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Sample records for ferrite nanoparticles prepared

  1. Magnetic hyperthermia heating of cobalt ferrite nanoparticles prepared by low temperature ferrous sulfate based method

    NASA Astrophysics Data System (ADS)

    Yadavalli, Tejabhiram; Jain, Hardik; Chandrasekharan, Gopalakrishnan; Chennakesavulu, Ramasamy

    2016-05-01

    A facile low temperature co-precipitation method for the synthesis of crystalline cobalt ferrite nanostructures using ferrous sulfate salt as the precursor has been discussed. The prepared samples were compared with nanoparticles prepared by conventional co-precipitation and hydrothermal methods using ferric nitrate as the precursor. X-ray diffraction studies confirmed the formation of cubic spinel cobalt ferrites when dried at 110 °C as opposed to conventional methods which required higher temperatures/pressure for the formation of the same. Field emission scanning electron microscope studies of these powders revealed the formation of nearly spherical nanostructures in the size range of 20-30 nm which were comparable to those prepared by conventional methods. Magnetic measurements confirmed the ferromagnetic nature of the cobalt ferrites with low magnetic remanance. Further magnetic hyperthermia studies of nanostructures prepared by low temperature method showed a rise in temperature to 50 °C in 600 s.

  2. Preparation and Characterization of Hexagonal W-type Barium Ferrite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Trif, László; Tolnai, Gyula; Sajó, István; Kálmán, Erika

    New chemical synthesis procedure for preparation of nickel-zinc doped W-type hexagonal, nickel-zinc doped barium ferrite nanoparticles has been developed, using the nitrate-citrate sol-gel auto-combustion method (NCSAM). The crystalline phase attributes, microstructure, morphology, thermal behavior of the as-burnt phase and the sintered powders were characterized using XRD, SEM, TG-DTA, FT-IR measurements. The pure W-type ferrite phase is formed during 4 h annealing at a temperature of 1 200 °C.

  3. Preparation of silica coated cobalt ferrite magnetic nanoparticles for the purification of histidine-tagged proteins

    NASA Astrophysics Data System (ADS)

    Aygar, Gülfem; Kaya, Murat; Özkan, Necati; Kocabıyık, Semra; Volkan, Mürvet

    2015-12-01

    Surface modified cobalt ferrite (CoFe2O4) nanoparticles containing Ni-NTA affinity group were synthesized and used for the separation of histidine tag proteins from the complex matrices through the use of imidazole side chains of histidine molecules. Firstly, CoFe2O4 nanoparticles with a narrow size distribution were prepared in an aqueous solution using the controlled co-precipitation method. In order to obtain small CoFe2O4 agglomerates, oleic acid and sodium chloride were used as dispersants. The CoFe2O4 particles were coated with silica and subsequently the surface of these silica coated particles (SiO2-CoFe2O4) was modified by amine (NH2) groups in order to add further functional groups on the silica shell. Then, carboxyl (-COOH) functional groups were added to the SiO2-CoFe2O4 magnetic nanoparticles through the NH2 groups. After that Nα,Nα-Bis(carboxymethyl)-L-lysine hydrate (NTA) was attached to carboxyl ends of the structure. Finally, the surface modified nanoparticles were labeled with nickel (Ni) (II) ions. Furthermore, the modified SiO2-CoFe2O4 magnetic nanoparticles were utilized as a new system that allows purification of the N-terminal His-tagged recombinant small heat shock protein, Tpv-sHSP 14.3.

  4. Magnetic studies of nickel ferrite nanoparticles prepared by sol-gel technique

    NASA Astrophysics Data System (ADS)

    Anumol, C. N.; Chithra, M.; Sahoo, Subasa C.

    2016-05-01

    Ni-ferrite nanoparticles were synthesized by sol-gel technique by varying the solvent concentration. X-ray diffraction studies confirmed the phase purity in the samples. The lattice constant and grain size were found to be in the range of 0.833-0.834 nm and 14-26 nm respectively. There was no systematic variation in magnetization value with the solvent concentration and grain size. The highest magnetization, remanence and coercivity values of 60 emu/g, 12 emu/g and 180 Oe respectively were observed at 300K in the present study for the sample prepared in 75ml of solvent. The observed magnetization value is 20% higher than the bulk value of 50 emu/g. The magnetization, coercivity and remanence values were enhanced at 60K compared to those at 300K. The observed high magnetization value in the nanoparticles can be explained on the basis of modified cation distribution in the lattice sites. The enhanced magnetic properties at 60K may be understood due to the reduced thermal fluctuation and increased anisotropy at low temperature.

  5. Magnetocaloric effect in ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Poddar, P.; Gass, J.; Rebar, D. J.; Srinath, S.; Srikanth, H.; Morrison, S. A.; Carpenter, E. E.

    2006-12-01

    A comparative study of the magnetocaloric effect (MCE) is reported in two different types of chemically synthesized magnetic nanoparticle systems—cobalt ferrite and manganese zinc ferrite with mean size around 5 and 15 nm, respectively. While CoFe 2O 4 nanoparticles were synthesized using co-precipitation, the Mn 0.68Zn 0.25Fe 2.07O 4 (MZFO) nanoparticles were prepared by reverse micelle technique using AOT as surfactant. Our results indicate that the change in entropy with the change in applied magnetic field (d S/d H) is reasonably large for this class of nanoparticles and has a wide distribution over a broad temperature range covering the region above and below the blocking temperature. The maximum entropy change is influenced by the particle size, overall distribution in anisotropy and magnetic moments.

  6. Highly aluminium doped barium and strontium ferrite nanoparticles prepared by citrate auto-combustion synthesis

    SciTech Connect

    Shirtcliffe, Neil J. . E-mail: neil.shirtcliffe@ntu.ac.uk; Thompson, Simon; O'Keefe, Eoin S.; Appleton, Steve; Perry, Carole C. . E-mail: carole.perry@ntu.ac.uk

    2007-02-15

    Aluminium doped barium and strontium hexaferrite nanoparticles BaAl {sub x}Fe{sub (12-x)}O{sub 19} and SrAl {sub x}Fe{sub (12-x)}O{sub 19} were synthesised via a sol-gel route using citric acid to complex the ions followed by an auto-combustion reaction. This method shows promise for the synthesis of complex ferrite powders with small particle size. It was found that around half of the iron could be substituted for aluminium in the barium ferrite with structure retention, whereas strontium aluminium ferrites could be produced with any aluminium content including total substitution of the iron. All synthesised materials consisted of particles smaller than 1 {mu}m, which is the size of a single magnetic domain, and various doping levels were achieved with the final elemental composition being within the bounds of experimental error. The materials show structural and morphological changes as they move from iron to aluminium ferrites. Such materials may be promising for imaging applications.

  7. Preparation of cobalt ferrite nanoparticles via a novel solvothermal approach using divalent iron salt as precursors

    SciTech Connect

    Ma, Jie; Green Bio- and Eco-Chem. Eng. Lab, University of Shanghai for Science and Technology ; Zhao, Jiantao; Li, Wenlie; Zhang, Shuping; Green Bio- and Eco-Chem. Eng. Lab, University of Shanghai for Science and Technology ; Tian, Zhenran; Basov, Sergey

    2013-02-15

    Graphical abstract: CoFe{sub 2}O{sub 4} nanoparticles are obtained via solvothermal approach using Fe{sup 2+} salt as iron resource. The magnetic properties can be modified by some additives. Display Omitted Highlights: ► CoFe{sub 2}O{sub 4} nanoparticles are synthesized by a facile one-step novel solvothermal method. ► The system is firstly performed in water–glycol mixture solvent with an ordinary air surrounding. ► The ferrous ions are used as iron source without adding oxidant. ► It is firstly found the low-coercivity CoFe{sub 2}O{sub 4} nanoparticles can be obtained with the help of some additives in the synthesis system. -- Abstract: Cobalt ferrite (CoFe{sub 2}O{sub 4}) nanoparticles are synthesized by a facile novel solvothermal method. The reactions are firstly performed in water–glycol system and Fe{sup 2+} salt is used as iron source without oxidant help. Some factors influenced the reactions, including temperature, reaction time, additives, are investigated. The samples are characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM), respectively. The magnetic properties of some samples are detected by vibrating sample magnetometry techniques (VSM). It is firstly found that the magnetism of cobalt ferrites nanomaterials can be modified by some additives. The coercivity of CoFe{sub 2}O{sub 4} nanoparticles evidently decreases from 600 to 50 Oe in the presence of PEG-4000 in the system.

  8. Preparation and characterization of MnZn-ferrite nanoparticles using reverse micelles

    NASA Astrophysics Data System (ADS)

    Morrison, S. A.; Cahill, C. L.; Carpenter, E. E.; Calvin, S.; Harris, V. G.

    2003-05-01

    Research on manganese zinc ferrites (MZFO) has undergone a renewal in recent years as advances in synthetic techniques promise smaller grain sizes and corresponding changes in material properties. Current techniques for nanoscale synthesis of ferrites, however, produce a broad distribution of particle sizes, thus limiting the density of compacted materials, and consequently altering coercivity [C. Rath et al., J. Appl. Phys. 91, 2211 (2002)]. To minimize porosity, bulk materials need to be pressed from uniform particles. Wet chemical synthesis performed in reverse micelles, in which pools of water are encased by surfactant molecules in an excess volume of oil, provides the greatest control over size and morphology. During synthesis, surfactant molecules keep particles separated and restrict particle growth. This affords greater control over the size and shape of the particles grown in the micelles and commonly results in highly uniform morphologies [J. P. Chen et al., J. Appl. Phys. 76, 6316 (1994); C. Liu et al., J. Phys. Chem. B. 104, 1141 (2000)]. As a first step, it is necessary to produce pure phase, nanosized ferrite particles, therefore in this study, analysis of the powder of a sample prepared by a reverse micelle technique is compared to a sample prepared by a traditional ceramic method. Future studies will focus on the porosity and subsequent material properties of compacted forms of the pure phase samples.

  9. Structural and magnetic properties of magnesium ferrite nanoparticles prepared via EDTA-based sol-gel reaction

    NASA Astrophysics Data System (ADS)

    Hussein, Shaban I.; Elkady, Ashraf S.; Rashad, M. M.; Mostafa, A. G.; Megahid, R. M.

    2015-04-01

    Magnesium ferrite (MgFe2O4) nanoparticles have been prepared, for the first time, by ethylene diamine tetraacetic acid (EDTA)-based sol-gel combustion method. The prepared ferrite system is calcined at 400, 500 and 600 °C. Thermo-gravimetric and differential thermal analysis (TGA-DTA), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, high resolution transmission electron microscopy (HRTEM) and vibrating sample magnetometry (VSM) were applied for elucidating the structural and magnetic properties of the prepared system. XRD patterns revealed that the prepared system have two spinel MgFe2O4 structures, namely cubic and tetragonal phases that are dependent on calcination temperature (Tc). The crystallite sizes varied from 8.933 to 41.583 nm, and from 1.379 to 292.565 nm for the cubic and tetragonal phases respectively depending on Tc. The deduced lattice parameters for the cubic and (tetragonal) systems are a=8.368, 8.365 and 8.377 and (a=7.011, 5.922, 5.908 and c=6.622, 8.456, 8.364) Å at Tc=400, 500 and 600 °C respectively. While the cation distribution of the cubic phase is found to be mixed spinel and Tc-dependent, it is an inverse spinel in the tetragonal phase where the Fe3+ ions occupy both the tetrahedral A- and octahedral B-sites in almost equal amount; the Mg2+ ions are found to occupy only the B-sites. The HRTEM and selected-area electron diffraction (SAED) revealed the detailed morphology of the nanoparticles, and confirmed their crystalline spinel structure. VSM indicated the existence of an appreciable fraction of superparamagnetic particles at room temperature, with pure superparamagnetic behavior observed for samples calcined at 400 °C. Besides, the magnetic properties are found to change by thermal treatment as a result of the varied phase concentration, cation distribution and lattice parameters. Thus, the new synthesis route used in this study by applying EDTA as an organic precursor for preparing MgFe2O4 nanoparticles at rather low temperatures proved to be efficient in obtaining nanoparticles with favorable structural and magnetic properties. Such properties would qualify them for several potential applications including e.g. in hyperthermia treatment, as contrast agents in magnetic resonance imaging (MRI), and in ferroelastomers technology.

  10. 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.

  11. Spin canting in ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Marx, J.; Huang, H.; Salih, K. S. M.; Thiel, W. R.; Schünemann, V.

    2016-12-01

    Recently, an easily scalable process for the production of small (3 -7 nm) monodisperse superparamagnetic ferrite nanoparticles MeFe2O4 (Me = Zn, Mn, Co) from iron metal and octanoic acid has been reported (Salih et al., Chem. Mater. 25 1430-1435 2013). Here we present a Mössbauer spectroscopic study of these ferrite nanoparticles in external magnetic fields of up to B = 5 T at liquid helium temperatures. Our analysis shows that all three systems show a comparable inversion degree and the cationic distribution for the tetrahedral A and the octahedral B sites has been determined to (Zn0.19Fe0.81) A [Zn0.81Fe1.19] B O4, (Mn0.15Fe0.85) A [Mn0.85Fe1.15] B O4 and (Co0.27Fe0.73) A [Co0.73Fe1.27] B O4. Spin canting occurs presumably in the B-sites and spin canting angles of 33°, 51° and 59° have been determined for the zinc, the manganese, and the cobalt ferrite nanoparticles.

  12. Ferrite Nanoparticles in Pharmacological Modulation of Angiogenesis

    NASA Astrophysics Data System (ADS)

    Deshmukh, Aparna; Radha, S.; Khan, Y.; Tilak, Priya

    2011-07-01

    Nanoparticles are being explored in the targeted drug delivery of pharmacological agents : angiogenesis being one such novel application which involves formation of new blood vessels or branching of existing ones. The present study involves the use of ferrite nanoparticles for precise therapeutic modulation of angiogenesis. The ferrite nanoparticles synthesized by co-precipitation of ferrous and ferric salts by a suitable base, were found to be 10-20 nm from X-ray diffraction and TEM measurements. The magnetization measurements showed superparamagnetic behavior of the uncoated nanoparticles. These ferrite nanoparticles were found to be bio-compatible with lymphocytes and neural cell lines from the biochemical assays. The chick chorioallantoic membrane(CAM) from the shell of fertile white Leghorn eggs was chosen as a model to study angiogenic activity. An enhancement in the angiogenic activity in the CAM due to addition of uncoated ferrite nanoparticles was observed.

  13. Magnetocaloric effect in ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Rebar, D.

    2005-03-01

    Miniaturization of the electronic devices for space, military and consumer applications requires cooling devices to be fabricated on a chip for power efficient, noise-free operations. Refrigeration based on the adiabatic-demagnetization has been used for several decades for cooling down to sub-kelvin temperatures. Superparamagnetic particles also hold tremendous potential towards this application. We have studied magnetocaloric effect (MCE) properties in chemically synthesized ferrite nanoparticles over a broad range in temperature and magnetic fields. Nanoparticles investigated include Fe3O4 (average size = 8 nm, synthesized using co-precipitation method), MnZnFe2O4 (average size = 15 nm, synthesized using reverse-micelle technique) and CoFe2O4 (average size 8 nm, synthesized using pyrolectic technique). The magnetic entropy change was calculated by applying Maxwell's relations to magnetization vs magnetic field curves at various temperatures. Our results indicate that the single-domain particles in their superparamagnetic state show a considerable entropy change near the blocking temperature. The influence of interactions on MCE effect will also be discussed. Work supported by NSF through Grant No. CTS-0408933

  14. Magnetic properties of superparamagnetic lithium ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Verma, Seema; Joy, P. A.

    2005-12-01

    Magnetic properties of lithium ferrite nanoparticles of size in the range of 4-50nm, synthesized by a low-temperature method, have been evaluated. A broad maximum at ˜220K in the temperature variation of the zero-field-cooled magnetization as well as the ac susceptibility and divergence of the zero-field-cooled and field-cooled magnetizations below this temperature indicate the superparamagnetic behavior of the lithium ferrite particles of size ˜4nm. On the other hand, at high temperatures, these particles show a cusp immediately below the Curie temperature of bulk lithium ferrite (895K). This anomalous magnetic behavior of the lithium ferrite nanoparticles, similar to that arising from the Hopkinson effect for bulk materials, is probed in detail and is explained in terms of the cumulative effect of the temperature variation of the anisotropy and particle size growth during the measurements at high temperatures.

  15. Preparation of ferrite-coated MFM cantilevers

    NASA Astrophysics Data System (ADS)

    Koblischka, M. R.; Kirsch, M.; Wei, J.; Sulzbach, T.; Hartmann, U.

    2007-09-01

    Ferrite-coated magnetic force microscopy (MFM) cantilevers were prepared for the use with a high-frequency MFM (HF-MFM) setup. The ferrite coatings were fabricated by means of radio frequency (RF) magnetron sputtering directly on the Si surface. Two types of ferrites were employed in this study: NiZnFe 2O 4 spinel and Co 2Z-type hexaferrite (Ba 3Co 2Fe 24O 41, BCFO). The typical thickness of the coatings was 50 nm. For comparison, ferrite samples on (1 0 0) and (1 1 1)-oriented Si substrates (analogous to the surfaces of the cantilevers) were prepared. Successful HF-MFM imaging was performed with both types of cantilevers using harddisk writer poles as samples. The HF-MFM images obtained by ferrite-coated cantilevers evidently reveal more details of the magnetic field distribution of the writer poles up to the GHz range than conventional CoCr-coated MFM cantilevers.

  16. Strong and moldable cellulose magnets with high ferrite nanoparticle content.

    PubMed

    Galland, Sylvain; Andersson, Richard L; Ström, Valter; Olsson, Richard T; Berglund, Lars A

    2014-11-26

    A major limitation in the development of highly functional hybrid nanocomposites is brittleness and low tensile strength at high inorganic nanoparticle content. Herein, cellulose nanofibers were extracted from wood and individually decorated with cobalt-ferrite nanoparticles and then for the first time molded at low temperature (<120 °C) into magnetic nanocomposites with up to 93 wt % inorganic content. The material structure was characterized by TEM and FE-SEM and mechanically tested as compression molded samples. The obtained porous magnetic sheets were further impregnated with a thermosetting epoxy resin, which improved the load-bearing functions of ferrite and cellulose material. A nanocomposite with 70 wt % ferrite, 20 wt % cellulose nanofibers, and 10 wt % epoxy showed a modulus of 12.6 GPa, a tensile strength of 97 MPa, and a strain at failure of ca. 4%. Magnetic characterization was performed in a vibrating sample magnetometer, which showed that the coercivity was unaffected and that the saturation magnetization was in proportion with the ferrite content. The used ferrite, CoFe2O4, is a magnetically hard material, demonstrated by that the composite material behaved as a traditional permanent magnet. The presented processing route is easily adaptable to prepare millimeter-thick and moldable magnetic objects. This suggests that the processing method has the potential to be scaled-up for industrial use for the preparation of a new subcategory of magnetic, low-cost, and moldable objects based on cellulose nanofibers. PMID:25331121

  17. Magnetoabsorption and magnetic hysteresis in Ni ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Hernández-Gómez, P.; Muñoz, J. M.; Valente, M. A.; Torres, C.; de Francisco, C.

    2013-01-01

    Nickel ferrite nanoparticles were prepared by a modified sol-gel technique employing coconut oil, and then annealed at different temperatures in 400-1200 °C range. This route of preparation has revealed to be one efficient and cheap technique to obtain high quality nickel ferrite nanosized powder. Sample particles sizes obtained with XRD data and Scherrer's formula lie in 13 nm to 138 nm, with increased size with annealing temperature. Hysteresis loops have been obtained at room temperature with an inductive method. Magnetic field induced microwave absorption in nanoscale ferrites is a recent an active area of research, in order to characterize and explore potential novel applications. In the present work microwave magnetoabsorption data of the annealed nickel ferrite nanoparticles are presented. These data have been obtained with a system based on a network analyzer that operates in the frequency range 0 - 8.5 GHz. At fields up to 400 mT we can observe a peak according to ferromagnetic resonance theory. Sample annealed at higher temperature exhibits different absorption, coercivity and saturation magnetization figures, revealing its multidomain character.

  18. Preparation and magnetic properties of Zn-Cu-Cr-La ferrite and its nanocomposites with polyaniline.

    PubMed

    Li, Liangchao; Liu, Hui; Wang, Yuping; Jiang, Jing; Xu, Feng

    2008-05-15

    Nanosized Zn(0.6)Cu(0.4)Cr(0.5)Fe(1.5-x)La(x)O(4) (x=0 - 0.06) ferrites doped with La are synthesized by a rheological phase reaction method. Polyaniline (PANI)/ferrite nanocomposites are prepared by in situ polymerization method. The structure, morphology and ferromagnetic property of ferrite powders and nanocomposites are characterized by X-ray powder diffractometer (XRD), transmission electron microscope (TEM), Fourier transform infrared spectra (FTIR), UV-visible spectroscopy (UV), thermogravimetric analysis (TGA) and vibrating sample magnetometer (VSM). The results indicate that the PANI and nanosized ferrite powders can be combined effectively. The polymers can reduce the agglomeration of nanosized ferrite particles to some extent, which is good for the dispersedness and stabilization of nanoparticles. The PANI/ferrite nanocomposites under applied magnetic field exhibit the hysteretic loops of the ferromagnetic nature. The magnetic properties of nanocomposites are tailored by controlling the ferrite content. PMID:18313067

  19. Ferrite nanoparticles for future heart diagnostics

    NASA Astrophysics Data System (ADS)

    Hong, Nguyen Hoa; Raghavender, A. T.; Ciftja, O.; Phan, M.-H.; Stojak, K.; Srikanth, H.; Zhang, Yin Hua

    2013-08-01

    Normally, CoFe2O4 has been known as ferromagnetic ferrite with a quite large magnetic moment. However, since we aim to inject the particles into the human body, we are also interested in ZnFe2O4 because in the human body, Fe and Zn exist, so that adding ZnFe2O4 is safer. In both cases, the nanoparticles are coated by silica in order to get rid of toxicity. Our main purpose is to test whether these nanoparticles affect the contractile function of heart cells. Our results on rat's heart cells have shown that both Zn and Co ferrites improved the contractility of heart cells. Notably, although both nanoparticles increased contraction and delayed relaxation, Co ferrites induced a greater contraction but with a slower relaxation. We can theoretically argue that the magnetization effects of the quantum dots have a considerable effect on the pulsating properties of the heart cells. Through this effect, the locally applied magnetic field is able to induce as well as turn on/off various regular beating patterns, thus, resetting the heart beatings.

  20. Microwave-assisted synthesis and characterization of nickel ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Carpenter, Gopal; Sen, Ravindra; Malviya, Nitin; Gupta, Nitish

    2015-08-01

    Nickel ferrite nanoparticles (NiFe2O4) were successfully prepared by microwave-assisted combustion method (MWAC) using citric Electron acid as a chelating agent. NiFe2O4 nanoparticles were characterized by X-ray diffraction (XRD) pattern, Scanning Microscopy (SEM), Fourier transform infrared (FTIR) and UV-Visible techniques. XRD analysis revealed that NiFe2O4 nanoparticles have spinel cubic structure with the average crystalline size of 26.38 nm. SEM analysis revealed random and porous structural morphology of particles and FTIR showed absorption bands related to octahedral and tetrahedral sites, in the range 400-600cm-1 which strongly favor the formation of NiFe2O4 nanoparticles. The optical band gap is determined by UV Visible method and found to be 5.4 eV.

  1. Atomic engineering of mixed ferrite and core-shell nanoparticles.

    PubMed

    Morrison, Shannon A; Cahill, Christopher L; Carpenter, Everett E; Calvin, Scott; Harris, Vincent G

    2005-09-01

    Nanoparticulate ferrites such as manganese zinc ferrite and nickel zinc ferrite hold great promise for advanced applications in power electronics. The use of these materials in current applications requires fine control over the nanoparticle size as well as size distribution to maximize their packing density. While there are several techniques for the synthesis of ferrite nanoparticles, reverse micelle techniques provide the greatest flexibility and control over size, crystallinity, and magnetic properties. Recipes for the synthesis of manganese zinc ferrite, nickel zinc ferrite, and an enhanced ferrite are presented along with analysis of the crystalline and magnetic properties. Comparisons are made on the quality of nanoparticles produced using different surfactant systems. The importance of various reaction conditions is explored with a discussion on the corresponding effects on the magnetic properties, particle morphology, stoichiometry, crystallinity, and phase purity. PMID:16193949

  2. Synthesis and characterization of Bismuth ferrite (BiFeO3) nanoparticles by solution evaporation method

    NASA Astrophysics Data System (ADS)

    Manzoor, A.; Afzal, A. M.; Umair, M.; Ali, Adnan; Rizwan, M.; Yaqoob, M. Z.

    2015-11-01

    Single phase Bismuth ferrite (BiFeO3) with high magnetization and polarization was synthesized by solution evaporation method (SEM) at room temperature. The influence of temperature and size of nanoparticles on magnetic properties was studied. The prepared Bismuth ferrite (BiFeO3) was characterized by X-ray diffraction (XRD) to investigate the structure and size of crystal. The average crystallite size of nanoparticles (NPs) as calculated by X-ray diffraction (XRD) falls in the range of 22-31 nm. The crystallite size of Bismuth ferrite increased as the temperature varied from 450 °C to 650 °C. Magnetic properties were studied by using physical properties measurement system (PPMS). It was also observed that the magnetic properties were directly related to the size and temperature of Bismuth ferrite nanoparticles. It has been investigated that the magnetization was decreased as the temperature and crystallite size increased.

  3. Structural and magnetic study of dysprosium substituted cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Kumar, Hemaunt; Srivastava, R. C.; Pal Singh, Jitendra; Negi, P.; Agrawal, H. M.; Das, D.; Hwa Chae, Keun

    2016-03-01

    The present work investigates the magnetic behavior of Dy3+ substituted cobalt ferrite nanoparticles. X-ray diffraction studies reveal presence of cubic spinel phases in these nanoparticles. Raman spectra of these nanoparticles show change in intensity of Raman bands, which reflects cation redistribution in cubic spinel lattice. Saturation magnetization and coercivity decrease with increase of Dy3+concentration in these nanoparticles. Room temperature Mössbauer measurements show the cation redistribution in these nanoparticles and corroborates the results obtained from Raman Spectroscopic measurements. Decrease in magnetization of Dy3+ substituted cobalt ferrite is attributed to the reduction in the magnetic interaction and cation redistribution.

  4. A biosensor system using nickel ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Singh, Prachi; Rathore, Deepshikha

    2016-05-01

    NiFe2O4 ferrite nanoparticles were synthesized by chemical co-precipitation method and the structural characteristics were investigated using X-ray diffraction technique, where single cubic phase formation of nanoparticles was confirmed. The average particle size of NiFe2O4 was found to be 4.9 nm. Nanoscale magnetic materials are an important source of labels for biosensing due to their strong magnetic properties which are not found in biological systems. This property of the material was exploited and the fabrication of the NiFe2O4 nanoparticle based biosensor was done in the form of a capacitor system, with NiFe2O4 as the dielectric material. The biosensor system was tested towards different biological materials with the help of electrochemical workstation and the same was analysed through Cole-Cole plot of NiFe2O4. The performance of the sensor was determined based on its sensitivity, response time and recovery time.

  5. A facile microwave synthetic route for ferrite nanoparticles with direct impact in magnetic particle hyperthermia.

    PubMed

    Makridis, A; Chatzitheodorou, I; Topouridou, K; Yavropoulou, M P; Angelakeris, M; Dendrinou-Samara, C

    2016-06-01

    The application of ferrite magnetic nanoparticles (MNPs) in medicine finds its rapidly developing emphasis on heating mediators for magnetic hyperthermia, the ever-promising "fourth leg" of cancer treatment. Usage of MNPs depends largely on the preparation processes to select optimal conditions and effective routes to finely tailor MNPs. Microwave heating, instead of conventional heating offers nanocrystals at significantly enhanced rate and yield. In this work, a facile mass-production microwave hydrothermal synthetic approach was used to synthesize stable ferromagnetic manganese and cobalt ferrite nanoparticles with sizes smaller than 14nm from metal acetylacetonates in the presence of octadecylamine. Prolonging the reaction time from 15 to 60min, led to ferrites with improved crystallinity while the sizes are slight increased. The high crystallinity magnetic nanoparticles showed exceptional magnetic heating parameters. In vitro application was performed using the human osteosarcoma cell line Saos-2 incubated with manganese ferrite nanoparticles. Hyperthermia applied in a two cycle process, while AC magnetic field remained on until the upper limit of 45°C was achieved. The comparative results of the AC hyperthermia efficiency of ferrite nanoparticles in combination with the in vitro study coincide with the magnetic features and their tunability may be further exploited for AC magnetic hyperthermia driven applications. PMID:27040263

  6. Copper ferrite nanoparticle-induced cytotoxicity and oxidative stress in human breast cancer MCF-7 cells.

    PubMed

    Ahamed, Maqusood; Akhtar, Mohd Javed; Alhadlaq, Hisham A; Alshamsan, Aws

    2016-06-01

    Copper ferrite (CuFe2O4) nanoparticles (NPs) are important magnetic materials currently under research due to their applicability in nanomedicine. However, information concerning the biological interaction of copper ferrite NPs is largely lacking. In this study, we investigated the cellular response of copper ferrite NPs in human breast cancer (MCF-7) cells. Copper ferrite NPs were prepared by co-precipitation technique with the thermal effect. Prepared NPs were characterized by X-ray diffraction (XRD), field emission transmission electron microscopy (FETEM) and dynamic light scattering (DLS). Characterization data showed that copper ferrite NPs were crystalline, spherical with smooth surfaces and average diameter of 15nm. Biochemical studies showed that copper ferrite NPs induce cell viability reduction and membrane damage in MCF-7 cells and degree of induction was dose- and time-dependent. High SubG1 cell population during cell cycle progression and MMP loss with a concomitant up-regulation of caspase-3 and caspase-9 genes suggested that copper ferrite NP-induced cell death through mitochondrial pathway. Copper ferrite NP was also found to induce oxidative stress in MCF-7 cells as indicated by reactive oxygen species (ROS) generation and glutathione depletion. Cytotoxicity due to copper ferrite NPs exposure was effectively abrogated by N-acetyl-cysteine (ROS scavenger) suggesting that oxidative stress could be the plausible mechanism of copper ferrite NPs toxicity. Further studies are underway to explore the toxicity mechanisms of copper ferrite NPs in different types of human cells. This study warrants further generation of extensive biointeraction data before their application in nanomedicine. PMID:26925725

  7. Transition metal-substituted cobalt ferrite nanoparticles for biomedical applications.

    PubMed

    Sanpo, Noppakun; Berndt, Christopher C; Wen, Cuie; Wang, James

    2013-03-01

    Transition metals of copper, zinc, chromium and nickel were substituted into cobalt ferrite nanoparticles via a sol-gel route using citric acid as a chelating agent. The microstructure and elemental composition were characterized using scanning electron microscopy combined with energy-dispersive X-ray spectroscopy. Phase analysis of transition metal-substituted cobalt ferrite nanoparticles was performed via X-ray diffraction. Surface wettability was measured using the water contact angle technique. The surface roughness of all nanoparticles was measured using profilometry. Moreover, thermogravimetric analysis and differential scanning calorimetry were performed to determine the temperature at which the decomposition and oxidation of the chelating agents took place. Results indicated that the substitution of transition metals influences strongly the microstructure, crystal structure and antibacterial property of the cobalt ferrite nanoparticles. PMID:23137676

  8. Exchange spring like magnetic behavior in cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Chithra, M.; Anumol, C. N.; Sahu, Baidyanath; Sahoo, Subasa C.

    2016-03-01

    Cobalt ferrite nanoparticles were prepared by sol-gel technique and were annealed at 900 °C in air for 2 h. Structural properties were studied by X-ray diffraction, Raman spectroscopy and Fourier transformed infrared spectroscopy. Scanning electron microscopy and transmission electron microscopy studies show presence of mostly two different sizes of grains in these samples. Magnetization value of 58.36 emu/g was observed at 300 K for the as prepared sample and an enhanced magnetization close to the bulk value of 80.59 emu/g was observed for the annealed sample. At 10 K a two stepped hysteresis loop showing exchange spring magnetic behavior was observed accompanied by very high values of coercivity and remanence. Two clear peaks were observed in the derivative of demagnetization curve in the as prepared sample where as two partially overlapped peaks were observed in the annealed sample. The observed magnetic properties can be understood on the basis of the grain size and their distribution leading to the different types of intergranular interactions in these nanoparticles.

  9. An Approach for Enhancement of Saturation Magnetization in Cobalt Ferrite Nanoparticles by Incorporation of Terbium Cation

    NASA Astrophysics Data System (ADS)

    Sodaee, Tahmineh; Ghasemi, Ali; Paimozd, Ebrahim; Paesano, Andrea; Morisako, Akimitsu

    2013-09-01

    Cobalt ferrite nanoparticles were synthesized by a reverse micelle process. The optimum processing conditions required to fabricate nanocrystalline cobalt ferrite using a reverse micelle technique, especially the effect of water-to-surfactant molar ratios including w = 8, 10, 12, and 14, pH values in the range of 8 to 11, and annealing temperatures in the range of 400°C to 800°C, were evaluated. x-Ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), vibrating-sample magnetometry, and superconducting quantum interference device analysis were employed to evaluate the structural and magnetic properties of synthesized nanoparticles. XRD analysis confirms that the nanoparticles have a single-phase cubic spinel structure. The average particle size increases with increasing pH value and annealing temperature. Magnetization study reveals that the cobalt ferrite nanoparticles exhibit a superparamagnetic trend. The zero-field-cooled magnetization curves of cobalt ferrite nanoparticles indicated that, with an increase in pH value, the blocking temperature increases. Based on the obtained optimum parameters, terbium-substituted cobalt ferrite nanoparticles with composition CoFe2- x Tb x O4 ( x = 0.1 to 0.5) were prepared by a reverse micelle process. XRD and field-emission scanning electron microscopy evaluation demonstrated that single-phase spinel ferrites with narrow size distribution were obtained. Mössbauer spectroscopy was used to determine the site preference of terbium cation. The results confirm that terbium cations were distributed at tetrahedral and octahedral sites, but with a preference for the former. It was observed that, with an increase in terbium content, the saturation magnetization increases.

  10. Investigation of structural, thermal and magnetic properties of cadmium substituted cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Venkata Reddy, Ch.; Byon, Chan; Narendra, B.; Baskar, D.; Srinivas, G.; Shim, Jaesool; Prabhakar Vattikuti, S. V.

    2015-06-01

    Cd substituted Cobalt ferrite nano particles are synthesis using co-precipitation method. The as prepared samples are calcinated at 300 and 600 °C respectively. The existence of single phase spinal cubic structure of the prepared ferrite material is confirmed by the powder XRD measurement. The surface morphology images, compositional features are studied by SEM with EDX, and TEM. From the FT-IR spectra the absorption bands observed at 595 and 402 cm-1 are attributed to vibrations of tetrahedral and octahedral complexes respectively. From the VSM data, parameters like magnetization, coercivity, remanent magnetization and remanent squareness are measured. The saturation magnetization value is increases with increasing calcination temperature. The DSC and TG-DTA curves reveal that the thermal stability of the prepared ferrite nanoparticles. The calcination temperature affects the crystallite size, morphology and magnetic properties of the samples.

  11. Dielectric properties of cobalt ferrite nanoparticles in ultrathin nanocomposite films.

    PubMed

    Alcantara, Gustavo B; Paterno, Leonardo G; Fonseca, Fernando J; Pereira-da-Silva, Marcelo A; Morais, Paulo C; Soler, Maria A G

    2013-12-01

    Multilayered nanocomposite films (thickness 50-90 nm) of cobalt ferrite nanoparticles (np-CoFe2O4, 18 nm) were deposited on top of interdigitated microelectrodes by the layer-by-layer technique in order to study their dielectric properties. For that purpose, two different types of nanocomposite films were prepared by assembling np-CoFe2O4 either with poly(3,4-ethylenedioxy thiophene):poly(styrene sulfonic acid) or with polyaniline and sulfonated lignin. Despite the different film architectures, the morphology of both was dominated by densely-packed layers of nanoparticles surrounded by polyelectrolytes. The dominant effect of np-CoFe2O4 was also observed after impedance spectroscopy measurements, which revealed that dielectric behavior of the nanocomposites was largely influenced by the charge transport across nanoparticle-polyelectrolyte interfaces. For example, nanocomposites containing np-CoFe2O4 exhibited a single low-frequency relaxation process, with time constants exceeding 15 ms. At 1 kHz, the dielectric constant and the dissipation factor (tan δ) of these nanocomposites were 15 and 0.15, respectively. These values are substantially inferior to those reported for pressed pellets made exclusively of similar nanoparticles. Impedance data were further fitted with equivalent circuit models from which individual contributions of particle's bulk and interfaces to the charge transport within the nanocomposites could be evaluated. The present study evidences that such nanocomposites display a dielectric behavior dissimilar from that exhibited by their individual counterparts much likely due to enlarged nanoparticle-polyelectrolyte interfaces. PMID:24145704

  12. Ferrite Nanoparticles, Films, Single Crystals, and Metamaterials: High Frequency Applications

    SciTech Connect

    Harris,V.

    2006-01-01

    Ferrite materials have long played an important role in power conditioning, conversion, and generation across a wide spectrum of frequencies (up to ten decades). They remain the preferred magnetic materials, having suitably low losses, for most applications above 1 MHz, and are the only viable materials for nonreciprocal magnetic microwave and millimeter-wave devices (including tunable filters, isolators, phase shifters, and circulators). Recently, novel processing techniques have led to a resurgence of research interest in the design and processing of ferrite materials as nanoparticles, films, single crystals, and metamaterials. These latest developments have set the stage for their use in emerging technologies that include cancer remediation therapies such as magnetohyperthermia, magnetic targeted drug delivery, and magneto-rheological fluids, as well as enhanced magnetic resonance imaging. With reduced dimensionality of nanoparticles and films, and the inherent nonequilibrium nature of many processing schemes, changes in local chemistry and structure have profound effects on the functional properties and performance of ferrites. In this lecture, we will explore these effects upon the fundamental magnetic and electronic properties of ferrites. Density functional theory will be applied to predict the properties of these ferrites, with synchrotron radiation techniques used to elucidate the chemical and structural short-range order. This approach will be extended to study the atomic design of ferrites by alternating target laser-ablation deposition. Recently, this approach has been shown to produce ferrites that offer attractive properties not found in conventionally grown ferrites. We will explore the latest research developments involving ferrites as related to microwave and millimeter-wave applications and the attempt to integrate these materials with semiconductor materials platforms.

  13. The role of cobalt ferrite magnetic nanoparticles in medical science.

    PubMed

    Amiri, S; Shokrollahi, H

    2013-01-01

    The nanotechnology industry is rapidly growing and promises that the substantial changes that will have significant economic and scientific impacts be applicable to a wide range of areas, such as aerospace engineering, nano-electronics, environmental remediation and medical healthcare. In this area, cobalt ferrite nanoparticles have been regarded as one of the competitive candidates because of their suitable physical, chemical and magnetic properties like the high anisotropy constant, high coercivity and high Curie temperature, moderate saturation magnetization and ease of synthesis. This paper introduces the magnetic properties, synthesis methods and some medical applications, including the hyperthermia, magnetic resonance imaging (MRI), magnetic separation and drug delivery of cobalt ferrite nanoparticles. PMID:25428034

  14. Corrosion behavior of magnetic ferrite coating prepared by plasma spraying

    SciTech Connect

    Liu, Yi; Wei, Shicheng Tong, Hui; Tian, Haoliang; Liu, Ming; Xu, Binshi

    2014-12-15

    Graphical abstract: The saturation magnetization (M{sub s}) of the ferrite coating is 34.417 emu/g while the M{sub s} value of the ferrite powder is 71.916 emu/g. It can be seen that plasma spray process causes deterioration of the room temperature soft magnetic properties. - Highlights: • Spinel ferrite coatings have been prepared by plasma spraying. • The coating consists of nanocrystalline grains. • The saturation magnetization of the ferrite coating is 34.417 emu/g. • Corrosion behavior of the ferrite coating was examined in NaCl solution. - Abstract: In this study, spray dried spinel ferrite powders were deposited on the surface of mild steel substrate through plasma spraying. The structure and morphological studies on the ferrite coatings were carried out using X-ray diffraction, scanning electron microscope and Raman spectroscopy. It was showed that spray dried process was an effective method to prepare thermal spraying powders. The coating showed spinel structure with a second phase of LaFeO{sub 3}. The magnetic property of the ferrite samples were measured by vibrating sample magnetometer. The saturation magnetization (M{sub s}) of the ferrite coating was 34.417 emu/g. The corrosion behavior of coating samples was examined by electrochemical impedance spectroscopy. EIS diagrams showed three corrosion processes as the coating immersed in 3.5 wt.% NaCl solution. The results suggested that plasma spraying was a promising technology for the production of magnetic ferrite coatings.

  15. High-Performance Ferrite Nanoparticles through Nonaqueous Redox Phase Tuning.

    PubMed

    Chen, Ritchie; Christiansen, Michael G; Sourakov, Alexandra; Mohr, Alan; Matsumoto, Yuri; Okada, Satoshi; Jasanoff, Alan; Anikeeva, Polina

    2016-02-10

    From magnetic resonance imaging to cancer hyperthermia and wireless control of cell signaling, ferrite nanoparticles produced by thermal decomposition methods are ubiquitous across biomedical applications. While well-established synthetic protocols allow for precise control over the size and shape of the magnetic nanoparticles, structural defects within seemingly single-crystalline materials contribute to variability in the reported magnetic properties. We found that stabilization of metastable wüstite in commonly used hydrocarbon solvents contributed to significant cation disorder, leading to nanoparticles with poor hyperthermic efficiencies and transverse relaxivities. By introducing aromatic ethers that undergo radical decomposition upon thermolysis, the electrochemical potential of the solvent environment was tuned to favor the ferrimagnetic phase. Structural and magnetic characterization identified hallmark features of nearly defect-free ferrite nanoparticles that could not be demonstrated through postsynthesis oxidation with nearly 500% increase in the specific loss powers and transverse relaxivity times compared to similarly sized nanoparticles containing defects. The improved crystallinity of the nanoparticles enabled rapid wireless control of intracellular calcium. Our work demonstrates that redox tuning during solvent thermolysis can generate potent theranostic agents through selective phase control in ferrites and can be extended to other transition metal oxides relevant to memory and electrochemical storage devices. PMID:26756463

  16. 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.

  17. Effect of heat treatment on microwave absorption properties of Ni-Zn-Mg-La ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Liu, Yi; Wei, Shicheng; Xu, Binshi; Wang, Yujiang; Tian, Haoliang; Tong, Hui

    2014-01-01

    Spinel structure Ni-Zn-Mg-La ferrites have been prepared by the sol-gel route and investigated as a radar absorbing material (RAM) in a frequency range of 1-18 GHz. The structure and morphological studies on the nanoparticles of the ferrites have been carried out using X-ray diffraction, scanning electron microscopy and X-ray photoelectron spectroscopy. The complex permeability and complex permittivity are measured by a network analyzer. The electromagnetic wave loss and microwave absorbing property are studied as a function of frequency, annealing temperature and thickness of the absorber. The results indicate that electromagnetic wave loss of the ferrite only annealed at 850 °C shows two peaks. The reflection loss varies with the change of the annealing temperature. The absorber annealed at 850 °C exhibits the best microwave absorbing properties, which is suitable for microwave absorption materials.

  18. Oriented attachment explains cobalt ferrite nanoparticle growth in bioinspired syntheses.

    PubMed

    Wolff, Annalena; Hetaba, Walid; Wißbrock, Marco; Löffler, Stefan; Mill, Nadine; Eckstädt, Katrin; Dreyer, Axel; Ennen, Inga; Sewald, Norbert; Schattschneider, Peter; Hütten, Andreas

    2014-01-01

    Oriented attachment has created a great debate about the description of crystal growth throughout the last decade. This aggregation-based model has successfully described biomineralization processes as well as forms of inorganic crystal growth, which could not be explained by classical crystal growth theory. Understanding the nanoparticle growth is essential since physical properties, such as the magnetic behavior, are highly dependent on the microstructure, morphology and composition of the inorganic crystals. In this work, the underlying nanoparticle growth of cobalt ferrite nanoparticles in a bioinspired synthesis was studied. Bioinspired syntheses have sparked great interest in recent years due to their ability to influence and alter inorganic crystal growth and therefore tailor properties of nanoparticles. In this synthesis, a short synthetic version of the protein MMS6, involved in nanoparticle formation within magnetotactic bacteria, was used to alter the growth of cobalt ferrite. We demonstrate that the bioinspired nanoparticle growth can be described by the oriented attachment model. The intermediate stages proposed in the theoretical model, including primary-building-block-like substructures as well as mesocrystal-like structures, were observed in HRTEM measurements. These structures display regions of substantial orientation and possess the same shape and size as the resulting discs. An increase in orientation with time was observed in electron diffraction measurements. The change of particle diameter with time agrees with the recently proposed kinetic model for oriented attachment. PMID:24605288

  19. Size-dependent magnetic properties of calcium ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Khanna, Lavanya; Verma, N. K.

