.; Galindo-Gonzalez, C.; Kasama, T.; Cervera, L.; Posfai, M.; Harrison, R. J.; Dunin-Borkowski, R. E.</p> <p>2007-12-01</p> <p>The behavior of magnetic particles in fluid environments is key to the acquisition of detrital remanence magnetization and is essential to a multitude of industrial applications. This study introduces a series of synthetic clay-<span class="hlt">magnetite</span> aggregates whose physical attributes can be tailored for controlled depositional experiments. We describe the mineralogical structure and magnetic behavior of montmorillonite platelets coated with nanometer-scale <span class="hlt">magnetite</span> crystals using both electron microscopy and rock magnetism techniques. Selected area electron diffraction of the <span class="hlt">magnetite</span> and the montmorillonite host shows no evidence of preferred orientation or oriented aggregation. Grain size distributions of <span class="hlt">magnetite</span> in three different clay-<span class="hlt">magnetite</span> assemblages were directly measured using conventional bright-field transmission electron microscopy. The spacing of the <span class="hlt">magnetite</span> grains and their three-dimensional distribution around individual clay platelets was imaged using a tomographic reconstruction generated from high-angle annular dark-field (HAADF) images. The grain size distributions determined from the bright-field images and the tomographic reconstruction agree within error with estimates derived from magnetic granulometry techniques based on magnetic hysteresis and low-field susceptibility measurements. All three samples behave superparamagnetically at room temperature, and display increasing levels of single domain behavior as the samples are cooled to liquid nitrogen temperatures (- 195°C). Off-axis electron holography images show that superparamagnetic grains are also stabilized into flux closure structures at -195°C. The average spacing between adjacent <span class="hlt">magnetite</span> crystals and the overall platelet shape of the aggregates creates an anisotropy of magnetic susceptibility that allows assemblages to align with external magnetic fields at room temperature. By adjusting the dimensions and concentrations of the <span class="hlt">magnetite</span> grains in these aggregates, we can create</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/biblio/1025420','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/biblio/1025420"><span id="translatedtitle">Electrophoretic mobility of <span class="hlt">magnetite</span> particles in high temperature water</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Vidojkovic, Sonja; Rodriguez-Santiago, V; Fedkin, Mark V.; Wesolowski, David J; Lvov, Serguei N.</p> <p>2011-01-01</p> <p><span class="hlt">Magnetite</span>(Fe3O4) isoneofthemostcommonoxidesformingdepositsandparticulatephasesin industrialhightemperaturewatercircuits.Itscolloidalcharacteristicsplayaprincipalroleinthe mechanismofdepositformationandcanbeusedascontrollingfactorstopreventorminimizedeposit formationanddamageofindustrialpipelinesduetounder-depositcorrosion.Inthisstudy,ahigh temperatureparticleelectrophoresistechniquewasemployedtomeasurethezetapotentialatthe <span class="hlt">magnetite</span>/waterinterface the parameterthatcontrolscolloidalstabilityofparticles,theiraggrega- tion, anddeposition.Themeasurementsweremadeattemperaturesupto200 1C overawiderangeofpH. The isoelectricpointsofmagnetite,atwhichthedepositionofparticlesisincreased,weredeterminedatpH 6.35, 6.00,5.25,and5.05fortemperatures25,100,150,and200 1C, respectively.Theobserved temperaturedependenceofzetapotentialandtheisoelectricpHpointofmagnetitecanhelptoexplain the extentofinteractionsbetweenthecolloidalparticlesandthesteelwallsurfacesunderhydro- thermalconditions,andindicatemethodsforcontrollingandmitigatingoxidedepositioninhigh temperaturewatercycles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20120011767','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20120011767"><span id="translatedtitle">The Origin of <span class="hlt">Magnetite</span> Crystals in ALH84001 Carbonate Disks</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Thomas-Keprta, K. L.; Clemett, S. J.; Wentworth, S. J.; McKay, D. S.; Gibson