    2013-06-01

    The union of nanotechnology with the other fields of science heralds the influx of many newer and better technologies, with the capability to revolutionize the human life. In the present work, calcium ferrite nanoparticles were synthesized by conventional sol-gel method and were characterised by X-ray diffraction, Transmission electron microscope, Vibrating sample magnetometer and Fourier transform infrared spectroscope. The synthesized nanoparticles were calcined at different temperatures and their magnetic behaviour was studied. The synthesized nanoparticles calcined at 900 °C were formed in the shape of capsules and exhibited mixed characteristics of ferrimagnetic and paramagnetic grains with magnetic saturation of 0.85 emu/g whereas nanoparticles calcined at 500 °C were spherical in shape and exhibited superparamagnetic characteristics with saturation magnetization of 37.67 emu/g.

  20. Preparation of highly anisotropic cobalt ferrite/silica microellipsoids using an external magnetic field.

    PubMed

    Abramson, Sébastien; Dupuis, Vincent; Neveu, Sophie; Beaunier, Patricia; Montero, David

    2014-08-01

    Magnetic cobalt ferrite/silica microparticles having both an original morphology and an anisotropic nanostructure are synthesized through the use of an external magnetic field and nanoparticles characterized by a high magnetic anisotropy. The association of these two factors implies that the ESE (emulsion and solvent evaporation) sol-gel method employed here allows the preparation of silica microellipsoids containing magnetic nanoparticles aggregated in large chains. It is clearly shown that without this combination, microspheres characterized by an isotropic distribution of the magnetic nanoparticles are obtained. While the chaining of the cobalt ferrite nanoparticles inside the silica matrix is related to the increase of their magnetic dipolar interactions, the ellipsoidal shape of the microparticles may be explained by the elongation of the sol droplets in the direction of the external magnetic field during the synthesis. Because of their highly anisotropic structure, these microparticles exhibit permanent magnetic moments, which are responsible, at a larger scale, for the existence of strong magnetic dipolar interactions. Therefore, when they are dispersed in water, the microellipsoids self-assemble into large and irregular chains. These interactions can be reinforced by the use of external magnetic field, allowing the preparation of very large permanent chains. This research illustrates how nanostructured particles exhibiting complex architectures can be elaborated through simple, fast, and low-cost methods, such as the use of external fields in combination with soft chemistry. PMID:25029515

  1. Micro Raman, Mossbauer and magnetic studies of manganese substituted zinc ferrite nanoparticles: Role of Mn

    NASA Astrophysics Data System (ADS)

    Thota, Suneetha; Kashyap, Subhash C.; Sharma, Shiv K.; Reddy, V. R.

    2016-04-01

    A series of Mn-Zn Ferrite nanoparticles (<15 nm) with formula MnxZn1-xFe2O4 (where x=0.00, 0.35, 0.50, 0.65) were successfully prepared by citrate-gel method at low temperature (400 °C). X-ray diffraction analysis confirmed the formation of single cubic spinel phase in these nanoparticles. The FESEM and TEM micrographs revealed the nanoparticles to be nearly spherical in shape and of fairly uniform size. The fractions of Mn2+, Zn2+ and Fe3+ cations occupying tetrahedral sites along with Fe occupying octahedral sites within the unit cell of different ferrite samples are estimated by room temperature micro-Raman spectroscopy. Low temperature Mossbauer measurement on Mn0.5Zn0.5Fe2O4 has reconfirmed the mixed spinel phase of these nanoparticles. Room temperature magnetization studies (PPMS) of Mn substituted samples showed superparamagnetic behavior. Manganese substitution for Zn in the ferrite caused the magnetization to increase from 04 to18 emu/g and Lande's g factor (estimated from ferromagnetic resonance measurement) from 2.02 to 2.12 when x was increased up to 0.50. The FMR has shown that higher Mn cationic substitution leads to increase in dipolar interaction and decrease in super exchange interaction. Thermomagnetic (M-T) and magnetization (M-H) measurements have shown that the increase in Mn concentration (up to x=0.50) enhances the spin ordering temperature up to 150 K (blocking temperature). Magnetocrystalline anisotropy in the nanoparticles was established by Mossbauer, ferromagnetic resonance and thermomagnetic measurements. The optimized substitution of manganese for zinc improves the magnetic properties and makes these nanoparticles a potential candidate for their applications in microwave region and biomedical field.

  2. Comparison of surface effects in SiO2 coated and uncoated nickel ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Nadeem, K.; Krenn, H.; Sarwar, W.; Mumtaz, M.

    2014-01-01

    Magnetic properties of uncoated and silica coated nickel ferrite nanoparticles of comparable sizes have been studied in detail. Silica coated and uncoated nanoparticles were prepared by sol-gel and co-precipitation methods, respectively. Average crystallite size determined by X-ray diffraction is 12 nm and 14 nm for the silica coated and uncoated nanoparticles, respectively. Normalized saturation magnetization value of the coated nanoparticles was found to be lower than of uncoated nanoparticles, while a comparable small coercivity is observed for both the samples. Zero field cooled/field cooled (ZFC/FC) measurements reveal that the average blocking temperature (TB) of coated nanoparticles is lower than of the uncoated nanoparticles and is shifted to lower temperatures at high field. Thermoremanent magnetization (TRM) measurement indicates that the relaxation of coated nanoparticles have not been influenced very much with increasing cooling field as compared to uncoated nanoparticles and is attributed to enhanced surface effects in coated nanoparticles. The main source of enhanced surface effects in the coated nanoparticles is foremost disordered surface spins due to silica matrix. Temperature dependent AC susceptibility exhibits two peaks for the coated nanoparticles' sample. First peak corresponds to blocking of huge core spin while second peak at lower temperature is may be due to enhanced surface effects (spin-glass behavior). All these findings such as lower saturation magnetization, faster shift of blocking temperature at high field, small effect of high magnetic field on magnetic relaxation, low temperature out-of-phase AC susceptibility peak for the coated nanoparticles signify enhanced surface effects in them as compared to uncoated nanoparticles.

  3. Surface effects in the magnetic properties of crystalline 3 nm ferrite nanoparticles chemically synthesized

    NASA Astrophysics Data System (ADS)

    Lima, E.; De Biasi, E.; Mansilla, M. Vasquez; Saleta, M. E.; Effenberg, F.; Rossi, L. M.; Cohen, R.; Rechenberg, H. R.; Zysler, R. D.

    2010-11-01

    We have systematically studied the magnetic properties of ferrite nanoparticles with 3, 7, and 11 nm of diameter with very narrow grain size distributions. Samples were prepared by the thermal decomposition of Fe(acac)3 in the presence of surfactants giving nanoparticles covered by oleic acid. High resolution transmission electron microscopy (HRTEM) images and XRD diffraction patterns confirms that all samples are composed by crystalline nanoparticles with the spinel structure expected for the iron ferrite. ac and dc magnetization measurements, as well in-field Mössbauer spectroscopy, indicate that the magnetic properties of nanoparticles with 11 and 7 nm are close to those expected for a monodomain, presenting large MS (close to the magnetite bulk). Despite the crystalline structure observed in HRTEM images, the nanoparticles with 3 nm are composed by a magnetically ordered region (core) and a surface region that presents a different magnetic order and it contains about 66% of Fe atoms. The high saturation and irreversibility fields in the M(H ) loops of the particles with 3 nm together with the misalignment at 120 kOe in the in-field Mössbauer spectrum of surface component indicate a high surface anisotropy for the surface atoms, which is not observed for the core. For T <10 K, we observe an increase in the susceptibility and of the magnetization for former sample, indicating that surface moments tend to align with applied field increasing the magnetic core size.

  4. Structural, dielectric and gas sensing behavior of Mn substituted spinel MFe2O4 (M=Zn, Cu, Ni, and Co) ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Ranjith Kumar, E.; Siva Prasada Reddy, P.; Sarala Devi, G.; Sathiyaraj, S.

    2016-01-01

    Spinel ferrite (MnZnFe2O4, MnCuFe2O4, MnNiFe2O4 and MnCoFe2O4) nanoparticles have been prepared by evaporation method. The annealing temperature plays an important role on changing particle size of the spinel ferrite nanoparticles was found out by X-ray diffraction and transmission electron microscopy. The role of manganese substitution in the spinel ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in dielectric properties have been measured in the frequency range of 100 kHz to 5 MHz. These spinel ferrites are decomposed to α-Fe2O3 after annealing above 550 °C in air. Through the characterization of the prepared powder, the effect of annealing temperature, chemical composition and preparation technique on the microstructure, particle size and dielectric properties of the Mn substituted spinel ferrite nanoparticles are discussed. Furthermore, Conductance response of Mn substituted MFe2O4 ferrite nanoparticles were measured by exposing the materials to reducing gas like liquefied petroleum gas (LPG).

  5. Cr(3+) substituted spinel ferrite nanoparticles with high coercivity.

    PubMed

    Zhang, Wei; Zuo, Xudong; Zhang, Dongmei; Wu, Chengwei; Silva, S Ravi P

    2016-06-17

    The low coercivity of spinel ferrites is a major barrier that significantly limits their use in high density magnetic recording applications. By controlling the substituting content of Cr(3+), in this article we describe how magnetic CoCr x Fe2-x O4 (0 < x < 1.2) nanoparticles with coercivity of up to 6.4 kOe were successfully obtained by the hydrothermal process. The high coercivity is attributed to the synergetic effects of magnetocrystalline anisotropy and the nanoscale size effect. X-ray diffraction analysis confirmed the spinel structure of the nanoparticles with transmission electron microscopy (TEM) suggesting regular tetragonal morphology. The TEM indicated an edge length ranging from 15 nm to 150 nm, which increases monotonically with increasing Cr content. Raman analyses supported the proposed model on the formation mechanism of the nanoparticles, i.e. heterogeneous and homogeneous nucleation. PMID:27159283

  6. Magnetic relaxation/stability of Co ferrite nanoparticles embedded in amorphous silica particles

    NASA Astrophysics Data System (ADS)

    Caizer, C.; ?ura, V.

    2006-06-01

    The investigated system consisted of Co ferrite nanoparticles embedded in amorphous SiO 2 particles, with ?=1% magnetic volume fraction. The M- H curve ( M is the magnetization and H is the external magnetic field) of the particle system, recorded at room temperature using a 50 Hz alternating magnetic field, showed a very wide hysteresis loop indicating a strong deviation from the theoretical Langevin curve. The structural phases and mean diameter of the nanoparticles were determined by X-ray diffraction and transmission electron microscopy. Structural analysis results and theoretical evaluations of the critical diameter under which the particle has a single-domain magnetic structure suggested that the factor accounting for the observed behavior is a high magnetic anisotropy (anisotropy constant around 1.610 5 Jm -3); even the volume of Co ferrite nanoparticles is within the superparamagnetic range. The observed behavior was explained assuming that the magnetic moments of nanoparticles could be blocked even at room temperature, due to the existence of a high (0.64 eV) energy barrier which cannot be exceeded by thermal activation alone (0.03 eV). The magnetic relaxation time (?=2.510-1 s) evaluated from experimental data was much longer than the experiment time (t=210-2 s), in agreement with the observed magnetic remanence. The Co ferrite nanoparticles embedded in amorphous SiO 2 showed stable magnetic single-domain structure in a very wide range of diameters (7.6-162 nm), and the particle shape appeared to be unimportant due to the high magnetic anisotropy. The results reported in the present paper demonstrate the existence of a relatively simple preparation method of interesting magnetic nanomaterials with potential application for magnetic recording media.

  7. Oxidative stress mediated apoptosis induced by nickel ferrite nanoparticles in cultured A549 cells.

    PubMed

    Ahamed, Maqusood; Akhtar, Mohd Javed; Siddiqui, Maqsood A; Ahmad, Javed; Musarrat, Javed; Al-Khedhairy, Abdulaziz A; AlSalhi, Mohamad S; Alrokayan, Salman A

    2011-05-10

    Due to the interesting magnetic and electrical properties with good chemical and thermal stabilities, nickel ferrite nanoparticles are being utilized in many applications including magnetic resonance imaging, drug delivery and hyperthermia. Recent studies have shown that nickel ferrite nanoparticles produce cytotoxicity in mammalian cells. However, there is very limited information concerning the toxicity of nickel ferrite nanoparticles at the cellular and molecular level. The aim of this study was to investigate the cytotoxicity, oxidative stress and apoptosis induction by well-characterized nickel ferrite nanoparticles (size 26 nm) in human lung epithelial (A549) cells. Nickel ferrite nanoparticles induced dose-dependent cytotoxicity in A549 cells demonstrated by MTT, NRU and LDH assays. Nickel ferrite nanoparticles were also found to induce oxidative stress evidenced by generation of reactive oxygen species (ROS) and depletion of antioxidant glutathione (GSH). Further, co-treatment with the antioxidant L-ascorbic acid mitigated the ROS generation and GSH depletion due to nickel ferrite nanoparticles suggesting the potential mechanism of oxidative stress. Quantitative real-time PCR analysis demonstrated that following the exposure of A549 cells to nickel ferrite nanoparticles, the level of mRNA expressions of cell cycle checkpoint protein p53 and apoptotic proteins (bax, caspase-3 and caspase-9) were significantly up-regulated, whereas the expression of anti-apoptotic proteins (survivin and bcl-2) were down-regulated. Moreover, activities of caspase-3 and caspase-9 enzymes were also significantly higher in nickel ferrite nanoparticles exposed cells. To the best of our knowledge this is the first report showing that nickel ferrite nanoparticles induced apoptosis in A549 cells through ROS generation and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways. PMID:21382431

  8. Preparation and magnetic properties of nano size nickel ferrite particles using hydrothermal method

    PubMed Central

    2012-01-01

    Background Nickel ferrite, a kind of soft magnetic materials is one of the most attracting class of materials due to its interesting and important properties and has many technical applications, such as in catalysis, sensors and so on. In this paper the synthesis of NiFe2O4 nanoparticles by the hydrothermal method is reported and the inhibition of surfactant (Glycerol or Sodium dodecyl sulfate) on the particles growth is investigated. Methods For investigation of the inhibition effect of surfactant on NiFe2O4 particles growth, the samples were prepared in presence of Glycerol and Sodium dodecyl sulfate. The X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM) and inductively coupled plasma atomic emission spectrometer (ICP-AES) techniques were used to characterize the samples. Results The results of XRD and ICP-AES show that the products were pure NiFe2O4 and also nanoparticles grow with increasing the temperature, while surfactant prevents the particle growth under the same condition. The average particle size was determined from the Scherrer's equation and TEM micrographs and found to be in the range of 50-60 nm that decreased up to 10-15 nm in presence of surfactant. The FT-IR results show two absorption bands near to 603 and 490 cm-1 for the tetrahedral and octahedral sites respectively. Furthermore, the saturated magnetization and coercivity of NiFe2O4 nanoparticles were in the range of 39.60 emu/g and 15.67 Qe that decreased for samples prepared in presence of surfactant. As well as, the nanoparticles exhibited a superparamagnetic behavior at room temperature. Conclusions Nanosized nickel ferrite particles were synthesized with and without surfactant assisted hydrothermal methods. The results show that with increasing of temperature, the crystallinity of nanoparticles is increased. In the presence of surfactants, the crystallinity of NiFe2O4 nanoparticles decreased in comparison with surfactant- free prepared samples. All of the nickel ferrite nanoparticles were superparamagnetic at room temperature. Graphical abstract PMID:22462726

  9. Influence of spherical assembly of copper ferrite nanoparticles on magnetic properties: orientation of magnetic easy axis.

    PubMed

    Chatterjee, Biplab K; Bhattacharjee, Kaustav; Dey, Abhishek; Ghosh, Chandan K; Chattopadhyay, Kalyan K

    2014-06-01

    The magnetic properties of copper ferrite (CuFe2O4) nanoparticles prepared via sol-gel auto combustion and facile solvothermal method are studied focusing on the effect of nanoparticle arrangement. Randomly oriented CuFe2O4 nanoparticles (NP) are obtained from the sol-gel auto combustion method, while the solvothermal method allows us to prepare iso-oriented uniform spherical ensembles of CuFe2O4 nanoparticles (NS). X-ray diffractometry (XRD), atomic absorption spectroscopy (AAS), infra-red (IR) spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), (57)Fe Mössbauer spectroscopy and vibrating sample magnetometer (VSM) are used to investigate the composition, microstructure and magnetic properties of as-prepared ferrite nanoparticles. The field-dependent magnetization measurement for the NS sample at low temperature exhibits a step-like rectangular hysteresis loop (M(R)/M(S) ~ 1), suggesting cubic anisotropy in the system, whereas for the NP sample, typical features of uniaxial anisotropy (M(R)/M(S) ~ 0.5) are observed. The coercive field (HC) for the NS sample shows anomalous temperature dependence, which is correlated with the variation of effective anisotropy (K(E)) of the system. A high-temperature enhancement of H(C) and K(E) for the NS sample coincides with a strong spin-orbit coupling in the sample as evidenced by significant modification of Cu/Fe-O bond distances. The spherical arrangement of nanocrystals at mesoscopic scale provokes a high degree of alignment of the magnetic easy axis along the applied field leading to a step-like rectangular hysteresis loop. A detailed study on the temperature dependence of magnetic anisotropy of the system is carried out, emphasizing the influence of the formation of spherical iso-oriented assemblies. PMID:24714977

  10. Cobalt ferrite nanoparticles in a mesoporous silicon dioxide matrix

    NASA Astrophysics Data System (ADS)

    Komogortsev, S. V.; Patrusheva, T. N.; Balaev, D. A.; Denisova, E. A.; Ponomarenko, I. V.

    2009-10-01

    We have studied magnetic nanoparticles of cobalt ferrite obtained by the extraction-pyrolysis method in a mesoporous silicon dioxide (MSM-41) molecular sieve matrix. The X-ray diffraction data show evidence for the formation of CoFe2O4 particles with a coherent scattering domain size of ˜40 nm. Measurements of the magnetization curves showed that powders consisting of these nanoparticles are magnetically hard materials with a coercive field of H c(4.2 K) = 9.0 kOe and H c(300 K) = 1.8 kOe and a reduced remanent magnetization of M r/ M s(4.2 K) = 0.83 and M r/ M s(300 K) = 0.49. The shape of the low-temperature (4.2 K) magnetization curves is adequately described in terms of the Stoner-Wohlfarth model for randomly oriented single-domain particles with a cubic magnetic anisotropy.

  11. Hydrothermal synthesis of fine stabilized superparamagnetic nanoparticles of Zn2+ substituted manganese ferrite

    NASA Astrophysics Data System (ADS)

    Zahraei, Maryam; Monshi, Ahmad; Morales, Maria del Puerto; Shahbazi-Gahrouei, Daryoush; Amirnasr, Mehdi; Behdadfar, Behshid

    2015-11-01

    Superparamagnetic Zn2+ substituted manganese ferrite Mn1-xZnxFe2O4 (x=0.3, 0.35, 0.4 and 0.45) nanoparticles (NPs) were synthesized via a direct, efficient and environmental friendly hydrothermal method. The synthesized NPs were characterized by X-ray powder diffractometry (XRD), transmission electron microscopy (TEM), thermo-gravimetry (TG) and vibrating sample magnetometry (VSM). The effects of various parameters such as the pH of reaction mixture, time and temperature of hydrothermal treatment and Zn substitution on the spinel phase formation, the magnetization, and the size of resulting NPs are discussed. The Zn2+ substituted manganese ferrite NPs obtained from hydrothermal process crystallized mainly in the spinel phase. Nevertheless, without citrate ions, the hematite phase appeared in the product. The monophase Zn2+ substituted manganese ferrite NPs hydrothermally prepared in the presence of citric acid had mean particle size of 7 nm and a narrow size distribution. Furthermore, the synthesized NPs can be used to prepare ferrofluids for biomedical applications due to their small size, good stability in aqueous medium (pH 7) and also high magnetization value.

  12. Polyethylene glycol coated CoFe2O4 nanoparticles: A potential spinel ferrite for biomedical applications

    NASA Astrophysics Data System (ADS)

    Humbe, Ashok V.; Birajdar, Shankar D.; Bhandari, J. M.; Waghule, N. N.; Bhagwat, V. R.; Jadhav, K. M.

    2015-06-01

    The structural and magnetic properties of the polyethylene glycol (PEG) coated cobalt spinel ferrite (CoFe2O4) nanoparticles have been reported in the present study. CoFe2O4 nanoparticles were prepared by sol-gel auto-combustion method using citric acid + ethylene glycol as a fuel. The prepared powder of cobalt ferrite nanoparticles was annealed at 600°C for 6h and used for further study. The structural characterization of CoFe2O4 nanoparticles were carried out by X-ray diffraction technique. The X-ray analysis confirmed the formation of single phase cubic spinel structure. The crystallite size, Lattice constant and X-ray density of the PEG coated CoFe2O4 nanoparticles were calculated by using XRD data. The presence of PEG on CoFe2O4 nanoparticles and reduced agglomeration in the CoFe2O4 nanoparticles were revealed by SEM studies. The magnetic properties were studied by pulse field hysteresis loop tracer technique at a room temperature. The magnetic parameters such as saturation magnetization, remanence magnetization, coercivity etc have been obtained. These magnetic parameters were get decreased by PEG coating.

  13. Photoacoustic and magnetoelastic property of cobalt ferrite nanoparticles and its attenuation with barium titanate coating

    NASA Astrophysics Data System (ADS)

    Betal, Soutik; Dutta, Moumita; Khachatryan, Edward; Cotica, Luiz; Nash, Kelly; Bhalla, Amar; Guo, Ruyan

    2015-08-01

    We report an experimental study, where Cobalt Ferrite (CoFe2O4) nanoparticles exhibit Photoacoustic (PA) emission peak intensity of 235.2V/J when analyzed under the Opto-Acoustic measurement setup. PA emission peak intensity decreases to 210V/J when AC Magnetic field is applied and further when Barium Titanate coated cobalt ferrite nanoparticles were analyzed, the PA peak further reduces to 68.76667V/J and with application of AC magnetic field the peak completely disappears. The measurement depicts the Photoacoustic and magnetoelastic behavior of cobalt ferrite nanoparticles.

  14. Effect of O-vacancies on magnetic properties of bismuth ferrite nanoparticles by solution evaporation method

    NASA Astrophysics Data System (ADS)

    Afzal, A. M.; Umair, M.; Dastgeer, G.; Rizwan, M.; Yaqoob, M. Z.; Rashid, R.; Munir, H. S.

    2016-02-01

    Bismuth ferrite is a multiferroic material which shows high magnetization and polarization at room temperature. In present work, the effect of Oxygen (O) vacancies on magnetic properties of bismuth ferrite nanoparticles is studied. Bismuth ferrite nanoparticles (BiFeO3) were synthesized by solution evaporation method (SEM) at room temperature. The sample was annealed under two different atmospheres such as in air and oxygen, to check the effect of O-vacancies on magnetic properties. The average crystallite size of Bismuth ferrite nanoparticles (NPs) as calculated by X-ray diffraction (XRD) falls in the range of 23-32 nm and 26-39 nm for the case of air and oxygen respectively. The crystallite size of bismuth ferrite nanoparticles increases as the temperature was varied from 450 °C to 650 °C. Further the influence of annealing temperature on the magnetic properties of the bismuth ferrite nanoparticles was also observed. It was concluded that the magnetic properties of Bismuth ferrite nanoparticles are directly interconnected to annealing atmosphere and annealing temperature. The magnetic properties were increased in the case of oxygen annealing, which actually leads in our case to an improvement of the crystallinity.

  15. Study of Zn-Cu Ferrite Nanoparticles for LPG Sensing

    PubMed Central

    Jain, Anuj; Baranwal, Ravi Kant; Bharti, Ajaya; Vakil, Z.; Prajapati, C. S.

    2013-01-01

    Nanostructured zinc-copper mixed ferrite was synthesized using sol-gel method. XRD patterns of different compositions of zinc-copper ferrite, Zn(1−x)CuxFe2O4 (x = 0.0, 0.25, 0.50, 0.75), revealed single phase inverse spinel ferrite in all the samples synthesized. With increasing copper concentration, the crystallite size was found to be increased from 28 nm to 47 nm. The surface morphology of all the samples studied by the Scanning Electron Microscopy there exhibits porous structure of particles throughout the samples. The pellets of the samples are prepared for LPG sensing characteristics. The sensing is carried out at different operating temperatures (200, 225, and 250°C) with the variation of LPG concentrations (0.2, 0.4, and 0.6 vol%). The maximum sensitivity of 55.33% is observed at 250°C operating for the 0.6 vol% LPG. PMID:23864833

  16. Room temperature optical and dielectric properties of Sr and Ni doped lanthanum ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Naseem, Swaleha; Khan, Wasi; Singh, B. R.; Naqvi, A. H.

    2015-06-01

    Strontium and nickel doped lanthanum ferrite (LaFeO3) nanoparticles (NPs) were prepared reverse micelle (RM) and calcinated at 700°C. Microstructural studies were carried by XRD and SEM/EDS techniques. The results of structural characterization show the formation of all samples in single phase without any impurity. Optical properties were studied by UV- visible spectroscopy and band gap energy was estimated 3.89 eV. Room temperature dielectric constant (ɛ') decreases abruptly at lower frequencies owing to the charge transport relaxation time. The observed behavior of the dielectric properties can be attributed on the basis of Koop's theory based on Maxwell-Wagner's two layer model in studied nanoparticles.

  17. Radiation induced structural and magnetic transformations in nanoparticle MnxZn(1-x)Fe2O4 ferrites

    NASA Astrophysics Data System (ADS)

    Naik, P. P.; Tangsali, R. B.; Sonaye, B.; Sugur, S.

    2015-07-01

    Nanoparticle magnetic materials are suitable for multiple modern high end medical applications like targeted drug delivery, gene therapy, hyperthermia and MR thermometry imaging. Majority of these applications are confined to use of Mn-Zn ferrite nanoparticles. These nanoparticles are normally left in the body after their requisite application. Preparing these nanoparticles is usually a much involved job. However with the development of the simple technique MnxZn1-xFe2O4 nanoparticles could be prepared with much ease. The nanoparticles of MnxZn1-xFe2O4 with (x=1.0, 0.7, 0.5, 0.3, 0.0) were prepared and irradiated with gamma radiation of various intensities ranging between 500 R to 10,000 R, after appropriate structural and magnetic characterization. Irradiated samples were investigated for structural and magnetic properties, as well as for structural stability and cation distribution. The irradiated nanoparticles exhibited structural stability with varied cation distribution and magnetic properties, dependent on gamma radiation dose. Surprisingly samples also exhibited quenching of lattice parameter and particle size. The changes introduced in the cation distribution, lattice constant, particle size and magnetic properties were found to be irreversible with time lapse and were of permanent nature exhibiting good stability even after several months. Thus the useful properties of nanoparticles could be enhanced on modifying the cation distribution inside the nanoparticles by application of gamma radiation.

  18. Cytotoxicity of nickel zinc ferrite nanoparticles on cancer cells of epithelial origin

    PubMed Central

    Al-Qubaisi, Mothanna Sadiq; Rasedee, Abdullah; Flaifel, Moayad Husein; Ahmad, Sahrim HJ; Hussein-Al-Ali, Samer; Hussein, Mohd Zobir; Eid, Eltayeb EM; Zainal, Zulkarnain; Saeed, Mohd; Ilowefah, Muna; Fakurazi, Sharida; Isa, Norhaszalina Mohd; Zowalaty, Mohamed Ezzat El

    2013-01-01

    In this study, in vitro cytotoxicity of nickel zinc (NiZn) ferrite nanoparticles against human colon cancer HT29, breast cancer MCF7, and liver cancer HepG2 cells was examined. The morphology, homogeneity, and elemental composition of NiZn ferrite nanoparticles were investigated by scanning electron microscopy, transmission electron microscopy, and energy dispersive X-ray spectroscopy, respectively. The exposure of cancer cells to NiZn ferrite nanoparticles (15.6–1,000 μg/mL; 72 hours) has resulted in a dose-dependent inhibition of cell growth determined by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. The quantification of caspase-3 and -9 activities and DNA fragmentation to assess the cell death pathway of the treated cells showed that both were stimulated when exposed to NiZn ferrite nanoparticles. Light microscopy examination of the cells exposed to NiZn ferrite nanoparticles demonstrated significant changes in cellular morphology. The HepG2 cells were most prone to apoptosis among the three cells lines examined, as the result of treatment with NiZn nanoparticles. In conclusion, NiZn ferrite nanoparticles are suggested to have potential cytotoxicity against cancer cells. PMID:23885175

  19. Microwave-hydrothermal synthesis of perovskite bismuth ferrite nanoparticles

    SciTech Connect

    Biasotto, G.; Simoes, A.Z.; Foschini, C.R.; Zaghete, M.A.; Varela, J.A.; Longo, E.

    2011-12-15

    Highlights: Black-Right-Pointing-Pointer BiFeO{sub 3} (BFO) nanoparticles were grown by hydrothermal microwave method (HTMW). Black-Right-Pointing-Pointer The soaking time is effective in improving phase formation. Black-Right-Pointing-Pointer Rietveld refinement reveals an orthorhombic structure. Black-Right-Pointing-Pointer The observed magnetism of the BFO crystallites is a consequence of particle size. Black-Right-Pointing-Pointer The HTMW is a genuine technique for low temperatures and short times of synthesis. -- Abstract: Hydrothermal microwave method (HTMW) was used to synthesize crystalline bismuth ferrite (BiFeO{sub 3}) nanoparticles (BFO) in the temperature of 180 Degree-Sign C with times ranging from 5 min to 1 h. BFO nanoparticles were characterized by means of X-ray analyses, FT-IR, Raman spectroscopy, TG-DTA and FE-SEM. X-ray diffraction results indicated that longer soaking time was benefit to refraining the formation of any impurity phases and growing BFO crystallites into almost single-phase perovskites. Typical FT-IR spectra for BFO nanoparticles presented well defined bands, indicating a substantial short-range order in the system. TG-DTA analyses confirmed the presence of lattice OH{sup -} groups, commonly found in materials obtained by HTMW process. Compared with the conventional solid-state reaction process, submicron BFO crystallites with better homogeneity could be produced at the temperature as low as 180 Degree-Sign C. These results show that the HTMW synthesis route is rapid, cost effective, and could be used as an alternative to obtain BFO nanoparticles in the temperature of 180 Degree-Sign C for 1 h.

  20. Direct dyes removal using modified magnetic ferrite nanoparticle

    PubMed Central

    2014-01-01

    The magnetic adsorbent nanoparticle was modified using cationic surface active agent. Zinc ferrite nanoparticle and cetyl trimethylammonium bromide were used as an adsorbent and a surface active agent, respectively. Dye removal ability of the surface modified nanoparticle as an adsorbent was investigated. Direct Green 6 (DG6), Direct Red 31 (DR31) and Direct Red 23 (DR23) were used. The characteristics of the adsorbent were studied using Fourier transform infrared (FTIR), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The effect of adsorbent dosage, initial dye concentration and salt was evaluated. In ternary system, dye removal of the adsorbent at 90, 120, 150 and 200 mg/L dye concentration was 63, 45, 30 and 23% for DR23, 97, 90, 78 and 45% for DR31 and 51, 48, 42 and 37% for DG6, respectively. It was found that dye adsorption onto the adsorbent followed Langmuir isotherm. The adsorption kinetic of dyes was found to conform to pseudo-second order kinetics. PMID:24991427

  1. Electromagnetic properties of NiZn ferrite nanoparticles and their polymer composites

    SciTech Connect

    Parsons, P.; Duncan, K.; Giri, A. K.; Xiao, J. Q.; Karna, S. P.

    2014-05-07

    The magnetic properties of polycrystalline NiZn ferrite nanoparticles synthesized using a polyol-reduction and coprecipitation reaction methods have been investigated. The effects on magnetization of synthesis approach, chemical composition, processing conditions, and on the size of nanoparticles on magnetization have been investigated. The measured room-temperature magnetization for the as-prepared magnetic nanoparticles (MNP) synthesized via polyol-reduction and coprecipitation is 69 Am{sup 2} kg{sup −1} and 14 Am{sup 2} kg{sup −1}, respectively. X-ray diffraction measurements confirm spinel structure of the particles with an estimated grain size of ∼80 nm obtained from the polyol-reduction and 28 nm obtained from these coprecipitation techniques. Upon calcination under atmospheric conditions at different temperatures between 800 °C and 1000 °C, the magnetization, M, of the coprecipitated MNP increases to 76 Am{sup 2} kg{sup −1} with an estimated grain size of 90 nm. The MNP-polymer nanocomposites made from the synthesized MNP in various loading fraction and high density polyethylene exhibit interesting electromagnetic properties. The measured permeability and permittivity of the magnetic nanoparticle-polymer nanocomposites increases with the loading fractions of the magnetic nanoparticles, suggesting control for impedance matching for antenna applications.

  2. Electrophoretic deposition of nickel zinc ferrite nanoparticles into microstructured patterns

    NASA Astrophysics Data System (ADS)

    Kelly, Stefan J.; Wen, Xiao; Arnold, David P.; Andrew, Jennifer S.

    2016-05-01

    Using DC electric fields, nickel-zinc ferrite (Ni0.5Zn0.5Fe2O4) nanoparticles (Dh =16.6 ± 3.6 nm) are electrophoretically deposited onto silicon substrates to form dense structures defined by photoresist molds. Parameters such as electric field, bath composition, and deposition time are tuned to produce films ranging in thickness from 177 to 805 nm. The deposited films exhibit soft magnetic properties with a saturation magnetization of 60 emu/g and a coercivity of 2.6 kA/m (33 Oe). Additionally, the influence of the photoresist mold on the deposit profile is studied, and patterned films with different shapes (lines, squares, circles, etc.) are demonstrated with feature sizes down to 5 μm.

  3. Effect of gamma irradiation on the structural and magnetic properties of Co–Zn spinel ferrite nanoparticles

    SciTech Connect

    Raut, Anil V.; Kurmude, D.V.; Shengule, D.R.; Jadhav, K.M.

    2015-03-15

    Highlights: • Co–Zn ferrite nanoparticles were examined before and after γ-irradiation. • Single phase cubic spinel structure of Co–Zn was confirmed by XRD data. • The grain size was reported in the range of 52–62 nm after γ-irradiation. • Ms, Hc, n{sub B} were reported to be increased after gamma irradiation. - Abstract: In this work, the structural and magnetic properties of Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} (0.0 ≤ x ≤ 1.0) ferrite nanoparticles were studied before and after gamma irradiation. The as-synthesized samples of Co–Zn ferrite nanoparticles prepared by sol–gel auto-combustion technique were analysed by XRD which suggested the single phase; cubic spinel structure of the material. Crystal defects produced in the spinel lattice were studied before and after Co{sup 60} γ-irradiation in a gamma cell with a dose rate of 0.1 Mrad/h in order to report the changes in structural and magnetic properties of the Co–Zn ferrite nanoparticles. The average crystallite size (t), lattice parameter (α) and other structural parameters of gamma-irradiated and un-irradiated Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} spinel ferrite system was calculated from XRD data. The morphological characterizations were performed using scanning electron microscopy (SEM). The magnetic properties were measured using pulse field hysteresis loop tracer by applying magnetic field of 1000 Oe, and the analysis of data obtained revealed that the magnetic property such as saturation magnetization (Ms), coecivity (Hc), magneton number (n{sub B}) etc. magnetic parameters were increased after irradiation.

  4. Synthesis and cytotoxicity study of magnesium ferrite-gold core-shell nanoparticles.

    PubMed

    Nonkumwong, Jeeranan; Pakawanit, Phakkhananan; Wipatanawin, Angkana; Jantaratana, Pongsakorn; Ananta, Supon; Srisombat, Laongnuan

    2016-04-01

    In this work, the core-magnesium ferrite (MgFe2O4) nanoparticles were prepared by hydrothermal technique. Completed gold (Au) shell coating on the surfaces of MgFe2O4 nanoparticles was obtained by varying core/shell ratios via a reduction method. Phase identification, morphological evolution, optical properties, magnetic properties and cytotoxicity to mammalian cells of these MgFe2O4 core coated with Au nanoparticles were examined by using a combination of X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy, UV-visible spectroscopy (UV-vis), vibrating sample magnetometry and resazurin microplate assay techniques. In general, TEM images revealed different sizes of the core-shell nanoparticles generated from various core/shell ratios and confirmed the completed Au shell coating on MgFe2O4 core nanoparticles via suitable core/shell ratio with particle size less than 100nm. The core-shell nanoparticle size and the quality of coating influence the optical properties of the products. The UV-vis spectra of complete coated MgFe2O4-Au core-shell nanoparticles exhibit the absorption bands in the near-Infrared (NIR) region indicating high potential for therapeutic applications. Based on the magnetic property measurement, it was found that the obtained MgFe2O4-Au core-shell nanoparticles still exhibit superparamagnetism with lower saturation magnetization value, compared with MgFe2O4 core. Both of MgFe2O4 and MgFe2O4-Au core-shell also showed in vitro non-cytotoxicity to mouse areola fibroblast (L-929) cell line. PMID:26838832

  5. Influence of Ce-Substitution on Structural, Magnetic and Electrical Properties of Cobalt Ferrite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Hashhash, A.; Kaiser, M.

    2016-01-01

    Nano-crystalline samples of cerium substituted cobalt ferrites with chemical formula CoCe x Fe2- x O4 (0.0 ≤ x ≤ 0.1) were prepared using the citrate auto-combustion method. The prepared ferrites were characterized by x-ray diffraction (XRD), Fourier transform infrared spectroscopy spectra (FTIR), transmission electron microscopy (TEM), and a vibrating sample magnetometer (VSM). The XRD patterns and FTIR spectra confirm that the prepared samples reveal the formation of a single-phase spinel structure. TEM micrographs showed that the particles are made up of spherical and elongated nano-metric shapes. A limitation of the size of nanoparticles is observed as the Ce3+ concentration increases. VSM measurements showed that the coercivity H c and magnetization values M s are strongly dependent on Ce3+ content and particle size. The values of H c lie in the range of (411-1600 G), which suggest that these samples are convenient for different applications. The alternating current electrical conductivity ( σ), dielectric permittivities ( ɛ', ɛ″), and dielectric loss tangent (tan δ) were studied at different ranges of frequency and temperature. The relation of conductivity with temperature revealed a semiconductor to semi-metallic behavior as cerium concentration increases. The variation in (tan δ) with frequency at different temperature shows abnormal behavior with more than one relaxation peak. The conduction mechanism used in the present study has been discussed in the light of cation-anion-cation interactions over the octahedral B-site.

  6. Chitosan-coated nickel-ferrite nanoparticles as contrast agents in magnetic resonance imaging

    NASA Astrophysics Data System (ADS)

    Ahmad, Tanveer; Bae, Hongsub; Iqbal, Yousaf; Rhee, Ilsu; Hong, Sungwook; Chang, Yongmin; Lee, Jaejun; Sohn, Derac

    2015-05-01

    We report evidence for the possible application of chitosan-coated nickel-ferrite (NiFe2O4) nanoparticles as both T1 and T2 contrast agents in magnetic resonance imaging (MRI). The coating of nickel-ferrite nanoparticles with chitosan was performed simultaneously with the synthesis of the nickel-ferrite nanoparticles by a chemical co-precipitation method. The coated nanoparticles were cylindrical in shape with an average length of 17 nm and an average width of 4.4 nm. The bonding of chitosan onto the ferrite nanoparticles was confirmed by Fourier transform infrared spectroscopy. The T1 and T2 relaxivities were 0.858±0.04 and 1.71±0.03 mM-1 s-1, respectively. In animal experimentation, both a 25% signal enhancement in the T1-weighted mage and a 71% signal loss in the T2-weighted image were observed. This demonstrated that chitosan-coated nickel-ferrite nanoparticles are suitable as both T1 and T2 contrast agents in MRI. We note that the applicability of our nanoparticles as both T1 and T2 contrast agents is due to their cylindrical shape, which gives rise to both inner and outer sphere processes of nanoparticles.

  7. Preparation of transparent conductors ferroelectric memory materials and ferrites

    DOEpatents

    Bhattacharya, R.N.; Ginley, D.S.

    1998-07-28

    A process is described for the preparation by electrodeposition of metal oxide film and powder compounds for ferroelectric memory materials and ferrites wherein the metal oxide includes a plurality of metals. The process comprises providing an electrodeposition bath, providing soluble salts of the metals to this bath, electrically energizing the bath to thereby cause formation of a recoverable film of metal on the electrode, recovering the resultant film as a film or a powder, and recovering powder formed on the floor of the bath. The films and powders so produced are subsequently annealed to thereby produce metal oxide for use in electronic applications. The process can be employed to produce metal-doped metal oxide film and powder compounds for transparent conductors. The process for preparation of these metal-doped metal oxides follows that described above.

  8. Preparation of transparent conductors ferroelectric memory materials and ferrites

    DOEpatents

    Bhattacharya, Raghu Nath; Ginley, David S.

    1998-01-01

    A process for the preparation by electrodeposition of metal oxide film and powder compounds for ferroelectric memory materials and ferrites wherein the metal oxide includes a plurality of metals. The process comprises providing an electrodeposition bath, providing soluble salts of the metals to this bath, electrically energizing the bath to thereby cause formation of a recoverable film of metal on the electrode, recovering the resultant film as a film or a powder, and recovering powder formed on the floor of the bath. The films and powders so produced are subsequently annealed to thereby produce metal oxide for use in electronic applications. The process can be employed to produce metal-doped metal oxide film and powder compounds for transparent conductors. The process for preparation of these metal-doped metal oxides follows that described above.

  9. Magnetic liposomes based on nickel ferrite nanoparticles for biomedical applications.

    PubMed

    Rodrigues, Ana Rita O; Gomes, I T; Almeida, Bernardo G; Araújo, J P; Castanheira, Elisabete M S; Coutinho, Paulo J G

    2015-07-21

    Nickel ferrite nanoparticles with superparamagnetic behavior at room temperature were synthesized using a coprecipitation method. These magnetic nanoparticles were either covered with a lipid bilayer, forming dry magnetic liposomes (DMLs), or entrapped in liposomes, originating aqueous magnetoliposomes (AMLs). A new and promising method for the synthesis of DMLs is described. The presence of the lipid bilayer in DMLs was confirmed by FRET (Förster Resonance Energy Transfer) measurements between the fluorescent-labeled lipids NBD-C12-HPC (NBD acting as a donor) included in the second lipid layer and rhodamine B-DOPE (acceptor) in the first lipid layer. An average donor-acceptor distance of 3 nm was estimated. Assays of the non-specific interactions of magnetoliposomes with biological membranes (modeled using giant unilamellar vesicles, GUVs) were performed. Membrane fusion between both aqueous and dry magnetoliposomes and GUVs was confirmed by FRET, which is an important result regarding applications of these systems both as hyperthermia agents and antitumor drug nanocarriers. PMID:26095537

  10. Magnetic properties of cobalt-ferrite nanoparticles embedded in polystyrene resin

    SciTech Connect

    Vaishnava, P. P.; Senaratne, U.; Buc, E.; Naik, R.; Naik, V. M.; Tsoi, G.; Wenger, L. E.; Boolchand, P.

    2006-04-15

    Samples of maghemite and cobalt-ferrite nanoparticles (sizes, 3-10 nm) were prepared by cross-linking sulfonated polystyrene resin with aqueous solutions of (1) FeCl{sub 2}, (2) 80%FeCl{sub 2}+20%CoCl{sub 2}, (3) FeCl{sub 3}, and (4) 80%FeCl{sub 3}+20%CoCl{sub 2} by volume. Chemical analysis, x-ray powder-diffraction, and {sup 57}Fe Moessbauer spectroscopic measurements show that samples 1 and 3 consist of {gamma}-Fe{sub 2}O{sub 3} nanoparticles (sizes, {approx}10 and 3 nm) and sample 2 and 4 consist of Co{sub x}Fe{sub 3-x}O{sub 4} nanoparticles (sizes, {approx}10 and 4 nm). The temperature dependence of the zero-field-cooled and field-cooled magnetizations at low temperatures, together with a magnetic hysteresis in the M versus H data below blocking temperatures, demonstrate superparamagnetic behavior. The introduction of Co in the iron oxide-resin matrix results in an increase in the blocking temperature of nanoparticles.

  11. Microstructural and Mössbauer properties of low temperature synthesized Ni-Cd-Al ferrite nanoparticles

    PubMed Central

    2011-01-01

    We report the influence of Al3+ doping on the microstructural and Mössbauer properties of ferrite nanoparticles of basic composition Ni0.2Cd0.3Fe2.5 - xAlxO4 (0.0 ≤ x ≤ 0.5) prepared through simple sol-gel method. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray, transmission electron microscopy (TEM), Fourier transformation infrared (FTIR), and Mössbauer spectroscopy techniques were used to investigate the structural, chemical, and Mössbauer properties of the grown nanoparticles. XRD results confirm that all the samples are single-phase cubic spinel in structure excluding the presence of any secondary phase corresponding to any structure. SEM micrographs show the synthesized nanoparticles are agglomerated but spherical in shape. The average crystallite size of the grown nanoparticles was calculated through Scherrer formula and confirmed by TEM and was found between 2 and 8 nm (± 1). FTIR results show the presence of two vibrational bands corresponding to tetrahedral and octahedral sites. Mössbauer spectroscopy shows that all the samples exhibit superparamagnetism, and the quadrupole interaction increases with the substitution of Al3+ ions. PMID:21851597

  12. Synthesis and Characterization of Cobalt Substituted Zinc Ferrite Nanoparticles by Microwave Combustion Method.

    PubMed

    Sundararajan, M; Kennedy, L John; Vijaya, J Judith

    2015-09-01

    Pure and cobalt doped zinc ferrites were prepared by microwave combustion method using L-arginine as a fuel. The prepared samples were characterized by various instrumental techniques such as X-ray powder diffractometry, high resolution scanning electron microscopy (HR-SEM), energy dispersive X-ray analysis, Fourier transformed infrared (FT-IR) spectroscopy, photoluminescence spectroscopy and UV-Visible diffuse reflectance spectroscopy. Vibrating sample magnetometry at room temperature was recorded to study the magnetic behavior of the samples. X-ray analysis confirmed the formation of zinc ferrites normal spinel-type structure with an average crystallite sizes in the range, 25.69 nm to 35.68 nm. The lattice parameters decreased as cobalt fraction was increased. The HR-SEM images showed nanoparticles are agglomerated. The estimated band gap energy value was found to decrease with an increase in cobalt content (1.87 to 1.62 eV). Broad visible emissions are observed in the photoluminescence spectra. A gradual increase in the coercivity and saturation magnetization (M(s)) were noted at relatively higher cobalt doping fractions. PMID:26716235

  13. Comparison effects and electron spin resonance studies of α-Fe2O4 spinel type ferrite nanoparticles.

    PubMed

    Bayrakdar, H; Yalçın, O; Cengiz, U; Özüm, S; Anigi, E; Topel, O

    2014-11-11

    α-Fe2O4 spinel type ferrite nanoparticles have been synthesized by cetyltrimethylammonium bromide (CTAB) and ethylenediaminetetraacetic acid (EDTA) assisted hydrothermal route by using NaOH solution. Electron spin resonance (ESR/EPR) measurements of α-Fe2O4 nanoparticles have been performed by a conventional x-band spectrometer at room temperature. The comparison effect of nanoparticles prepared by using CTAB and EDTA in different α-doping on the structural and morphological properties have been investigated in detail. The effect of EDTA-assisted synthesis for α-Fe2O4 nanoparticles are refined, and thus the spectroscopic g-factor are detected by using ESR signals. These samples can be considered as great benefits for magnetic recording media, electromagnetic and drug delivery applications. PMID:24858357

  14. Comparison effects and electron spin resonance studies of α-Fe2O4 spinel type ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Bayrakdar, H.; Yalçın, O.; Cengiz, U.; Özüm, S.; Anigi, E.; Topel, O.

    2014-11-01

    α-Fe2O4 spinel type ferrite nanoparticles have been synthesized by cetyltrimethylammonium bromide (CTAB) and ethylenediaminetetraacetic acid (EDTA) assisted hydrothermal route by using NaOH solution. Electron spin resonance (ESR/EPR) measurements of α-Fe2O4 nanoparticles have been performed by a conventional x-band spectrometer at room temperature. The comparison effect of nanoparticles prepared by using CTAB and EDTA in different α-doping on the structural and morphological properties have been investigated in detail. The effect of EDTA-assisted synthesis for α-Fe2O4 nanoparticles are refined, and thus the spectroscopic g-factor are detected by using ESR signals. These samples can be considered as great benefits for magnetic recording media, electromagnetic and drug delivery applications.

  15. Mn-Zn Ferrite Powder Preparation by Hydrothermal Process from Used Dry Batteries

    NASA Astrophysics Data System (ADS)

    Liu, Chung‑Wen; Lin, Cheng‑Hsiung; Fu, Yen‑Pei

    2006-05-01

    In this study, we propose a new process to synthesize Mn-Zn ferrite, using oxides of manganese and zinc extracted from used dry batteries, and ferrous chloride waste solution from iron plants or electronic plants recycled as starting raw materials. It is found that Mn-Zn ferrite powder prepared by the hydrothermal process from used dry batteries revealed the formation of cubic ferrite with a saturation magnetization (MS) of 58.8 emu/g.

  16. High-frequency electromagnetic properties of the manganese ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Zeng, Min; Liu, Jue; Yue, Ming; Yang, Haozhe; Dong, Hangrong; Tang, Wukui; Jiang, He; Liu, Xiaofang; Yu, Ronghai

    2015-05-01

    Manganese (MnFe2O4) nanoparticles are prepared via a facile solvothermal method. The electromagnetic properties are investigated in 1-18 GHz, indicating the MnFe2O4 nanoparticles are the promising materials to be applied as microwave absorbers. The wave absorbing mechanism can be attributed to the dielectric loss, magnetic loss, and the synergetic effect. The permittivity dispersion behavior is explained by Debye dipolar relation expression. The complex permeability is analyzed using Landau-Lifshitz-Gilbert equation. Natural resonance, exchange resonance, and eddy current loss arise at different frequencies.

  17. Structural, dielectric and magnetic properties of Gd substituted manganese ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Murugesan, C.; Sathyamoorthy, B.; Chandrasekaran, G.

    2015-08-01

    Gd3+ ion-substituted manganese ferrite nanoparticles with the chemical formula MnGdxFe2-xO4 (x = 0.0, 0.05, and 0.1) were synthesized by sol-gel auto combustion method. Thermal stability of the as-prepared sample was analyzed using thermo gravimetric and differential thermal analysis (TG-DTA) and the result reveals that the prepared sample is thermally stable above 300 °C. Structural and morphology studies were performed using powder x-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Indexed PXRD patterns confirm the formation of pure cubic spinel structure. The average crystallite sizes calculated using Sherrer’s formula decreased from 47 nm to 32 nm and lattice constant was enhanced from 8.407 Å to 8.432 Å. The FTIR spectrum of manganese ferrite shows a high frequency vibrational band at 564 cm-1 assigned to tetrahedral site and a low frequency vibrational band at 450 cm-1 assigned to octahedral site which are shifted to 556 cm-1 and 439 cm-1 for Gd3+ substitution and confirm the incorporation of Gd3+ into manganese ferrite. SEM analysis shows the presence of agglomerated spherical shaped particles at the surface. Room temperature dielectric and magnetic properties were studied using broadband dielectric spectroscopy (BDS) and vibrating sample magnetometry (VSM). Frequency dependent dielectric constant, ac conductivity and tan delta were found to increase with Gd3+ ion substitution. The measured values of saturation magnetization decrease from 46.6 emu g-1 to 41 emu g-1 with increase in Gd3+ concentration and coercivity decreases from 179.5 Oe to 143 Oe.

  18. Polyvinyl alcohol functionalized cobalt ferrite nanoparticles for biomedical applications

    NASA Astrophysics Data System (ADS)

    Salunkhe, A. B.; Khot, V. M.; Thorat, N. D.; Phadatare, M. R.; Sathish, C. I.; Dhawale, D. S.; Pawar, S. H.

    2013-01-01

    In the present work, cobalt ferrite nanoparticles (CoFe2O4 NPs) have been synthesized by combustion method. The surface of the CoFe2O4 NPs was modified with biocompatible polyvinyl alcohol (PVA). To investigate effect and nature of coating on the surface of CoFe2O4 NPs, the NPs were characterized X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA). The transmission electron microscopy (TEM) and dynamic light scattering (DLS) results demonstrate the monodispersed characteristics of CoFe2O4 NPs after surface modification with PVA. The decrease in contact angle from 162° to 50° with PVA coating on NPs indicates the transition from hydrophobic nature to hydrophilic. The Magnetic properties measurement system (MPMS) results show that the NPs have ferromagnetic behavior with high magnetization of 75.04 and 71.02 emu/g of uncoated and coated CoFe2O4 NPs respectively. These PVA coated NPs exhibit less toxicity over uncoated CoFe2O4 NPs up to 1.8 mg mL-1 when tested with mouse fibroblast L929 cell line.

  19. Embryotoxicity of cobalt ferrite and gold nanoparticles: a first in vitro approach.

    PubMed

    Di Guglielmo, Claudia; López, David Ramos; De Lapuente, Joaquín; Mallafre, Joan Maria Llobet; Suàrez, Miquel Borràs

    2010-09-01

    Nanoparticles (NPs) are emerging as promising biomedical tools thanks to their peculiar characteristics. Our purpose was to investigate the embryotoxicity of cobalt ferrite and gold NPs through the Embryonic Stem Cell Test (EST). The EST is an in vitro standard assay, which permits to classify substances as strongly, weakly or non-embryotoxic. Due to the particular physical-chemical nature of nanoparticles, we introduced a modification to the standard protocol exposing the Embryonic Stem Cells (ES-D3) to nanoparticles only during the first 5 days of the assay. Moreover, we proposed a method to discriminate and compare the embryotoxicity of the substances within the weakly embryotoxic range. Our ID(50) results permit to classify cobalt ferrite nanoparticles coated with gold and silanes as non-embryotoxic. The remaining nanoparticles have been classified as weakly embryotoxic in this decreasing order: gold salt (HAuCl(4).3H(2)O)>cobalt ferrite salt (CoFe(2)O(4))>cobalt ferrite nanoparticles coated with silanes (Si-CoFe)>gold nanoparticles coated with hyaluronic acid (HA-Au). PMID:20566333

  20. Structural and magnetic properties correlated with cation distribution of Mo-substituted cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Heiba, Z. K.; Mostafa, Nasser Y.; Abd-Elkader, Omar H.

    2014-11-01

    Mo-substituted cobalt ferrite nanoparticles; CoFe2-2xMoxO4 (0.0≤x≤0.3) were prepared by a one-step solution combustion synthesis technique. The reactants were metal nitrates and glycine as a fuel. The samples were characterized using an X-ray diffraction (XRD), a transmission electron microscope (TEM) and a vibrating sample magnetometer (VSM). XRD analysis revealed a pure single phase of cubic spinel ferrites for all samples with x up to 0.3. The lattice parameter decreases with Mo6+ substitution linearly up to x=0.15, then nonlinearly for x≥0.2. Rietveld analysis and saturation magnetization (Ms) revealed that Mo6+ replaced Fe3+ in the tetrahedral A-sites up to x=0.15, then it replaced Fe3+ in both A-sites and B-sites for x≥0.2. The saturation magnetization (Ms) increases with increasing Mo6+ substitution up to x=0.15 then decreases. The crystallite size decreased while the microstrain increased with increasing Mo6+ substitution. Inserting Mo6+ produces large residents of defects and cation vacancies.

  1. Evaluation of nickel ferrite nanoparticles coated with oleylamine by NMR relaxation measurements and magnetic hyperthermia.

    PubMed

    Menelaou, M; Georgoula, K; Simeonidis, K; Dendrinou-Samara, C

    2014-03-01

    Nickel ferrite nanoparticles were synthesized via a facile solvothermal approach. Oleylamine (OAm) was used in all synthetic procedures as a stabilizing agent and solvent. By varying the polarity of the solvents, hydrophobic NiFe2O4 nanoparticles coated with OAm of relatively similar sizes (9-11.7 nm) and in a range of magnetization values (32.0-53.5 emu g(-1)) were obtained. The as-prepared hydrophobic nanoparticles were characterized by XRD, TEM, SEM, TGA and VSM and converted to hydrophilic by two different approaches. The addition of a positively charged ligand (cetyltrimethyl ammonium bromide, CTAB) and the ligand exchange procedure (2,3-dimercaptosuccinic acid, DMSA) have been successfully applied. The aqueous suspensions of NiFe2O4@CTAB and NiFe2O4@DMSA showed good colloidal stability after a long period of time. The different surface modification affected both the NMR relaxometric measurements and the hyperthermia effects. In both techniques CTAB modification demonstrated higher r2 relaxivity (278.9 s(-1) mM(-1) in an NMR spectrometer at 11.7 T) and SAR values (423.4 W g(-1) at an applied AC field with a particle concentration of 0.5 mg mL(-1)). The results indicate that a coating with a larger molecule as CTAB under the same size, shape and magnetization of NiFe2O4 NPs gave rise to NMR relaxometric properties and heating efficacy. PMID:24413465

  2. Spin-flop transition, magnetic and microwave absorption properties of α-Fe2O4 spinel type ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Yalçın, Orhan; Bayrakdar, Harun; Özüm, Songül

    2013-10-01

    We have prepared NiFe2O4, CoFe2O4, Ni0.6Zn0.4Fe2O4 and ZnFe2O4 spinel type ferrite nanoparticles by surfactant-assisted hydrothermal process using cetyltrimethylammonium bromide (CTAB). The spin-flop transition, magnetic, dielectric and permittivity characterizations have been investigated. The spin-flop transition occurs from antiferromagnetic state to mixed state and then ferromagnetic state for Zn doped samples. The spin-flop transition occurs in the temperature range of 50-250 K. The ionic conduction, dipolar relaxation, atomic polarization and electronic polarization are the main mechanisms that contribute to the permittivity of a dielectric material. The permittivity increases with increasing frequency. This suggests a resonance behavior, which is expected when the ferrite samples are highly conductive and skin effect become significant. These samples will provide great benefits for electromagnetic applications and electromagnetic interference shielding characteristics.

  3. Control of the saturation temperature in magnetic heating by using polyethylene-glycol-coated rod-shaped nickel-ferrite (NiFe2O4) nanoparticles

    NASA Astrophysics Data System (ADS)

    Iqbal, Yousaf; Bae, Hongsub; Rhee, Ilsu; Hong, Sungwook

    2016-02-01

    Polyethylene-glycol (PEG)-coated nickel-ferrite nanoparticles were prepared for magnetic hyperthermia applications by using the co-precipitation method. The PEG coating occurred during the synthesis of the nanoparticles. The coated nanoparticles were rod-shaped with an average length of 16 nm and an average diameter of 4.5 nm, as observed using transmission electron microscopy. The PEG coating on the surfaces of the nanoparticles was confirmed from the Fourier-transform infrared spectra. The nanoparticles exhibited superparamagnetic characteristics with negligible coercive force. Further, magnetic heating effects were observed in aqueous solutions of the coated nanoparticles. The saturation temperature could be controlled at 42 ℃ by changing the concentration of the nanoparticles in the aqueous solution. Alternately, the saturation temperature could be controlled for a given concentration of nanoparticles by changing the intensity of the magnetic field. The Curie temperature of the nanoparticles was estimated to be 495 ℃. These results for the PEG-coated nickel-ferrite nanoparticles showed the possibility of utilizing them for controlled magnetic hyperthermia at 42 ℃.

  4. The superspin glass transition in zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Kaman, O.; Ko?nkov, T.; Jirk, Z.; Maryko, M.; Veverka, M.

    2015-05-01

    Nanoparticles of the ZnxFe3-xO4 (x = 0.3-0.4) spinel phase having 5 and 15 nm size were synthesized by thermal decomposition of the respective acetylacetonates in a high boiling-point solvent employing surfactants. The collective behaviour of the nanoparticles was probed by dc and ac magnetic measurements of tightly compressed pellets of the particles and silica coated products which were prepared by reverse microemulsion technique. The assembly of bare 5 nm particles remains in the superparamagnetic state with Curie-Weiss characteristics down to 35 K when a rather sharp freezing of superspins is detected. The larger particles show a similar but more diffusive transition at 250 K. The cores encapsulated into the diamagnetic silica do not exhibit glassy freezing.

  5. Preparation and investigation of dc conductivity and relative permeability of epoxy/Li-Ni-Zn ferrite composites

    NASA Astrophysics Data System (ADS)

    Darwish, M. A.; Saafan, S. A.; El-Kony, D.; Salahuddin, N. A.

    2015-07-01

    Ferrite nanoparticles - having the compositions Li(x/2)(Ni0.5Zn0.5)(1-x)Fe(2+x/2)O4 (x=0, 0.2, 0.3) - have been prepared by the co-precipitation method. The prepared powders have been divided into groups and sintered at different temperatures (373 K, 1074 K and 1473 K). X-Ray diffraction analysis (XRD) for all samples has confirmed the formation of the desired ferrites with crystallite sizes within the nanoscale (<100 nm). The dc conductivity, the relative permeability and the magnetization of the ferrite samples have been investigated and according to the results, the sample Li0.15(Ni0.5Zn0.5)0.7 Fe2.15O4 sintered at 1473 K has been chosen to prepare the composites. The particle size of this sample has been recalculated by using JEOL JEM-100SX transmission electron microscope and it has been found about 64.7 nm. Then, a pure epoxy sample and four pristine epoxy resin /Li0.15(Ni0.5Zn0.5)0.7 Fe2.15O4 composites have been prepared using different ferrite contents (20%, 30%, 40%, and 50%) wt.%. These samples have been characterized by Fourier transform infrared (FTIR) spectroscopy and their dc conductivity, relative permeability and magnetization have also been investigated. The obtained results indicate that the investigated composites may be promising candidates for practical applications such as EMI suppressor and high frequency applications.

  6. Zinc ferrite nanoparticle as a magnetic catalyst: Synthesis and dye degradation

    SciTech Connect

    Mahmoodi, Niyaz Mohammad

    2013-10-15

    Graphical abstract: Photocatalytic degradation of Reactive Red 198 and Reactive Red 120 by the synthesized zinc ferrite nanoparticle. - Highlights: • Magnetic zinc ferrite nanoparticle was synthesized and characterized. • Photocatalytic dye degradation by magnetic nanoparticle was studied. • Formate, acetate and oxalate were detected as dominant dye degradation aliphatic intermediates. • Nitrate and sulfate ions were detected as mineralization products of dyes. • Zinc ferrite nanoparticle was an effective magnetic photocatalyst to degrade dyes. - Abstract: In this paper, magnetic zinc ferrite (ZnFe{sub 2}O{sub 4}) nanoparticle was synthesized and its photocatalytic dye degradation ability from colored wastewater was studied. Reactive Red 198 (RR198) and Reactive Red 120 (RR120) were used as model dyes. The characteristics of ZnFe{sub 2}O{sub 4} were investigated using Fourier transform infrared (FTIR), X-ray diffraction (XRD) and scanning electron microscope (SEM). Photocatalytic dye degradation by ZnFe{sub 2}O{sub 4} was studied by UV–vis spectrophotometer and ion chromatography (IC). The effects of ZnFe{sub 2}O{sub 4} dosage, initial dye concentration and salt on dye degradation were evaluated. Formate, acetate and oxalate anions were detected as dominant aliphatic intermediate. Inorganic anions (nitrate and sulfate anions) were detected as dye mineralization products. The results indicated that ZnFe{sub 2}O{sub 4} could be used as a magnetic photocatalyst to degrade dyes from colored wastewater.

  7. Probing bismuth ferrite nanoparticles by hard x-ray photoemission: Anomalous occurrence of metallic bismuth

    SciTech Connect

    Chaturvedi, Smita; Rajendra, Ranguwar; Ballav, Nirmalya; Kulkarni, Sulabha; Sarkar, Indranil; Shirolkar, Mandar M.; Jeng, U-Ser; Yeh, Yi-Qi

    2014-09-08

    We have investigated bismuth ferrite nanoparticles (∼75 nm and ∼155 nm) synthesized by a chemical method, using soft X-ray (1253.6 eV) and hard X-ray (3500, 5500, and 7500 eV) photoelectron spectroscopy. This provided an evidence for the variation of chemical state of bismuth in crystalline, phase pure nanoparticles. X-ray photoelectron spectroscopy analysis using Mg Kα (1253.6 eV) source showed that iron and bismuth were present in both Fe{sup 3+} and Bi{sup 3+} valence states as expected for bismuth ferrite. However, hard X-ray photoelectron spectroscopy analysis of the bismuth ferrite nanoparticles using variable photon energies unexpectedly showed the presence of Bi{sup 0} valence state below the surface region, indicating that bismuth ferrite nanoparticles are chemically inhomogeneous in the radial direction. Consistently, small-angle X-ray scattering reveals a core-shell structure for these radial inhomogeneous nanoparticles.

  8. Magnetic properties of conducting polymer doped with manganese zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Poddar, P.; Wilson, J. L.; Srikanth, H.; Morrison, S. A.; Carpenter, E. E.

    2004-10-01

    The magnetic properties of superparamagnetic particles are influenced by the supporting matrix. We have systematically studied the DC magnetic properties of loosely packed manganese-zinc ferrite (Mn0.68Zn0.25Fe2.07O3) nanoparticles synthesized using a reverse micelle technique. The results have been compared with those for particles suspended in paraffin wax and embedded in a polypyrrole matrix. The polypyrrole-doped particles were prepared using an in situ ultraviolet irradiation method and spin-coated into thin films. The loosely packed particles showed no resolvable coercivity even well below the blocking temperature. On the other hand, the same particles in wax showed the opening up of a large coercivity below the blocking temperature. However, both the samples showed characteristic superparamagnetic transition peaks in the temperature-dependent susceptibility nearly at the same temperature. The particles in the polypyrrole matrix showed a remarkable increase in the blocking temperature and large hysteresis at 300 K. The structural characterization of the polymer-doped sample showed clustering of the nanoparticles.

  9. Magnesium-zinc ferrite nanoparticles: effect of copper doping on the structural, electrical and magnetic properties.

    PubMed

    Zaki, H M; Al-Heniti, S; Umar, Ahmad; Al-Marzouki, F; Abdel-Daiem, A; Elmosalami, T A; Dawoud, H A; Al-Hazmi, F S; Ata-Allah, S S

    2013-06-01

    In this paper, Mg0.5Zn0.5-Cu(x)Fe2O4 ferrites nanoparticles were synthesized by facile co-precipitation route and characterized in detail in terms of their structural, electrical and magnetic properties as a function of Cu concentration. The prepared samples have cubic spinel phase as confirmed by X-ray diffraction patterns. The decrease of the lattice constant and increase of X-ray density indicate the solubility of Cu ions in the spinel lattice. The AC conductivity measurements between 300 K and 773 K at different frequencies 1 KHz up to 1 MHz, showed two different behaviors as semiconductor-like at high temperature and frequency depending behavior associated with dispersion phenomena at low temperatures. The conduction mechanism in the system is influenced by Cu concentration and the dominant one is the hopping conduction mechanism. Dielectric measurements at the same conditions of temperatures and frequencies exhibited that the dielectric loss increases with increasing the temperature and decreasing the frequency indicating the semiconducting nature of the ferrite compounds. An anomalous behavior of the dielectric loss is observed in samples with high Cu content which explained in terms of resonance between frequency accompanied the electronic hopping and the frequency of the external electric field. The analysis of Mössbauer spectra revealed that copper free compound is super-paramagnetically relaxed in nature and zinc free compound demonstrates ferrimagnetic order. Moreover, hyperfine field spectrum shows the migration of Cu ions from octahedral to tetrahedral site in zinc free compound. PMID:23862448

  10. Ferromagnetic resonance behavior of spark plasma sintered Ni-Zn ferrite nanoparticles produced by a chemical route

    NASA Astrophysics Data System (ADS)

    Valenzuela, R.; Beji, Z.; Herbst, F.; Ammar, S.

    2011-04-01

    Ferrite nanoparticles of composition Zn0.5Ni0.5Fe2O4 were prepared by forced hydrolysis in a polyol (polyol process) from the corresponding iron, nickel, and zinc acetates. Synthesis conditions allowed for obtaining polycrystalline epitaxial clusters of about 22 nm in size with an average crystal size of about 5 nm. These powders were subsequently consolidated by spark plasma sintering (SPS) technique under a pressure of 80 MPa and temperatures in the 350 to 500 °C range for short periods (5 to 10 min). Densities reached 92% to 94% of the theoretical density. Particle size remained smaller than 61 nm, even for the highest temperature. Ferromagnetic resonance experiments at 77 K showed broadened resonance lines. In contrast with powdered nanoparticles, these high-density bodies can be used in many high-frequency applications.

  11. Structural and magnetic properties of cobalt-doped iron oxide nanoparticles prepared by solution combustion method for biomedical applications.

    PubMed

    Venkatesan, Kaliyamoorthy; Rajan Babu, Dhanakotti; Kavya Bai, Mane Prabhu; Supriya, Ravi; Vidya, Radhakrishnan; Madeswaran, Saminathan; Anandan, Pandurangan; Arivanandhan, Mukannan; Hayakawa, Yasuhiro

    2015-01-01

    Cobalt-doped iron oxide nanoparticles were prepared by solution combustion technique. The structural and magnetic properties of the prepared samples were also investigated. The average crystallite size of cobalt ferrite (CoFe2O4) magnetic nanoparticle was calculated using Scherrer equation, and it was found to be 16±5 nm. The particle size was measured by transmission electron microscope. This value was found to match with the crystallite size calculated by Scherrer equation corresponding to the prominent intensity peak (311) of X-ray diffraction. The high-resolution transmission electron microscope image shows clear lattice fringes and high crystallinity of cobalt ferrite magnetic nanoparticles. The synthesized magnetic nanoparticles exhibited the saturation magnetization value of 47 emu/g and coercivity of 947 Oe. The anti-microbial activity of cobalt ferrite nanoparticles showed better results as an anti-bacterial agent. The affinity constant was determined for the nanoparticles, and the cytotoxicity studies were conducted for the cobalt ferrite nanoparticles at different concentrations and the results are discussed. PMID:26491320

  12. Structural and magnetic properties of cobalt-doped iron oxide nanoparticles prepared by solution combustion method for biomedical applications

    PubMed Central

    Venkatesan, Kaliyamoorthy; Rajan Babu, Dhanakotti; Kavya Bai, Mane Prabhu; Supriya, Ravi; Vidya, Radhakrishnan; Madeswaran, Saminathan; Anandan, Pandurangan; Arivanandhan, Mukannan; Hayakawa, Yasuhiro

    2015-01-01

    Cobalt-doped iron oxide nanoparticles were prepared by solution combustion technique. The structural and magnetic properties of the prepared samples were also investigated. The average crystallite size of cobalt ferrite (CoFe2O4) magnetic nanoparticle was calculated using Scherrer equation, and it was found to be 16±5 nm. The particle size was measured by transmission electron microscope. This value was found to match with the crystallite size calculated by Scherrer equation corresponding to the prominent intensity peak (311) of X-ray diffraction. The high-resolution transmission electron microscope image shows clear lattice fringes and high crystallinity of cobalt ferrite magnetic nanoparticles. The synthesized magnetic nanoparticles exhibited the saturation magnetization value of 47 emu/g and coercivity of 947 Oe. The anti-microbial activity of cobalt ferrite nanoparticles showed better results as an anti-bacterial agent. The affinity constant was determined for the nanoparticles, and the cytotoxicity studies were conducted for the cobalt ferrite nanoparticles at different concentrations and the results are discussed. PMID:26491320

  13. 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

  14. Electrical and optical properties of gadolinium doped bismuth ferrite nanoparticles

    SciTech Connect

    Mukherjee, A. Banerjee, M. Basu, S.; Pal, M.

    2014-04-24

    Multiferroic bismuth ferrite (BFO) and gadolinium (Gd) doped bismuth ferrite had been synthesized by a sol-gel method. Particle size had been estimated by Transmission electron microscopy (TEM) and found to decrease with Gd doping. We studied the temperature and frequency dependence of impedance and electric modulus and calculated the grain and grain boundary resistance and capacitance of the investigated samples. We observed that electrical activation energy increases for all the doped samples. Optical band gap also increases for the doped samples which can be used in photocatalytic application of BFO.

  15. The anti-microbial activity of titania-nickel ferrite composite nanoparticles

    NASA Astrophysics Data System (ADS)

    Rana, S.; Misra, R. D. K.

    2005-12-01

    A novel approach to synthesize a new generation of composite nanoparticles consisting of a photocatalytic shell of anatase-titania and a magnetic core of nickel ferrite has been adopted combining reverse micelle and chemical hydrolysis techniques. Titania is an effective anti-microbial agent that can be directly sprayed on infected areas of the human body or environment. Unfortunately, titania is an electrical insulator and is difficult to extract from the sprayed surface after treatment. The titania photocatalytic shell provides good antimicrobial capability that renders the bacteria inactive and removes the organic pollutants, while the nickel ferrite magnetic core enables controlled delivery of composite nanoparticles through the application of a small magnetic field, encouraging their application as removable anti-microbial photocatalyst nanoparticles.

  16. Structure of Oxide Nanoparticles in Fe-16Cr MA/ODS Ferritic Steel

    SciTech Connect

    Hsiung, L; Fluss, M; Kimura, A

    2010-04-06

    Oxide nanoparticles in Fe-16Cr ODS ferritic steel fabricated by mechanical alloying (MA) method have been examined using high-resolution transmission electron microscopy (HRTEM) techniques. A partial crystallization of oxide nanoparticles was frequently observed in as-fabricated ODS steel. The crystal structure of crystalline oxide particles is identified to be mainly Y{sub 4}Al{sub 2}O{sub 9} (YAM) with a monoclinic structure. Large nanoparticles with a diameter larger than 20 nm tend to be incoherent and have a nearly spherical shape, whereas small nanoparticles with a diameter smaller than 10 nm tend to be coherent or semi-coherent and have faceted boundaries. The oxide nanoparticles become fully crystallized after prolonged annealing at 900 C. These results lead us to propose a three-stage formation mechanism of oxide nanoparticles in MA/ODS steels.

  17. Magnetic properties of bio-synthesized zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Yeary, Lucas W.; Moon, Ji-Won; Rawn, Claudia J.; Love, Lonnie J.; Rondinone, Adam J.; Thompson, James R.; Chakoumakos, Bryan C.; Phelps, Tommy J.

    2011-12-01

    The magnetic properties of zinc ferrite (Zn-substituted magnetite, ZnyFe1-yFe2O4) formed by a microbial process compared favorably with chemically synthesized materials. A metal reducing bacterium, Thermoanaerobacter, strain TOR-39 was incubated with ZnxFe1-xOOH (x=0.01, 0.1, and 0.15) precursors and produced nanoparticulate zinc ferrites. Composition and crystalline structure of the resulting zinc ferrites were verified using X-ray fluorescence, X-ray diffraction, transmission electron microscopy, and neutron diffraction. The average composition from triplicates gave a value for y of 0.02, 0.23, and 0.30 with the greatest standard deviation of 0.02. Average crystallite sizes were determined to be 67, 49, and 25 nm, respectively. While crystallite size decreased with more Zn substitution, the lattice parameter and the unit cell volume showed a gradual increase in agreement with previous literature values. The magnetic properties were characterized using a superconducting quantum interference device magnetometer and were compared with values for the saturation magnetization (Ms) reported in the literature. The averaged Ms values for the triplicates with the largest amount of zinc (y=0.30) gave values of 100.1, 96.5, and 69.7 emu/g at temperatures of 5, 80, and 300 K, respectively indicating increased magnetic properties of the bacterially synthesized zinc ferrites.

  18. Magnetic properties of bio-synthesized zinc ferrite nanoparticles

    SciTech Connect

    Yeary, Lucas W; Moon, Ji Won; Rawn, Claudia J; Love, Lonnie J; Rondinone, Adam Justin; Thompson, James R; Chakoumakos, Bryan C; Phelps, Tommy Joe

    2011-01-01

    The magnetic properties of zinc ferrite (Zn-substituted magnetite, Zn{sub y}Fe{sub 1-y}Fe{sub 2}O{sub 4}) formed by a microbial process compared favorably with chemically synthesized materials. A metal reducing bacterium, Thermoanaerobacter, strain TOR-39 was incubated with Zn{sub x}Fe{sub 1-x}OOH (x=0.01, 0.1, and 0.15) precursors and produced nanoparticulate zinc ferrites. Composition and crystalline structure of the resulting zinc ferrites were verified using X-ray fluorescence, X-ray diffraction, transmission electron microscopy, and neutron diffraction. The average composition from triplicates gave a value for y of 0.02, 0.23, and 0.30 with the greatest standard deviation of 0.02. Average crystallite sizes were determined to be 67, 49, and 25 nm, respectively. While crystallite size decreased with more Zn substitution, the lattice parameter and the unit cell volume showed a gradual increase in agreement with previous literature values. The magnetic properties were characterized using a superconducting quantum interference device magnetometer and were compared with values for the saturation magnetization (M{sub s}) reported in the literature. The averaged M{sub s} values for the triplicates with the largest amount of zinc (y=0.30) gave values of 100.1, 96.5, and 69.7 emu/g at temperatures of 5, 80, and 300 K, respectively indicating increased magnetic properties of the bacterially synthesized zinc ferrites.

  19. Chemical methodologies for preparation of micron and nanometer scale ferrites--a mini review of patents.

    PubMed

    Pant, Prita; Bhuvaneswari, Sundararaman; Ghosh, Narendra Nath

    2008-01-01

    Ferrites, with wide range of chemical compositions, have been studied extensively over the years as they have a plethora of applications such as magnetic read/write heads, transformer cores, antennas, microwave absorbers, deflecting yoke, high frequency transformers, catalysis, pigments etc. Particles of submicron size have attracted the attention of scientists and technologists in different fields because they exhibit many unique physical properties as compared to those of bulk materials and are in great demand. Traditional high temperature solid-state method for preparation of ferrites is associated with several limitations. The quest for synthesis of ultrafine ferrite materials has led to the development of various preparative methods. Several patents disclose different wet chemical techniques namely sol-gel, coprecipitation, hydrothermal, combustion, spray pyrolysis etc for preparation of variety of ferrites for wide range of applications. In this mini-review, several patented chemical methods have been discussed critically with specific examples along with the effect of synthetic routes on particle size formation. Applications of ferrite powders with different compositions prepared by the above mentioned patented methods have also been discussed in this review. PMID:19076039

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

    NASA Astrophysics Data System (ADS)

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

    2010-12-01

    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 10-14-10-15/cm3) 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.

  1. Structural, dielectric and magnetic properties of nickel substituted cobalt ferrite nanoparticles: Effect of nickel concentration

    NASA Astrophysics Data System (ADS)

    Velhal, Ninad B.; Patil, Narayan D.; Shelke, Abhijeet R.; Deshpande, Nishad G.; Puri, Vijaya R.

    2015-09-01

    Nickel substituted cobalt ferrite nanoparticles with composition Co1-xNixFe2O4 (0.0 ≤ x ≤ 1.0) was synthesized using simple, low temperature auto combustion method. The X-ray diffraction patterns reveal the formation of cubic phase spinel structure. The crystallite size varies from 30-44 nm with the nickel content. Porous and agglomerated morphology of the bulk sample was displayed in the scanning electron microscopy. Micro Raman spectroscopy reveals continuous shift of Eg and Eg(2) stokes line up to 0.8 Ni substitution. The dispersion behavior of the dielectric constant with frequency and the semicircle nature of the impedance spectra show the cobalt nickel ferrite to have high resistance. The ferromagnetic nature is observed in all the samples, however, the maximum saturation magnetization was achieved by the 0.4 Ni substituted cobalt ferrite, which is up to the 92.87 emu/gm at 30K.

  2. Structural and magnetic studies of the nickel doped CoFe2O4 ferrite nanoparticles synthesized by the chemical co-precipitation method

    NASA Astrophysics Data System (ADS)

    Kumar, Ashok; Yadav, Nisha; Rana, Dinesh S.; Kumar, Parmod; Arora, Manju; Pant, R. P.

    2015-11-01

    The physical properties of nickel doped cobalt ferrite nanoparticles NixCo1-xFe2O4 (x=0.5, 0.75, 0.9) derived by the chemical co-precipitation route are characterized by XRD, FTIR, TEM, EPR, search coil and ac susceptibility techniques to develop stable kerosene based ferrofluid. XRD patterns and TEM images confirm the single phase formation of NixCo1-xFe2O4 nanoparticles whose crystallite size increases and lattice parameters decreases with the increase in Ni content. EPR resonance signal peak-to-peak line width and resonance field value decreases with the increase in Ni concentration in these samples. The broad nature of resonance signal is attributed to the ferromagnetic nature of the as-prepared nanoparticles and the increase in super exchange interaction among Ni2+-O-Co2+ facilitate the shifting of resonance value to lower field. The hysteresis loops of these nickel doped cobalt ferrite analogs exhibits highly magnetic nature of these nanoparticles at ambient temperature whose saturation magnetization, coerecivity and remanence magnetization decreases linearly with the increase in Ni-concentration in cobalt ferrite. The magnetic susceptibility with temperature curve shows increasing trend of blocking temperature with rise in nickel ion concentration.

  3. Magnetic Silver-Coated Ferrite Nanoparticles and Their Application in Thick Films

    NASA Astrophysics Data System (ADS)

    Liu, Jianguo; Huang, Baling; Li, Xiangyou; Li, Ping; Zeng, Xiaoyan

    2010-12-01

    Magnetic silver-coated ferrite nanoparticles with 39.8% weight gain (relative to ferrite nanopowder coated by a silver layer) were synthesized by electroless deposition of silver on ferrite nanopowder. The mechanism of the electroless deposition was explored in terms of pretreatment, sensitization, activation, and the reduction of silver-ammonia complexes. Experiments showed that the optimal deposition conditions were a temperature of 50°C, pH value of 10 to 12, duration of 65 min with ethanol plus polyethylene glycol as additives, and ultrasonic vibration as a method of dispersing the nanoparticles. From transmission electron microscopy (TEM) images, it was observed that as-synthesized nanoparticles had a core-shell structure with a particle size of 35 nm to 90 nm and a shell thickness of 5 nm to 20 nm. X-ray diffraction (XRD) analysis confirmed that only ferrite and metallic silver were present in the product. Electrical resistance and magnetic hysteresis measurements demonstrated that the nanoparticles were both electrically conductive (volume electrical resistivity on the order of 10-4 Ω cm to 10-3 Ω cm when compressed to pressure of 2 × 10 6 Pa) and possessed ferrimagnetic properties. After a thick-film paste, obtained with the nanoparticles as the functional phase, was directly written and sintered, scanning electron microscopy (SEM) analysis and electrical resistance measurements of conductive lines in the acquired array pattern showed that an electrically conductive network with some defects and cavities was formed, with a volume electrical resistivity of 1 × 10-4 Ω cm to 1 × 10-3 Ω cm.

  4. Galactosylated manganese ferrite nanoparticles for targeted MR imaging of asialoglycoprotein receptor.

    PubMed

    Yang, Seung-Hyun; Heo, Dan; Lee, Eugene; Kim, Eunjung; Lim, Eun-Kyung; Lee, Young Han; Haam, Seungjoo; Suh, Jin-Suck; Huh, Yong-Min; Yang, Jaemoon; Park, Sahng Wook

    2013-11-29

    Cancer cells can express specific biomarkers, such as cell membrane proteins and signaling factors. Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The asialoglycoprotein receptor (ASGPr) was selected as a biomarker for hepatoma cells and the ASGPr-targetable imaging agent bearing a galactosyl group was prepared using manganese ferrite nanoparticles (MFNP) and galactosylgluconic acid. The utility of the ASGPr-targetable imaging agent, galactosylated MFNP (G-MFNP) was assessed by several methods in ASGPr-expressing HepG2 cells as target cells and ASGPr-deficient MCF7 cells. Physical and chemical properties of G-MFNP were examined using Fourier-transform infrared spectroscopy, dynamic light scattering, zeta potential analysis, and transmission electron microscopy. No significant cytotoxicity was observed in either cell line. Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. We suggest that these results will be useful in strategies for cancer diagnoses based on magnetic resonance imaging. PMID:24192299

  5. Manifestation of weak ferromagnetism and photocatalytic activity in bismuth ferrite nanoparticles

    SciTech Connect

    Sakar, M.; Balakumar, S.; Saravanan, P.; Jaisankar, S. N.

    2013-02-05

    Bismuth ferrite (BFO) nanoparticles were synthesized by auto-ignition technique with and without adding ignition fuel such as citric acid. The presence of citric acid in the reaction mixture yielded highly-magnetic BFO/{gamma}-Fe{sub 2}O{sub 3} nanocomposite. When this composite was annealed to 650 Degree-Sign C, a single phase BFO was formed with average crystallite size of 50 nm and showed weak ferromagnetic behavior. Conversely, the phase pure BFO prepared without adding citric acid exhibited antiferromagnetism because of its larger crystallite size of around 70 nm. The visible-light driven photocatalytic activity of both the pure BFO and BFO/{gamma}-Fe{sub 2}O{sub 3} nanocomposite were examined by degrading methyl orange dye. The pure BFO showed a moderate photocatalytic activity; while BFO/{gamma}-Fe{sub 2}O{sub 3} nanocomposite showed enhanced activity. This could be probably due to the optimal band gap ratio between BFO and {gamma}-Fe{sub 2}O{sub 3} phases reduced the recombination of electron-hole pairs which aided in the enhancement of photocatalytic activity.

  6. Study Of Structural And Dielectric Properties Of Ni-Mg Ferrite Nanoparticles

    SciTech Connect

    Nongjai, Razia; Batoo, Khalid Mujasam; Khan, Shakeel

    2010-12-01

    Ferrite nanoparticles of basic composition Ni{sub 0.7}Mg{sub 0.3}Fe{sub 2-x}Al{sub x}O{sub 4}(0.0{<=}x{<=}0.5) were prepared through citrate gel method and characterized using XRD, TEM and dielectric spectroscopy techniques. The dielectric properties were studied as a function of frequency (42 Hz-5 MHz) at room temperature. The average particle size has been found between 8-17 nm. The dispersion in dielectric properties and ac conductivity ({sigma}{sub ac}), with frequency reveals that the dispersion is due to Maxwell-Wagner type of interfacial polarization in general and the hopping of charge between Fe{sup 2+} and Fe{sup 3+} as well as between Ni{sup 2+} and Ni{sup 3+} ions at B-sites. The dielectric loss tangent (tan {delta}) shows abnormal behavior for the compositions 0.3, 0.4 and 0.5 which has been explained in the light of Rezlescue model.

  7. Galactosylated manganese ferrite nanoparticles for targeted MR imaging of asialoglycoprotein receptor

    NASA Astrophysics Data System (ADS)

    Yang, Seung-Hyun; Heo, Dan; Lee, Eugene; Kim, Eunjung; Lim, Eun-Kyung; Lee, Young Han; Haam, Seungjoo; Suh, Jin-Suck; Huh, Yong-Min; Yang, Jaemoon; Park, Sahng Wook

    2013-11-01

    Cancer cells can express specific biomarkers, such as cell membrane proteins and signaling factors. Thus, finding biomarkers and delivering diagnostic agents are important in the diagnosis of cancer. In this study, we investigated a biomarker imaging agent for the diagnosis of hepatic cancers. The asialoglycoprotein receptor (ASGPr) was selected as a biomarker for hepatoma cells and the ASGPr-targetable imaging agent bearing a galactosyl group was prepared using manganese ferrite nanoparticles (MFNP) and galactosylgluconic acid. The utility of the ASGPr-targetable imaging agent, galactosylated MFNP (G-MFNP) was assessed by several methods in ASGPr-expressing HepG2 cells as target cells and ASGPr-deficient MCF7 cells. Physical and chemical properties of G-MFNP were examined using Fourier-transform infrared spectroscopy, dynamic light scattering, zeta potential analysis, and transmission electron microscopy. No significant cytotoxicity was observed in either cell line. Targeting ability was assessed using flow cytometry, magnetic resonance imaging, inductively coupled plasma atomic emission spectroscopy, absorbance analysis, dark-field microscopy, Prussian blue staining, and transmission electron microscopy. We demonstrated that G-MFNP target successfully and bind to ASGPr-expressing HepG2 cells specifically. We suggest that these results will be useful in strategies for cancer diagnoses based on magnetic resonance imaging.

  8. Spherical barium ferrite nanoparticles and hexaferrite single crystals for information data storage and RF devices

    NASA Astrophysics Data System (ADS)

    Jalli, Jeevan Prasad

    Since their discovery in the early 1950's hexagonal ferrites or hexaferrites have been studied for a long time because of their technological applications, such as microwave devices and high density magnetic recording media. In this dissertation efforts have been made to address these two applications by developing nanosized spherical barium ferrite particles for advanced magnetic recording media, and hexaferrite single crystals for low loss RF devices. Accordingly, this dissertation consists of two parts; part one spherical barium ferrite nanoparticles for information data storage media, and part two hexaferrite single crystals for RF devices. Part I. Spherical Barium Ferrite Nanoparticles Hexagonal barium ferrite (H-BaFe) nanoparticles are good candidates for particulate recording media due to their high uniaxial magnetocrystalline anisotropy, excellent chemical stability, and narrow switching field distribution. One major disadvantage of using H-BaFe particles for particulate recording media is their poor dispersion and a high degree of stacking that deteriorate the recording capability by creating large media noise and surface roughness. One way to solve and improve the recording performance of H-BaFe media is employing substantially nanosized spherical barium ferrite (S­BaFe) particles. Spherical shaped particles have low aspect ratio and only form a point-to-point contact, unlike the H-BaFe particles. Therefore, using S-BaFe particles not only decrease the degree of magnetic interaction between the particles but also can substantially increases the recording performance by improving the dispersion and SNR of the particles in the magnetic media. In this dissertation, two different approaches were employed successfully to synthesize S-BaFe nanoparticles in the range of 20-45 nm. Part II. Hexaferrite Single Crystals As wireless communication systems are flourishing, and the operating frequencies are increasing, there is a great demand for RF devices such as circulators and isolators. Traditional RF devices using spinel or garnets are disadvantageous in the millimeter range frequencies, since they require a strong external bias field provided by external permanent magnets. A promising approach to circumvent this problem is to use the high crystalline anisotropy field in the hexaferrites. Single crystals of M and Y-type hexaferrites show promising results with their low microwave losses and excellent magnetic and physical properties. In this dissertation efforts to grow, high-quality bulk M and Y-type single crystals with the aim to study and improve their magnetic and microwave properties with respect to different cation dopant elements is reported. Also, a liquid phase epitaxial technique was developed to grow thick barium ferrite films onto semiconductor substrates. Finally, magnetic domain patterns on bulk M-type single crystals was studied by using a magnetic force microscopy technique.

  9. Microstructural, magnetic and electric properties of mixed Cs-Zn ferrites prepared by solution combustion method

    NASA Astrophysics Data System (ADS)

    Gupta, Manik; Randhawa, B. S.

    2012-07-01

    Nanosized zinc substituted ferrites with composition Cs0.5-x/2ZnxMn0.05Fe2.45-x/2O4 (x = 0-0.5) were prepared by solution combustion route. The ferrites obtained have been characterized by powder XRD, Mössbauer spectroscopy and Transmission Electron Microscope (TEM). Magnetic and electrical properties have also been studied. Powder X-ray diffraction analysis shows the formation of single phase cubic spinel structure. The saturation magnetization (Ms) initially exhibits an upward trend followed by a regular decrease with increasing diamagnetic Zn content. Curie temperature shows a downward trend with Zn content. The Mössbauer spectra display transition from ferrimagnetic to super-paramagnetic phase with increasing 'x' value. The temperature dependence resistivity shows regular decrease with temperature reflecting semiconductor behaviour of the ferrite samples. The permittivity (ɛ') and tangent loss (tan δ) measured at room temperature as a function of frequency shows the expected ferrite behaviour. TEM studies indicate the formation of nanosized ferrite particles. These results demonstrate promising features of Cs-Zn ferrites in microwave applications.

  10. Preparation of DPPE-Stabilized Gold Nanoparticles

    ERIC Educational Resources Information Center

    Dungey, Keenan E.; Muller, David P.; Gunter, Tammy

    2005-01-01

    An experiment is presented that introduces students to nanotechnology through the preparation of nanoparticles and their visualization using transmission electron microscopy (TEM). The experiment familiarizes the students with nonaqueous solvents, biphasic reactions, phase-transfer agents, ligands to stabilize growing nanoparticles, and bidentate

  11. Preparation of DPPE-Stabilized Gold Nanoparticles

    ERIC Educational Resources Information Center

    Dungey, Keenan E.; Muller, David P.; Gunter, Tammy

    2005-01-01

    An experiment is presented that introduces students to nanotechnology through the preparation of nanoparticles and their visualization using transmission electron microscopy (TEM). The experiment familiarizes the students with nonaqueous solvents, biphasic reactions, phase-transfer agents, ligands to stabilize growing nanoparticles, and bidentate…

  12. Laccase immobilized manganese ferrite nanoparticle: synthesis and LSSVM intelligent modeling of decolorization.

    PubMed

    Mahmoodi, Niyaz Mohammad; Arabloo, Milad; Abdi, Jafar

    2014-12-15

    Laccase was immobilized onto manganese ferrite nanoparticle (MFN) and dye decolorization from single and binary systems was studied. The characteristics of laccase immobilized manganese ferrite nanoparticle (LIMFN) were investigated using Fourier transform infrared (FTIR) and scanning electron microscopy (SEM). Direct red 31 (DR31), Acid blue 92 (AB92) and Direct green 6 (DG6) were used. A least square support vector machine (LSSVM) was developed to predict the decolorization efficiency of various single and binary systems based on the obtained laboratory data under different experimental conditions. Statistical and graphical quality measures were also employed to evaluate the performance and accuracy of the developed intelligent models. It is shown that the predictions of the designed LSSVM models are in close agreement with the experimental data. The effects of LIMFN dosage, pH and dye concentration on dye decolorization from single and binary systems were evaluated. Decolorization kinetics followed Michaelis-Menten Model. PMID:25282090

  13. Inter-particle interactions and magnetism in manganese-zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Poddar, P.; Srikanth, H.; Morrison, S. A.; Carpenter, E. E.

    2005-03-01

    Manganese-zinc ferrite (Mn xZn 1-xFe 2O 4) nanoparticles were synthesized by reverse micelle technique using two different surfactant media—(1) bis-(2-ethylhexl) sodium sulfosuccinate (AOT) and (2) mix of nonylphenol poly(oxyethylene) 5 and nonylphenol poly(oxyethylene) 9 (NP) followed by annealing of precursors to remove the surfactant coating and to obtain better crystalline phase. A comparison of the magnetic properties showed distinct differences in blocking temperature, coercivity and saturation magnetization. Radio-frequency (RF) transverse susceptibility (TS) measurements were in agreement with the static magnetization data. Our precise TS measurements further revealed features associated with anisotropy fields that were dependent on the grain size, crystallinity and inter-particle interactions. Overall, we have demonstrated that RF TS is an excellent probe of the dynamic magnetization and influence of effects such as crystallinity and inter-particle interactions in soft ferrite nanoparticles.

  14. Faraday rotation of cobalt ferrite nanoparticle polymer composite films at cryogenic temperatures.

    PubMed

    Demir, Veysi; Gangopadhyay, Palash; Norwood, Robert A; Peyghambarian, Nasser

    2014-04-01

    This paper investigates the behavior of the Verdet constant for cobalt ferrite (CoFe₂O₄) nanoparticles polymer composite films at low temperatures using a 532 nm laser source. An experimental setup for Faraday rotation (FR) at low temperatures is introduced and FRs were measured at various temperatures. Verdet constants were deduced from the paramagnetic model for terbium gallium garnet glass where ~4× improvement was observed at 40° K for CoFe₂O₄ composite film. PMID:24787165

  15. Magnetic properties of nanocomposites based on opal matrices with embedded ferrite-spinel nanoparticles

    NASA Astrophysics Data System (ADS)

    Rinkevich, A. B.; Korolev, A. V.; Samoylovich, M. I.; Klescheva, S. M.; Perov, D. V.

    2016-02-01

    Magnetic properties of nanocomposites based on opal matrices with ferrite-spinel nanoparticles embedded have been investigated in temperature range from 2 to 300 K. The magnetization curves and hysteresis loops as well as the temperature dependence of magnetic moment and the temperature and frequency dependences of AC susceptibility have been measured. The results of magnetic measurements are compared to X-ray analysis and electron microscopy investigations.

  16. Experimental evidence of surface effects in the magnetic dynamics behavior of ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Sousa, E. C.; Alves, C. R.; Aquino, R.; Sousa, M. H.; Goya, G. F.; Rechenberg, H. R.; Tourinho, F. A.; Depeyrot, J.

    2005-03-01

    The magnetic dynamics behavior of copper and nickel ferrite nanoparticles used in the magnetic fluid elaboration and with mean sizes between 3.5 to 10.4 nm is investigated by measurements of magnetic hysteretic properties and zero field cooling (ZFC) susceptibility. The dependence of the irreversibility field, inversely proportional to the particle size, clearly indicates that the magnetic anisotropy of our particles finds its origin on the surface layer.

  17. New methods for lipid nanoparticles preparation.

    PubMed

    Corrias, Francesco; Lai, Francesco

    2011-09-01

    Lipid nanoparticles have attracted many researchers during recent years due to the excellent tolerability and advantages compared to liposomes and polymeric nanoparticles. High pressure homogenization is the main technique used to prepare solid lipid nanoparticles (SLN) encapsulating different type of drugs, however this method involves some critical process parameters. For this reason and in order to overcome patented methods, different production techniques for lipid nanoparticles have been widely investigated in recent years (last decade). The paper reviews new methods for lipid nanoparticles preparation, and their recent applications in pharmaceutical field, especially focusing on coacervation, microemulsions templates, supercritical fluid technology, phase-inversion temperature (PIT) techniques. References of the most relevant literature and patents published by various research groups on these fields are provided. PMID:21834772

  18. Cobalt Zinc Ferrite Nanoparticles as a Potential Magnetic Resonance Imaging Agent: An In vitro Study

    PubMed Central

    Ghasemian, Zeinab; Shahbazi-Gahrouei, Daryoush; Manouchehri, Sohrab

    2015-01-01

    Background: Magnetic Nanoparticles (MNP) have been used for contrast enhancement in Magnetic Resonance Imaging (MRI). In recent years, research on the use of ferrite nanoparticles in T2 contrast agents has shown a great potential application in MR imaging. In this work, Co0.5Zn0.5Fe2O4 and Co0.5Zn0.5Fe2O4-DMSA magnetic nanoparticles, CZF-MNPs and CZF-MNPs-DMSA, were investigated as MR imaging contrast agents. Methods: Cobalt zinc ferrite nanoparticles and their suitable coating, DMSA, were investigated under in vitro condition. Human prostate cancer cell lines (DU145 and PC3) with bare (uncoated) and coated magnetic nanoparticles were investigated as nano-contrast MR imaging agents. Results: Using T2-weighted MR images identified that signal intensity of bare and coated MNPs was enhanced with increasing concentration of MNPs in water. The values of 1/T2 relaxivity (r2) for bare and coated MNPs were found to be 88.46 and 28.80 (mM−1 s−1), respectively. Conclusion: The results show that bare and coated MNPs are suitable as T2-weighted MR imaging contrast agents. Also, the obtained r2/r1 values (59.3 and 50) for bare and coated MNPs were in agreement with the results of other previous relevant works. PMID:26140183

  19. Catalysts prepared from copper-nickel ferrites for the steam reforming of methanol

    NASA Astrophysics Data System (ADS)

    Huang, Yung-Han; Wang, Sea-Fue; Tsai, An-Pang; Kameoka, Satoshi

    2015-05-01

    In this study, Fe3O4-supported Cu and Ni catalysts are prepared through reduction of Cu-Ni (Ni1-xCuxFe2O4) ferrites. The Cu-Ni ferrites, synthesized using a solid-state reaction method, are reduced at temperatures from 240 °C to 500 °C in a H2 atmosphere. All ferrites are characterized with granular morphology and a smooth particle surface before reduction. For the CuFe2O4, Ni0.5Cu0.5Fe2O4 and NiFe2O4 ferrites reduced at 240, 300, and 400 °C, respectively, nanosized Cu and/or Ni particles (5-32 nm) and mesopores (5-30 nm) are distributed and adhered on the surfaces of Fe3O4 supports. After increasing the reduction temperature of NiFe2O4 ferrite to 500 °C, the Ni particles and mesopores disappear from the Fe3O4 surfaces, which is due to the formation of a Fe-Ni alloy covering on the Fe3O4 surfaces. The CuFe2O4 ferrite after H2 reduction at 240 °C exhibits the highest H2 production rate of 149 ml STP/min g-cat at 360 °C. The existence of Ni content in the Cu-Ni ferrites enhances the reverse water gas shift reaction, and raises the CO selectivity while reducing the CO2 selectivity. Formation of a Fe-Ni alloy exaggerates the trend and poisons the H2 production rate.

  20. Bacterially synthesized ferrite nanoparticles for magnetic hyperthermia applications.

    PubMed

    Céspedes, Eva; Byrne, James M; Farrow, Neil; Moise, Sandhya; Coker, Victoria S; Bencsik, Martin; Lloyd, Jonathan R; Telling, Neil D

    2014-11-01

    Magnetic hyperthermia uses AC stimulation of magnetic nanoparticles to generate heat for cancer cell destruction. Whilst nanoparticles produced inside magnetotactic bacteria have shown amongst the highest reported heating to date, these particles are magnetically blocked so that strong heating occurs only for mobile particles, unless magnetic field parameters are far outside clinical limits. Here, nanoparticles extracellularly produced by the bacteria Geobacter sulfurreducens are investigated that contain Co or Zn dopants to tune the magnetic anisotropy, saturation magnetization and nanoparticle sizes, enabling heating within clinical field constraints. The heating mechanisms specific to either Co or Zn doping are determined from frequency dependent specific absorption rate (SAR) measurements and innovative AC susceptometry simulations that use a realistic model concerning clusters of polydisperse nanoparticles in suspension. Whilst both particle types undergo magnetization relaxation and show heating effects in water under low AC frequency and field, only Zn doped particles maintain relaxation combined with hysteresis losses even when immobilized. This magnetic heating process could prove important in the biological environment where nanoparticle mobility may not be possible. Obtained SARs are discussed regarding clinical conditions which, together with their enhanced MRI contrast, indicate that biogenic Zn doped particles are promising for combined diagnostics and cancer therapy. PMID:25232657

  1. Bacterially synthesized ferrite nanoparticles for magnetic hyperthermia applications

    NASA Astrophysics Data System (ADS)

    Céspedes, Eva; Byrne, James M.; Farrow, Neil; Moise, Sandhya; Coker, Victoria S.; Bencsik, Martin; Lloyd, Jonathan R.; Telling, Neil D.

    2014-10-01

    Magnetic hyperthermia uses AC stimulation of magnetic nanoparticles to generate heat for cancer cell destruction. Whilst nanoparticles produced inside magnetotactic bacteria have shown amongst the highest reported heating to date, these particles are magnetically blocked so that strong heating occurs only for mobile particles, unless magnetic field parameters are far outside clinical limits. Here, nanoparticles extracellularly produced by the bacteria Geobacter sulfurreducens are investigated that contain Co or Zn dopants to tune the magnetic anisotropy, saturation magnetization and nanoparticle sizes, enabling heating within clinical field constraints. The heating mechanisms specific to either Co or Zn doping are determined from frequency dependent specific absorption rate (SAR) measurements and innovative AC susceptometry simulations that use a realistic model concerning clusters of polydisperse nanoparticles in suspension. Whilst both particle types undergo magnetization relaxation and show heating effects in water under low AC frequency and field, only Zn doped particles maintain relaxation combined with hysteresis losses even when immobilized. This magnetic heating process could prove important in the biological environment where nanoparticle mobility may not be possible. Obtained SARs are discussed regarding clinical conditions which, together with their enhanced MRI contrast, indicate that biogenic Zn doped particles are promising for combined diagnostics and cancer therapy.Magnetic hyperthermia uses AC stimulation of magnetic nanoparticles to generate heat for cancer cell destruction. Whilst nanoparticles produced inside magnetotactic bacteria have shown amongst the highest reported heating to date, these particles are magnetically blocked so that strong heating occurs only for mobile particles, unless magnetic field parameters are far outside clinical limits. Here, nanoparticles extracellularly produced by the bacteria Geobacter sulfurreducens are investigated that contain Co or Zn dopants to tune the magnetic anisotropy, saturation magnetization and nanoparticle sizes, enabling heating within clinical field constraints. The heating mechanisms specific to either Co or Zn doping are determined from frequency dependent specific absorption rate (SAR) measurements and innovative AC susceptometry simulations that use a realistic model concerning clusters of polydisperse nanoparticles in suspension. Whilst both particle types undergo magnetization relaxation and show heating effects in water under low AC frequency and field, only Zn doped particles maintain relaxation combined with hysteresis losses even when immobilized. This magnetic heating process could prove important in the biological environment where nanoparticle mobility may not be possible. Obtained SARs are discussed regarding clinical conditions which, together with their enhanced MRI contrast, indicate that biogenic Zn doped particles are promising for combined diagnostics and cancer therapy. Electronic supplementary information (ESI) available: Further details of the cluster model of polydisperse nanoparticles used for the AC susceptibility simulations (Fig. S1 to S3). Examples of the heating curves and the linear fit used to determine the SAR values are shown in Fig. S4. Fig. S5 exhibits the energy loss per mass of iron during magnetic hyperthermia (from SAR values) normalized to H2 and frequency for further comparison among samples. Fig. S6 shows the comparison between the simulations of AC susceptibility spectra including regions below and above the experimental frequency range for MNA, Zn0.2 and Zn0.4 nanoparticles suspended in solvents with different viscosities (water, glycerol and a hypothetical high viscous solvent). Fig. S7 exhibits a comparison among the simulated χ'' susceptibility of MNA, Zn0.2 and Zn0.4 nanoparticles (a) in water and (b) in glycerol. See DOI: 10.1039/c4nr03004d

  2. Structural and magnetic properties of cadmium substituted manganese ferrites prepared by hydrothermal route

    NASA Astrophysics Data System (ADS)

    Mostafa, Nasser Y.; Zaki, Z. I.; Heiba, Z. K.

    2013-03-01

    Cd-substituted manganese ferrite Mn1-xCdxFe2O4 powders with x having values 0.0, 0.1, 0.3 and 0.5 have been synthesized by hydrothermal route at 180 °C in presence of NaOH as mineralizer. The obtained ferrite samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and vibrating sample magnetometer (VSM). The XRD analysis showed that pure single phases of cubic ferrites were obtained with x upto 0.3. However, sample with x≥0.5 showed hexagonal phase of cadmium hydroxide (Cd(OH)2) besides the ferrite phase. The increase in Cd-substitution upto x=0.3 leads to an increase in the lattice parameter as well as the average crystallite size of the prepared ferrites. The average crystallite size increased by increasing the Cd-content and was in the range of 39-57 nm. According to VSM results, the saturation magnetization increased with Cd ion substitution.

  3. Adsorption of Pb(2+) from aqueous solution using spinel ferrite prepared from steel pickling sludge.

    PubMed

    Fang, Binbin; Yan, Yubo; Yang, Yang; Wang, Fenglian; Chu, Zhen; Sun, Xiuyun; Li, Jiansheng; Wang, Lianjun

    2016-01-01

    In this paper, spinel ferrite with high crystallinity and high saturation magnetization was successfully prepared from steel pickling sludge by adding iron source and precipitator in the hydrothermal condition. The obtained spinel ferrite was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), vibrating sample magnetometer (VSM), and Zeta potential methods and investigated as an adsorbent for removal of Pb(2+) from aqueous solution. Batch experiments were performed by varying the pH values, contact time, temperature and initial metal concentration. The result of pH impact showed that the adsorption of Pb(2+) was a pH dependent process, and the pH 5.8 ± 0.2 was found to be the optimum condition. The achieved experimental data were analyzed with various kinetic and isotherm models. The kinetic studies revealed that Pb(2+) adsorption onto spinel ferrite followed a pseudo-second order model, and the Langmuir isotherm model provided the perfect fit to the equilibrium experimental data. At different temperatures, the maximum Pb(2+) adsorption capacities calculated from the Langmuir equation were in the range of 126.5-175.4 mg/g, which can be in competition with other adsorbents. The thermodynamic results showed that the spinel ferrite could spontaneously and endothermically adsorb Pb(2+) from aqueous solution. The regeneration studies showed that spinel ferrite could be used five times (removal efficiency (%) >90%) by desorption with HNO3 reagent. PMID:26942534

  4. Effects of magnetic cobalt ferrite nanoparticles on biological and artificial lipid membranes

    PubMed Central

    Drašler, Barbara; Drobne, Damjana; Novak, Sara; Valant, Janez; Boljte, Sabina; Otrin, Lado; Rappolt, Michael; Sartori, Barbara; Iglič, Aleš; Kralj-Iglič, Veronika; Šuštar, Vid; Makovec, Darko; Gyergyek, Sašo; Hočevar, Matej; Godec, Matjaž; Zupanc, Jernej

    2014-01-01

    Background The purpose of this work is to provide experimental evidence on the interactions of suspended nanoparticles with artificial or biological membranes and to assess the possibility of suspended nanoparticles interacting with the lipid component of biological membranes. Methods 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) lipid vesicles and human red blood cells were incubated in suspensions of magnetic bare cobalt ferrite (CoFe2O4) or citric acid (CA)-adsorbed CoFe2O4 nanoparticles dispersed in phosphate-buffered saline and glucose solution. The stability of POPC giant unilamellar vesicles after incubation in the tested nanoparticle suspensions was assessed by phase-contrast light microscopy and analyzed with computer-aided imaging. Structural changes in the POPC multilamellar vesicles were assessed by small angle X-ray scattering, and the shape transformation of red blood cells after incubation in tested suspensions of nanoparticles was observed using scanning electron microscopy and sedimentation, agglutination, and hemolysis assays. Results Artificial lipid membranes were disturbed more by CA-adsorbed CoFe2O4 nanoparticle suspensions than by bare CoFe2O4 nanoparticle suspensions. CA-adsorbed CoFe2O4-CA nanoparticles caused more significant shape transformation in red blood cells than bare CoFe2O4 nanoparticles. Conclusion Consistent with their smaller sized agglomerates, CA-adsorbed CoFe2O4 nanoparticles demonstrate more pronounced effects on artificial and biological membranes. Larger agglomerates of nanoparticles were confirmed to be reactive against lipid membranes and thus not acceptable for use with red blood cells. This finding is significant with respect to the efficient and safe application of nanoparticles as medicinal agents. PMID:24741305

  5. Synthesis, Characterization and in Vitro Evaluation of Manganese Ferrite (MnFe₂O₄) Nanoparticles for Their Biocompatibility with Murine Breast Cancer Cells (4T1).

    PubMed

    Kanagesan, Samikannu; Aziz, Sidek Bin Ab; Hashim, Mansor; Ismail, Ismayadi; Tamilselvan, Subramani; Alitheen, Noorjahan Banu Binti Mohammed; Swamy, Mallappa Kumara; Purna Chandra Rao, Bandaru

    2016-01-01

    Manganese ferrite (MnFe₂O₄) magnetic nanoparticles were successfully prepared by a sol-gel self-combustion technique using iron nitrate and manganese nitrate, followed by calcination at 150 °C for 24 h. Calcined sample was systematically characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and vibrational sample magnetometry (VSM) in order to identify the crystalline phase, functional group, morphology, particle size, shape and magnetic behavior. It was observed that the resultant spinal ferrites obtained at low temperature exhibit single phase, nanoparticle size and good magnetic behavior. The study results have revealed the existence of a potent dose dependent cytotoxic effect of MnFe₂O₄ nanoparticles against 4T1 cell lines at varying concentrations with IC50 values of 210, 198 and 171 μg/mL after 24 h, 48 h and 72 h of incubation, respectively. Cells exposed to higher concentrations of nanoparticles showed a progressive increase of apoptotic and necrotic activity. Below 125 μg/mL concentration the nanoparticles were biocompatible with 4T1 cells. PMID:26978339

  6. Comparative cytotoxic response of nickel ferrite nanoparticles in human liver HepG2 and breast MFC-7 cancer cells.

    PubMed

    Ahamed, Maqusood; Akhtar, Mohd Javed; Alhadlaq, Hisham A; Khan, M A Majeed; Alrokayan, Salman A

    2015-09-01

    Nickel ferrite nanoparticles (NPs) have received much attention for their potential applications in biomedical fields such as magnetic resonance imaging, drug delivery and cancer hyperthermia. However, little is known about the toxicity of nickel ferrite NPs at the cellular and molecular levels. In this study, we investigated the cytotoxic responses of nickel ferrite NPs in two different types of human cells (i.e., liver HepG2 and breast MCF-7). Nickel ferrite NPs induced dose-dependent cytotoxicity in both types of cells, which was demonstrated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazoliumbromide (MTT), neutral red uptake (NRU) and lactate dehydrogenase (LDH) assays. Nickel ferrite NPs were also found to induce oxidative stress, which was evident by the depletion of glutathione and the induction of reactive oxygen species (ROS) and lipid peroxidation. The mitochondrial membrane potential due to nickel ferrite NP exposure was also observed. The mRNA levels for the tumor suppressor gene p53 and the apoptotic genes bax, CASP3 and CASP9 were up-regulated, while the anti-apoptotic gene bcl-2 was down-regulated following nickel ferrite NP exposure. Furthermore, the activities of apoptotic enzymes (caspase-3 and caspase-9) were also higher in both types of cells treated with nickel ferrite NPs. Cytotoxicity induced by nickel ferrite was efficiently prevented by N-acetyl cysteine (ROS scavenger) treatment, which suggested that oxidative stress might be one of the possible mechanisms of nickel ferrite NP toxicity. We also observed that MCF-7 cells were slightly more susceptible to nickel ferrite NP exposure than HepG2 cells. This study warrants further investigation to explore the potential mechanisms of different cytotoxic responses of nickel ferrite NPs in different cell lines. PMID:25966046

  7. Enhancement in magnetic properties of magnesium substituted bismuth ferrite nanoparticles

    SciTech Connect

    Xu, Jianlong; Xie, Dan E-mail: RenTL@mail.tsinghua.edu.cn; Teng, Changjiu; Zhang, Xiaowen; Zhang, Cheng; Sun, Yilin; Ren, Tian-Ling E-mail: RenTL@mail.tsinghua.edu.cn; Zeng, Min; Gao, Xingsen; Zhao, Yonggang

    2015-06-14

    We report a potential way to effectively improve the magnetic properties of BiFeO{sub 3} (BFO) nanoparticles through Mg{sup 2+} ion substitution at the Fe-sites of BFO lattice. The high purity and structural changes induced by Mg doping are confirmed by X-ray powder diffractometer and Raman spectra. Enhanced magnetic properties are observed in Mg substituted samples, which simultaneously exhibit ferromagnetic and superparamagnetic properties at room temperature. A physical model is proposed to support the observed ferromagnetism of Mg doped samples, and the superparamagnetic properties are revealed by the temperature dependent magnetization measurements. The improved magnetic properties and soft nature obtained by Mg doping in BFO nanoparticles demonstrate the possibility of BFO nanoparticles to practical applications.

  8. Method to prepare nanoparticles on porous mediums

    DOEpatents

    Vieth, Gabriel M. [Knoxville, TN; Dudney, Nancy J. [Oak Ridge, TN; Dai, Sheng [Knoxville, TN

    2010-08-10

    A method to prepare porous medium decorated with nanoparticles involves contacting a suspension of nanoparticles in an ionic liquid with a porous medium such that the particles diffuse into the pores of the medium followed by heating the resulting composition to a temperature equal to or greater than the thermal decomposition temperature of the ionic liquid resulting in the removal of the liquid portion of the suspension. The nanoparticles can be a metal, an alloy, or a metal compound. The resulting compositions can be used as catalysts, sensors, or separators.

  9. Studying the effect of Zn-substitution on the magnetic and hyperthermic properties of cobalt ferrite nanoparticles.

    PubMed

    Mameli, V; Musinu, A; Ardu, A; Ennas, G; Peddis, D; Niznansky, D; Sangregorio, C; Innocenti, C; Thanh, Nguyen T K; Cannas, C

    2016-05-21

    The possibility to finely control nanostructured cubic ferrites (M(II)Fe2O4) paves the way to design materials with the desired magnetic properties for specific applications. However, the strict and complex interrelation among the chemical composition, size, polydispersity, shape and surface coating renders their correlation with the magnetic properties not trivial to predict. In this context, this work aims to discuss the magnetic properties and the heating abilities of Zn-substituted cobalt ferrite nanoparticles with different zinc contents (ZnxCo1-xFe2O4 with 0 < x < 0.6), specifically prepared with similar particle sizes (∼7 nm) and size distributions having the crystallite size (∼6 nm) and capping agent amount of 15%. All samples have high saturation magnetisation (Ms) values at 5 K (>100 emu g(-1)). The increase in the zinc content up to x = 0.46 in the structure has resulted in an increase of the saturation magnetisation (Ms) at 5 K. High Ms values have also been revealed at room temperature (∼90 emu g(-1)) for both CoFe2O4 and Zn0.30Co0.70Fe2O4 samples and their heating ability has been tested. Despite a similar saturation magnetisation, the specific absorption rate value for the cobalt ferrite is three times higher than the Zn-substituted one. DC magnetometry results were not sufficient to justify these data, the experimental conditions of SAR and static measurements being quite different. The synergic combination of DC with AC magnetometry and (57)Fe Mössbauer spectroscopy represents a powerful tool to get new insights into the design of suitable heat mediators for magnetic fluid hyperthermia. PMID:27121263

  10. Online monitoring of cell metabolism to assess the toxicity of nanoparticles: the case of cobalt ferrite.

    PubMed

    Mariani, Valentina; Ponti, Jessica; Giudetti, Guido; Broggi, Francesca; Marmorato, Patrick; Gioria, Sabrina; Franchini, Fabio; Rauscher, Hubert; Rossi, François

    2012-05-01

    Different in vitro assays are successfully used to determine the relative cytotoxicity of a broad range of compounds. Nevertheless, different research groups have pointed out the difficulty in using the same tests to assess the toxicity of nanoparticles (NPs). In this study, we evaluated the possible use of a microphysiometer, Bionas 2500 analyzing system Bionas GmbH®, to detect in real time changes in cell metabolisms linked to NPs exposure. We focused our work on response changes of fibroblast cultures linked to exposure by cobalt ferrite NPs and compared the results to conventional in vitro assays. The measurements with the microphysiometer showed a cobalt ferrite cytotoxic effect, confirmed by the Colony Forming Efficiency assay. In conclusion, this work demonstrated that the measurement of metabolic parameters with a microphysiometer is a promising method to assess the toxicity of NPs and offers the advantage to follow on-line the cell metabolic changes. PMID:21495878

  11. Investigations of cations distributions and morphology of cobalt ferrite magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Chandekar, Kamlesh V.; Kant, K. Mohan

    2016-05-01

    Cobalt ferrite nanoparticles were synthesized by co-precipitation method and structural properties was investigated by X-ray diffraction (XRD) at room temperature. X-ray diffraction data was used to determine lattice parameter, X-ray density, distributions of cations among tetrahedral and octahedral sites, site radii, ionic radii and bond length of inverse spinel cobalt ferrite. XRD analysis revealed crystallinity and high intense peak correspond to cubic inverse spinel structure with average crystalline size measured by X-ray line profile fitting was found to be 13nm for most intense peak (311). The surface morphology and microstructural feature was investigated by TEM analysis which revealed that particle size varying from 12-22 nm with selected electron diffraction pattern (SAED).

  12. Method for preparing spherical ferrite beads and use thereof

    DOEpatents

    Lauf, Robert J.; Anderson, Kimberly K.; Montgomery, Frederick C.; Collins, Jack L.

    2002-01-01

    The invention allows the fabrication of small, dense, highly polished spherical beads of hexagonal ferrites with selected compositions for use in nonreciprocal microwave and mm-wave devices as well as in microwave absorbent or reflective coatings, composites, and the like. A porous, generally spherical bead of hydrous iron oxide is made by a sol-gel process to form a substantially rigid bead having a generally fine crystallite size and correspondingly finely distributed internal porosity. The resulting gel bead is washed and hydrothermally reacted with a soluble alkaline earth salt (typically Ba or Sr) under conditions of elevated temperature and pressure to convert the bead into a mixed hydrous iron-alkaline earth oxide while retaining the generally spherical shape. This mixed oxide bead is then washed, dried, and calcined to produce the desired (BaFe.sub.12 O.sub.19 or SrFe.sub.12 O.sub.19) crystal structure. The calcined bead is then sintered to form a dense bead of the BaFe.sub.12 O.sub.19 and SrFe.sub.12 O.sub.19 phase suitable for polishing and incorporation into various microwave devices and components.

  13. Biocompatible mesoporous silica-coated superparamagnetic manganese ferrite nanoparticles for targeted drug delivery and MR imaging applications.

    PubMed

    Sahoo, Banalata; Devi, K Sanjana P; Dutta, Sujan; Maiti, Tapas K; Pramanik, Panchanan; Dhara, Dibakar

    2014-10-01

    Multifunctional mesoporous silica-coated superparamagnetic manganese ferrite (MnFe2O4) nanoparticles (M-MSN) were synthesized and evaluated for targeted drug delivery and magnetic resonance imaging (MRI) applications. MnFe2O4 nanoparticles were prepared by solvothermal route and were silica-coated by surface silylation using sol-gel reactions. Subsequently, silylation was done using (3-aminopropyl)triethoxysilane in presence of a surfactant (CTAB), followed by selective etching of the surfactant molecules that resulted in amine-functionalized superparamagnetic nanoparticles (NH2-MSN). Further modification of the surface of the NH2-MSN with targeting (folate) or fluorescent (RITC) molecules resulted in M-MSN. The formation of the M-MSN was proved by several characterization techniques viz. XRD, XPS, HRTEM, FESEM, VSM, BET surface area measurement, FTIR, and UV-Vis spectroscopy. The M-MSN were loaded with anticancer drug Doxorubicin and the efficacy of the DOX loaded M-MSN was evaluated through in vitro cytotoxicity, fluorescence microscopy, and apoptosis studies. The in vivo biocompatibility of the M-MSN was demonstrated in a mice-model system. Moreover, the M-MSN also acted as superior MRI contrast agent owing to a high magnetization value as well as superparamagnetic behavior at room temperature. These folate-conjugated nanoparticles (FA-MSN) exhibited stronger T2-weighted MRI contrast towards HeLa cells as compared to the nanoparticles without folate conjugation, justifying their potential importance in MRI based diagnosis of cancer. Such M-MSN with a magnetic core required for MRI imaging, a porous shell for carrying drug molecules, a targeting moeity for cancer cell specificity and a fluorescent molecule for imaging, all integrated into a single system, may potentially serve as an excellent material in biomedical applications. PMID:24980623

  14. Study of the preparation of NI-Mn-Zn ferrite using spent NI-MH and alkaline Zn-Mn batteries

    NASA Astrophysics Data System (ADS)

    Xi, Guoxi; Xi, Yuebin; Xu, Huidao; Wang, Lu

    2016-01-01

    Magnetic nanoparticles of Ni-Mn-Zn ferrite have been prepared by a sol-gel method making use of spent Ni-MH and Zn-Mn batteries as source materials. Characterization by X-ray diffraction was carried out to study the particle size. The presence of functional groups was identified by Fourier transform infrared spectroscopy. From studies by thermogravimetry and differential scanning calorimetry, crystallization occurred at temperatures above 560 °C. The magnetic properties of the final products were found to be directly influenced by the average particle size of the product. The Ms values increase and the Hc values decrease as the size of the Ni-Mn-Zn ferrite particles increases.

  15. Correlating size and composition-dependent effects with magnetic, Mössbauer, and pair distribution function measurements in a family of catalytically active ferrite nanoparticles

    DOE PAGESBeta

    Wong, Stanislaus; Papaefthymiou, Georgia C.; Lewis, Crystal S.; Han, Jinkyu; Zhang, Cheng; Li, Qiang; Shi, Chenyang; Abeykoon, A. M.Milinda; Billinge, Simon J.L.; Stach, Eric; et al

    2015-05-06

    The magnetic spinel ferrites, MFe₂O₄ (wherein 'M' = a divalent metal ion such as but not limited to Mn, Co, Zn, and Ni), represent a unique class of magnetic materials in which the rational introduction of different 'M's can yield correspondingly unique and interesting magnetic behaviors. Herein we present a generalized hydrothermal method for the synthesis of single-crystalline ferrite nanoparticles with 'M' = Mg, Fe, Co, Ni, Cu, and Zn, respectively, which can be systematically and efficaciously produced simply by changing the metal precursor. Our protocol can moreover lead to reproducible size control by judicious selection of various surfactants. Asmore » such, we have probed the effects of both (i) size and (ii) chemical composition upon the magnetic properties of these nanomaterials using complementary magnetometry and Mössbauer spectroscopy techniques. The structure of the samples was confirmed by atomic PDF analysis of X-ray and electron powder diffraction data as a function of particle size. These materials retain the bulk spinel structure to the smallest size (i.e., 3 nm). In addition, we have explored the catalytic potential of our ferrites as both (a) magnetically recoverable photocatalysts and (b) biological catalysts, and noted that many of our as-prepared ferrite systems evinced intrinsically higher activities as compared with their iron oxide analogues.« less

  16. Correlating size and composition-dependent effects with magnetic, Mössbauer, and pair distribution function measurements in a family of catalytically active ferrite nanoparticles

    SciTech Connect

    Wong, Stanislaus; Papaefthymiou, Georgia C.; Lewis, Crystal S.; Han, Jinkyu; Zhang, Cheng; Li, Qiang; Shi, Chenyang; Abeykoon, A. M.Milinda; Billinge, Simon J.L.; Stach, Eric; Thomas, Justin; Guerrero, Kevin; Munayco, Pablo; Munayco, Jimmy; Scorzelli, Rosa B.; Burnham, Philip; Viescas, Arthur J; Tiano, Amanda L.

    2015-05-06

    The magnetic spinel ferrites, MFe₂O₄ (wherein 'M' = a divalent metal ion such as but not limited to Mn, Co, Zn, and Ni), represent a unique class of magnetic materials in which the rational introduction of different 'M's can yield correspondingly unique and interesting magnetic behaviors. Herein we present a generalized hydrothermal method for the synthesis of single-crystalline ferrite nanoparticles with 'M' = Mg, Fe, Co, Ni, Cu, and Zn, respectively, which can be systematically and efficaciously produced simply by changing the metal precursor. Our protocol can moreover lead to reproducible size control by judicious selection of various surfactants. As such, we have probed the effects of both (i) size and (ii) chemical composition upon the magnetic properties of these nanomaterials using complementary magnetometry and Mössbauer spectroscopy techniques. The structure of the samples was confirmed by atomic PDF analysis of X-ray and electron powder diffraction data as a function of particle size. These materials retain the bulk spinel structure to the smallest size (i.e., 3 nm). In addition, we have explored the catalytic potential of our ferrites as both (a) magnetically recoverable photocatalysts and (b) biological catalysts, and noted that many of our as-prepared ferrite systems evinced intrinsically higher activities as compared with their iron oxide analogues.

  17. Correlating size and composition-dependent effects with magnetic, Mssbauer, and pair distribution function measurements in a family of catalytically active ferrite nanoparticles

    SciTech Connect

    Wong, Stanislaus; Papaefthymiou, Georgia C.; Lewis, Crystal S.; Han, Jinkyu; Zhang, Cheng; Li, Qiang; Shi, Chenyang; Abeykoon, A. M.Milinda; Billinge, Simon J.L.; Stach, Eric; Thomas, Justin; Guerrero, Kevin; Munayco, Pablo; Munayco, Jimmy; Scorzelli, Rosa B.; Burnham, Philip; Viescas, Arthur J; Tiano, Amanda L.

    2015-05-06

    The magnetic spinel ferrites, MFe?O? (wherein 'M' = a divalent metal ion such as but not limited to Mn, Co, Zn, and Ni), represent a unique class of magnetic materials in which the rational introduction of different 'M's can yield correspondingly unique and interesting magnetic behaviors. Herein we present a generalized hydrothermal method for the synthesis of single-crystalline ferrite nanoparticles with 'M' = Mg, Fe, Co, Ni, Cu, and Zn, respectively, which can be systematically and efficaciously produced simply by changing the metal precursor. Our protocol can moreover lead to reproducible size control by judicious selection of various surfactants. As such, we have probed the effects of both (i) size and (ii) chemical composition upon the magnetic properties of these nanomaterials using complementary magnetometry and Mssbauer spectroscopy techniques. The structure of the samples was confirmed by atomic PDF analysis of X-ray and electron powder diffraction data as a function of particle size. These materials retain the bulk spinel structure to the smallest size (i.e., 3 nm). In addition, we have explored the catalytic potential of our ferrites as both (a) magnetically recoverable photocatalysts and (b) biological catalysts, and noted that many of our as-prepared ferrite systems evinced intrinsically higher activities as compared with their iron oxide analogues.

  18. Citric Acid Fuctionalized Magnetic Ferrite Nanoparticles for Photocatalytic Degradation of Azo Dye.

    PubMed

    Mahto, Triveni Kumar; Roy, Anurag; Sahoo, Banalata; Sahu, Sumanta Kumar

    2015-01-01

    In this study different magnetic ferrite nanoparticles (MFe2O4, where M = Fe, Mn, Zn) were synthesized through an aqueous coprecipitation method and then functionalized with citric acid for the degradation of azo dye present in industrial waste water. Here we evaluated the role of citric acid for photocatalytic application. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and the catalytic activity in degradation of methyl orange (MO) was evaluated. The rate of MO degradation in different magnetic systems was determined by UV-Vis spectroscopy. The effect of active parameters (pH, initial MO concentration and effect of sunlight) on degradation performance was investigated. For the first time, citric acid chemistry is successfully exploited to develop a photocatalyst that can successfully degrade the dyes. This citric acid functionalized magnetic ferrite nanoparticles are very much effective for photocalytic degradation of dye and also these can be recollected with the help of permanent magnet for successive uses. PMID:26328345

  19. HRTEM Study of Oxide Nanoparticles in K3-ODS Ferritic Steel Developed for Radiation Tolerance

    SciTech Connect

    Hsiung, L; Fluss, M; Tumey, S; Kuntz, J; El-Dasher, B; Wall, M; Choi, W; Kimura, A; Willaime, F; Serruys, Y

    2009-11-02

    Crystal and interfacial structures of oxide nanoparticles and radiation damage in 16Cr-4.5Al-0.3Ti-2W-0.37 Y{sub 2}O{sub 3} ODS ferritic steel have been examined using high-resolution transmission electron microscopy (HRTEM) techniques. Oxide nanoparticles with a complex-oxide core and an amorphous shell were frequently observed. The crystal structure of complex-oxide core is identified to be mainly monoclinic Y{sub 4}Al{sub 2}O{sub 9} (YAM) oxide compound. Orientation relationships between the oxide and the matrix are found to be dependent on the particle size. Large particles (> 20 nm) tend to be incoherent and have a spherical shape, whereas small particles (< 10 nm) tend to be coherent or semi-coherent and have a faceted interface. The observations of partially amorphous nanoparticles and multiple crystalline domains formed within a nanoparticle lead us to propose a three-stage mechanism to rationalize the formation of oxide nanoparticles containing core/shell structures in as-fabricated ODS steels. Effects of nanoparticle size and density on cavity formation induced by (Fe{sup 8+} + He{sup +}) dual-beam irradiation are briefly addressed.

  20. HRTEM Study of the Role of Nanoparticles in ODS Ferritic Steel

    SciTech Connect

    Hsiung, L; Tumey, S; Fluss, M; Serruys, Y; Willaime, F

    2011-08-30

    Structures of nanoparticles and their role in dual-ion irradiated Fe-16Cr-4.5Al-0.3Ti-2W-0.37Y{sub 2}O{sub 3} (K3) ODS ferritic steel produced by mechanical alloying (MA) were studied using high-resolution transmission electron microscopy (HRTEM) techniques. The observation of Y{sub 4}Al{sub 2}O{sub 9} complex-oxide nanoparticles in the ODS steel imply that decomposition of Y{sub 2}O{sub 3} in association with internal oxidation of Al occurred during mechanical alloying. HRTEM observations of crystalline and partially crystalline nanoparticles larger than {approx}2 nm and amorphous cluster-domains smaller than {approx}2 nm provide an insight into the formation mechanism of nanoparticles/clusters in MA/ODS steels, which we believe involves solid-state amorphization and re-crystallization. The role of nanoparticles/clusters in suppressing radiation-induced swelling is revealed through TEM examinations of cavity distributions in (Fe + He) dual-ion irradiated K3-ODS steel. HRTEM observations of helium-filled cavities (helium bubbles) preferably trapped at nanoparticle/clusters in dual-ion irradiated K3-ODS are presented.

  1. [Superparamagnetic Cobalt Ferrite Nanoparticles "Blow up" Spatial Ordering of Double-stranded DNA Molecules].

    PubMed

    Yevdokimov, Yu M; Pershina, A G; Salyanov, V I; Magaeva, A A; Popenko, V I; Shtykova, E V; Dadinova, L A; Skuridin, S G

    2015-01-01

    The formation of cholesteric liquid-crystalline dispersions formed by double-stranded DNA molecules, handled by positively charged superparamagnetic cobalt ferrite nanoparticles, as well as action of these nanoparticles on DNA dispersion, are considered. The binding of magnetic nanoparticles to the linear double-stranded DNA in solution of high ionic strength (0.3 M NaCl) and subsequent phase exclusion of these complexes from polyethylene glycol-containing solutions lead to their inability to form dispersions, whose particles do possess the spatially twisted arrangement of neighboring double-stranded DNA molecules. The action of magnetic nanoparticles on DNA dispersion (one magnetic nanoparticle per one double-stranded DNA molecule) results in such "perturbation" of DNA structure at sites of magnetic nanoparticles binding that the regular spatial structure of DNA dispersion particles "blows up"; this process is accompanied by disappearance of both abnormal optical activity and characteristic Bragg maximum on the small-angle X-ray scattering curve. Allowing with the fact that the physicochemical properties of the DNA liquid-crystalline dispersion particles reflect features of spatial organization of these molecules in chromosomes of primitive organisms, it is possible, that the found effect can have the relevant biological consequences. PMID:26349206

  2. HRTEM study of oxide nanoparticles in K3-ODS ferritic steel developed for radiation tolerance

    NASA Astrophysics Data System (ADS)

    Hsiung, L.; Fluss, M.; Tumey, S.; Kuntz, J.; El-Dasher, B.; Wall, M.; Choi, B.; Kimura, A.; Willaime, F.; Serruys, Y.

    2011-02-01

    Crystal and interfacial structures of oxide nanoparticles and radiation damage in 16Cr-4.5Al-0.3Ti-2W-0.37 Y 2O 3 ODS ferritic steel have been examined using high-resolution transmission electron microscopy (HRTEM) techniques. Oxide nanoparticles with a complex-oxide core and an amorphous shell were frequently observed. The crystal structure of complex-oxide core is identified to be mainly monoclinic Y 4Al 2O 9 (YAM) oxide compound. Orientation relationships between the oxide and the matrix are found to be dependent on the particle size. Large particles (>20 nm) tend to be incoherent and have a spherical shape, whereas small particles (<10 nm) tend to be coherent or semi-coherent and have a faceted interface. The observations of partially amorphous nanoparticles and multiple crystalline domains formed within a nanoparticle lead us to propose a three-stage mechanism to rationalize the formation of oxide nanoparticles containing core/shell structures in as-fabricated ODS steels. Effects of nanoparticle size and density on cavity formation induced by (Fe 8+ + He +) dual-beam irradiation are briefly addressed.

  3. Preparation and characterization of Mg nanoparticles

    SciTech Connect

    Song Meirong; Chen Miao Zhang Zhijun

    2008-05-15

    In this paper, Mg nanoparticles were prepared in tetrahydrofuran via lithium reduction of the corresponding Mg salt. X-ray diffraction and scanning electron microscope investigations confirm the formation of hexagonal phase Mg particles with an average size of 300 nm. X-ray photoelectron spectrometer analysis indicates that the as-prepared Mg nanoparticles are covered with a protecting layer consisting of residue solvents, naphthalene and Mg(OH){sub 2}, which slows down further oxidation under ambient conditions. Thermal analysis shows that the rapid oxidation and nitridation processes of the particles take place at around 500 deg. C and 553 deg. C, respectively. Furthermore, the addition of a small amount of magnesium nanoparticles remarkably catalyzes the decomposition process of ammonium perchlorate by lowering the decomposition temperature and enhancing its heat output.

  4. Synchrotron study on load partitioning between ferrite/martensite and nanoparticles of a 9Cr ODS steel

    NASA Astrophysics Data System (ADS)

    Mo, Kun; Zhou, Zhangjian; Miao, Yinbin; Yun, Di; Tung, Hsiao-Ming; Zhang, Guangming; Chen, Weiying; Almer, Jonathan; Stubbins, James F.

    2014-12-01

    Oxide dispersion strengthened (ODS) steels exhibit exceptional radiation resistance and high-temperature creep strength when compared to traditional ferritic and ferritic/martensitic (F/M) steels. Their excellent mechanical properties result from very fine nanoparticles dispersed within the matrix. In this work, we applied a high-energy synchrotron radiation X-ray to study the deformation process of a 9Cr ODS steel. The load partitioning between the ferrite/martensite and the nanoparticles was observed during sample yielding. During plastic deformation, the nanoparticles experienced a dramatic loading process, and the internal stress on the nanoparticles increased to a maximum value of 3.7 GPa, which was much higher than the maximum applied stress (∼986 MPa). After necking, the loading capacity of the nanoparticles was significantly decreased due to a debonding of the particles from the matrix, as indicated by a decline in lattice strain/internal stress. Due to the load partitioning, the ferrite/martensite slightly relaxed during early yielding, and slowly strained until failure. This study develops a better understanding of loading behavior for various phases in the ODS F/M steel.

  5. Highly coercive cobalt ferrite nanoparticles-CuTl-1223 superconductor composites

    NASA Astrophysics Data System (ADS)

    Jabbar, Abdul; Qasim, Irfan; Khan, Shahid A.; Nadeem, K.; Waqee-ur-Rehman, M.; Mumtaz, M.; Zeb, F.

    2015-03-01

    We explored the effects of highly coercive cobalt ferrite (CoFe2O4) nanoparticles addition on structural, morphological, and superconducting properties of Cu0.5Tl0.5Ba2Ca2Cu3O10-δ (CuTl-1223} matrix. Series of (CoFe2O4)x/CuTl-1223 (x=0 2.0 wt%) composites samples were synthesized and were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) absorption spectroscopy, and dc-resistivity versus temperature measurements. The magnetic behavior of CoFe2O4 nanoparticles was determined by MH-loops with the help of superconducting quantum interference device (SQUID). MH-loops analysis showed that these nanoparticles exhibit high saturation magnetization (86 emu/g) and high coercivity (3350 Oe) at 50 K. The tetragonal structure of host CuTl-1223 superconducting matrix was not altered after the addition of CoFe2O4 nanoparticles, which gave us a clue that these nanoparticles had occupied the inter-granular sites (grain-boundaries) and had filled the pores. The increase of mass density with increasing content of these nanoparticles in composites can also be an evidence of filling up the voids in the matrix. The resistivity versus temperature measurements showed an increase in zero resistivity critical {Tc(0)}, which could be most probably due to improvement of weak-links by the addition of these nanoparticles. But the addition of these nanoparticles beyond an optimum level caused the agglomeration and produced additional stresses in material and suppressed the superconductivity.

  6. Surface spin-glass in cobalt ferrite nanoparticles dispersed in silica matrix

    NASA Astrophysics Data System (ADS)

    Zeb, F.; Sarwer, W.; Nadeem, K.; Kamran, M.; Mumtaz, M.; Krenn, H.; Letofsky-Papst, I.

    2016-06-01

    Surface effects in cobalt ferrite (CoFe2O4) nanoparticles dispersed in a silica (SiO2) matrix were studied by using AC and DC magnetization. Nanoparticles with different concentration of SiO2 were synthesized by using sol-gel method. Average crystallite size lies in the range 25-34 nm for different SiO2 concentration. TEM image showed that particles are spherical and elongated in shape. Nanoparticles with higher concentration of SiO2 exhibit two peaks in the out-of-phase ac-susceptibility. First peak lies in the high temperature regime and corresponds to average blocking temperature of the nanoparticles. Second peak lies in the low temperature regime and is attributed to surface spin-glass freezing in these nanoparticles. Low temperature peak showed SiO2 concentration dependence and was vanished for large uncoated nanoparticles. The frequency dependence of the AC-susceptibility of low temperature peak was fitted with dynamic scaling law which ensures the presence of spin-glass behavior. With increasing applied DC field, the low temperature peak showed less shift as compared to blocking peak, broaden, and decreased in magnitude which also signifies its identity as spin-glass peak for smaller nanoparticles. M-H loops showed the presence of more surface disorder in nanoparticles dispersed in 60% SiO2 matrix. All these measurements revealed that surface effects become strengthen with increasing SiO2 matrix concentration and surface spins freeze in to spin-glass state at low temperatures.

  7. An integrated study of thermal treatment effects on the microstructure and magnetic properties of Zn-ferrite nanoparticles

    SciTech Connect

    Antic, Bratislav; Perovic, Marija; Kremenovic, Aleksandar; Blanusa, Jovan; Spasojevic, Vojislav; Vulic, Predrag; Bessais, Lotfi; Bozin, Emil S

    2015-09-30

    The evolution of the magnetic state, crystal structure and microstructure parameters of nanocrystalline zinc–ferrite, tuned by thermal annealing of ~4 nm nanoparticles, was systematically studied by complementary characterization methods. Structural analysis of neutron and synchrotron x-ray radiation data revealed a mixed cation distribution in the nanoparticle samples, with the degree of inversion systematically decreasing from 0.25 in an as-prepared nanocrystalline sample to a non-inverted spinel structure with a normal cation distribution in the bulk counterpart. The results of DC magnetization and Mossbauer spectroscopy experiments indicated a superparamagnetic relaxation in ~4 nm nanoparticles, albeit with different freezing temperatures Tf of 27.5 K and 46 K, respectively. The quadrupole splitting parameter decreases with the annealing temperature due to cation redistribution between the tetrahedral and octahedral sites of the spinel structure and the associated defects. DC magnetization measurements indicated the existence of significant interparticle interactions among nanoparticles (‘superspins’). Additional confirmation for the presence of interparticle interactions was found from the fit of the Tf(H) dependence to the AT line, from which a value of the anisotropy constant of Keff = 5.6 × 105 erg cm-3 was deduced. Further evidence for strong interparticle interactions was found from AC susceptibility measurements, where the frequency dependence of the freezing temperature Tf(ƒ) was satisfactory described by both Vogel–Fulcher and dynamic scaling theory, both applicable for interacting systems. The parameters obtained from these fits suggest collective freezing of magnetic moments at Tf .

  8. Preparation and characterization of Ni-Zn ferrite + polymer nanocomposites using mechanical milling method

    NASA Astrophysics Data System (ADS)

    Raju, P.; Murthy, S. R.

    2013-12-01

    The insulating properties of Ni-Zn ferrites can be improved by the addition of various types of insulating materials such as polymers, ceramics, etc. In this connection, ferrite-polymer composites have been subjected to extensive research, because they have many applications: electromagnetic interference shielding, rechargeable battery, electrodes and sensors, and microwave absorption. Electrical and magnetic properties of such composites will depend on the size, shape and amount of filler addition. In this paper, we report the preparation and characterization of nanocomposites of Ni-Zn ferrite + paraformaldehyde. These nanocomposites were prepared by using mechanical milling method and characterized by X-ray powder diffraction, scanning electron microscopy (SEM) and Fourier transform infrared spectrometer. The particle size estimated from SEM pictures for composites varies from 36 to 60 nm. Magnetic properties were measured on nanocomposites at room temperature. The complex permittivity and permeability were measured over a wide frequency range from 1 MHz to 1.8 GHz at room temperature. From our studies, it is observed that both the values of permittivity and permeability decrease with an increase in polymer content.

  9. Manganese ferrite-based nanoparticles induce ex vivo, but not in vivo, cardiovascular effects.

    PubMed

    Nunes, Allancer D C; Ramalho, Laylla S; Souza, Alvaro P S; Mendes, Elizabeth P; Colugnati, Diego B; Zufelato, Nícholas; Sousa, Marcelo H; Bakuzis, Andris F; Castro, Carlos H

    2014-01-01

    Magnetic nanoparticles (MNPs) have been used for various biomedical applications. Importantly, manganese ferrite-based nanoparticles have useful magnetic resonance imaging characteristics and potential for hyperthermia treatment, but their effects in the cardiovascular system are poorly reported. Thus, the objectives of this study were to determine the cardiovascular effects of three different types of manganese ferrite-based magnetic nanoparticles: citrate-coated (CiMNPs); tripolyphosphate-coated (PhMNPs); and bare magnetic nanoparticles (BaMNPs). The samples were characterized by vibrating sample magnetometer, X-ray diffraction, dynamic light scattering, and transmission electron microscopy. The direct effects of the MNPs on cardiac contractility were evaluated in isolated perfused rat hearts. The CiMNPs, but not PhMNPs and BaMNPs, induced a transient decrease in the left ventricular end-systolic pressure. The PhMNPs and BaMNPs, but not CiMNPs, induced an increase in left ventricular end-diastolic pressure, which resulted in a decrease in a left ventricular end developed pressure. Indeed, PhMNPs and BaMNPs also caused a decrease in the maximal rate of left ventricular pressure rise (+dP/dt) and maximal rate of left ventricular pressure decline (-dP/dt). The three MNPs studied induced an increase in the perfusion pressure of isolated hearts. BaMNPs, but not PhMNPs or CiMNPs, induced a slight vasorelaxant effect in the isolated aortic rings. None of the MNPs were able to change heart rate or arterial blood pressure in conscious rats. In summary, although the MNPs were able to induce effects ex vivo, no significant changes were observed in vivo. Thus, given the proper dosages, these MNPs should be considered for possible therapeutic applications. PMID:25031535

  10. Manganese ferrite-based nanoparticles induce ex vivo, but not in vivo, cardiovascular effects

    PubMed Central

    Nunes, Allancer DC; Ramalho, Laylla S; Souza, Álvaro PS; Mendes, Elizabeth P; Colugnati, Diego B; Zufelato, Nícholas; Sousa, Marcelo H; Bakuzis, Andris F; Castro, Carlos H

    2014-01-01

    Magnetic nanoparticles (MNPs) have been used for various biomedical applications. Importantly, manganese ferrite-based nanoparticles have useful magnetic resonance imaging characteristics and potential for hyperthermia treatment, but their effects in the cardiovascular system are poorly reported. Thus, the objectives of this study were to determine the cardiovascular effects of three different types of manganese ferrite-based magnetic nanoparticles: citrate-coated (CiMNPs); tripolyphosphate-coated (PhMNPs); and bare magnetic nanoparticles (BaMNPs). The samples were characterized by vibrating sample magnetometer, X-ray diffraction, dynamic light scattering, and transmission electron microscopy. The direct effects of the MNPs on cardiac contractility were evaluated in isolated perfused rat hearts. The CiMNPs, but not PhMNPs and BaMNPs, induced a transient decrease in the left ventricular end-systolic pressure. The PhMNPs and BaMNPs, but not CiMNPs, induced an increase in left ventricular end-diastolic pressure, which resulted in a decrease in a left ventricular end developed pressure. Indeed, PhMNPs and BaMNPs also caused a decrease in the maximal rate of left ventricular pressure rise (+dP/dt) and maximal rate of left ventricular pressure decline (−dP/dt). The three MNPs studied induced an increase in the perfusion pressure of isolated hearts. BaMNPs, but not PhMNPs or CiMNPs, induced a slight vasorelaxant effect in the isolated aortic rings. None of the MNPs were able to change heart rate or arterial blood pressure in conscious rats. In summary, although the MNPs were able to induce effects ex vivo, no significant changes were observed in vivo. Thus, given the proper dosages, these MNPs should be considered for possible therapeutic applications. PMID:25031535

  11. Study of Ni-Zn Ferrite Prepared From Citrate Precursor

    NASA Astrophysics Data System (ADS)

    Sudheesh, V. D.; Vinesh, A.; Lakshmi, N.; Venugopalan, K.

    2011-07-01

    Ni0.5Zn0.5Fe2O4 prepared using citrate precursor method and calcined at different temperatures is studied using X-ray diffraction (XRD), Mössbauer spectroscopy and DC magnetization. Magnetization study shows that critical size of the sample is around 50 nm. Mössbauer studies confirm that there is no change in the cation distribution with calcining and also that a particle size distribution exists in samples calcined at higher temperatures. Thus the change in magnetic properties can be entirely attributed to structural parameters due to variation in size leading to different core-spin ratio, grain boundary effects etc.

  12. Synthesis of nickel–zinc ferrite magnetic nanoparticle and dye degradation using photocatalytic ozonation

    SciTech Connect

    Mahmoodi, Niyaz Mohammad; Bashiri, Marziyeh; Moeen, Shirin Jebeli

    2012-12-15

    Graphical abstract: Display Omitted Highlights: ► Nickel–zinc ferrite magnetic nanoparticle (NZFMN) was synthesized and characterized. ► Dye degradation by photocatalytic ozonation using NZFMN was studied. ► Formate, acetate and oxalate were detected as dominant dye degradation aliphatic intermediates. ► Nitrate, sulfate and chloride ions were detected as mineralization products of dyes. ► NZFMN was an effective magnetic nanocatalyst to degrade dyes. -- Abstract: In this paper, nickel–zinc ferrite magnetic nanoparticle (NZFMN) was synthesized and its dye degradation ability using photocatalytic ozonation was investigated. The NZFMN was characterized by X-ray diffraction (XRD), scanning electron microscopic (SEM), Fourier transforms infrared (FTIR) and alternative gradient force magnetometer (AGFM). Reactive Red 198 (RR198) and Direct Green 6 (DG6) were used as dye models. UV–vis and ion chromatography (IC) analyses were employed to study dye degradation. The effects of operational parameters on decolorization such as NZFMN dosage, dye concentration, salt and pH were studied. RR198 and DG6 were completely decolorized (100%) by photocatalytic ozonation using NZFMN. Formate, acetate and oxalate anions were detected as dominant aliphatic intermediates. Nitrate, sulfate and chloride ions were detected as mineralization products of dyes. Results showed that the photocatalytic ozonation using NZFMN was a very effective method for dye degradation.

  13. Synthesis, structural and magnetic behavior studies of Zn-Al substituted cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Zare, Samad; Ati, Ali A.; Dabagh, Shadab; Rosnan, R. M.; Othaman, Zulkafli

    2015-06-01

    A series of nano-sized Zn-Al substituted cobalt ferrite Co(1-x)Zn(x)Fe2-xAlxO4 with 0.0 ⩽ x ⩽ 1.0 have been synthesized by chemical co-precipitation technique. The XRD spectra revealed the single phase spinel structure of Co(1-x)Zn(x)Fe2-xAlxO4 with average size of nanoparticles are estimated to be 17-30 nm. These are small enough to achieve the suitable signal to noise ratio, which is important in the high-density recording media. The FTIR spectra show the characteristic of two strong absorption bands at 560-600 cm-1 corresponds to the intrinsic stretching vibrations of the metal at the tetrahedral site and lowest band is observed at 370-410 cm-1 corresponds to octahedral site. The crystalline structures of nanoparticles composite were characterized by Field Emission Scanning Electron Microscopy (FE-SEM). The magnetic properties such as saturation magnetization, remanence magnetization, and coercivity were calculated from the hysteresis loops. Saturation magnetization were found to increase up to x = 0.4 while remanence magnetization and coercivity continuously decrease with increasing Zn-Al concentration. The stability in coercivity while increase in saturation magnetization confirms that the Co0.6Zn0.4Fe1.6Al0.4O4 ferrite sample is suitable for applications in high-density recording media.

  14. Ultrafast and continuous synthesis of crystalline ferrite nanoparticles in supercritical ethanol

    NASA Astrophysics Data System (ADS)

    Pascu, Oana; Marre, Samuel; Aymonier, Cyril; Roig, Anna

    2013-02-01

    Magnetic nanoparticles (NPs) are of increasing interest in various industrially relevant products. For these, the development of greener and faster approaches facilitating scaling-up production is of paramount importance. Here, we report a novel, green and potentially scalable approach for the continuous and ultrafast (90 s) synthesis of superparamagnetic ferrite NPs (MnFe2O4, Fe3O4) in supercritical ethanol (scEtOH) at a fairly moderate temperature (260 °C). ScEtOH exhibits numerous advantages such as its production from bio-resources, its lack of toxicity and its relatively low supercritical coordinates (pc = 6.39 MPa and Tc = 243 °C), being therefore appropriate for the development of sustainable technologies. The present study is completed by the investigation of both in situ and ex situ NP surface functionalization. The as-obtained nanoparticles present good crystallinity, sizes below 8 nm, superparamagnetic behavior at room temperature and high saturation magnetization. Moreover, depending on the capping strategy, the ferrite NPs present extended (for in situ coated NPs) or short-term (for ex situ coated NPs) colloidal stability.

  15. In-situ high-pressure x-ray diffraction study of zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Ferrari, S.; Kumar, R. S.; Grinblat, F.; Aphesteguy, J. C.; Saccone, F. D.; Errandonea, D.

    2016-06-01

    We have studied the high-pressure structural behavior of zinc ferrite (ZnFe2O4) nanoparticles by powder X-ray diffraction measurements up to 47 GPa. We found that the cubic spinel structure of ZnFe2O4 remains up to 33 GPa and a phase transition is induced beyond this pressure. The high-pressure phase is indexed to an orthorhombic CaMn2O4-type structure. Upon decompression the low- and high-pressure phases coexist. The compressibility of both structures was also investigated. We have observed that the lattice parameters of the high-pressure phase behave anisotropically upon compression. Further, we predict possible phase transition around 55 GPa. For comparison, we also studied the compression behavior of magnetite (Fe3O4) nanoparticles by X-ray diffraction up to 23 GPa. Spinel-type ZnFe2O4 and Fe3O4 nanoparticles have a bulk modulus of 172 (20) GPa and 152 (9) GPa, respectively. This indicates that in both cases the nanoparticles do not undergo a Hall-Petch strengthening.

  16. Janus nanoparticles: preparation, characterization, and applications.

    PubMed

    Song, Yang; Chen, Shaowei

    2014-02-01

    In chemical functionalization of colloidal particles, the functional moieties are generally distributed rather homogeneously on the particle surface. Recently, a variety of synthetic protocols have been developed in which particle functionalization may be carried out in a spatially controlled fashion, leading to the production of structurally asymmetrical particles. Janus particles represent the first example in which the two hemispheres exhibit distinctly different chemical and physical properties, which is analogous to the dual-faced Roman god, Janus. Whereas a variety of methods have been reported for the preparation of (sub)micron-sized polymeric Janus particles, it has remained challenging for the synthesis and (unambiguous) structural characterization of much smaller nanometer-sized Janus particles. Herein, several leading methods for the preparation of nanometer-sized Janus particles are discussed and the important properties and applications of these Janus nanoparticles in electrochemistry, sensing, and catalysis are highlighted. Some perspectives on research into functional patchy nanoparticles are also given. PMID:24376180

  17. Synthesis of cobalt ferrite nanoparticles from thermolysis of prospective metal-nitrosonaphthol complexes and their photochemical application in removing methylene blue

    NASA Astrophysics Data System (ADS)

    Tavana, Jalal; Edrisi, Mohammad

    2016-03-01

    In this study, cobalt ferrite (CoFe2O4) nanoparticles were synthesized by two novel methods. The first method is based on the thermolysis of metal-NN complexes. In the second method, a template free sonochemical treatment of mixed cobalt and iron chelates of α-nitroso-β-naphthol (NN) was applied. Products prepared through method 1 were spherical, with high specific surface area (54.39 m2 g-1) and small average crystalline size of 13 nm. However, CoFe2O4 nanoparticles prepared by method 2 were in random shapes, a broad range of crystalline sizes and a low specific surface area of 25.46 m2 g-1 though highly pure. A Taguchi experimental design was implemented in method 1 to determine and obtain the optimum catalyst. The structural and morphological properties of products were investigated by x-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, Fourier transform infrared, Brunauer-Emmett-Teller and dynamic laser light scattering. The crystalline size calculations were performed using Williamson-Hall method on XRD spectrum. The photocatalytic activity of the optimum nanocrystalline cobalt ferrite was investigated for degradation of a representative pollutant, methylene blue (MB), and visible light as energy source. The results showed that some 92% degradation of MB could be achieved for 7 h of visible light irradiation.

  18. Nanocrystalline magnesium ferrite prepared for photocatalytic applications by using the polymerized complex method

    NASA Astrophysics Data System (ADS)

    Dom, Rekha; Borse, Pramod H.; Hong, Kyong-Soo; Choi, Seyong; Lee, Byeong Seob; Ha, Myoung Gyu; Kim, Jong Pil; Jeong, Euh Duck; Kim, Hyun Gyu

    2015-11-01

    Magnesium ferrite (MgFe2O4) exhibiting a spinel phase was synthesized by using the polymerized complex and the solid-state reaction methods, and its physico-chemical properties were studied to explore the water-splitting under visible light photons. The study revealed the potential for using MgFe2O4 particles for photo-catalytic application. The structural study provided information on ferrite nano-crystallites fabricated by using the polymer complex method. The morphological studies demonstrated that, in contrast to the solid-state reaction method, a homogenous, monodispersed ferrite photocatalyst could be formed by using the polymerized complex method. The optical study revealed a larger visible-light absorption capability for the nanosized MgFe2O4 photocatalysts prepared by using the polymer complex methods, and indicated a red-shift of the bandgap by 0.06 eV as compared to the bandgap of the bulk. These nanocrystallites were highly photoactive with respect to the photodegradation and photocatalytic hydrogen evolution applications. The electrochemical analysis showed that they exhibited favorable bandedge positions suitable for photocatalytic H2 evolution. Thus, nanocrystalline MgFe2O4 is an active visible-light photocatalyst, that might be useful for the decomposition of water.

  19. Synthesis, magnetic and optical properties of core/shell Co1-xZnxFe2O4/SiO2 nanoparticles

    PubMed Central

    2011-01-01

    The optical properties of multi-functionalized cobalt ferrite (CoFe2O4), cobalt zinc ferrite (Co0.5Zn0.5Fe2O4), and zinc ferrite (ZnFe2O4) nanoparticles have been enhanced by coating them with silica shell using a modified Stber method. The ferrites nanoparticles were prepared by a modified citrate gel technique. These core/shell ferrites nanoparticles have been fired at temperatures: 400C, 600C and 800C, respectively, for 2 h. The composition, phase, and morphology of the prepared core/shell ferrites nanoparticles were determined by X-ray diffraction and transmission electron microscopy, respectively. The diffuse reflectance and magnetic properties of the core/shell ferrites nanoparticles at room temperature were investigated using UV/VIS double-beam spectrophotometer and vibrating sample magnetometer, respectively. It was found that, by increasing the firing temperature from 400C to 800C, the average crystallite size of the core/shell ferrites nanoparticles increases. The cobalt ferrite nanoparticles fired at temperature 800C; show the highest saturation magnetization while the zinc ferrite nanoparticles coated with silica shell shows the highest diffuse reflectance. On the other hand, core/shell zinc ferrite/silica nanoparticles fired at 400C show a ferromagnetic behavior and high diffuse reflectance when compared with all the uncoated or coated ferrites nanoparticles. These characteristics of core/shell zinc ferrite/silica nanostructures make them promising candidates for magneto-optical nanodevice applications. PMID:21774807

  20. Bimetallic nanoparticles: Preparation, properties, and biomedical applications.

    PubMed

    Nasrabadi, Hamid Tayefi; Abbasi, Elham; Davaran, Soodabeh; Kouhi, Mohammad; Akbarzadeh, Abolfazl

    2016-01-01

    Many studies of non-supported bimetallic nanoparticle (BMNP) dispersions, stabilized by ligands or polymers, and copolymers, were started only about 10 years ago. Several preparative procedures have been proposed, and full characterizations on BMNPs have been approved. Studies on BMNPs received huge attention from both scientific and technological communities because most of the NPs' catalytic activity depends on their structural aspects. In this study, we focus on the preparation, properties, and bio-application of BMNPs and introduction of the recent advance in these NPs. PMID:25203939

  1. Productive encounter: molecularly imprinted nanoparticles prepared using magnetic templates.

    PubMed

    Berghaus, Melanie; Mohammadi, Reza; Sellergren, Börje

    2014-08-18

    Synthesis of core-shell nanoparticles by surface initiated reversible addition fragmentation chain transfer polymerization in presence of a chiral template conjugated to magnetic nanoparticles is reported. The approach leads to imprinted nanoparticles featuring enantioselectivity and enhanced affinity compared to nanoparticles prepared using free template. PMID:24983025

  2. Iron-based soft magnetic composites with Mn-Zn ferrite nanoparticles coating obtained by sol-gel method

    NASA Astrophysics Data System (ADS)

    Wu, Shen; Sun, Aizhi; Xu, Wenhuan; Zhang, Qian; Zhai, Fuqiang; Logan, Philip; Volinsky, Alex A.

    2012-11-01

    This paper focuses on iron-based soft magnetic composites which were synthesized by utilizing Mn-Zn ferrite nanoparticles to coat iron powder. The nanocrystalline iron powders, with an average particle diameter of 20 nm, were obtained via the sol-gel method. Scanning electron microscopy, energy dispersive X-ray spectroscopy and distribution maps show that the iron particle surface is covered with a thin layer of Mn-Zn ferrites. Mn-Zn ferrite uniformly coated the surface of the powder particles, resulting in a reduced imaginary permeability, increased electrical resistivity and a higher operating frequency of the synthesized magnets. Mn-Zn ferrite coated samples have higher permeability and lower magnetic loss when compared with the non-magnetic epoxy resin coated compacts. The real part of permeability increases by 33.5% when compared with the epoxy resin coated samples at 10 kHz. The effects of heat treatment temperature on crystalline phase formation and on the magnetic properties of the Mn-Zn ferrite were investigated via X-ray diffraction and a vibrating sample magnetometer. Ferrites decomposed to FeO and MnO after annealing above 400 °C in nitrogen; thus it is the optimum annealing temperature to attain the desired permeability.

  3. Magnetic nanoparticle assembly arrays prepared by hierarchical self-assembly on a patterned surface.

    PubMed

    Wen, Tianlong; Zhang, Dainan; Wen, Qiye; Zhang, Huaiwu; Liao, Yulong; Li, Qiang; Yang, Qinghui; Bai, Feiming; Zhong, Zhiyong

    2015-03-21

    Inverted pyramid hole arrays were fabricated by photolithography and used as templates to direct the growth of colloidal nanoparticle assemblies. Cobalt ferrite nanoparticles deposit in the holes to yield high quality pyramid magnetic nanoparticle assembly arrays by carefully controlling the evaporation of the carrier fluid. Magnetic measurements indicate that the pyramid magnetic nanoparticle assembly arrays preferentially magnetize perpendicular to the substrate. PMID:25712606

  4. Synthesis and characterization of CoFe2O4 ferrite nanoparticles obtained by an electrochemical method.

    PubMed

    Mazarío, E; Herrasti, P; Morales, M P; Menéndez, N

    2012-09-01

    Uniform size cobalt ferrite nanoparticles have been synthesized in one step using an electrochemical technique. Synthesis parameters such as the current density, temperature and stirring were optimized to produce pure cobalt ferrite. The nanoparticles have been investigated by means of magnetic measurements, Mössbauer spectroscopy, x-ray powder diffraction and transmission electron microscopy. The average size of the electrosynthesized samples was controlled by the synthesis parameters and this showed a rather narrow size distribution. The x-ray analysis shows that the CoFe(2)O(4) obtained presents a totally inverse spinel structure. The magnetic properties of the stoichiometric nanoparticles show ferromagnetic behavior at room temperature with a coercivity up to 6386 Oe and a saturation magnetization of 85 emu g(-1). PMID:22894928

  5. Preparation of medical magnetic nanobeads with ferrite particles encapsulated in a polyglycidyl methacrylate (GMA) for bioscreening

    SciTech Connect

    Nishibiraki, H.; Kuroda, C.S.; Maeda, M.; Matsushita, N.; Abe, M.; Handa, H.

    2005-05-15

    Ferrite nanoparticles (an intermediate between Fe{sub 3}O{sub 4} and {gamma}-Fe{sub 2}O{sub 3}), {approx}7 nm in diameter, were embedded in beads of a mixed polymer of styrene (St) and glycidyl methacrylate (GMA) by emulsifier-free emulsion polymerization method. The beads were coated with GMA by a seeded polymerization method in order to suppress nonspecific protein binding on the surfaces; GMA exhibits very low nonspecific protein binding, which is required for carriers used for bioscreening. The beads have diameters of 180{+-}50 nm and saturation magnetizations of 28 emu/g, exceeding commercially available polymer-coated beads of micron size having a weaker saturation magnetization ({approx}12 emu/g)

  6. Structural characterization of microwave-synthesized zinc-substituted cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Parmar, Harshida; Desai, Rucha; Upadhyay, R. V.

    2011-07-01

    Microwave combustion technique modified by post treatment procedure is used to synthesize single-phase spinel ferrites of cobalt, zinc, and substituted magnetic nanoparticles of typical size 390 Å. The post treatment does not alter the crystal structure but increases the crystallinity. This is confirmed by powder x-ray diffraction and Fourier Transform Infrared (FTIR) studies. Citric acid is used as a fuel. The fresh synthesized sample shows an impurity phase in x-ray and in FTIR. This is due to the unreacted citrate molecule adsorbed on the particle surface. It is shown that by treating the sample with 0.1 M HCl, we can eliminate the impurity phase, and one can obtain a pure single phase. The magnetization at 8 kOe increases by nearly 8% after the removal of impurity. In order to remove surface adsorbed OH- ion, samples are treated with NaCl and heated to 200°C for four hours. The XRD result indicates that after the treatment neither the crystallite size nor the distribution changes, but it removes OH- ion. This is also confirmed by FTIR analysis. Thus, this modified technique can be used to synthesize pure nanocrystalline samples of spinel ferrites.

  7. Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode.

    PubMed

    Dimitrijević, Teodora; Vulić, Predrag; Manojlović, Dragan; Nikolić, Aleksandar S; Stanković, Dalibor M

    2016-07-01

    In this study, a novel electrochemical sensor for quantification of ascorbic acid with amperometric detection in physiological conditions was constructed. For this purpose, cobalt and nickel ferrites were synthesized using microwave and ultrasound assistance, characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray powder diffraction (XRPD), and used for modification of glassy carbon paste electrode (GCPE). It was shown that introducing these nanoparticles to the structure of GCPE led to increasing analytical performance. Co ferrite modified GCPE (CoFeGCPE) showed better characteristics toward ascorbic acid sensing. The limit of detection (LOD) obtained by sensor was calculated to be 0.0270 mg/L, with linear range from 0.1758 to 2.6010 mg/L. This sensor was successfully applied for practical analysis, and the obtained results demonstrated that the proposed procedure could be a promising replacement for the conventional electrode materials and time-consuming and expensive separation methods. PMID:27059753

  8. Giant antiresonance in electromagnetic wave reflection from a 3D structure with ferrite spinel nanoparticles

    NASA Astrophysics Data System (ADS)

    Ustinov, V. V.; Rinkevich, A. B.; Perov, D. V.; Burkhanov, A. M.; Samoylovich, M. I.; Kleshcheva, S. M.; Kuznetsov, E. A.

    2013-04-01

    We analyze the microwave properties of nanocomposite materials obtained by embedding opal matrices (regular packing of SiO2 spheres about 250 nm in diameter) of ferrite spinel nanoparticles in the interspherical space. It is found that the main reason for microwave changes is the magnetic resonance in a nanocomposite. In addition to the resonance, antiresonance also takes place, which is manifested as a minimum of absorbed power at frequencies higher than a certain frequency characteristic of the given type of ferrite particles. Antiresonance appears in the fields smaller than the resonance field. The amplitude of the reflected signal in antiresonance increases fourfold. The measurements are taken in the frequency range from 26 to 38 GHz. The change in the moduli of transmission and reflection coefficients in the external magnetic field in a rectangular waveguide containing a nanocomposite is analyzed. The modulus of the wave transmittance through a rectangular resonator with a nanocomposite specimen is measured. The structural analysis of nanocomposites is carried out. In addition, the magnetization curves and hysteresis loops are measured.

  9. Effect of Ni2+ substitution on structural and magnetic properties of Ni-Zn ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Srinivas, Ch.; Tirupanyam, B. V.; Satish, A.; Seshubai, V.; Sastry, D. L.; Caltun, O. F.

    2015-05-01

    A series of co-precipitated NixZn1-xFe2O4 (x=0.5, 0.6, 0.7) ferrite nanoparticles heat treated at 200 °C were produced in order to understand the influence of substitution level on structural and magnetic properties including magnetocrystalline anisotropy. The XRD, FE-SEM, VSM and FC-ZFC techniques were used to characterize the samples. It is observed that as Ni2+ concentration increases crystallite size (D), saturation magnetization (Ms) and blocking temperature (TB) and decreases coercive field (Hc). All particles exhibit superparamagnetism at room temperature and hence lie in the single domain range. The magnetic anisotropy constant (K) is estimated to be maximum for Ni0.5Zn0.5Fe2O4 sample, whose particle size is the smallest. The results are interpreted presuming the presence of core shell interactions and/or cation redistribution that influence the magnetic properties of these ferrite nano particles.

  10. Competing magnetic interactions in nickel ferrite nanoparticle clusters: Role of magnetic interactions

    NASA Astrophysics Data System (ADS)

    Malik, Rakesh; Annapoorni, S.; Lamba, Subhalakshmi; Sharma, Parmanand; Inoue, Akihisa

    2008-09-01

    The magnetic behavior of nickel ferrite nanoparticles of different sizes was studied by annealing nickel ferrite powders at temperatures ranging from 300 to 900 °C. Transmission electron microscopy studies show that the average particle sizes change from ˜8 to ˜120 nm with increasing annealing temperatures. The x-ray diffraction patterns of the annealed samples reveal that a single phase is retained. Hysteresis measurements performed up to a field of 10 kOe show a tendency toward saturation. The saturation magnetization is found to increase with annealing temperature (particle size) with the magnetization tending toward the bulk value for powders annealed at 900 °C. Zero field cooled-field cooled measurements performed at 0.5 kOe indicate the presence of a superparamagnetic phase up to an annealing temperature of 700 °C with blocking temperatures in the range of 150-330 K. Numerical simulations are carried out using an interacting model of an array of single domain magnetic particles to explain the change in the magnetic behavior of the samples with annealing temperature and to estimate the anisotropy of the system. Our studies indicate that the observed magnetic behavior can be explained by the changes in the anisotropy of the system and the dominance of the short range interparticle exchange interactions over the long range dipolar interactions with increasing particle sizes. This change in the interaction profile is further confirmed by the Henkel plots for the particles annealed at different temperatures.

  11. Synergetic effect of size and morphology of cobalt ferrite nanoparticles on proton relaxivity.

    PubMed

    N, Venkatesha; Srivastava, Chandan; Hegde, Veena

    2014-12-01

    Cobalt ferrite nanoparticles with average sizes of 14, 9 and 6 nm were synthesised by the chemical co-precipitation technique. Average particle sizes were varied by changing the chitosan surfactant to precursor molar ratio in the reaction mixture. Transmission electron microscopy images revealed a faceted and irregular morphology for the as-synthesised nanoparticles. Magnetic measurements revealed a ferromagnetic nature for the 14 and 9 nm particles and a superparamagnetic nature for the 6 nm particles. An increase in saturation magnetisation with increasing particle size was noted. Relaxivity measurements were carried out to determine T2 value as a function of particle size using nuclear magnetic resonance measurements. The relaxivity coefficient increased with decrease in particle size and decrease in the saturation magnetisation value. The observed trend in the change of relaxivity value with particle size was attributed to the faceted nature of as-synthesised nanoparticles. Faceted morphology results in the creation of high gradient of magnetic field in the regions adjacent to the facet edges increasing the relaxivity value. The effect of edges in increasing the relaxivity value increases with decrease in the particle size because of an increase in the total number of edges per particle dispersion. PMID:25429495

  12. Effect of particle size on structural, magnetic and dielectric properties of manganese substituted nickel ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Kumar, E. Ranjith; Kamzin, Aleksandr S.; Prakash, T.

    2015-03-01

    Mn substituted NiFe2O4 ferrite nanoparticles (Mn-NiFe2O4) were synthesized by the auto-combustion method. Their actions were carried out at different fuel ratios (50%, 75% and 100%). The nanoparticles have been investigated by X-ray powder diffraction, scanning electron microscopy and transmission electron microscopy. The average crystallite size of the synthesized and annealed samples was between 25 and 75 nm, which were found to be dependent on both fuel ratio and annealing temperatures. However, lattice parameters, interplanar spacing and grain size were controlled by varying the fuel ratio. Magnetic characterizations of the nanoparticles were carried out using a vibrating sample magnetometer at room temperature. The saturation magnetization was computed and found to lie between 6 emu/g and 57 emu/g depending on the particle size of the studied sample. The coercivity was found to exhibit non-monotonic behavior with the particle size. Such behavior can be accounted for by the combination between surface anisotropy and thermal energies. The value of dielectric constant and dielectric loss was found to exhibit almost linear dependence on the particle size.

  13. Fabrication of a glucose biosensor based on citric acid assisted cobalt ferrite magnetic nanoparticles.

    PubMed

    Krishna, Rahul; Titus, Elby; Chandra, Sudeshna; Bardhan, Neel Kanth; Krishna, Rohit; Bahadur, Dhirendra; Gracio, José

    2012-08-01

    A novel and practical glucose biosensor was fabricated with immobilization of Glucose oxidase (GOx) enzyme on the surface of citric acid (CA) assisted cobalt ferrite (CF) magnetic nanoparticles (MNPs). This innovative sensor was constructed with glassy carbon electrode which is represented as (GOx)/CA-CF/(GCE). An explicit high negative zeta potential value (-22.4 mV at pH 7.0) was observed on the surface of CA-CF MNPs. Our sensor works on the principle of detection of H2O2 which is produced by the enzymatic oxidation of glucose to gluconic acid. This sensor has tremendous potential for application in glucose biosensing due to the higher sensitivity 2.5 microA/cm2-mM and substantial increment of the anodic peak current from 0.2 microA to 10.5 microA. PMID:22962799

  14. Cellular distribution and degradation of cobalt ferrite nanoparticles in Balb/3T3 mouse fibroblasts.

    PubMed

    Marmorato, Patrick; Ceccone, Giacomo; Gianoncelli, Alessandra; Pascolo, Lorella; Ponti, Jessica; Rossi, François; Salomé, Murielle; Kaulich, Burkhard; Kiskinova, Maya

    2011-11-30

    The effect of the concentration of cobalt ferrite (CoFe(2)O(4)) nanoparticles (NPs) on their intracellular location and distribution has been explored by synchrotron radiation X-ray and fluorescence microscopy (SR-XRF) monitoring the evolution of NPs elemental composition as well. In cells exposed to low concentrations of CoFe(2)O(4) NPs, the NPs preferentially segregate in the perinuclear region preserving their initial chemical content. At concentrations exceeding 500 μM the XRF spectra indicate the presence of Co and Fe also in the nuclear region, accompanied by sensible changes in the cellular morphology. The increase of the Co/Fe ratio measured in the nuclear compartment indicates that above certain concentrations the CoFe(2)O(4) NPs intracellular distribution could be accompanied by biodegradation resulting in Co accumulation in the nucleus. PMID:21925252

  15. Aqueous synthesis and transmission electron microscopy observation of seed-grown spherical ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Tanaka, T.; Tada, M.; Nakagawa, T.; Abe, M.

    2012-03-01

    Uniform-sized spherical iron ferrite nanoparticles grew on seed crystals in an aqueous solution containing sucrose. Using the seed crystals which were highly dispersed in acidic or alkaline seed-crystal suspension without relation to pH of the suspension, we widely controlled the particle diameter in the range 20-200 nm by changing the additive amount of the seed crystals. By transmission electron microscopy observation and X-ray diffraction analysis, it indicated that the particles were highly crystalline but not amorphous. Selected area diffraction patterns of the particles by using transmission electron microscope revealed that the particles were composed of one to several crystals. Thus we provided the evidence that the particles grew on clusters composed of one to several seed crystals to which those of several dozen seed crystals were disintegrated.

  16. Solvothermal synthesis of cobalt ferrite nanoparticles loaded on multiwalled carbon nanotubes for magnetic resonance imaging and drug delivery.

    PubMed

    Wu, Huixia; Liu, Gang; Wang, Xue; Zhang, Jiamin; Chen, Yu; Shi, Jianlin; Yang, Hong; Hu, He; Yang, Shiping

    2011-09-01

    Multiwalled carbon nanotube (MWCNT)/cobalt ferrite (CoFe(2)O(4)) magnetic hybrids were synthesized by a solvothermal method. The reaction temperature significantly affected the structure of the resultant MWCNT/CoFe(2)O(4) hybrids, which varied from 6nm CoFe(2)O(4) nanoparticles uniformly coated on the nanotubes at 180°C to agglomerated CoFe(2)O(4) spherical particles threaded by MWCNTs and forming necklace-like nanostructures at 240°C. Based on the superparamagnetic property at room temperature and high hydrophilicity, the MWCNT/CoFe(2)O(4) hybrids prepared at 180°C (MWCNT/CoFe(2)O(4)-180) were further investigated for biomedical applications, which showed a high T(2) relaxivity of 152.8 Fe mM(-1)s(-1) in aqueous solutions, a significant negative contrast enhancement effect on cancer cells and, more importantly, low cytotoxicity and negligible hemolytic activity. The anticancer drug doxorubicin (DOX) can be loaded onto the hybrids and subsequently released in a sustained and pH-responsive way. The DOX-loaded hybrids exhibited notable cytotoxicity to HeLa cancer cells due to the intracellular release of DOX. These results suggest that MWCNT/CoFe(2)O(4)-180 hybrids may be used as both effective magnetic resonance imaging contrast agents and anticancer drug delivery systems for simultaneous cancer diagnosis and chemotherapy. PMID:21664499

  17. Development of phosphonate modified Fe 1-x MnxFe2O4 mixed ferrite nanoparticles: novel peroxidase mimetics in enzyme linked immunosorbent assay.

    PubMed

    Bhattacharya, Dipsikha; Baksi, Ananya; Banerjee, Indranil; Ananthakrishnan, Rajakumar; Maiti, Tapas K; Pramanik, Panchanan

    2011-10-30

    A highly facile and feasible strategy on the fabrication of advanced intrinsic peroxidase mimetics based on Mn(2+) doped mixed ferrite (Mn(II)(x)Fe(II)(1-x)Fe(III)(2)O(4)) nanoparticles was demonstrated for the quantitative and sensitive detection of mouse IgG (as a model analyte). Mn(2+) doped Fe(1-x)Mn(x)Fe(2)O(4) nanoparticles were synthesized using varying ratios of Mn(2+):Fe(2+) ions and characterized by the well known complementary techniques. The increase of Mn(2+) proportion had remarkably enhanced the peroxidase activity and magnetism. The catalytic activity of mixed ferrites was found to follow Michaelis-Menten kinetics and was noticeably higher than native Fe(3)O(4). The calculated K(m) and K(cat) exhibited strong affinity with substrates which were remarkably higher than similar sized native magnetite nanoparticles and horseradish peroxidase (HRP). These findings stimulated us to develop carboxyl modified Fe(1-x)Mn(x)Fe(2)O(4) nanoparticles using phosphonomethyl immunodiacetic acid (PMIDA) to engineer PMIDA-Fe(1-x)Mn(x)Fe(2)O(4) fabricated enzyme linked immunosorbent assay (ELISA). Results of both PMIDA-Fe(1-x)Mn(x)Fe(2)O(4) linked ELISA revealed that the enhancements in absorbance during the catalysis of enzyme substrate were linearly proportional to the concentration of mouse IgG within the range between 0.1 μg/ml and 2.5 μg/ml. Further, this detection was ten times lower than previous reports and the detection limit of mouse IgG was 0.1 μg/ml. The advantages of our fabricated artificial peroxidase mimetics are combined of low cost, easy to prepare, better stability and tunable catalytic activity. Moreover, this method provides a new horizon for the development of promising analytical tools in the application of biocatalysis, bioassays, and bioseparation. PMID:22063549

  18. Superior electro-optic response in multiferroic bismuth ferrite nanoparticle doped nematic liquid crystal device.

    PubMed

    Nayek, Prasenjit; Li, Guoqiang

    2015-01-01

    A superior electro-optic (E-O) response has been achieved when multiferroic bismuth ferrite (BiFeO3/BFO) nanoparticles (NPs) were doped in nematic liquid crystal (NLC) host E7 and the LC device was addressed in the large signal regime by an amplitude modulated square wave signal at the frequency of 100 Hz. The optimized concentration of BFO is 0.15 wt%, and the corresponding total optical response time (rise time + decay time) for a 5 μm-thick cell is 2.5 ms for ~7 V(rms). This might be exploited for the construction of adaptive lenses, modulators, displays, and other E-O devices. The possible reason behind the fast response time could be the visco-elastic constant and restoring force imparted by the locally ordered LCs induced by the multiferroic nanoparticles (MNPs). Polarized optical microscopic textural observation shows that the macroscopic dislocation-free excellent contrast have significant impact on improving the image quality and performance of the devices. PMID:26041701

  19. Superior electro-optic response in multiferroic bismuth ferrite nanoparticle doped nematic liquid crystal device

    PubMed Central

    Nayek, Prasenjit; Li, Guoqiang

    2015-01-01

    A superior electro-optic (E-O) response has been achieved when multiferroic bismuth ferrite (BiFeO3/BFO) nanoparticles (NPs) were doped in nematic liquid crystal (NLC) host E7 and the LC device was addressed in the large signal regime by an amplitude modulated square wave signal at the frequency of 100 Hz. The optimized concentration of BFO is 0.15 wt%, and the corresponding total optical response time (rise time + decay time) for a 5 μm-thick cell is 2.5 ms for ~7 Vrms. This might be exploited for the construction of adaptive lenses, modulators, displays, and other E-O devices. The possible reason behind the fast response time could be the visco-elastic constant and restoring force imparted by the locally ordered LCs induced by the multiferroic nanoparticles (MNPs). Polarized optical microscopic textural observation shows that the macroscopic dislocation-free excellent contrast have significant impact on improving the image quality and performance of the devices. PMID:26041701

  20. Nickel Ferrite Nanoparticles Anchored onto Silica Nanofibers for Designing Magnetic and Flexible Nanofibrous Membranes.

    PubMed

    Hong, Feifei; Yan, Chengcheng; Si, Yang; He, Jianxin; Yu, Jianyong; Ding, Bin

    2015-09-16

    Many applications proposed for magnetic silica nanofibers require their assembly into a cellular membrane structure. The feature to keep structure stable upon large deformation is crucial for a macroscopic porous material which functions reliably. However, it remains a key issue to realize robust flexibility in two-dimensional (2D) magnetic silica nanofibrous networks. Here, we report that the combination of electrospun silica nanofibers with zein dip-coating can lead to the formation of flexible, magnetic, and hierarchical porous silica nanofibrous membranes (SNM). The 290 nm diameter silica nanofibers act as templates for the uniform anchoring of nickel ferrite nanoparticles (size of 50 nm). Benefiting from the homogeneous and stable nanofiber-nanoparticle composite structure, the resulting magnetic SNM can maintain their structure integrity under repeated bending as high as 180° and can facilely recover. The unique hierarchical structure also provides this new class of silica membrane with integrated properties of ultralow density, high porosity, large surface area, good magnetic responsiveness, robust dye adsorption capacity, and effective emulsion separation performance. Significantly, the synthesis of such fascinating membranes may provide new insight for further application of silica in a self-supporting, structurally adaptive, and 2D membrane form. PMID:26301575

  1. Mössbauer spectroscopy, magnetic characteristics, and reflection loss analysis of nickel-strontium substituted cobalt ferrite nanoparticles

    SciTech Connect

    Ghasemi, Ali; Paesano, Andrea; Cerqueira Machado, Carla Fabiana; Shirsath, Sagar E.; Liu, Xiaoxi; Morisako, Akimitsu

    2014-05-07

    In current research work, Co{sub 1-x}Ni{sub x/2}Sr{sub x/2}Fe{sub 2}O{sub 4} (x = 0–1 in a step of 0.2) ferrite nanoparticles were synthesized by a sol-gel method. According to the evolution in the subspectral areas obtained from Mössbauer spectroscopy, it was found that the relaxing iron belongs mostly to the site B, since the Mössbauer fraction of site A does not vary appreciably. With an increase in Ni-Sr substitution contents in cobalt ferrite, the coercivity and saturation of magnetization decrease. Variation of reflection loss versus frequency in microwave X-band demonstrates that the reflection peak shifts to lower frequency by adding substituted cations and the synthesized nanoparticles can be considered for application in electromagnetic wave absorber technology.

  2. Incorporation of cobalt-ferrite nanoparticles into a conducting polymer in aqueous micellar medium: strategy to get photocatalytic composites.

    PubMed

    Endrődi, Balázs; Hursán, Dorottya; Petrilla, Liliána; Bencsik, Gábor; Visy, Csaba; Chams, Amani; Maslah, Nabiha; Perruchot, Christian; Jouini, Mohamed

    2014-01-01

    In this study an easy strategy for conducting polymer based nanocomposite formation is presented through the deposition of cobalt-ferrite (CoFe(2)O(4)) containing poly(3,4-ethylenedioxythiophene) (PEDOT) thin layers. The electrochemical polymerization has been performed galvanostatically in an aqueous micellar medium in the presence of the nanoparticles and the surface active Triton X-100. The nanoparticles have been characterized by Transmission electron microscopy (TEM), the thin layers has been studied by applying Scanning electron microscopy (SEM), and X-ray diffraction (XRD), and the basic electrochemical properties have been also determined. Moreover, electrocatalytic activity of the composite was demonstrated in the electrooxidation reaction of dopamine (DA). The enhanced sensitivity - related to the cobalt-ferrite content - and the experienced photocatalyitic activity are promising for future application. PMID:25125121

  3. Cation distribution and magnetic properties in chromium-substituted nickel ferrites prepared using aerosol route

    SciTech Connect

    Singhal, Sonal Chandra, Kailash

    2007-01-15

    Cation distribution have been investigated using X-ray diffraction, magnetic and Moessbauer spectral studies in chromium-substituted nickel ferrites prepared by aerosol route. Cation distribution indicates that the chromium atom occupy octahedral site upto x=0.8, and then also enters into tetrahedral site. The saturation magnetization decreases linearly with the increase of chromium concentration due to the diamagnetic nature of the Cr{sup 3+}. However, interesting behaviour is observed in the coercivity. Initially it increases slowly with the chromium concentration but when x>0.8 a very large increase has been observed. This was attributed to the specific cation distribution of Cr{sup 3+} which results an unquenched orbital angular momentum and a large anisotropy. Room temperature Moessbauer spectra of as obtained samples exhibited a broad doublet resolved into two doublets corresponding to the surface and internal region atoms. The samples annealed at 1200 deg. C show broad sextets, which were fitted with different sextets, indicating different local environment of both tetrahedral and octahedral coordinated iron cation. - Graphical abstract: Hysterisis loop of chromium-substituted nickel ferrites after annealing at 1200 deg. C.

  4. Curie temperature and magnetic properties of aluminum doped barium ferrite particles prepared by ball mill method

    NASA Astrophysics Data System (ADS)

    Chen, Daming; Harward, Ian; Baptist, Joshua; Goldman, Sara; Celinski, Zbigniew

    2015-12-01

    Barium ferrite has attracted considerable interest in the fields of permanent magnets and perpendicular magnetic recording due to its strong uniaxial anisotropy and high Curie temperature (Tc). We prepared aluminum doped barium ferrite ceramics (BaAlxFe12-xO19, 0≤x≤6) by the ball mill method. The powder was milled for 96 h, and after forming pellets, annealed for 48 h in air at 1000 °C. The X-ray diffraction (XRD) data show that there are only single hexagonal phases in the samples without any impurity phase. The crystal lattice constants, a and c, were calculated by Cohen's method. Both a and c decrease with increasing x, ranging from 0.588 nm and 2.318 nm to 0.573 nm and 2.294 nm, respectively. A Vibrating Sample Magnetometer (VSM) and Superconducting Quantum Interference Device (SQUID) were used to investigate Tc and magnetic properties of BaFe12-xAlxO19. It is found that Tc decreases with increasing x, from 425 °C to 298 °C. It is also found that the saturated magnetization (4πMs) decreases with increasing x, while the coercivity (Hc) increases with the increase in x. The anisotropy field was also determined from the SQUID measurement.

  5. Preparation and characterization of uniform near IR polystyrene nanoparticles.

    PubMed

    Pellach, Michal; Margel, Shlomo

    2014-01-01

    Biomaterials for in vivo fluorescence imaging are required to be biocompatible, nontoxic, photostable and highly fluorescent. Fluorescence must be in the near infrared (NIR) region of the electromagnetic spectrum to avoid absorption and autofluorescence of endogenous tissues. NIR fluorescent polystyrene nanoparticles may be considered ideal biomaterials for in vivo imaging applications. These NIR nanoparticles were prepared by a swelling process of polystyrene template nanoparticles with a hydrophobic NIR dye dissolved in a water-miscible swelling solvent, a method developed for preparation of nonbiodegradable nanoparticles, for NIR fluorescent bioimaging applications. This method overcomes common problems that occur with dye entrapment during nanoparticle formation such as loss of fluorescence and size polydispersity. Fluorescence intensity of the nanoparticles was found to be size dependent, and was optimized for differently sized nanoparticles. The resulting NIR nanoparticles were also found to be more fluorescent and highly photostable compared to the free dye in solution, showing their potential as biomaterials for in vivo fluorescence imaging. PMID:24460556

  6. Effects of Thermal Annealing on Structural and Magnetic Properties of Lithium Ferrite Nanoparticles

    SciTech Connect

    Jovic, Natasa G.; Masadeh, Ahmad S.; Kremenovic, Aleksandar S.; Antic, Bratislav V.; Blanusa, Jovan L.; Cvjeticanin, Nikola D.; Goya, Gerardo F.; Antisari, Marco Vittori; Bozin, Emil S.

    2010-01-12

    Pure, crystalline, {approx}10 nm lithium ferrite phase (Li{sub 0.5}Fe{sub 2.5}O{sub 4}), was successfully synthesized at very low temperature using a modified combustion method. The crystal structure and microstructure evolution of this system upon annealing were monitored by a careful investigation of X-ray diffractograms collected on a synchrotron source. Comparative analysis of the results obtained from the full profile Rietveld method (in reciprocal space) and the pair distribution function method (in direct space) was carried out. Nanocrystalline samples exhibit similar crystal structure, on average, with a partial ordering of Li{sup +} and Fe{sup 3+} ions between octahedral 4b and 12d sites on the spinel crystal lattice (space group P4{sub 3}32). After annealing at 973 K, cation distribution changes to a completely ordered, resembling that which is seen in the bulk lithium ferrite. The PDF analysis reveals abnormally high values of oxygen atomic displacement parameters in tetrahedral 8c sites (O1) indicating a significant disordering of the O1 network and suggests migration of lithium ions from 4b sites to the outer layers of nanoparticles. Analysis of room temperature Moessbauer spectra has shown that the hyperfine field for Fe{sup 3+} ions in tetrahedral 8c sites is the most sensitive on increasing the particle size and improving the crystallinity. From the differential thermal analysis, it was found that a lower driving force is required to induce an order-disorder phase transition in nanocrystalline samples, compared to the bulk-like sample, presumably due to the higher crystal disordering in these samples.

  7. Recent advances in nanosized Mn-Zn ferrite magnetic fluid hyperthermia for cancer treatment.

    PubMed

    Lin, Mei; Huang, Junxing; Sha, Min

    2014-01-01

    This paper reviews the recent research and development of nanosized manganese zinc (Mn-Zn) ferrite magnetic fluid hyperthermia (MFH) for cancer treatment. Mn-Zn ferrite MFH, which has a targeted positioning function that only the temperature of tumor tissue with magnetic nanoparticles can rise, while normal tissue without magnetic nanoparticles is not subject to thermal damage, is a promising therapy for cancer. We introduce briefly the composition and properties of magnetic fluid, the concept of MFH, and features of Mn-Zn ferrite magnetic nanoparticles for MFH such as thermal bystander effect, universality, high specific absorption rate, the targeting effect of small size, uniformity of hyperthermia temperature, and automatic temperature control and constant temperature effect. Next, preparation methods of Mn-Zn ferrite magnetic fluid are discussed, and biocompatibility and biosecurity of Mn-Zn ferrite magnetic fluid are analyzed. Then the applications of nanosized Mn-Zn ferrite MFH in cancer are highlighted, including nanosized Mn-Zn ferrite MFH alone, nanosized Mn-Zn ferrite MFH combined with As2O3 chemotherapy, and nanosized Mn-Zn ferrite MFH combined with radiotherapy. Finally, the combination application of nanosized Mn-Zn ferrite MFH and gene-therapy is conceived, and the challenges and perspectives for the future of nanosized Mn-Zn ferrite MFH for oncotherapy are discussed. PMID:24730298

  8. Magnetic studies of Li-Zn ferrites prepared by citrate precursor method

    NASA Astrophysics Data System (ADS)

    Soibam, Ibetombi; Phanjoubam, Sumitra; Sharma, H. B.; Sarma, H. N. K.; Prakash, C.

    2009-11-01

    Ferrites having the general formula Li 0.5-0.5xZn xFe 2.5-0.5xO 4 where 0≤ x≤0.6 in steps of 0.2 were prepared by the citrate precursor method. The Curie temperature measured shows a decrease with increasing Zn concentration. Experimental results show that the room temperature initial permeability increases with the increase in the concentration of zinc. The initial permeability has also been studied as a function of frequency in the range of 100 Hz-1 MHz. The real part of initial permeability referred as initial permeability and the imaginary part of initial permeability better known as permeability loss show dispersion with frequency. Possible mechanism contributing to the above processes is discussed.

  9. Preparation and Characterisation of Highly Loaded Fluorescent Chitosan Nanoparticles

    PubMed Central

    Katas, Haliza; Mui Wen, Chan

    2011-01-01

    Chitosan (CS) nanoparticles have been developed as a versatile drug delivery system to transport drugs, genes, proteins, and peptides into target sites. Demands on fluorescent nanoparticles have increased recently due to various applications in medical and stem-cell-based researches. In this study, fluorescent CS nanoparticles were prepared by a mild method, namely, complex coacervation. Entrapment efficiency of sulforhodamine (SR101) loaded into CS nanoparticles was investigated to evaluate their capacity in incorporating fluorescent molecule. Particle size of produced fluorescent nanoparticles was in the range of 600–700 nm, and their particle size was highly dependent on the CS molecular weight as well as concentration. A high entrapment efficiency of SR101 into CS nanoparticles could also be obtained when it was dissolved in methanol. In conclusion, highly loaded fluorescent CS nanoparticles could be easily prepared using complex coacervation method and therefore can be applied in various medical researches. PMID:22389847

  10. Structural and magnetic properties of Zn-substituted cobalt ferrites prepared by co-precipitation method.

    PubMed

    Yaseneva, Polina; Bowker, Michael; Hutchings, Graham

    2011-11-01

    Zn substituted cobalt ferrite spinels with the general formula Zn(x)Co(1-x)Fe(2)O(4) (with x varying from 0 to 0.5) were synthesized by a co-precipitation method and calcined at 500 °C and 800 °C. It was found that Zn substitution has a big effect in decreasing the Curie temperature (T(c)), from around 440 °C for the undoped sample to ~180 °C with x = 0.5. However, these values were also strongly affected by the pre-calcination temperature of the samples, thus T(C) shifts from ~275 °C for the x = 0.3 sample to ~296 °C after calcination at 500 °C and 800 °C respectively. These effects are due to facilitation of demagnetisation by substitution of the non-magnetic Zn ions and by production of very small nanoparticles. The latter are removed by higher temperature calcinations and so T(C) increases. PMID:21952718

  11. Preliminary evaluation of a 99mTc labeled hybrid nanoparticle bearing a cobalt ferrite core: in vivo biodistribution.

    PubMed

    Psimadas, Dimitrios; Baldi, Giovanni; Ravagli, Costanza; Bouziotis, Penelope; Xanthopoulos, Stavros; Franchini, Mauro Comes; Georgoulias, Panagiotis; Loudos, George

    2012-08-01

    Magnetic nanoparticles have become important tools for imaging a wide range of diseases, improving drug delivery and applying hyperthermic treatment. Iron oxide based nanoparticles have been widely examined, unlike cobalt ferrite based ones. Herein, monodisperse and stable CoFe2O4 nanoparticles have been produced, coated and further stabilized using ethyl 12-(hydroxyamino)-12-oxododecanoate, poly(lactic-co-glycolic acid) and bovine serum albumin. The final product, NBRh1, was fully characterized and has been directly radiolabeled with 99mTc using SnCl1 as the reducing agent in high yields. In vitro stability and hyperthermic properties of 99mTC-NBRh1 were encouraging for further application in low frequencies hyperthermia and biomagnetic applications. In vivo evaluation followed after injection in healthy mice. The planar and SPECT imaging data as well as the biodistribution results were in accordance, showing high liver and spleen uptake as expected starting almost immediately after administration. In conclusion the preliminary results for nanoparticles bearing a cobalt ferrite core justify further investigations towards potential hyperthermic applications, drug transportation and liver or spleen imaging. PMID:22852467

  12. Enhanced biomedical heat-triggered carriers via nanomagnetism tuning in ferrite-based nanoparticles

    NASA Astrophysics Data System (ADS)

    Angelakeris, M.; Li, Zi-An; Hilgendorff, M.; Simeonidis, K.; Sakellari, D.; Filippousi, M.; Tian, H.; Van Tendeloo, G.; Spasova, M.; Acet, M.; Farle, M.

    2015-05-01

    Biomedical nanomagnetic carriers are getting a higher impact in therapy and diagnosis schemes while their constraints and prerequisites are more and more successfully confronted. Such particles should possess a well-defined size with minimum agglomeration and they should be synthesized in a facile and reproducible high-yield way together with a controllable response to an applied static or dynamic field tailored for the specific application. Here, we attempt to enhance the heating efficiency in magnetic particle hyperthermia treatment through the proper adjustment of the core-shell morphology in ferrite particles, by controlling exchange and dipolar magnetic interactions at the nanoscale. Thus, core-shell nanoparticles with mutual coupling of magnetically hard (CoFe2O4) and soft (MnFe2O4) components are synthesized with facile synthetic controls resulting in uniform size and shell thickness as evidenced by high resolution transmission electron microscopy imaging, excellent crystallinity and size monodispersity. Such a magnetic coupling enables the fine tuning of magnetic anisotropy and magnetic interactions without sparing the good structural, chemical and colloidal stability. Consequently, the magnetic heating efficiency of CoFe2O4 and MnFe2O4 core-shell nanoparticles is distinctively different from that of their counterparts, even though all these nanocrystals were synthesized under similar conditions. For better understanding of the AC magnetic hyperthermia response and its correlation with magnetic-origin features we study the effect of the volume ratio of magnetic hard and soft phases in the bimagnetic core-shell nanocrystals. Eventually, such particles may be considered as novel heating carriers that under further biomedical functionalization may become adaptable multifunctional heat-triggered nanoplatforms.

  13. Photodynamic Anticancer Activities of Multifunctional Cobalt Ferrite Nanoparticles in Various Cancer Cells.

    PubMed

    Park, Bong Joo; Choi, Kyong-Hoon; Nam, Ki Chang; Ali, Anser; Min, Joe Eun; Son, Hyungbin; Uhm, Han S; Kim, Ho-Joong; Jung, Jin-Seung; Choi, Eun Ha

    2015-02-01

    To develop novel multifunctional magnetic nanoparticles (MNPs) with good magnetic properties, biocompatibility, and anticancer activities by photodynamic therapy (PDT), we synthesized multifunctional cobalt ferrite (CoFe2O4) nanoparticles (CoFe2O4-HPs-FAs) functionalized by coating them with hematoporphyrin (HP) for introducing photo-functionality and by conjugating with folic acid (FA) for targeting cancer cells. We evaluated the activities of the CoFe2O4-HPs-FAs by checking magnetic resonance imaging (MRI) in vitro, its biocompatibility, and photodynamic anticancer activities on FA receptor (FR)-positive and FR-negative cancer cell lines, Hela, KB, MCF-7, and PC-3 cells, to use for clinical applications. In this study, we have demonstrated that the CoFe2O4-HPs-FAs have good MRI and biocompatibility with non-cytotoxicity, and remarkable photodynamic anticancer activities at very low concentrations regardless of cell types. Particularly, the photo-killing abilities in 3.13 μg/mL of CoFe2O4-HPs-FAs were measured to be 91.8% (p < 0.002) for Hela, 94.5% (p < 0.007) for KB, 79.1% (p < 0.003) for MCF-7, and 71.3% (p < 0.006) for PC-3. The photodynamic anticancer activities in 6.25 and 12.5 μg/mL of CoFe2O4-HPs-FAs were measured to be over 95% (p < 0.004) to almost 100% regardless of cell types. The newly developed multifunctional CoFe2O4-HPs-FAs are effective for PDT and have potential as therapeutic agents for MRI-based PDT, because they have a high saturation value of magnetization and superparamagnetism. PMID:26349298

  14. Improved electrical properties of cadmium substituted cobalt ferrites nano-particles for microwave application

    NASA Astrophysics Data System (ADS)

    Ahmad, Rabia; Hussain Gul, Iftikhar; Zarrar, Muhammad; Anwar, Humaira; khan Niazi, Muhammad Bilal; Khan, Azim

    2016-05-01

    Cadmium substituted cobalt ferrites with formula CdxCo1-xFe2O4 (x=0.0, 0.2, 0.35, 0.5), have been synthesized by wet chemical co-precipitation technique. Electrical, morphological and Structural properties of the samples have been studied using DC electrical resistivity and Impedance analyzer, Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD), respectively. XRD, SEM and AFM have been used to study the structural parameters such as measured density, lattice constant, X-ray density, crystallite size and morphology of the synthesized nano-particles. Debye-Scherrer formula has been used for the estimation of crystallite sizes. The estimated crystallite sizes were to be 15-19±2 nm. Hopping length of octahedral and tetrahedral sites have been calculated using indexed XRD data. The porosity and lattice constant increased as Cd2+concentration increases. DC electrical resistivity was performed using two probe technique. The decrease of resistivity with temperature confirms the semiconducting nature of the samples. The dielectric properties variation has been studied at room temperature as a function of frequency. Variation of dielectric properties from 100 Hz to 5 MHz has been explained on the basis of Maxwell and Wagner's model and hoping of electrons on octahedral sites. To separates the grains boundary and grains of the system CdxCo1-xFe2O4 the impedance analysis were performed.

  15. Assessment of Immunotoxicity of Dextran Coated Ferrite Nanoparticles in Albino Mice

    PubMed Central

    Syama, Santhakumar; Gayathri, Viswanathan; Mohanan, Parayanthala Valappil

    2015-01-01

    In this study, dextran coated ferrite nanoparticles (DFNPs) of size <25 nm were synthesized, characterized, and evaluated for cytotoxicity, immunotoxicity, and oxidative stress by in vitro and in vivo methods. Cytotoxicity was performed in vitro using splenocytes with different concentrations of DFNPs. Gene expression of selected cytokines (IL-1, IL-10, and TNF β) secretion by splenocytes was evaluated. Also, 100 mg of DFNPs was injected intraperitoneally to 18 albino mice for immunological stimulations. Six animals each were sacrificed at the end of 7, 14, and 21 days. Spleen was subjected to immunotoxic response and liver was analyzed for antioxidant parameters (lipid peroxidation, reduced glutathione, glutathione peroxidase, superoxide dismutase, and glutathione reductase). The results indicated that DFNPs failed to induce any immunological reactions and no significant alternation in antioxidant defense mechanism. Also, mRNA expression of the cytokines revealed an increase in IL-10 expression and subsequent decreased expression of IL-1 and TNF β. Eventually, DNA sequencing of liver actin gene revealed base alteration in nonconserved regions (10–20 bases) of all the treated groups when compared to control samples. Hence, it can be concluded that the DFNPs were nontoxic at the cellular level and nonimmunotoxic when exposed intraperitoneally to mice. PMID:26576301

  16. Water-soluble superparamagnetic manganese ferrite nanoparticles for magnetic resonance imaging.

    PubMed

    Yang, Hong; Zhang, Cuixia; Shi, Xiangyang; Hu, He; Du, Xiaoxia; Fang, Yong; Ma, Yanbin; Wu, Huixia; Yang, Shiping

    2010-05-01

    We report here a thermal decomposition approach to the synthesis of water-soluble superparamagnetic manganese ferrite (MnFe(2)O(4)) nanoparticles (NPs) for magnetic resonance (MR) imaging applications. In this approach, tetraethylene glycol was utilized as a coordination and stabilization agent, rendering the NPs water-soluble and stable. The formed NPs had a diameter of 7 nm with a narrow size distribution, and were superparamagnetic with a saturated magnetization (Ms) of 39 emu/g. In vitro cytotoxicity test revealed that the MnFe(2)O(4) NPs were biocompatible at a particle concentration below 200 microg/mL. The transverse relaxivity of MnFe(2)O(4) NPs in water and cells after incubation were determined to be 189.3mm(-1)s(-1) and 36.8mm(-1)s(-1) based on iron concentration, respectively. In vivo MR imaging studies in conjunction with inductively coupled plasma-atomic emission spectroscopy showed that the MnFe(2)O(4) NPs were preferentially accumulated in liver after intravenous injection for 4h. This suggests that the developed MnFe(2)O(4) NPs can serve as a sensitive MR imaging contrast agent for liver imaging. By appropriately modifying or functionalizing the surface of the NPs, these particles may be used for MR detection of other diseases. PMID:20144480

  17. High-Performance Flexible Organic Nano-Floating Gate Memory Devices Functionalized with Cobalt Ferrite Nanoparticles.

    PubMed

    Jung, Ji Hyung; Kim, Sunghwan; Kim, Hyeonjung; Park, Jongnam; Oh, Joon Hak

    2015-10-01

    Nano-floating gate memory (NFGM) devices are transistor-type memory devices that use nanostructured materials as charge trap sites. They have recently attracted a great deal of attention due to their excellent performance, capability for multilevel programming, and suitability as platforms for integrated circuits. Herein, novel NFGM devices have been fabricated using semiconducting cobalt ferrite (CoFe2O4) nanoparticles (NPs) as charge trap sites and pentacene as a p-type semiconductor. Monodisperse CoFe2O4 NPs with different diameters have been synthesized by thermal decomposition and embedded in NFGM devices. The particle size effects on the memory performance have been investigated in terms of energy levels and particle-particle interactions. CoFe2O4 NP-based memory devices exhibit a large memory window (≈73.84 V), a high read current on/off ratio (read I(on)/I(off)) of ≈2.98 × 10(3), and excellent data retention. Fast switching behaviors are observed due to the exceptional charge trapping/release capability of CoFe2O4 NPs surrounded by the oleate layer, which acts as an alternative tunneling dielectric layer and simplifies the device fabrication process. Furthermore, the NFGM devices show excellent thermal stability, and flexible memory devices fabricated on plastic substrates exhibit remarkable mechanical and electrical stability. This study demonstrates a viable means of fabricating highly flexible, high-performance organic memory devices. PMID:26153227

  18. Magnetic phase transitions in ferrite nanoparticles characterized by electron spin resonance

    SciTech Connect

    Flores-Arias, Yesica Vázquez-Victorio, Gabriela; Ortega-Zempoalteca, Raul; Acevedo-Salas, Ulises; Valenzuela, Raul; Ammar, Souad

    2015-05-07

    Ferrite magnetic nanoparticles in the composition Zn{sub 0.7}Ni{sub 0.3}Fe{sub 2}O{sub 4} were synthesized by the polyol method, with an average size of 8 nm. Electron spin resonance (ESR) measurements were carried out at a frequency of 9.45 GHz in the 100–500 K temperature range. Obtained results exhibited a characteristic ESR signal in terms of resonance field, H{sub res}, linewidth, ΔH, and peak ratio, R, for each magnetic phase. At low temperatures, the ferrimagnetic phase showed low H{sub res}, broad ΔH, and asymmetric R. At high temperatures, these parameters exhibited opposite values: high H{sub res}, small ΔH, and R ∼ 1. For intermediate temperatures, a different phase was observed, which was identified as a superparamagnetic phase by means of zero-field cooling-field cooling and hysteresis loops measurements. The observed differences were explained in terms of the internal fields and especially due to the cubic anisotropy in the ordered phase.

  19. Green preparation and catalytic application of Pd nanoparticles

    NASA Astrophysics Data System (ADS)

    Xu, Lang; Wu, Xing-Cai; Zhu, Jun-Jie

    2008-07-01

    A green strategy for the facile preparation and effective stabilization of Pd nanoparticles has been developed by using D-glucose as the reducing and stabilizing agents. The UV/vis absorption spectroscopy, transmission electron microscopy (TEM), x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and zeta potential measurements were used to characterize the as-prepared Pd nanoparticles. It was found that the D-glucose concentration and pH value had an important effect on the size distribution and stability of the nanoparticles. Further, the Pd nanoparticles exhibited good catalytic properties in the degradation of azo dyes.

  20. Preparation of drug nanoparticles by emulsion evaporation method

    NASA Astrophysics Data System (ADS)

    Hoa, Le Thi Mai; Chi, Nguyen Tai; Triet, Nguyen Minh; Thanh Nhan, Le Ngoc; Mau Chien, Dang

    2009-09-01

    Polymeric drug nanoparticles were prepared by emulsion solvent evaporation method. In this study, prepared the polymeric drug nanoparticles consist of ketoprofen and Eudragit E 100. The morphology structure was investigated by scanning electron microscopy (SEM). The interactions between the drug and polymer were investigated by Fourier transform infrared spectroscopy (FTIR). The size distribution was measured by means of Dynamic Light Scattering. The nanoparticles have an average size of about 150 nm. The incorporation ability of drugs in the polymeric nanoparticles depended on the integration between polymer and drug as well as the glass transition temperature of the polymer.

  1. Magnetic studies of CuFe2O4 nanoparticles prepared by co-precipitation method

    NASA Astrophysics Data System (ADS)

    Subha, A.; Shalini, M. Govindaraj; Sahoo, Subasa C.

    2016-05-01

    Cu-ferrite nanoparticles were synthesized by co-precipitation method and were annealed at different temperatures ranging from 400 to l000°C in air for 4 hours. The as-prepared sample and the sample annealed at 400°C showed small peaks of cubic Cu-ferrite in X-ray diffraction studies. For the intermediate temperature 600°C, some additional peaks of α-Fe2O3 were observed. As the annealing temperature increased further only tetragonal Cu-ferrite peaks were observed. In all the samples some traces of CuO was noted. Grain size was increased from 2lnm for the as prepared sample to 42nm for the sample annealed at l000°C. Spontaneous magnetization value was found to be very small for the as prepared sample and it was increased monotonically with the increase in annealing temperature. Maximum magnetization of 29.7emu/g was observed at 300K for the sample annealed at l000°C. The remanent magnetization was increased with the increase in annealing temperature up to 900°C and then decreased whereas for the coercivity a peak was observed for the sample annealed at 800°C. The highest coercivity of l402 Oe was observed at 300K for the sample annealed at 800°C. As the measurement temperature decreased from 300K to 60K, magnetization and coercivity values were increased. The observed magnetic behaviour may be understood on the basis of phase transformation, grain growth with the increase in annealing temperature and reduced thermal energy at low measurement temperature.

  2. Volume-labeled nanoparticles and methods of preparation

    DOEpatents

    Wang, Wei; Gu, Baohua; Retterer, Scott T; Doktycz, Mitchel J

    2015-04-21

    Compositions comprising nanosized objects (i.e., nanoparticles) in which at least one observable marker, such as a radioisotope or fluorophore, is incorporated within the nanosized object. The nanosized objects include, for example, metal or semi-metal oxide (e.g., silica), quantum dot, noble metal, magnetic metal oxide, organic polymer, metal salt, and core-shell nanoparticles, wherein the label is incorporated within the nanoparticle or selectively in a metal oxide shell of a core-shell nanoparticle. Methods of preparing the volume-labeled nanoparticles are also described.

  3. Adsorption of Cu2+ ions using chitosan-modified magnetic Mn ferrite nanoparticles synthesized by microwave-assisted hydrothermal method

    NASA Astrophysics Data System (ADS)

    Meng, Yuying; Chen, Deyang; Sun, Yitao; Jiao, Dongling; Zeng, Dechang; Liu, Zhongwu

    2015-01-01

    Chitosan-modified Mn ferrite nanoparticles were synthesized by a one-step microwave-assisted hydrothermal method. These Mn ferrite magnetic composite nanoparticles were employed to absorb Cu2+ ions in water. XRD verified the spinel structure of the MnFe2O4 nanoparticles. Chitosan modification does not result in any phase change of MnFe2O4. FTIR and zeta potentials curves for all samples suggest that chitosan can be successfully coated on the Mn ferrites. TEM characterization showed that the modified MnFe2O4 nanoparticles have a cubic shape with a mean diameter of ∼100 nm. For adsorption behavior, the effects of experiment parameters such as solution pH value, contact time and initial Cu2+ ions concentration on the adsorption efficiency were systematically investigated. The results showed that increasing solution pH value and extending contact time are favorable for improving adsorption efficiency. Especially, adsorption efficiency can reach up to 100% and 96.7% after 500 min adsorption at pH 6.5 for the solutions with initial Cu2+ ions concentration of 50 mg/L and 100 mg/L. Adsorption data fits well with the Langmuir isotherm models with a maximum adsorption capacity (qm) and a Langmuir adsorption equilibrium constant (K) of 65.1 mg/g and 0.090 L/mg, respectively. The adsorption kinetic agrees well with pseudo second order model with the pseudo second rate constants (K2) of 0.0468 and 0.00189 g/mg/min for solutions with initial Cu2+ ions of 50 and 100 mg/L, respectively.

  4. Nanoparticles of Molybdenum Chlorophyllin Photosensitizer and Magnetic Citrate-Coated Cobalt Ferrite Complex Available to Hyperthermia and Photodynamic Therapy Clinical Trials

    NASA Astrophysics Data System (ADS)

    Primo, Fernando L.; Cordo, Paloma L. A. G.; Neto, Alberto F.; Morais, Paulo C.; Tedesco, Antonio C.

    2010-12-01

    This study report on the synthesis and characterization of molybdenum chlorophyllin (Mo-Chl) compounds associated in a complex with magnetic nanoparticles (citrate-coated cobalt ferrite), the latter prepared as a biocompatible magnetic fluid (MF). The complex material was developed for application as a synergic drug for cancer treatment using Photodynamic Therapy (PDT) and Hyperthermia (HPT). Chlorophyllin was obtained from alkaline extraction of Ilex paraguariensis following molybdenum insertion from hydrolysis with molybdate sodium. Fluorescence quantum yield (Φf) of Mo-Chl/dimethyl-sulphoxide (DMSO) was lower than 0.1, with a lifetime of 5.0 ns, as obtained from time-correlated single-photon counting technique. The oxygen quantum yield of Mo-Chl was carried out using laser flash-photolysis studies in homogeneous medium saturated with O2(g) (ΦΔ = 0.50). Cellular viability was also evaluated via the classical MTT assay using gingival fibroblasts cells as a biological model. Studies performed with the complex Mo-Chl (5.0 μmol.L-1)/MF at different magnetic nanoparticle concentrations (ranging from 1012 to 1015 particle.mL-1) revealed a cellular viability of approximately 95% for the ideal magnetic material concentration of 1×10 particle.mL-1. The present study shows that natural photosensitizers molecules Mo-Chl used in association with magnetic nanoparticles represent a promising generation of drug developed to work synergistically in the treatment of neoplastic tissues using PDT and HPT.

  5. Adsorption of cobalt ferrite nanoparticles within layer-by-layer films: a kinetic study carried out using quartz crystal microbalance.

    PubMed

    Alcantara, Gustavo B; Paterno, Leonardo G; Afonso, André S; Faria, Ronaldo C; Pereira-da-Silva, Marcelo A; Morais, Paulo C; Soler, Maria A G

    2011-12-28

    The paper reports on the successful use of the quartz crystal microbalance technique to assess accurate kinetics and equilibrium parameters regarding the investigation of in situ adsorption of nanosized cobalt ferrite particles (CoFe(2)O(4)--10.5 nm-diameter) onto two different surfaces. Firstly, a single layer of nanoparticles was deposited onto the surface provided by the gold-coated quartz resonator functionalized with sodium 3-mercapto propanesulfonate (3-MPS). Secondly, the layer-by-layer (LbL) technique was used to build multilayers in which the CoFe(2)O(4) nanoparticle-based layer alternates with the sodium sulfonated polystyrene (PSS) layer. The adsorption experiments were conducted by modulating the number of adsorbed CoFe(2)O(4)/PSS bilayers (n) and/or by changing the CoFe(2)O(4) nanoparticle concentration while suspended as a stable colloidal dispersion. Adsorption of CoFe(2)O(4) nanoparticles onto the 3-MPS-functionalized surface follows perfectly a first order kinetic process in a wide range (two orders of magnitude) of nanoparticle concentrations. These data were used to assess the equilibrium constant and the adsorption free energy. Alternatively, the Langmuir adsorption constant was obtained while analyzing the isotherm data at the equilibrium. Adsorption of CoFe(2)O(4) nanoparticles while growing multilayers of CoFe(2)O(4)/PSS was conducted using colloidal suspensions with CoFe(2)O(4) concentration in the range of 10(-8) to 10(-6) (moles of cobalt ferrite per litre) and for different numbers of cycles n = 1, 3, 5, and 10. We found the adsorption of CoFe(2)O(4) nanoparticles within the CoFe(2)O(4)/PSS bilayers perfectly following a first order kinetic process, with the characteristic rate constant growing with the increase of CoFe(2)O(4) nanoparticle concentration and decreasing with the rise of the number of LbL cycles (n). Additionally, atomic force microscopy was employed for assessing the LbL film roughness and thickness. We found the film thickness increasing from about 20 to 120 nm while shifting from 3 to 10 CoFe(2)O(4)/PSS bilayers, using the 8.9 × 10(-6) (moles of cobalt ferrite per litre) suspension. PMID:22025281

  6. Comparing highly ordered monolayers of nanoparticles fabricated using electrophoretic deposition: Cobalt ferrite nanoparticles versus iron oxide nanoparticles

    DOE PAGESBeta

    Dickerson, James H.; Krejci, Alex J.; Garcia, Adriana -Mendoza; Sun, Shouheng; Pham, Viet Hung

    2015-08-01

    Ordered assemblies of nanoparticles remain challenging to fabricate, yet could open the door to many potential applications of nanomaterials. Here, we demonstrate that locally ordered arrays of nanoparticles, using electrophoretic deposition, can be extended to produce long-range order among the constituents. Voronoi tessellations along with multiple statistical analyses show dramatic increases in order compared with previously reported assemblies formed through electric field-assisted assembly. As a result, based on subsequent physical measurements of the nanoparticles and the deposition system, the underlying mechanisms that generate increased order are inferred.

  7. Impact of Nd3+ in CoFe2O4 spinel ferrite nanoparticles on cation distribution, structural and magnetic properties

    NASA Astrophysics Data System (ADS)

    Yadav, Raghvendra Singh; Havlica, Jaromir; Masilko, Jiri; Kalina, Lukas; Wasserbauer, Jaromir; Hajdúchová, Miroslava; Enev, Vojtěch; Kuřitka, Ivo; Kožáková, Zuzana

    2016-02-01

    Nd3+ doped cobalt ferrite nanoparticles have been synthesized by starch-assisted sol-gel auto-combustion method. The significant role played by Nd3+ added to cobalt ferrite in changing cation distribution and further in influencing structural and magnetic properties, was explored and reported. The crystal structure formation and crystallite size were studied from X-ray diffraction studies. The microstructural features were investigated by field emission scanning electron microscopy and transmission electron microscopy that demonstrates the nanocrystalline grain formation with spherical morphology. An infrared spectroscopy study shows the presence of two absorption bands related to tetrahedral and octahedral group complexes within the spinel ferrite lattice system. The change in Raman modes in synthesized ferrite system were observed with Nd3+ substitution, particle size and cation redistribution. The impact of Nd3+ on cation distribution of Co2+ and Fe3+ at octahedral and tetrahedral sites in spinel ferrite cobalt ferrite nanoparticles was investigated by X-ray photoelectron spectroscopy. Room temperature magnetization measurements showed that the saturation magnetization and coercivity increase with addition of Nd3+ substitution in cobalt ferrite.

  8. Enhanced Néel temperature in Mn ferrite nanoparticles linked to growth-rate-induced cation inversion.

    PubMed

    Yang, Aria; Chinnasamy, C N; Greneche, J M; Chen, Yajie; Yoon, Soack D; Chen, Zhaohui; Hsu, Kailin; Cai, Zhuhua; Ziemer, Kate; Vittoria, C; Harris, V G

    2009-05-01

    Mn ferrite (MnFe(2)O(4)) nanoparticles, having diameters from 4 to 50 nm, were synthesized using a modified co-precipitation technique in which mixed metal chloride solutions were added to different concentrations of boiling NaOH solutions to control particle growth rate. Thermomagnetization measurements indicated an increase in Néel temperature corresponding to increased particle growth rate and particle size. The Néel temperature is also found to increase inversely proportionally to the cation inversion parameter, delta, appearing in the formula (Mn(1-delta)Fe(delta))(tet)[Mn(delta)Fe(2-delta)](oct)O(4). These results contradict previously published reports of trends between Néel temperature and particle size, and demonstrate the dominance of cation inversion in determining the strength of superexchange interactions and subsequently Néel temperature in ferrite systems. The particle surface chemistry, structure, and magnetic spin configuration play secondary roles. PMID:19420627

  9. Structural, dielectric and magnetic properties of cobalt ferrite prepared using auto combustion and ceramic route

    NASA Astrophysics Data System (ADS)

    Murugesan, C.; Perumal, M.; Chandrasekaran, G.

    2014-09-01

    Cobalt ferrite is synthesized by using low temperature auto combustion and high temperature ceramic methods. The prepared samples have values of lattice constant equal to 8.40 Å and 8.38 Å for auto combustion and ceramic methods respectively. The FTIR spectrum of samples of the auto combustion method shows a high frequency vibrational band at 580 cm-1 assigned to tetrahedral site and a low frequency vibrational band at 409 cm-1 assigned to octahedral site which are shifted to 590 cm-1 and 412 cm-1 for the ceramic method sample. SEM micrographs of samples show a substantial difference in surface morphology and size of the grains between the two methods. The frequency dependent dielectric constant and ac conductivity of the samples measured from 1 Hz to 2 MHz at room temperature are reported. The room temperature magnetic hysteresis parameters of the samples are measured using VSM. The measured values of saturation magnetization, coercivity and remanent magnetization are 42 emu/g, 1553 Oe, 18.5 emu/g for the auto combustion method, 66.7 emu/g, 379.6 Oe, and 17.3 emu/g for the ceramic method, respectively. The difference in preparation methods and size of the grains causes interesting changes in electrical and magnetic properties.

  10. Positron annihilation and magnetic properties studies of copper substituted nickel ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Kargar, Z.; Asgarian, S. M.; Mozaffari, M.

    2016-05-01

    Single phase copper substituted nickel ferrite Ni1-xCuxFe2O4 (x = 0.0, 0.1, 0.3 and 0.5) nanoparticles were synthesized by the sol-gel method. TEM images of the samples confirm formation of nano-sized particles. The Rietveld refinement of the X-ray diffraction patterns showed that lattice constant increase with increase in copper content from 8.331 for x = 0.0 to 8.355 Å in x = 0.5. Cation distribution of samples has been determined by the occupancy factor, using Rietveld refinement. The positron lifetime spectra of the samples were convoluted into three lifetime components. The shortest lifetime is due to the positrons that do not get trapped by the vacancy defects. The second lifetime is ascribed to annihilation of positrons in tetrahedral (A) and octahedral (B) sites in spinel structure. It is seen that for x = 0.1 and 0.3 samples, positron trapped within vacancies in A sites, but for x = 0.0 and 0.5, the positrons trapped and annihilated within occupied B sites. The longest lifetime component attributed to annihilation of positrons in the free volume between nanoparticles. The obtained results from coincidence Doppler broadening spectroscopy (CDBS) confirmed the results of positron annihilation lifetime spectroscopy (PALS) and also showed that the vacancy clusters concentration for x = 0.3 is more than those in other samples. Average defect density in the samples, determined from mean lifetime of annihilated positrons reflects that the vacancy concentration for x = 0.3 is maximum. The magnetic measurements showed that the saturation magnetization for x = 0.3 is maximum that can be explained by Néel's theory. The coercivity in nanoparticles increased with increase in copper content. This increase is ascribed to the change in anisotropy constant because of increase of the average defect density due to the substitution of Cu2+ cations and magnetocrystalline anisotropy of Cu2+ cations. Curie temperature of the samples reduces with increase in copper content which can be explained based on Néel's theory.

  11. A novel sonication route to prepare anthracene nanoparticles

    SciTech Connect

    Kang Peng; Chen Chunnian; Hao Lingyun; Zhu Chunling; Hu Yuan; Chen Zuyao

    2004-04-02

    A novel sonication method has been successfully developed for the preparation of anthracene nanoparticles. The as-prepared nanoparticles are characterized using transmission electron microscopy, ultraviolet-visible absorption spectroscopy, fluorescence excitation and emission spectroscopy. Nanoparticles prepared with sonication are smaller and better dispersed than with magnetic stirring. Surfactants cetyltrimethylammonium bromide, bis(2-ethylhexyl)sodium sulfosuccinate, sodium dodecyl sulfonate and polyvinylpyrrolidone are used to control the size and morphology. Excimer band is found at 445 and 472 nm and possible mechanism is discussed.

  12. Polyethylene glycol as an alternative polymer solvent for nanoparticle preparation.

    PubMed

    Ali, Mohamed Ehab; Lamprecht, Alf

    2013-11-01

    Solvent toxicity is one of the major drawbacks in the preparation of polymeric nanoparticles today. Here, polyethylene glycols (PEGs) are proposed as non-toxic solvents for the preparation of polymeric nanoparticles. Based on a preparation process similar to the solvent displacement technique, several process parameters were examined for their effects on the properties of the prepared nanoparticles by this method to achieve the optimum preparation conditions. The investigated parameters included polymer type and concentration, volume and temperature of the dispersing phase, methods of dispersing the solvent phase into the non-solvent phase, duration and speed of stirring and washing by dialysis. Ammonio methacrylate copolymer (Eudragit RL), poly-lactide-co-glycolide (PLGA), and PEG-PLGA were found to be successful polymer candidates for the preparation of nanoparticles by this method. Nanoparticles with diameters ranging from 80 to 400 nm can be obtained. The encapsulation efficiencies of bovine serum albumin, and lysozyme as model proteins were ranging from 7.3±2.2% to 69.3±1.8% depending on the strength of polymer-protein interaction. Biological assays confirmed a full lysozyme activity after the preparation process. PEG proved to be a suitable non-toxic solvent for the preparation of polymeric protein-loaded nanoparticles, maintaining the integrity of protein. PMID:23958752

  13. Comparison of structural and electrical properties of Co{sup 2+}doped Mn-Zn soft nano ferrites prepared via coprecipitation and hydrothermal methods

    SciTech Connect

    Anwar, Humaira; Maqsood, Asghari

    2014-01-01

    Graphical abstract: - Highlights: • Coprecipitation and hydrothermal synthesis of Co{sup 2+} doped Mn-Zn ferrites. • Dielectric measurements at 3 MHz and 1 GHz frequencies. • Enhanced DC electrical resistivity for samples prepared from hydrothermal technique. • Impedance studies for the prepared samples showing major contribution due to grains. - Abstract: A series of Co doped Mn-Zn ferrites compounds with the formula Mn{sub 0.5}Zn{sub 0.5−x}Co{sub x}Fe{sub 2}O{sub 4} (x = 0, 0.15, 0.25, 0.35 and 0.50) were successfully synthesized by polyethylene glycol-assisted coprecipitation and hydrothermal methods. The structural characterization of the samples was done using X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) and Fourier transform infrared spectroscopy (FTIR). All the samples found to have cubic spinel structure. The average crystallite size of all nanoparticles were estimated using Scherrer's formula and found to lie between 10 and 25 ± 3 nm with small size distribution of particles prepared by hydrothermal method. The FTIR spectrum showed two absorption bands of tetrahedral and octahedral metal-oxygen sites. DC electrical resistivity varied from 4.12 × 10{sup 7} to 8.32 × 10{sup 10} ohm cm with cobalt doping. The dielectric measurements were performed from 20 Hz to 3 MHz and from 1 MHz to 1 GHz frequency ranges. The value of dielectric constant (ε′) varies from 15.54 to 106.25 (1 MHz) and 6.73–16.48 (1 GHz) for all the samples at room temperature. Impedance spectroscopy was carried out from 20 Hz to 3 MHz, at room temperature to study the grains and grain boundaries effect.

  14. Electrospinning preparation, characterization and magnetic properties of cobalt-nickel ferrite (Co(1-x)Ni(x)Fe2)O4) nanofibers.

    PubMed

    Xiang, Jun; Chu, Yanqiu; Shen, Xiangqian; Zhou, Guangzhen; Guo, Yintao

    2012-06-15

    Uniform Co(1-)(x)Ni(x)Fe(2)O(4) (x=0.0, 0.2, 0.4, 0.6, 0.8 and 1.0) nanofibers with average diameter of 110 nm and length up to several millimeters were prepared by calcination of electrospun precursor nanofibers containing polymer and inorganic salts. The as-spun and calcined nanofibers were characterized in detail by TG-DTA, XRD, FE-SEM, TEM, SAED and VSM, respectively. The effect of composition of the nanofibers on the structure and magnetic properties were investigated. The nanofibers are formed through assembling magnetic nanoparticles with poly(vinyl pyrrolidone) as the structure-directing template. The structural characteristics and magnetic properties of the resultant nanofibers vary with chemical composition and can be tuned by adjusting the Co/Ni ratio. Both lattice parameter and particle size decrease gradually with increasing nickel concentration. The saturation magnetization and coercivity lie in the range 29.3-56.4 emu/g and 210-1255 Oe, respectively, and both show a monotonously decreasing behavior with the increase in nickel concentration. Such changes in magnetic properties can mainly be attributed to the lower magnetocrystalline anisotropy and the smaller magnetic moment of Ni(2+) ions compared to Co(2+) ions. Furthermore, the coercivity of Co-Ni ferrite nanofibers is found to be superior to that of the corresponding nanoparticle counterparts, presumably due to their large shape anisotropy. These novel one-dimensional Co-Ni ferrite magnetic nanofibers can potentially be used in micro-/nanoelectronic devices, microwave absorbers and sensing devices. PMID:22456275

  15. Observation of magnetic anomalies in one-step solvothermally synthesized nickel-cobalt ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Datt, Gopal; Sen Bishwas, Mousumi; Manivel Raja, M.; Abhyankar, A. C.

    2016-02-01

    Magnetic anomalies corresponding to the Verwey transition and reorientation of anisotropic vacancies are observed at 151 K and 306 K, respectively, in NiCoFe2O4 nanoparticles (NPs) synthesized by a modified-solvothermal method followed by annealing. Cationic disorder and spherical shape induced non-stoichiometry suppress the Verwey transition in the as-synthesized NPs. On the other hand, reorientation of anisotropic vacancies is quite robust. XRD and electron microscopy investigations confirm a single phase spinel structure and the surface morphology of the as-synthesized NPs changes from spherical to octahedral upon annealing. Rietveld analysis reveals that the Ni2+ ions migrate from tetrahedral (A) to octahedral (B) sites upon annealing. The Mössbauer results show canted spins in both the NPs and the strength of superexchange is stronger in Co-O-Fe than Ni-O-Fe. Magnetic force images show that the as-synthesised NPs are single-domain whereas the annealed NPs are multi-domain octahedral particles. The FMR study reveals that both the NPs have a broad FMR line-width; and resonance properties are consistent with the random anisotropy model. The broad inhomogeneous FMR line-width, observation of the Verwey transition, tuning of the magnetic domain structure as well as the magnetic properties suggest that the NiCoFe2O4 ferrite NPs may be promising for future generation spintronics, magneto-electronics, and ultra-high-density recording media as well as for radar absorbing applications.Magnetic anomalies corresponding to the Verwey transition and reorientation of anisotropic vacancies are observed at 151 K and 306 K, respectively, in NiCoFe2O4 nanoparticles (NPs) synthesized by a modified-solvothermal method followed by annealing. Cationic disorder and spherical shape induced non-stoichiometry suppress the Verwey transition in the as-synthesized NPs. On the other hand, reorientation of anisotropic vacancies is quite robust. XRD and electron microscopy investigations confirm a single phase spinel structure and the surface morphology of the as-synthesized NPs changes from spherical to octahedral upon annealing. Rietveld analysis reveals that the Ni2+ ions migrate from tetrahedral (A) to octahedral (B) sites upon annealing. The Mössbauer results show canted spins in both the NPs and the strength of superexchange is stronger in Co-O-Fe than Ni-O-Fe. Magnetic force images show that the as-synthesised NPs are single-domain whereas the annealed NPs are multi-domain octahedral particles. The FMR study reveals that both the NPs have a broad FMR line-width; and resonance properties are consistent with the random anisotropy model. The broad inhomogeneous FMR line-width, observation of the Verwey transition, tuning of the magnetic domain structure as well as the magnetic properties suggest that the NiCoFe2O4 ferrite NPs may be promising for future generation spintronics, magneto-electronics, and ultra-high-density recording media as well as for radar absorbing applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr06791j

  16. Long-circulating PEGylated manganese ferrite nanoparticles for MRI-based molecular imaging.

    PubMed

    Pernia Leal, Manuel; Rivera-Fernández, Sara; Franco, Jaime M; Pozo, David; de la Fuente, Jesús M; García-Martín, María Luisa

    2015-02-01

    Magnetic resonance based molecular imaging has emerged as a very promising technique for early detection and treatment of a wide variety of diseases, including cancer, neurodegenerative disorders, and vascular diseases. The limited sensitivity and specificity of conventional MRI are being overcome by the development of a new generation of contrast agents, using nanotechnology approaches, with improved magnetic and biological properties. In particular, for molecular imaging, high specificity, high sensitivity, and long blood circulation times are required. Furthermore, the lack of toxicity and immunogenicity together with low-cost scalable production are also necessary to get them into the clinics. In this work, we describe a facile, robust and cost-effective ligand-exchange method to synthesize dual T1 and T2 MRI contrast agents with long circulation times. These contrast agents are based on manganese ferrite nanoparticles (MNPs) between 6 and 14 nm in size covered by a 3 kDa polyethylene glycol (PEG) shell that leads to a great stability in aqueous media with high crystallinity and magnetization values, thus retaining the magnetic properties of the uncovered MNPs. Moreover, the PEGylated MNPs have shown different relaxivities depending on their size and the magnetic field applied. Thus, the 6 nm PEGylated MNPs are characterized by a low r2/r1 ratio of 4.9 at 1.5 T, hence resulting in good dual T1 and T2 contrast agents under low magnetic fields, whereas the 14 nm MNPs behave as excellent T2 contrast agents under high magnetic fields (r2 = 335.6 mM(-1) s(-1)). The polymer core shell of the PEGylated MNPs minimizes their cytotoxicity, and allows long blood circulation times. This combination of cellular compatibility and excellent T2 and r2/r1 values under low magnetic fields, together with long circulation times, make these nanomaterials very promising contrast agents for molecular imaging. PMID:25554363

  17. Observation of magnetic anomalies in one-step solvothermally synthesized nickel-cobalt ferrite nanoparticles.

    PubMed

    Datt, Gopal; Sen Bishwas, Mousumi; Manivel Raja, M; Abhyankar, A C

    2016-02-25

    Magnetic anomalies corresponding to the Verwey transition and reorientation of anisotropic vacancies are observed at 151 K and 306 K, respectively, in NiCoFe2O4 nanoparticles (NPs) synthesized by a modified-solvothermal method followed by annealing. Cationic disorder and spherical shape induced non-stoichiometry suppress the Verwey transition in the as-synthesized NPs. On the other hand, reorientation of anisotropic vacancies is quite robust. XRD and electron microscopy investigations confirm a single phase spinel structure and the surface morphology of the as-synthesized NPs changes from spherical to octahedral upon annealing. Rietveld analysis reveals that the Ni(2+) ions migrate from tetrahedral (A) to octahedral (B) sites upon annealing. The Mössbauer results show canted spins in both the NPs and the strength of superexchange is stronger in Co-O-Fe than Ni-O-Fe. Magnetic force images show that the as-synthesised NPs are single-domain whereas the annealed NPs are multi-domain octahedral particles. The FMR study reveals that both the NPs have a broad FMR line-width; and resonance properties are consistent with the random anisotropy model. The broad inhomogeneous FMR line-width, observation of the Verwey transition, tuning of the magnetic domain structure as well as the magnetic properties suggest that the NiCoFe2O4 ferrite NPs may be promising for future generation spintronics, magneto-electronics, and ultra-high-density recording media as well as for radar absorbing applications. PMID:26880070

  18. Load partitioning between ferrite/martensite and dispersed nanoparticles of a 9Cr ferritic/martensitic (F/M) ODS steel at high temperatures

    SciTech Connect

    Zhang, Guangming; Mo, Kun; Miao, Yinbin; Liu, Xiang; Almer, Jonathan; Zhou, Zhangjian; Stubbins, James F.

    2015-06-18

    In this study, a high-energy synchrotron radiation X-ray technique was used to investigate the tensile deformation processes of a 9Cr-ODS ferritic/martensitic (F/M) steel at different temperatures. Two minor phases within the 9Cr-ODS F/M steel matrix were identified as Y2Ti2O7 and TiN by the high-energy X-ray diffraction, and confirmed by the analysis using energy dispersive X-ray spectroscopy (EDS) of scanning transmission electron microscope (STEM). The lattice strains of the matrix and particles were measured through the entire tensile deformation process. During the tensile tests, the lattice strains of the ferrite/martensite and the particles (TiN and Y2Ti2O7) showed a strong temperature dependence, decreasing with increasing temperature. Analysis of the internal stress at three temperatures showed that the load partitioning between the ferrite/martensite and the particles (TiN and Y2Ti2O7) was initiated during sample yielding and reached to a peak during sample necking. At three studied temperatures, the internal stress of minor phases (Y2Ti2O7 and TiN) was about 2 times that of F/M matrix at yielding position, while the internal stress of Y2Ti2O7 and TiN reached about 4.5-6 times and 3-3.5 times that of the F/M matrix at necking position, respectively. It indicates that the strengthening of the matrix is due to minor phases (Y2Ti2O7 and TiN), especially Y2Ti2O7 particles. Although the internal stresses of all phases decreased with increasing temperature from RT to 600 degrees C, the ratio of internal stresses of each phase at necking position stayed in a stable range (internal stresses of Y2Ti2O7 and TiN were about 4.5-6 times and 3-3.5 times of that of F/M matrix, respectively). The difference between internal stress of the F/M matrix and the applied stress at 600 degrees C is slightly lower than those at RI and 300 degrees C, indicating that the nanoparticles still have good strengthening effect at 600 degrees C. (C) 2015 Elsevier B.V. All rights reserved.

  19. Preparation of linoleic acid capped gold nanoparticles and their spectra

    NASA Astrophysics Data System (ADS)

    Das, Ratan; Nath, Siddhartha S.; Bhattacharjee, Ramendu

    2010-11-01

    Gold nanoparticles have been prepared through the chemical reduction of tetrachloroaurate ions by ethanol with linoleic acid as a protecting layer to the nanoparticles. X-Ray diffraction study and transmission electron microscopy (TEM) reveal that the particles are mostly spherical in shape with an average size of nearly 10 nm. The UV/vis absorption spectra show absorption maximum at 510 nm, which is due to surface plasmon resonance (SPR). Photoluminescence spectra of gold nanoparticles have also been analysed, which show an emission peak at 770 nm when illuminated at 550 nm. The most important fact is that the produced nanoparticles remain stable for more than 1 week.

  20. Zero-valent iron nanoparticles preparation

    SciTech Connect

    Oropeza, S.; Corea, M.; Gmez-Yez, C.; Cruz-Rivera, J.J.; Navarro-Clemente, M.E.

    2012-06-15

    Graphical abstract: Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}] at room temperature and a pressure of 3 atm. The synthesized nanoparticles were spherical and had diameters less than 5 nm. Highlights: ? Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}]. ? The conditions of reaction were at room temperature and a pressure of 3 atm. ? The synthesized nanoparticles were spherical and had diameters less than 5 nm. -- Abstract: Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}] at room temperature and a pressure of 3 atm. To monitor the reaction, a stainless steel pressure reactor lined with PTFE and mechanically stirred was designed. This design allowed the extraction of samples at different times, minimizing the perturbation in the system. In this way, the shape and the diameter of the nanoparticles produced during the reaction were also monitored. The results showed the production of zero-valent iron nanoparticles that were approximately 5 nm in diameter arranged in agglomerates. The agglomerates grew to 900 nm when the reaction time increased up to 12 h; however, the diameter of the individual nanoparticles remained almost the same. During the reaction, some byproducts constituted by amino species acted as surfactants; therefore, no other surfactants were necessary.

  1. Novel Methods of Lipidic Nanoparticle Preparation and Drug Loading

    NASA Astrophysics Data System (ADS)

    Maitani, Y.

    2013-09-01

    In improving cancer chemotherapy, lipidic nanoparticle systems for drug delivery, such as liposomes and emulsions, have received much attention because they are capable of delivering their drug payload selectively to cancer cells and of circulating for a long period in the bloodstream. In addition, lipidic nanoparticles have been examined for use in gene delivery as a non-viral vector. Preparation methods of particles and drug loading methods are crucial for the physicochemical properties of nanoparticles, which are the key aspects for pharmaceutical applications. This review describes new preparation methods for nanoparticles and a loading method for drugs using nanotechnology, including an evaluation of nanoparticles from the point of drug release for applications in cancer therapy and gene delivery.

  2. Oriented Y-type hexagonal ferrite thin films prepared by chemical solution deposition

    SciTech Connect

    Buršík, J.; Kužel, R.; Knížek, K.; Drbohlav, I.

    2013-07-15

    Thin films of Ba{sub 2}Zn{sub 2}Fe{sub 12}O{sub 22} (Y) hexaferrite were prepared through the chemical solution deposition method on SrTiO{sub 3}(1 1 1) (ST) single crystal substrates using epitaxial SrFe{sub 12}O{sub 19} (M) hexaferrite thin layer as a seed template layer. The process of crystallization was mainly investigated by means of X-ray diffraction and atomic force microscopy. A detailed inspection revealed that growth of seed layer starts through the break-up of initially continuous film into isolated grains with expressive shape anisotropy and hexagonal habit. The vital parameters of the seed layer, i.e. thickness, substrate coverage, crystallization conditions and temperature ramp were optimized with the aim to obtain epitaxially crystallized Y phase. X-ray diffraction Pole figure measurements and Φ scans reveal perfect parallel in-plane alignment of SrTiO{sub 3} substrate and both hexaferrite phases. - Graphical abstract: XRD pole figure and AFM patterns of Ba{sub 2}Zn{sub 2}Fe{sub 12}O{sub 22} thin film epitaxially grown on SrTiO{sub 3}(1 1 1) single crystal using seeding layer templating. - Highlights: • Single phase Y-type hexagonal ferrite thin films were prepared by CSD method. • Seed M layer breaks into isolated single crystal islands and serves as a template. • Large seed grains grow by consuming the grains within the bulk of recoated film. • We explained the observed orientation relation of epitaxial domains. • Epitaxial growth on SrTiO{sub 3}(1 1 1) with relation (0 0 1){sub M,Y}//(1 1 1){sub ST}+[1 0 0]{sub M,Y}//[2 −1 −1]{sub ST}.

  3. Antifungal activity of gold nanoparticles prepared by solvothermal method

    SciTech Connect

    Ahmad, Tokeer; Wani, Irshad A.; Lone, Irfan H.; Ganguly, Aparna; Manzoor, Nikhat; Ahmad, Aijaz; Ahmed, Jahangeer; Al-Shihri, Ayed S.

    2013-01-15

    Graphical abstract: Gold nanoparticles (7 and 15 nm) of very high surface area (329 and 269 m{sup 2}/g) have been successfully synthesized through solvothermal method by using tin chloride and sodium borohydride as reducing agents. As-prepared gold nanoparticles shows very excellent antifungal activity against Candida isolates and activity increases with decrease in the particle size. Display Omitted Highlights: ► Effect of reducing agents on the morphology of gold nanoparticles. ► Highly uniform and monodisperse gold nanoparticles (7 nm). ► Highest surface area of gold nanoparticles (329 m{sup 2/}g). ► Excellent antifungal activity of gold nanoparticles against Candida strains. -- Abstract: Gold nanoparticles have been successfully synthesized by solvothermal method using SnCl{sub 2} and NaBH{sub 4} as reducing agents. X-ray diffraction studies show highly crystalline and monophasic nature of the gold nanoparticles with face centred cubic structure. The transmission electron microscopic studies show the formation of nearly spherical gold nanoparticles of average size of 15 nm using SnCl{sub 2}, however, NaBH{sub 4} produced highly uniform, monodispersed and spherical gold nanoparticles of average grain size of 7 nm. A high surface area of 329 m{sup 2}/g for 7 nm and 269 m{sup 2}/g for 15 nm gold nanoparticles was observed. UV–vis studies assert the excitations over the visible region due to transverse and longitudinal surface plasmon modes. The gold nanoparticles exhibit excellent size dependant antifungal activity and greater biocidal action against Candida isolates for 7 nm sized gold nanoparticles restricting the transmembrane H{sup +} efflux of the Candida species than 15 nm sized gold nanoparticles.

  4. Preparation of silver nanoparticles by laser ablation in polyvinylpyrrolidone solutions

    NASA Astrophysics Data System (ADS)

    Tsuji, Takeshi; Thang, D.-H.; Okazaki, Yuuki; Nakanishi, Masataka; Tsuboi, Yasuyuki; Tsuji, Masaharu

    2008-06-01

    We performed laser ablation of a silver plate in polyvinylpyrrolidone (PVP) aqueous solutions to prepare silver nanoparticles. Secondary laser irradiation onto the prepared colloidal solutions was also carried out. It was revealed that the formation efficiency was increased by addition of PVP as well as the stability of nanoparticles. The result of shadowgraph measurements suggested that the increased ablation efficiency by PVP is attributable to increased secondary etching efficiency by the solvent-confined plasma toward the silver plate. On the other hand, the size decrease of the nanoparticles by addition of PVP was more remarkable during the secondary irradiation process than in the laser ablation (nanoparticle preparation) process. This result indicates that emitted materials interact less sufficiently with PVP molecules in the laser ablation process than in the secondary laser irradiation process.

  5. Preparations of Platinum Nanoparticles and Their Catalytic Performances.

    PubMed

    Jung, Sang Chul; Nahm, Seung Won; Jung, Ho Young; Park, Young-Kwon; Seo, Seong Gyu; Kim, Sang Chai

    2015-07-01

    This work investigates the effect of reducing agents and stabilizing agent on the preparation of platinum nanoparticles. We used H2PtCl6 as a precursor and hydrogen and sodium borohydride as reducing agents to prepare colloidal platinum nanoparticles. Polyvinylpyrrolidones (PVPs) is used as a stabilizing agent. Hydrogen and sodium borohydride are used as reducing agents. The prepared platinum nanoparticles are characterized by transmission electron microscopy (TEM) and X-ray diffractometer (XRD). The concentrations of the precursor and the stabilizing agent influence the size of platinum nanoparticles, while the reducing agents influence the morphologies and structures of platinum nanoparticles. Supported platinum catalysts (CPt-NaBH4, CPt-H2) are prepared from colloidal platinum nanoparticles and γ-Al2O3. For comparison, another supported platinum catalyst (IPt) is prepared by the conventional impregnation method with an aqueous H2PtCL6 solution and γ-AL2O3. The catalytic activities of CPts are superior to that of IPt on the basis of benzene conversion. PMID:26373160

  6. Anhydride functionalised calcium ferrite nanoparticles: a new selective magnetic material for enrichment of lead ions from water and food samples.

    PubMed

    Pirouz, Mojgan Jafari; Beyki, Mostafa Hossein; Shemirani, Farzaneh

    2015-03-01

    In this research a sonochemistry route for manufacture of uniform nanocrystalline CaFe2O4 and its anhydride functionalisation were reported. The potential of raw and modified material as a magnetically separable sorbent in selective enrichment of lead ions from water and food samples is outlined. This material was characterised using FT-IR, XRD, SEM and VSM techniques. The SEM and VSM results indicated that the calcium ferrite nanoparticles are sphere-like particles possessing superparamagnetic properties with an average diameter of 40 nm. Various analytical parameters, including pH, contact time, type and concentration of eluent, adsorption capacity, sample volume and interference of ions, were optimised. Following a modification by anhydride, calcium ferrite selectivity toward lead ions was raised more than twofold compared to the unmodified nanoparticles. Finally a pre-concentration procedure was applied for determination of trace Pb(II) in canned tuna fish, canned tomato paste, parsley, milk and well-water samples with satisfactory results. PMID:25306327

  7. Microwave-absorbing characteristics of epoxy resin composites containing nanoparticles of NiZn- and NiCuZn-ferrites

    NASA Astrophysics Data System (ADS)

    Aphesteguy, J. C.; Damiani, Abel; DiGiovanni, Dalmas; Jacobo, S. E.

    2009-10-01

    NiZn- and NiCuZn-ferrite nanoparticles (50-70 nm) with the chemical formula Ni 0.5 Zn 0.5Fe 2O 4 (NiZn) and Ni 0.35Cu 0.15Zn 0.5Fe 2O 4 (NiCuZn) were synthesized by a combustion synthesis method. The nanocrystallite of these materials was characterized by structural and magnetic methods. Saturation magnetization increases from 83 emu/g (NiZn) to 91 emu/g (NiCuZn). Magnetic permeability and dielectric permittivity were measured on sintered samples (pellets and toroids) in the frequency range of 1 MHz-1.8 GHz. Reflection losses ( RL) for both samples were calculated from complex permeability and permittivity. Cu substitution in NiZn-ferrite enhances permeability and RL. In order to explore microwave-absorbing properties in X-band, magnetic nanoparticles were mixed with an epoxy resin to be converted into a microwave-absorbing composite and microwave behaviors of both materials were studied using a microwave vector network analyzer from 7.5 to 13.5 GHz. Cu substitution diminishes absorption intensity in the range 11.5-12.5 GHz.

  8. Low temperature-fired Ni-Cu-Zn ferrite nanoparticles through auto-combustion method for multilayer chip inductor applications

    PubMed Central

    2012-01-01

    Ferrite nanoparticles of basic composition Ni0.7-xZnxCu0.3Fe2O4 (0.0 ≤ x ≤ 0.2, x = 0.05) were synthesized through auto-combustion method and were characterized for structural properties using X-ray diffraction [XRD], scanning electron microscopy, transmission electron microscopy, and Fourier transform infrared spectroscopy [FT-IR]. XRD analysis of the powder samples sintered at 600°C for 4 h showed the cubic spinel structure for ferrites with a narrow size distribution from 28 to 32 nm. FT-IR showed two absorption bands (v1 and v2) that are attributed to the stretching vibration of tetrahedral and octahedral sites. The effect of Zn doping on the electrical properties was studied using dielectric and impedance spectroscopy at room temperature. The dielectric parameters (ε', ε″, tanδ, and σac) show their maximum value for 10% Zn doping. The dielectric constant and loss tangent decrease with increasing frequency of the applied field. The results are explained in the light of dielectric polarization which is similar to the conduction phenomenon. The complex impedance shows that the conduction process in grown nanoparticles takes place predominantly through grain boundary volume. PACS: 75.50.Gg; 78.20; 77.22.Gm. PMID:22316055

  9. Preparation of silver nanoparticles at low temperature

    NASA Astrophysics Data System (ADS)

    Mishra, Mini; Chauhan, Pratima

    2016-04-01

    Silver from ancient time is used as antimicrobial agent in the bulk form but now with the advancement in nanotechnology silver in the form of nanoparticles shown potential effect against microbes which make us easy to fight with many diseases plants and animals. In this work silver nanoparticles were synthesized by chemical routes using sodium borohydride as reducing agent at low temperature. The particles were characterized through UV-Visible spectroscopy as well as X-Ray Diffraction. The UV-visible spectra of silver nanoparticles exhibited absorption at 425 cm; the crystallite size of the particles is between 19nm to 39nm. EDAX graph shows two peaks of silver and oxygen. Water absorbed by silver nanoparticles was removed by the calcinations.

  10. Environmentally friendly preparation of metal nanoparticles

    EPA Science Inventory

    The book chapter summarizes the “state of the art” in the exploitation of various environmentally-friendly synthesis approaches, reaction precursors and conditions to manufacture metal and metal oxide nanoparticles for a vast variety of purposes.

  11. Environmentally friendly preparation of metal nanoparticles

    EPA Science Inventory

    The book chapter summarizes the state of the art in the exploitation of various environmentally-friendly synthesis approaches, reaction precursors and conditions to manufacture metal and metal oxide nanoparticles for a vast variety of purposes.

  12. Hemoglobin loaded polymeric nanoparticles: preparation and characterizations.

    PubMed

    Dessy, Alberto; Piras, Anna M; Schirò, Giorgio; Levantino, Matteo; Cupane, Antonio; Chiellini, Federica

    2011-05-18

    In the present work polymeric nanoparticles based on Poly (maleic anhydride-alt-butyl vinyl ether) 5% grafted with m-PEG (2000) and 95% grafted with 2-methoxyethanol (VAM41-PEG) were loaded with human hemoglobin (Hb) and characterized from a physicochemical point of view. The assessment of structural and functional features of the loaded Hb was performed and the effect of the introduction of different reducing agents as aimed at minimizing Hb oxidation during the nanoparticles formulation process, was also investigated. Nanoparticles possessing an average diameter of 138±10 nm and physicochemical features suitable for this kind of application were successfully obtained. Although the oxidation of the protein was not avoided during its loading into nanoparticles, the presence of acidic moieties in the polymeric structure is proposed to be directly involved in the protein inactivation mechanism. PMID:21443949

  13. Fabrication of silver-coated cobalt ferrite nanocomposite and the study of its antibacterial activity

    NASA Astrophysics Data System (ADS)

    Kooti, M.; Saiahi, S.; Motamedi, H.

    2013-05-01

    A new silver coated cobalt ferrite nanocomposite, Ag@CoFe2O4, was prepared by a two-step procedure. In the first step, cobalt ferrite nanoparticles were synthesized by a combustion method using glycine as a fuel. This ferrite was then coated with nanosilver via chemical reduction of Ag+ solution. The as-synthesized Ag@CoFe2O4 was characterized by X-ray diffraction, transmission electron microscopy, and vibrating sample magnetometer. The antibacterial activity of this composite was investigated against some Gram-positive and Gram-negative bacteria and compared with those of silver nanoparticles and some standard antibacterial drugs.

  14. Preparation and characterization of hollow glass microspheres coated by CoFe{sub 2}O{sub 4} nanoparticles using urea as precipitator via coprecipitation method

    SciTech Connect

    Pang Xiaofen; Fu Wuyou; Yang Haibin Zhu Hongyang; Xu Jing; Li Xiang; Zou Guangtian

    2009-02-04

    The composite of hollow glass microspheres coated by CoFe{sub 2}O{sub 4} nanoparticles has been successfully prepared using urea as precipitator via coprecipitation method. The resultant composites were characterized by X-ray diffraction, field emission scanning electron microscope and vibrating sample magnetometer. The results showed that the slow decomposition of urea could be beneficial to form uniform and entire cobalt ferrite coating layer on the surface of hollow glass microspheres. The smoothest morphology was obtained for the sample prepared from 0.7 M urea, while the sample prepared from 1.0 M urea had the thickest shell. This indicated that there was a competition between the morphology and thickness of the coated microspheres. A possible formation mechanism of hollow glass microspheres coated with cobalt ferrite was proposed. The magnetic properties of the samples were also investigated.

  15. Structure and magnetic properties of Co and Ni nano-ferrites prepared by a two step direct microemulsions synthesis

    NASA Astrophysics Data System (ADS)

    Pulišová, P.; Kováč, J.; Voigt, A.; Raschman, P.

    2013-09-01

    Nano-particles of CoFe2O4, NiFe2O4 and Co0.5Ni0.5Fe2O4 were synthesized by a two step microemulsion precipitation where inverse micelles of water in hexanol were stabilized using cetyltrimethylammonium bromide. Powder X-ray diffraction analysis and Transmission electron microscopy measurements provided data to clarify the crystal structure and size of the produced nano-particles. Different measurements of magnetic properties at low temperatures of 2 K revealed that nano-particles of NiFe2O4 represent magnetically soft ferrite with a coercivity ∼40 kA/m, whereas nano-particles of CoFe2O4 and Co0.5Ni0.5Fe2O4 were magnetically harder with a coercivity of 815 and 947 kA/m, respectively. Additionally zero field cooling and field cooling measurements provided data for estimating the blocking temperature of the materials produced. For NiFe2O4 this temperature is lower, 23 K. The blocking temperature of CoFe2O4 of 238 K and Co0.5Ni0.5Fe2O4 of 268 K are higher in comparison with NiFe2O4.

  16. Preparation and characterization of stearic acid-pullulan nanoparticles.

    PubMed

    Kim, In-Sook; Oh, In-Joon

    2010-05-01

    For a new anticancer drug carrier, we synthesized 4 compositions of amphiphilic stearic acidconjugated pullulan (SAP) and characterized them with FT-IR spectroscopy. Crystalline changes were verified by x-ray diffraction patterns before and after synthesis of the SAP conjugate. SAP nanoparticles were prepared by a diafiltration method, and the fluorescence spectroscopy using pyrene showed particle self-assembly in water. SAP nanoparticles were spherical in TEM photos, and particle size ranged between 200 approximately 500 nm in photon correlation spectroscopy. Release of all-trans-retinoic acid from the SAP nanoparticles was maintained over 5 weeks. For further study in vivo, we tested the cytotoxicity of SAP nanoparticles using an MTT assay, and cytotoxicity was augmented as the molar mass of stearic acid increased in human liver carcinoma HepG2 cells. Therefore, SAP nanoparticles might be a promising longterm delivery carrier for hydrophobic therapeutic molecules with the appropriate composition. PMID:20512475

  17. Structure, morphology and magnetic properties of Mg((x))Zn((1 - x))Fe2O4 ferrites prepared by polyol and aqueous co-precipitation methods: a low-toxicity alternative to Ni((x))Zn((1 - x))Fe2O4 ferrites.

    PubMed

    Daigle, A; Modest, J; Geiler, A L; Gillette, S; Chen, Y; Geiler, M; Hu, B; Kim, S; Stopher, K; Vittoria, C; Harris, V G

    2011-07-29

    The synthesis and properties of Mg((x))Zn((1 - x))Fe(2)O(4) spinel ferrites as a low-toxicity alternative to the technologically significant Ni((x))Zn((1 - x))Fe(2)O(4) ferrites are reported. Ferrite nanoparticles have been formed through both the polyol and aqueous co-precipitation methods that can be readily adapted to industrial scale synthesis to satisfy the demand of a variety of commercial applications. The structure, morphology and magnetic properties of Mg((x))Zn((1 - x))Fe(2)O(4) were studied as a function of composition and particle size. Scanning electron microscopy images show particles synthesised by the aqueous co-precipitation method possess a broad size distribution (i.e. ? 80-120 nm) with an average diameter of the order of 100 nm 20 nm and could be produced in high process yields of up to 25 g l(-1). In contrast, particles synthesised by the polyol-based co-precipitation method possess a narrower size distribution with an average diameter in the 30 nm 5 nm range but are limited to smaller yields of ? 6 g l(-1). Furthermore, the polyol synthesis method was shown to control average particle size by varying the length of the glycol surfactant chain. Particles prepared by both methods are compared with respect to their phase purity, crystal structure, morphology, magnetic properties and microwave properties. PMID:21719975

  18. Structure, morphology and magnetic properties of Mg(x) Zn(1 - x)Fe2O4 ferrites prepared by polyol and aqueous co-precipitation methods: a low-toxicity alternative to Ni(x)Zn(1 - x)Fe2O4 ferrites

    NASA Astrophysics Data System (ADS)

    Daigle, A.; Modest, J.; Geiler, A. L.; Gillette, S.; Chen, Y.; Geiler, M.; Hu, B.; Kim, S.; Stopher, K.; Vittoria, C.; Harris, V. G.

    2011-07-01

    The synthesis and properties of Mg(x)Zn(1 - x)Fe2O4 spinel ferrites as a low-toxicity alternative to the technologically significant Ni(x)Zn(1 - x)Fe2O4 ferrites are reported. Ferrite nanoparticles have been formed through both the polyol and aqueous co-precipitation methods that can be readily adapted to industrial scale synthesis to satisfy the demand of a variety of commercial applications. The structure, morphology and magnetic properties of Mg(x)Zn(1 - x)Fe2O4 were studied as a function of composition and particle size. Scanning electron microscopy images show particles synthesised by the aqueous co-precipitation method possess a broad size distribution (i.e. ~ 80-120 nm) with an average diameter of the order of 100 nm ± 20 nm and could be produced in high process yields of up to 25 g l - 1. In contrast, particles synthesised by the polyol-based co-precipitation method possess a narrower size distribution with an average diameter in the 30 nm ± 5 nm range but are limited to smaller yields of ~ 6 g l - 1. Furthermore, the polyol synthesis method was shown to control average particle size by varying the length of the glycol surfactant chain. Particles prepared by both methods are compared with respect to their phase purity, crystal structure, morphology, magnetic properties and microwave properties.

  19. Preparation of magnetic fluorescent hollow nanoparticles with multi-layer

    NASA Astrophysics Data System (ADS)

    Sun, Xiuxue; Zhang, Jimei; Dai, Zhao; Li, Ping; Zhou, Wen; Zheng, Guo

    2009-07-01

    A kind of novel magnetic fluorescent hollow nanoparticles with multi-layer shells by layer-by-layer self-assembly process was presented in this paper. Non-crosslinking poly(acrylic acid) (PAA) nanoparticles as core with 250 nm in diameters were prepared by distillation-precipitation polymerization in acetonitrile with 2, 2'-Azobisisobutyronitrile (AIBN) as initiator and without any stabilizer and crosslinker. Then 4-vinylpyridine (4-VPy) as monomer was selfassembled on the surface of PAA nanoparticles because of hydrogen-bonding effect between the surface carboxyl of PAA nanoparticles and pyridine of 4-VPy. The 4-VPy as first shell layer were crosslinked by ethylene glycol dimethacrylate (EGDMA) by seeds distillation-precipitation polymerization in acetonitrile. The core/shell structure of this kind of nanoparticles was investigated by FT-IR and TEM. We can find that the products had an absorption peak at 1641 cm-1 from the FT-IR, which showed that the vinyl groups had been connected in the polyAA microspheres. After that, the non-crosslinking PAA core was removed under a solution of sodium hydroxide in ethanol-water. On the other hand, CdTe quantum dots (QDs) with about 3 nm in diameters as shell were prepared in aqueous solution with 3- mercaptopropionic acid (MPA) as stabilizer and 1, 6-hexylenediamime modified Fe3O4 nanoparticles with about 11 nm in diameters as core were synthesized in water respectively. Because of the hydrogen-bonding between the surface carboxyl of MPA on CdTe QDs and the amino on Fe3O4 nanoparticles, the core/shell magnetic-fluorescent nanoparticles were obtained. Then, the magnetic-fluorescent nanoparticles as second shell layer were self-assembled on the hollow 4VPy nanoparticles.

  20. Long-circulating PEGylated manganese ferrite nanoparticles for MRI-based molecular imaging

    NASA Astrophysics Data System (ADS)

    Pernia Leal, Manuel; Rivera-Fernández, Sara; Franco, Jaime M.; Pozo, David; de La Fuente, Jesús M.; García-Martín, María Luisa

    2015-01-01

    Magnetic resonance based molecular imaging has emerged as a very promising technique for early detection and treatment of a wide variety of diseases, including cancer, neurodegenerative disorders, and vascular diseases. The limited sensitivity and specificity of conventional MRI are being overcome by the development of a new generation of contrast agents, using nanotechnology approaches, with improved magnetic and biological properties. In particular, for molecular imaging, high specificity, high sensitivity, and long blood circulation times are required. Furthermore, the lack of toxicity and immunogenicity together with low-cost scalable production are also necessary to get them into the clinics. In this work, we describe a facile, robust and cost-effective ligand-exchange method to synthesize dual T1 and T2 MRI contrast agents with long circulation times. These contrast agents are based on manganese ferrite nanoparticles (MNPs) between 6 and 14 nm in size covered by a 3 kDa polyethylene glycol (PEG) shell that leads to a great stability in aqueous media with high crystallinity and magnetization values, thus retaining the magnetic properties of the uncovered MNPs. Moreover, the PEGylated MNPs have shown different relaxivities depending on their size and the magnetic field applied. Thus, the 6 nm PEGylated MNPs are characterized by a low r2/r1 ratio of 4.9 at 1.5 T, hence resulting in good dual T1 and T2 contrast agents under low magnetic fields, whereas the 14 nm MNPs behave as excellent T2 contrast agents under high magnetic fields (r2 = 335.6 mM-1 s-1). The polymer core shell of the PEGylated MNPs minimizes their cytotoxicity, and allows long blood circulation times. This combination of cellular compatibility and excellent T2 and r2/r1 values under low magnetic fields, together with long circulation times, make these nanomaterials very promising contrast agents for molecular imaging.Magnetic resonance based molecular imaging has emerged as a very promising technique for early detection and treatment of a wide variety of diseases, including cancer, neurodegenerative disorders, and vascular diseases. The limited sensitivity and specificity of conventional MRI are being overcome by the development of a new generation of contrast agents, using nanotechnology approaches, with improved magnetic and biological properties. In particular, for molecular imaging, high specificity, high sensitivity, and long blood circulation times are required. Furthermore, the lack of toxicity and immunogenicity together with low-cost scalable production are also necessary to get them into the clinics. In this work, we describe a facile, robust and cost-effective ligand-exchange method to synthesize dual T1 and T2 MRI contrast agents with long circulation times. These contrast agents are based on manganese ferrite nanoparticles (MNPs) between 6 and 14 nm in size covered by a 3 kDa polyethylene glycol (PEG) shell that leads to a great stability in aqueous media with high crystallinity and magnetization values, thus retaining the magnetic properties of the uncovered MNPs. Moreover, the PEGylated MNPs have shown different relaxivities depending on their size and the magnetic field applied. Thus, the 6 nm PEGylated MNPs are characterized by a low r2/r1 ratio of 4.9 at 1.5 T, hence resulting in good dual T1 and T2 contrast agents under low magnetic fields, whereas the 14 nm MNPs behave as excellent T2 contrast agents under high magnetic fields (r2 = 335.6 mM-1 s-1). The polymer core shell of the PEGylated MNPs minimizes their cytotoxicity, and allows long blood circulation times. This combination of cellular compatibility and excellent T2 and r2/r1 values under low magnetic fields, together with long circulation times, make these nanomaterials very promising contrast agents for molecular imaging. Electronic supplementary information (ESI) available: Additional experimental details including TEM images of MNPs, size distribution graphs, thermogravimetric curves, FTIR spectra, and XRD patterns of MNPs. See DOI: 10.1039/c4nr05781c

  1. Influence of various surfactants on magnetic property of cobalt ferrite prepared by Co-precipitation technique

    NASA Astrophysics Data System (ADS)

    Solanki, Neha; Khatri, Hemal; Jotania, R. B.

    2016-05-01

    Cobalt Ferrite (CoFe2O4) particles were synthesised using a Co-precipitation method. Influence of three different surfactants i.e. (1) Cationic - CTAB (Cetyl Tri-Methyl Ammonium Bromide), (2) Anionic - SDBS (Sodium Dodecyl Benzene Sulphonate) and (3) Nonionic - Triton X-100, on magnetic property of Cobalt Ferrite were investigated. Magnetic property of Cobalt ferrite powder was studied at room temperature using Vibrating Sample Measurements (VSM) technique under an applied magnetic field of 15kOe. The results show maximum value of saturation magnetization - Ms (81.87 emu/g) for the sample synthesised without surfactant and Coercivity value found maximum (2086 kOe) for the sample synthesized in presence of surfactant SDBS.

  2. Crystal structures and magnetic properties of polyethylene glycol (PEG-4000) and silica-encapsulated nickel ferrite (NiFe2O4) nanoparticles

    NASA Astrophysics Data System (ADS)

    Shofiah, Siti; Muflihatun, Suharyadi, Edi

    2016-04-01

    Crystal structures and magnetic properties of polyethylene glycol (PEG-4000) and silica encapsulated nickel ferrite (NiFe2O4) nanoparticles comparable sizes have been studied in detail. NiFe2O4 were prepared by co-precipitation methods. Crystalline size is 4.8 ± 0.2 nm became 1.6 ± 0.1 nm and 10.6 ± 0.3 nm after encapsulated PEG-4000 and silica, respectively. Transmission electron microscopy (TEM) showed that encapsulated PEG-4000 and silica decreased agglomeration, controlled shape of nanoparticles more spherical and dispersed. Coercivity of NiFe2O4 was 46.2 Oe and then increased after encapsulated PEG-4000 to 47.8 Oe can be related to the multi-domains of NiFe2O4 as influence the crystalline size was decreased. Meanwhile, after encapsulated silica, coercivity of NiFe2O4 became 93 Oe as influence the crystalline size was increased at single-domains due to its strong shape anisotropy. Magnetization value decreased from 5.7 emu/g to 5.3 emu/g and 3.6 emu/g after encapsulated PEG-4000 and silica, respectively. The remanent magnetization showed decreasing when saturation magnetization decreased, and conversely. However, it also depends on presence of α-Fe2O3 phases and their material non magnetic of encapsulating. Based on the result, The magnetic properties exhibit a strong dependence on the crystalline size as influence PEG-4000 and silica encapsulated NiFe2O4 nanoparticles.

  3. Preparation and Properties of Various Magnetic Nanoparticles

    PubMed Central

    Drbohlavova, Jana; Hrdy, Radim; Adam, Vojtech; Kizek, Rene; Schneeweiss, Oldrich; Hubalek, Jaromir

    2009-01-01

    The fabrications of iron oxides nanoparticles using co-precipitation and gadolinium nanoparticles using water in oil microemulsion method are reported in this paper. Results of detailed phase analysis by XRD and Mössbauer spectroscopy are discussed. XRD analysis revealed that the crystallite size (mean coherence length) of iron oxides (mainly γ-Fe2O3) in the Fe2O3 sample was 30 nm, while in Fe2O3/SiO2 where the ε-Fe2O3 phase dominated it was only 14 nm. Gd/SiO2 nanoparticles were found to be completely amorphous, according to XRD. The samples showed various shapes of hysteresis loops and different coercivities. Differences in the saturation magnetization (MS) correspond to the chemical and phase composition of the sample materials. However, we observed that MS was not reached in the case of Fe2O3/SiO2, while for Gd/SiO2 sample the MS value was extremely low. Therefore we conclude that only unmodified Fe2O3 nanoparticles are suitable for intended biosensing application in vitro (e.g. detection of viral nucleic acids) and the phase purification of this sample for this purpose is not necessary. PMID:22574017

  4. Preparation of Chitosan Nanoparticles: A Study of Influencing Factors

    NASA Astrophysics Data System (ADS)

    Thakur, Anupama; Taranjit

    2011-12-01

    Chitosan (CS), a cationic polysaccharide, offers great advantages for ionic interactions with negatively charged species such as sodium tripolyphosphate (STPP) leading to the formation of biocompatible crosslinked chitosan nanoparticles In the present work, an attempt has been made to systematically study the following factors influencing the ionotropic gelation of chitosan with STPP to produce CS nanoparticles: effect of pH of solution, CS concentration, STPP concentration and CS/STPP ratio. The results show that with the increase in CS concentration, the yield of the nanoparticle decreases whereas size increases. The mean size of the prepared nanoparticles varied between 120 to 720 nm and zeta potential between +14 mV to +53 mV . Nanoparticle size and yield was found to be strongly dependent on solution pH. Nanoparticle size decreased with increase in solution pH from 4 to 5 and yield was found to be maximum at pH = 5. With increase in STPP concentration, the size and yield of the nanoparticle increased. The potential of CS nanoparticles to trap amoxicillin trihydrate, taken as the model drug, was also studied. The maximum drug loading capacity was found to be 35% at a solution pH = 5 for 0.2% CS and 0.086% STPP.

  5. Effect of zinc concentration on the structural and magnetic properties of mixed Co-Zn ferrites nanoparticles synthesized by sol/gel method

    NASA Astrophysics Data System (ADS)

    Ben Ali, M.; El Maalam, K.; El Moussaoui, H.; Mounkachi, O.; Hamedoun, M.; Masrour, R.; Hlil, E. K.; Benyoussef, A.

    2016-01-01

    Synthesization of zinc-substituted cobalt ferrites nano-particles Co1-xZnxFe2O4 (x=0.0-0.3) has been achieved by the sol/gel method. The characterization of the synthesized nano-particles has been done by X-ray diffractometry (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FITR). The relation between the composition and magnetic properties has been investigated by Magnetic Properties Measurement System (MPMS). The results revealed that the nanoparticles size is in the range of 11-28 nm. It was found that the zinc substitution in cobalt ferrite increases saturation magnetization from 60.92 emu/g (x=0) to 74.67 emu/g (x=0.3). Nevertheless, zinc concentrations cause a significant decrease in coercivity.

  6. Synthesis and magnetic properties of CoFe{sub 2}O{sub 4} spinel ferrite nanoparticles doped with lanthanide ions

    SciTech Connect

    Kahn, Myrtil L.; Zhang, Z. John

    2001-06-04

    Lanthanide ions have been doped into cobalt spinel ferrites using an oil-in-water micellar method to form CoLn{sub 0.12}Fe{sub 1.88}O{sub 4} nanoparticles with Ln=Ce, Sm, Eu, Gd, Dy, or Er. Doping with lanthanide ions (Ln{sup III}) modulates the magnetic properties of cobalt spinel ferrite nanoparticles. In particular cases of Gd{sup 3+} or Dy{sup 3+} ions, a dramatic increase in the blocking temperature and coercivity is observed. Indeed, the introduction of only 4% of Gd{sup 3+} ions increases the blocking temperature {similar_to}100 K and the coercivity 60%. Initial studies on the magnetic properties of these doped nanoparticles clearly demonstrate that the relationship between the modulation of magnetic properties and the nature of doped Ln{sup III} ions is interesting but very complex. {copyright} 2001 American Institute of Physics.

  7. Effect of pH value on electromagnetic loss properties of Co-Zn ferrite prepared via coprecipitation method

    NASA Astrophysics Data System (ADS)

    Huang, Xiaogu; Zhang, Jing; Wang, Wei; Sang, Tianyi; Song, Bo; Zhu, Hongli; Rao, Weifeng; Wong, Chingping

    2016-05-01

    In this paper, the cobalt zinc ferrite was prepared by coprecipitation method at different pH conditions. The influence of pH values on the coprecipitation reaction was theoretically analyzed at first. The calculated results showed that the pH values should be controlled in the range of 9-11 to form the stable precipitation. The XRD investigation was used to further confirm the formation of the composite on specific pH values. In addition, the morphological study revealed that the average particle size of the composite decreased from 40 nm to 30 nm when the pH value increased from 9-11. The variation of microstructure plays a critical role in controlling the electromagnetic properties. From the electromagnetic analysis, the dielectric loss factor was 0.02-0.07 and magnetic loss factor was 0.2-0.5 for the composite synthesized at pH of 9, which presents dramatically improved dielectric loss and magnetic loss properties than the samples prepared at pH of 10 and 11. The as-prepared cobalt zinc ferrite are highly promising to be used as microwave absorption materials.

  8. Effect of heat treatment on structural and Mössbauer spectroscopic properties of coprecipitated Mn0.5Ni0.5Fe2O4 ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Srinivas, Ch.; Tirupanyam, B. V.; Meena, S. S.; Babu, Ch. Seshu; Sastry, D. L.

    2015-06-01

    Results obtained in a systamatic study by X-ray diffraction and Mösssbauer spectroscopy on the structural and magnetic properties on Mn0.5Ni0.5Fe2O4 ferrite nanoparticles heat treated at 200 °C, 500 °C and 800 °C are reported. Average crystallite sizes are estimated to be in the range (2.6nm - 12.8nm). It is observed that crystallite sizes increase with increase in sintering temperature and random variation in lattice parameter was observed. At relatively low sintering temperatures the samples exhibit superparamagnetism and complete ferrite phase was observed at higher heat treatment.

  9. Microwave absorption properties of polymer composites with amorphous Fe-B and Ni-Zn-Co ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Shimba, Kazuaki; Yuki, Shozo; Tezuka, Nobuki; Sugimoto, Satoshi

    2013-06-01

    Nowadays, many communication devices use GHz-range microwaves, which cause serious issues, such as electromagnetic interference. For the prevention of these problems, microwave absorbers consisting of polymer composites with magnetic particles have received attention. With the current trend being to miniaturize devices, thin microwave absorber are now required. This paper reports that polymer composites with amorphous Fe-B submicrometer particles and Ni-Zn-Co ferrite nanoparticles showed a permeability of µ r ' = 8.0-9.0 at 1.0 GHz and a resonant frequency of f r = 1.8-2.4 GHz. They also exhibited good microwave absorption properties at 0.7-1.4 GHz for thicknesses of 2.5-3.9 mm.

  10. Preparation of platinum nanoparticle catalyst for propane dehydrogenation.

    PubMed

    Li, Jun; Wang, Jun; Ma, Zhanhua; Sun, Lanyi; Hu, Yangdong

    2014-09-01

    Supported Pt nanoparticle catalysts were prepared by combing a chemical reduction method with an ultrasonic sonication loading method. Several techniques including transmission electron microscopy (TEM), nitrogen sorption technique and pyridine adsorption Fourier-transform infrared (Py-IR) were applied to characterize the physicochemical properties of these catalysts. The catalytic performance of catalysts was evaluated in the dehydrogenation of propane. The influence of the preparation method of Pt nanoparticles, the ratio of Polyvinyl Pyrrolidone (PVP) to Pt, loading method and different supports on the catalytic performance was investigated. PVP is useful for controlling the size of Pt nanoparticles and a PVP/Pt ratio of 15 is favorable to achieve a good catalytic performance. NaBH4 reduction is better than ethanol refluxing in preparing Pt nanoparticles. The ultrasonic sonication is effective to load the Pt nanoparticles onto the support channels. The mesoporous alumina proved to be a good catalyst support due to its high surface area and unique pore structure. PMID:25924358

  11. Preparation, characterization and optimization of glipizide controlled release nanoparticles

    PubMed Central

    Emami, J.; Boushehri, M.S. Shetab; Varshosaz, J.

    2014-01-01

    The purpose of the present study was to develop glipizide controlled release nanoparticles using alginate and chitosan thorough ionotropic controlled gelation method. Glipizide is a frequently prescribed second generation sulfonylurea which lowers the blood glucose in type-two diabetics. Quick absorption of the drug from the gastrointestinal tract along with short half- life of elimination makes it a good candidate for controlled release formulations. Alginate-chitosan nanoparticles (ACNP) are convenient controlled delivery systems for glipizide, due to both the release limiting properties of the system, and the bioadhesive nature of the polymers. In the present study, glipizide loaded alginate-chitosan nanoparticles (GlACNP) were prepared, and the particle characteristics including particle size (PS), zeta potential (ZP), entrapment efficiency (EE%), loading percent (LP), and mean release time (MRT), as well as the morphology of the nanoparticles, the drug-excipient compatibility, and the release kinetics along with the drug diffusion mechanism were evaluated. The results suggested that ionotropic controlled gelation method offers the possibility of preparing the nanoparticles in mild conditions in an aqueous environment, and can lead to the preparation of particles with favorable size, controlled release characteristics, and high entrapment efficiency, serving as a convenient delivery system for glipizide. The particle and release characteristics can be efficiently optimized using the Box-Behnken design. Based on the findings of the present study, it is expected that this novel formulation be a superior therapeutic alternative to the currently available glipizide delivery systems. PMID:25657802

  12. Synthesis, magnetic and optical properties of core/shell Co1- x Zn x Fe2O4/SiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Girgis, Emad; Wahsh, Mohamed Ms; Othman, Atef Gm; Bandhu, Lokeshwar; Rao, Kv

    2011-07-01

    The optical properties of multi-functionalized cobalt ferrite (CoFe2O4), cobalt zinc ferrite (Co0.5Zn0.5Fe2O4), and zinc ferrite (ZnFe2O4) nanoparticles have been enhanced by coating them with silica shell using a modified Stöber method. The ferrites nanoparticles were prepared by a modified citrate gel technique. These core/shell ferrites nanoparticles have been fired at temperatures: 400°C, 600°C and 800°C, respectively, for 2 h. The composition, phase, and morphology of the prepared core/shell ferrites nanoparticles were determined by X-ray diffraction and transmission electron microscopy, respectively. The diffuse reflectance and magnetic properties of the core/shell ferrites nanoparticles at room temperature were investigated using UV/VIS double-beam spectrophotometer and vibrating sample magnetometer, respectively. It was found that, by increasing the firing temperature from 400°C to 800°C, the average crystallite size of the core/shell ferrites nanoparticles increases. The cobalt ferrite nanoparticles fired at temperature 800°C; show the highest saturation magnetization while the zinc ferrite nanoparticles coated with silica shell shows the highest diffuse reflectance. On the other hand, core/shell zinc ferrite/silica nanoparticles fired at 400°C show a ferromagnetic behavior and high diffuse reflectance when compared with all the uncoated or coated ferrites nanoparticles. These characteristics of core/shell zinc ferrite/silica nanostructures make them promising candidates for magneto-optical nanodevice applications.

  13. Platinum adlayered ruthenium nanoparticles, method for preparing, and uses thereof

    DOEpatents

    Tong, YuYe; Du, Bingchen

    2015-08-11

    A superior, industrially scalable one-pot ethylene glycol-based wet chemistry method to prepare platinum-adlayered ruthenium nanoparticles has been developed that offers an exquisite control of the platinum packing density of the adlayers and effectively prevents sintering of the nanoparticles during the deposition process. The wet chemistry based method for the controlled deposition of submonolayer platinum is advantageous in terms of processing and maximizing the use of platinum and can, in principle, be scaled up straightforwardly to an industrial level. The reactivity of the Pt(31)-Ru sample was about 150% higher than that of the industrial benchmark PtRu (1:1) alloy sample but with 3.5 times less platinum loading. Using the Pt(31)-Ru nanoparticles would lower the electrode material cost compared to using the industrial benchmark alloy nanoparticles for direct methanol fuel cell applications.

  14. Preparation of mesoporous cadmium sulfide nanoparticles with moderate pore size

    SciTech Connect

    Han Zhaohui Zhu, Huaiyong; Shi, Jeffrey; Parkinson, Gordon; Lu, G.Q.

    2007-03-15

    The preparation of cadmium sulfide nanoparticles that have a moderate pore size is reported. This preparation method involves a hydrothermal process that produces a precursor mixture and a following acid treatment of the precursor to get the porous material. The majority of the particles have a pore size close to 20nm, which complements and fills in the gap between the existing cadmium sulfide materials, which usually have a pore size either less than 10nm or are well above 100nm.

  15. Visualization of internalization of functionalized cobalt ferrite nanoparticles and their intracellular fate.

    PubMed

    Bregar, Vladimir B; Lojk, Jasna; Suštar, Vid; Veranič, Peter; Pavlin, Mojca

    2013-01-01

    In recent years, nanoparticles (NPs) and related applications have become an intensive area of research, especially in the biotechnological and biomedical fields, with magnetic NPs being one of the promising tools for tumor treatment and as MRI-contrast enhancers. Several internalization and cytotoxicity studies have been performed, but there are still many unanswered questions concerning NP interactions with cells and NP stability. In this study, we prepared functionalized magnetic NPs coated with polyacrylic acid, which were stable in physiological conditions and which were also nontoxic short-term. Using fluorescence, scanning, and transmission electron microscopy, we were able to observe and determine the internalization pathways of polyacrylic acid-coated NPs in Chinese hamster ovary cells. With scanning electron microscopy we captured what might be the first step of NPs internalization - an endocytic vesicle in the process of formation enclosing NPs bound to the membrane. With fluorescence microscopy we observed that NP aggregates were rapidly internalized, in a time-dependent manner, via macropinocytosis and clathrin-mediated endocytosis. Inside the cytoplasm, aggregated NPs were found enclosed in acidified vesicles accumulated in the perinuclear region 1 hour after exposure, where they stayed for up to 24 hours. High intracellular loading of NPs in the Chinese hamster ovary cells was obtained after 24 hours, with no observable toxic effects. Thus polyacrylic acid-coated NPs have potential for use in biotechnological and biomedical applications. PMID:23486857

  16. Preparation of metallic nanoparticles by irradiation in starch aqueous solution

    NASA Astrophysics Data System (ADS)

    NemÅ£anu, Monica R.; Braşoveanu, Mirela; Iacob, Nicuşor

    2014-11-01

    Colloidal silver nanoparticles (AgNPs) were synthesized in a single step by electron beam irradiation reduction of silver ions in aqueous solution containing starch. The nanoparticles were characterized by spectrophotocolorimetry and compared with those obtained by chemical (thermal) reduction method. The results showed that the smaller sizes of AgNPs were prepared with higher yields as the irradiation dose increased. The broadening of particle size distribution occurred by increasing of irradiation dose and dose rate. Chromatic parameters such as b* (yellow-blue coordinate), C* (chroma) and ΔEab (total color difference) could characterize the nanoparticles with respect of their concentration. Hue angle ho was correlated to the particle size distribution. Experimental data of the irradiated samples were also subjected to factor analysis using principal component extraction and varimax rotation in order to reveal the relation between dependent variables and independent variables and to reduce their number. The radiation-based method provided silver nanoparticles with higher concentration and narrower size distribution than those produced by chemical reduction method. Therefore, the electron beam irradiation is effective for preparation of silver nanoparticles using starch aqueous solution as dispersion medium.

  17. Preparation of metallic nanoparticles by irradiation in starch aqueous solution

    SciTech Connect

    Nemţanu, Monica R. Braşoveanu, Mirela Iacob, Nicuşor

    2014-11-24

    Colloidal silver nanoparticles (AgNPs) were synthesized in a single step by electron beam irradiation reduction of silver ions in aqueous solution containing starch. The nanoparticles were characterized by spectrophotocolorimetry and compared with those obtained by chemical (thermal) reduction method. The results showed that the smaller sizes of AgNPs were prepared with higher yields as the irradiation dose increased. The broadening of particle size distribution occurred by increasing of irradiation dose and dose rate. Chromatic parameters such as b* (yellow-blue coordinate), C* (chroma) and ΔE{sub ab} (total color difference) could characterize the nanoparticles with respect of their concentration. Hue angle h{sup o} was correlated to the particle size distribution. Experimental data of the irradiated samples were also subjected to factor analysis using principal component extraction and varimax rotation in order to reveal the relation between dependent variables and independent variables and to reduce their number. The radiation-based method provided silver nanoparticles with higher concentration and narrower size distribution than those produced by chemical reduction method. Therefore, the electron beam irradiation is effective for preparation of silver nanoparticles using starch aqueous solution as dispersion medium.

  18. On the Structure and Some Properties of LaCo Co-substituted NiZn Ferrites Prepared Using the Standard Ceramic Technique

    NASA Astrophysics Data System (ADS)

    Niu, Xiaofei; Liu, Xiansong; Huang, Xin; Huang, Kai; Ma, Yuqi; Huang, Feng; Lv, Farui

    2016-04-01

    Zn0.5Ni0.5-xCoxFe2-yLayO4 ferrites (with x=0, 0.02 and y=0, 0.02) were prepared by an industrial method using the standard ceramic technique and sintered at 1,250°C in air. X-ray diffraction (XRD) was used to obtain the phase formation of the NiZn ferrites. The microstructure of ferrites was investigated by scanning electron microscopy (SEM). The XRD reveals that lattice parameter (a) is decreased and a secondary phase (LaFeO3) is formed in the La-Co co-substituted NiZn ferrite sample, meanwhile, the grain size (D) of this sample decreased obviously by observing SEM photographs. Vibrating sample magnetometry (VSM), B-H analyzer, impedance analyzer and electrometer were carried out in order to characterize some properties of the ferrites. This investigation indicates that, La-Co co-substituted NiZn ferrite sample has higher power loss (Pcv) than other samples at low frequency with an increase in coercive field (Hc) and magnetocrystalline anisotropy (K1), a decrease in initial permeability (μi) and saturation magnetization (Ms). However, at high frequency, the power loss of La-Co co-substituted sample is low, which is attributed to high resistivity (ρ), small grain size (D), less number of Fe2+ ions and low porosity (P).

  19. 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.

  20. Copper(0) nanoparticles supported on silica-coated cobalt ferrite magnetic particles: cost effective catalyst in the hydrolysis of ammonia-borane with an exceptional reusability performance.

    PubMed

    Kaya, Murat; Zahmakiran, Mehmet; Ozkar, Saim; Volkan, Mürvet

    2012-08-01

    Herein we report the development of a new and cost-effective nanocomposite catalyst for the hydrolysis of ammonia-borane (NH(3)BH(3)), which is considered to be one of the most promising solid hydrogen carriers because of its high gravimetric hydrogen storage capacity (19.6% wt) and low molecular weight. The new catalyst system consisting of copper nanoparticles supported on magnetic SiO(2)/CoFe(2)O(4) particles was reproducibly prepared by wet-impregnation of Cu(II) ions on SiO(2)/CoFe(2)O(4) followed by in situ reduction of the Cu(II) ions on the surface of magnetic support during the hydrolysis of NH(3)BH(3) and characterized by ICP-MS, XRD, XPS, TEM, HR-TEM and N(2) adsorption-desorption technique. Copper nanoparticles supported on silica coated cobalt(II) ferrite SiO(2)/CoFe(2)O(4) (CuNPs@SCF) act as highly active catalyst in the hydrolysis of ammonia-borane, providing an initial turnover frequency of TOF = 2400 h(-1) at room temperature, which is not only higher than all the non-noble metal catalysts but also higher than the majority of the noble metal based homogeneous and heterogeneous catalysts employed in the same reaction. More importantly, they were easily recovered by using a permanent magnet in the reactor wall and reused for up to 10 recycles without losing their inherent catalytic activity significantly, which demonstrates the exceptional reusability of the CuNPs@SCF catalyst. PMID:22856878

  1. Preparation and Characterization of Chitosan Nanoparticles for Zidovudine Nasal Delivery.

    PubMed

    Barbi, Mariana Da Silva; Carvalho, Flávia Chiva; Kiill, Charlene Priscila; Barud, Hernane Da Silva; Santagneli, Sílvia Helena; Ribeiro, Sidney José Lima; Gremião, Maria Palmira Daflon

    2015-01-01

    Zidovudine (AZT) is the antiretroviral drug most frequently used for the treatment of Acquired Immunodeficiency Syndrome. Its low oral bioavailability demands the development of innovative strategies to overcome the first pass metabolism. The nasal route is an option for enhanced therapeutic efficacy and to reduce the extent of the first-pass effect. In this article, AZT loaded chitosan nanoparticles were prepared by a modified ionotropic gelation method with sodium tripolyphosphate. The increase proportion of CS (NP1 10:01 (w/w)) promoted the formation of smaller nanoparticles (260 nm), while raising the proportion of TPP (NP2 5:1 w/w) increased the nanoparticles size (330 nm). The incorporation of AZT increased the nanoparticles size for both AZT-loaded nanoparticles AZT-loaded NP1 (406 nm) and AZT-loaded NP2 (425 nm). The incorporation of AZT into NP1 did not change the electrophoretic mobility, however, in AZT-loaded NP2 there was a significant increase. The positive surface of the nanoparticles is very important for the mucoadhesive properties due interaction with the sialic groups of the mucin. Nuclear resonance magnetic data showed that the higher concentration of chitosan in the nanoparticles favored the interaction of few phosphate units (pyrophosphate) by ionic interaction Scanning electron microscopy, revealed that the nanoparticles are nearly spherical shape with porous surface. The entrapment efficiency of AZT, was 17.58% ± 1.48 and 11.02% ± 2.05 for NP1 and NP2, respectively. The measurement of the mucoadhesion force using mucin discs and nasal tissue obtained values of NP1 = 2.12 and NP2 = 4.62. In vitro permeation study showed that the nanoparticles promoted an increase in the flux of the drug through the nasal mucosa. In view of these results, chitosan nanoparticles were found to be a promising approach for the incorporation of hydrophilic drugs and these results suggest that the CS-containing nanoparticles have great potential for nasal AZT administration. PMID:26328451

  2. Effect of filler loading of nickel zinc ferrite on the tensile properties of PLA nanocomposites

    NASA Astrophysics Data System (ADS)

    Shahdan, Dalila; Ahmad, Sahrim Hj

    2013-05-01

    The mechanical strength of magnetic polymer nanocomposite (MPNC) of nickel zinc (NiZn) ferrite nanoparticles incorporated with polylactic acid (PLA) and liquid natural rubber (LNR) as compatibilizer is reported. The matrix was prepared from PLA and LNR in the ratio of 90:10. The MPNC were prepared at constant mixing temperature at 180°C, mixing time of 15 min. and mixing speed of 100 rpm. In order to achieve a good dispersion of NiZn ferrite in the matrix, firstly an ultrasonic treatment had been employed to mix the LNR and NiZn ferrite for 1 hour. The MPNC of PLA/LNR/NiZn ferrite then were prepared via Thermo Haake internal mixer using melt-blending method from different filler loading from 1-5 wt% NiZn ferrite. The result of tensile tests showed that as the filler loading increases the tensile strength also increases until an optimum value of filler loading was reached. The Young's modulus, tensile strength and elongation at break have also increased. The study proves that NiZn ferrite is excellent reinforcement filler in PLA matrix. Scanning electron micrograph (SEM) and energy dispersive X-ray spectroscopy (EDX) were meant to show the homogeneity dispersion of nanoparticles within the matrix and to confirm the elemental composition of NiZn ferrites-PLA/LNR nanocomposites respectively.

  3. Preparation of cobalt-zinc ferrite (Co{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}) nanopowder via combustion method and investigation of its magnetic properties

    SciTech Connect

    Yousefi, M.H.; Manouchehri, S.; Arab, A.; Mozaffari, M.; Physics Department, Razi University, Taghbostah, Kermanshah ; Amiri, Gh. R.; Department of Plasma Physics, Science and Research Branch, Islamic Azad University, Tehran ; Amighian, J.

    2010-12-15

    Research highlights: {yields} Cobalt-zinc ferrite was prepared by combustion method. {yields} Properties of the sample were characterized by several techniques. {yields} Curie temperature was determined to be 350 {sup o}C. -- Abstract: Cobalt-zinc ferrite (Co{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}) was prepared by combustion method, using cobalt, zinc and iron nitrates. The crystallinity of the as-burnt powder was developed by annealing at 700 {sup o}C. Crystalline phase was investigated by XRD. Using Williamson-Hall method, the average crystallite sizes for nanoparticles were determined to be about 27 nm before and 37 nm after annealing, and residual stresses for annealed particles were omitted. The morphology of the annealed sample was investigated by TEM and the mean particle size was determined to be about 30 nm. The final stoichiometry of the sample after annealing showed good agreement with the initial stoichiometry using atomic absorption spectrometry. Magnetic properties of the annealed sample such as saturation magnetization, remanence magnetization, and coercivity measured at room temperature were 70 emu/g, 14 emu/g, and 270 Oe, respectively. The Curie temperature of the sample was determined to be 350 {sup o}C using AC-susceptibility technique.

  4. Absorption and Decomposition of CO2 by Active Ferrites Prepared by Atmospheric Plasma Spraying

    NASA Astrophysics Data System (ADS)

    Li, Shaowei; He, Zhida; Zheng, Yanjun; Chen, Changfeng

    2015-12-01

    Active ferrites, which play an important role in the catalytic decomposition of CO2, have been fabricated by atmospheric plasma spraying to incorporate FeO and anoxic iron oxide [Fe3O4-δ (0 < δ < 1)]. The complexity of phase composition, especially the presence of FeO, gives the resulting powder a greater ability to decompose CO2 when compared to hydrogen-reduced Fe3O4 or Fe2O3 particles. Spraying distance is found to play an important role in modulating the decomposition ability of the powders, while elevated temperatures can also enhance the catalytic decomposition of CO2.

  5. Preparation, structural and morphological studies of Ni doped titania nanoparticles.

    PubMed

    Rajamannan, B; Mugundan, S; Viruthagiri, G; Shanmugam, N; Gobi, R; Praveen, P

    2014-07-15

    TiO2 nanoparticles doped with different weight percentages (4%, 8%, 12% and 16%) of nickel contents were prepared by a modified sol-gel method using Titanium tetra iso propoxide and nickel nitrate as precursors and 2-propanol as a solvent. X-ray diffraction studies show that the as prepared and annealed products show anatase structure with average particle sizes running between of 8 and 16 nm. FTIR results demonstrate the presence of strong chemical bonding at the interface of TiO2 nanoparticles. The optical properties of bare and doped samples were carried out using UV-DRS and photoluminescence measurements. The surface morphology and the element constitution of the nickel doped TiO2 nanoparticles were studied by scanning electron microscope attached with energy dispersive X-ray spectrometer arrangement. The non linear optical properties of the products were confirmed by Kurtz second harmonic generation (SHG) test and the output power generated by the nanoparticle was compared with that of potassium di hydrogen phosphate (KDP). PMID:24667428

  6. Preparation, structural and morphological studies of Ni doped titania nanoparticles

    NASA Astrophysics Data System (ADS)

    Rajamannan, B.; Mugundan, S.; Viruthagiri, G.; Shanmugam, N.; Gobi, R.; Praveen, P.

    2014-07-01

    TiO2 nanoparticles doped with different weight percentages (4%, 8%, 12% and 16%) of nickel contents were prepared by a modified sol-gel method using Titanium tetra iso propoxide and nickel nitrate as precursors and 2-propanol as a solvent. X-ray diffraction studies show that the as prepared and annealed products show anatase structure with average particle sizes running between of 8 and 16 nm. FTIR results demonstrate the presence of strong chemical bonding at the interface of TiO2 nanoparticles. The optical properties of bare and doped samples were carried out using UV-DRS and photoluminescence measurements. The surface morphology and the element constitution of the nickel doped TiO2 nanoparticles were studied by scanning electron microscope attached with energy dispersive X-ray spectrometer arrangement. The non linear optical properties of the products were confirmed by Kurtz second harmonic generation (SHG) test and the output power generated by the nanoparticle was compared with that of potassium di hydrogen phosphate (KDP).

  7. Preparation of silver nanoparticles using tryptophan and its formation mechanism.

    PubMed

    Zaheer, Zoya; Malik, Maqsood Ahmad; Al-Nowaiser, F M; Khan, Zaheer

    2010-12-01

    A non-toxic route was used for the preparation of silver nanoparticles using tryptophan (Trp) as reducing/stabilizing agent in the presence of cetyltrimethyl ammonium bromide (CTAB). Role of water soluble neutral polymer poly(vinylpyrrolidone) (PVP) has been studied on the growth of yellow colour silver nanoparticle formation. The synthesized nanostructures were characterized by UV-Visible absorption spectroscopy, transmission electron microscopy (TEM) by observing the size and distribution of silver nanoparticles. As the reaction proceeded, particles grew up to about 10 and 20 nm in the presence and absence of PVP, respectively, as determined by TEM. The formed nanoparticles showed the highest absorption plasmon band at 425 nm. Rate of silver sol formation increases with the [Trp], [CTAB] and [PVP], reaching a limiting value and then decreases with the increase in concentrations of these reagents. It was observed that nanoparticles are spherical, aggregated and poly dispersed in the absence and presence of PVP, respectively. On the basis of kinetic data, a suitable mechanism is proposed and discussed for the silver sol formation. PMID:20801004

  8. Facile preparation of superhydrophobic surfaces based on metal oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Bao, Xue-Mei; Cui, Jin-Feng; Sun, Han-Xue; Liang, Wei-Dong; Zhu, Zhao-Qi; An, Jin; Yang, Bao-Ping; La, Pei-Qing; Li, An

    2014-06-01

    A novel method for fabrication of superhydrophobic surfaces was developed by facile coating various metal oxide nanoparticles, including ZnO, Al2O3 and Fe3O4, on various substrates followed by treatment with polydimethylsiloxane (PDMS) via chemical vapor deposition (CVD) method. Using ZnO nanoparticles as a model, the changes in the surface chemical composition and crystalline structures of the metal oxide nanoparticles by PDMS treatment were investigated by X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR) analysis. The results show that the combination of the improved surface roughness generated from of the nanoparticles aggregation with the low surface-energy of silicon-coating originated from the thermal pyrolysis of PDMS would be responsible for the surface superhydrophobicity. By a simple dip-coating method, we show that the metal oxide nanoparticles can be easily coated onto the surfaces of various textural and dimensional substrates, including glass slide, paper, fabric or sponge, for preparation of superhydrophobic surfaces for different purpose. The present strategy may provide an inexpensive and new route to surperhydrophobic surfaces, which would be of technological significance for various practical applications especially for separation of oils or organic contaminates from water.

  9. Preparation of platinum nanoparticles in liquids by laser ablation method

    NASA Astrophysics Data System (ADS)

    Binh Nguyen, The; Dinh Nguyen, Thanh; Nguyen, Quang Dong; Trinh Nguyen, Thi

    2014-09-01

    Platinum (Pt) nanoparticles were prepared in solutions of ethanol and TSC (trisodium citrate—Na3C6H5O7.nH2O) in water by laser ablation method using Nd:YAG laser. The role of laser fluence, laser wavelength and concentration of surfactant liquids in laser ablation process were investigated. The morphology, size distribution and optical properties of the Pt nanoparticles (NPs) were observed by transmission electron microscopy (TEM), UV-vis spectrometer and x-ray diffraction measurements. The average diameter of Pt NPs prepared in ethanol and TSC solutions ranges around 7-9 nm and 10-12 nm, respectively. The results showed advantages of the laser ablation method.

  10. Development of cobalt ferrite powder preparation employing the sol-gel technique and its structural characterisation

    NASA Astrophysics Data System (ADS)

    Sajjia, M.; Oubaha, M.; Prescott, T.; Olabi, A. G.

    2010-06-01

    This work focuses on the development of a method to make nano cobalt ferrite powder using a solgel process. A particular emphasis is devoted to the understanding of the role of the chemical parameters involved in the solgel technique, and of the heat treatment on the structures and morphologies of the materials obtained. Several samples of cobalt ferrite powder were obtained by varying the initial parameters of the process in addition to the heat treatment temperature. Xray diffraction and scanning electron microscopy were used to identify the structure and morphology of samples demonstrating the influence of the initial parameters. DTA/TGA was carried out on one sample to identify important reaction temperatures during the heat treatment. The average particle size, as estimated for one sample by the full width at half maximum (FWHM) of the strongest Xray diffraction (XRD) peak, was found to be about 45 nm. It has been found that the chelating agent and the crosslinker have a critical influence on the resultant structure, the particle size and the particle size distribution.

  11. Self-assembled mesoporous Co and Ni-ferrite spherical clusters consisting of spinel nanocrystals prepared using a template-free approach.

    PubMed

    Yu, Byong Yong; Kwak, Seung-Yeop

    2011-10-21

    Based on a self-assembly strategy, spherical mesoporous cobalt and nickel ferrite nanocrystal clusters with a large surface area and narrow size distribution were successfully synthesized for the first time via a template-free solvothermal process in ethylene glycol and subsequent heat treatment. In this work, the mesopores in the ferrite clusters were derived mainly from interior voids between aggregated primary nanoparticles (with crystallite size of less than 7 nm) and disordered particle packing domains. The concentration of sodium acetate is shown herein to play a crucial role in the formation of mesoporous ferrite spherical clusters. These ferrite clusters were characterized in detail using wide-angle X-ray diffraction, thermogravimetric-differential thermal analysis, (57)Fe Mössbauer spectroscopy, X-ray photoelectron spectroscopy, field-emission scanning electron microscopy, standard and high-resolution transmission electron microscopy, and other techniques. The results confirmed the formation of both pure-phase ferrite clusters with highly crystalline spinel structure, uniform size (about 160 nm) and spherical morphology, and worm-like mesopore structures. The BET specific surface areas and mean pore sizes of the mesoporous Co and Ni-ferrite clusters were as high as 160 m(2) g(-1) and 182 m(2) g(-1), and 7.91 nm and 6.87 nm, respectively. A model for the formation of the spherical clusters in our system is proposed on the basis of the results. The magnetic properties of both samples were investigated at 300 K, and it was found that these materials are superparamagnetic. PMID:21904731

  12. Gold nanoparticles prepared using cape aloe active components.

    PubMed

    Krpetić, Zeljka; Scarì, Giorgio; Caneva, Enrico; Speranza, Giovanna; Porta, Francesca

    2009-07-01

    A novel use of two components of Cape aloe, aloin A and aloesin, acting as stabilizers in the preparation of gold and silver nanoparticles, is reported. Stable water-soluble particles of different size and shape are prepared by varying the reaction conditions, temperature, reaction time, and reducing agents. Characterization of the obtained particles is performed using UV-visible, attenuated total reflection Fourier transform infrared (ATR-FTIR), and 1H NMR spectroscopies and transmission electron microscopy (TEM). The efficient cellular uptake of 50 nm sized aloin A and aloesin stabilized gold particles into macrophages and HeLa cells was investigated, proposing these particles as nanovehicles. PMID:19505092

  13. Magnetic nanoparticles: preparation, physical properties, and applications in biomedicine

    PubMed Central

    2012-01-01

    Finally, we have addressed some relevant findings on the importance of having well-defined synthetic strategies developed for the generation of MNPs, with a focus on particle formation mechanism and recent modifications made on the preparation of monodisperse samples of relatively large quantities not only with similar physical features, but also with similar crystallochemical characteristics. Then, different methodologies for the functionalization of the prepared MNPs together with the characterization techniques are explained. Theorical views on the magnetism of nanoparticles are considered. PMID:22348683

  14. Nickel-doped cobalt ferrite nanoparticles: efficient catalysts for the reduction of nitroaromatic compounds and photo-oxidative degradation of toxic dyes

    NASA Astrophysics Data System (ADS)

    Singh, Charanjit; Goyal, Ankita; Singhal, Sonal

    2014-06-01

    This study deals with the exploration of NixCo1-xFe2O4 (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) ferrite nanoparticles as catalysts for reduction of 4-nitrophenol and photo-oxidative degradation of Rhodamine B. The ferrite samples with uniform size distribution were synthesized using the reverse micelle technique. The structural investigation was performed using powder X-ray diffraction, high-resolution transmission electron microscopy, energy dispersive X-ray and scanning tunneling microscopy. The spherical particles with ordered cubic spinel structure were found to have the crystallite size of 4-6 nm. Diffused UV-visible reflectance spectroscopy was employed to investigate the optical properties of the synthesized ferrite nanoparticles. The surface area calculated using BET method was found to be highest for Co0.4Ni0.6Fe2O4 (154.02 m2 g-1). Co0.4Ni0.6Fe2O4 showed the best catalytic activity for reduction of 4-nitrophenol to 4-aminophenol in the presence of NaBH4 as reducing agent, whereas CoFe2O4 was found to be catalytically inactive. The reduction reaction followed pseudo-first order kinetics. The effect of varying the concentration of catalyst and NaBH4 on the reaction rates was also scrutinized. The photo-oxidative degradation of Rhodamine B, enhanced oxidation efficacy was observed with the introduction of Ni2+ in to the cobalt ferrite lattice due to octahedral site preference of Ni2+. Almost 99% degradation was achieved in 20 min using NiFe2O4 nanoparticles as catalyst.

  15. Nickel-doped cobalt ferrite nanoparticles: efficient catalysts for the reduction of nitroaromatic compounds and photo-oxidative degradation of toxic dyes.

    PubMed

    Singh, Charanjit; Goyal, Ankita; Singhal, Sonal

    2014-07-21

    This study deals with the exploration of NixCo₁-xFe₂O₄ (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) ferrite nanoparticles as catalysts for reduction of 4-nitrophenol and photo-oxidative degradation of Rhodamine B. The ferrite samples with uniform size distribution were synthesized using the reverse micelle technique. The structural investigation was performed using powder X-ray diffraction, high-resolution transmission electron microscopy, energy dispersive X-ray and scanning tunneling microscopy. The spherical particles with ordered cubic spinel structure were found to have the crystallite size of 4-6 nm. Diffused UV-visible reflectance spectroscopy was employed to investigate the optical properties of the synthesized ferrite nanoparticles. The surface area calculated using BET method was found to be highest for Co₀.₄Ni₀.₆Fe₂O₄ (154.02 m(2) g(-1)). Co₀.₄Ni₀.₆Fe₂O₄ showed the best catalytic activity for reduction of 4-nitrophenol to 4-aminophenol in the presence of NaBH4 as reducing agent, whereas CoFe₂O₄ was found to be catalytically inactive. The reduction reaction followed pseudo-first order kinetics. The effect of varying the concentration of catalyst and NaBH₄ on the reaction rates was also scrutinized. The photo-oxidative degradation of Rhodamine B, enhanced oxidation efficacy was observed with the introduction of Ni(2+) in to the cobalt ferrite lattice due to octahedral site preference of Ni(2+). Almost 99% degradation was achieved in 20 min using NiFe₂O₄ nanoparticles as catalyst. PMID:24902783

  16. Preparation and magnetic properties of BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrite

    NASA Astrophysics Data System (ADS)

    Wang, Yan; Huang, Ying; Wang, Qiufen

    2012-09-01

    Nanocomposite of hard (BaFe12O19)/soft ferrite (Ni0.8Zn0.2Fe2O4) have been prepared by the sol-gel process. The nanocomposite ferrite are formed when the calcining temperature is above 800 °C. It is found that the magnetic properties strongly depend on the presintering treatment and calcining temperature. The “bee waist” type hysteresis loops for samples disappear when the presintering temperature is 400 °C and the calcination temperature reaches 1100 °C owing to the exchange-coupling interaction. The remanence of BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrite with the mass ratio of 5:1 is higher than a single phase ferrite. The specific saturation magnetization, remanence magnetization and coercivity are 63 emu/g, 36 emu/g and 2750 G, respectively. The exchange-coupling interaction in the BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrite is discussed.

  17. Preparation and Magnetic Properties of SrFe12O19 Ferrites Suitable for Use in Self-Biased LTCC Circulators

    NASA Astrophysics Data System (ADS)

    Peng, Long; Hu, Yue-Bin; Guo, Cheng; Li, Le-Zhong; Wang, Rui; Hu, Yun; Tu, Xiao-Qiang

    2015-01-01

    Strontium ferrites with different Bi2O3 content are prepared by the solid phase method, and their magnetic properties are investigated primarily. The Bi2O3 additive and sintering temperature separately exhibit a strong effect on the sintering density, crystal structure, and magnetic properties of the ferrites. As to the ferrites with 3 wt% Bi2O3, the relatively high sintering density ρs, saturation magnetization Ms, and intrinsic coercivity Hci can be obtained at a low sintering temperature of 900°C even much lower. Furthermore, the effective magnetic anisotropy constant Keff and magnetic anisotropy field Ha of the ferrites are calculated from the magnetization curve by the law of approach to saturation. It is suggested that the low-temperature sintered SrFe12O19 ferrites with Ms of 285.6 kA/m and Ha of 1564.6 kA/m possess a significant potentiality for applying in the self-biased low-temperature co-fired ceramics circulators from 34 to 40 GHz.

  18. Mssbauer and magnetization studies of nickel ferrite nanoparticles synthesized by the microwave-combustion method

    NASA Astrophysics Data System (ADS)

    Mahmoud, M. H.; Elshahawy, A. M.; Makhlouf, Salah A.; Hamdeh, H. H.

    2013-10-01

    Nanocrystalline nickel ferrite was synthesized from its stoichiometric metal nitrates and urea mixtures, using a microwave assisted combustion method. The process was a convenient, inexpensive and an efficient method for formation of NiFe2O4 nanomaterials. Effect of urea/metal nitrates ratio on the obtained phases, particle size and magnetic properties has been investigated by various techniques. Saturation magnetization of 50 emu/g was observed at room temperature for larger particles, and it decreases with decreasing particle size. The coercivity attains a maximum value of 170 Oe when the particle size was ~20 nm, and decreases with increasing particle size. Mssbauer spectra measured at RT for some representative samples show a combination of ordered and superparamagnetic behavior, whereas those collected at 20 K elucidate the nature of the obtained phases and cation distribution.

  19. Preparation of solid lipid nanoparticles using a membrane contactor.

    PubMed

    Charcosset, Catherine; El-Harati, Assma; Fessi, Hatem

    2005-11-01

    Solid lipid nanoparticles (SLN) were introduced at the beginning of the 1990s, as an alternative to solid nanoparticles, emulsions and liposomes in cosmetic and pharmaceutical preparations. The present study investigates a new process for the preparation of SLN using a membrane contactor. The lipid phase is pressed, at a temperature above the melting point of the lipid, through the membrane pores allowing the formation of small droplets. The aqueous phase circulates inside the membrane module, and sweeps away the droplets forming at the pore outlets. SLN are formed by the following cooling of the preparation to room temperature. The influence of process parameters (aqueous phase and lipid phase temperatures, aqueous phase cross-flow velocity and lipid phase pressure, membrane pore size) on the SLN size and on the lipid phase flux is investigated. It is shown that the membrane contactor allows the preparation of SLN with a lipid phase flux between 0.15 and 0.35 m3/h m2, and a mean SLN size between 70 and 215 nm. The advantages of this new process are its facility of use, the control of the SLN size by an appropriate choice of process parameters, and its scaling-up abilities. PMID:16169111

  20. Preparation of nanoferrites and their applications.

    PubMed

    Hazra, S; Ghosh, N N

    2014-02-01

    Ferrites have a plethora of applications in the myriad fields of technology. Ferrites are widely used in conventional electronic, electrical, and magnetic devices. For the past two decades, since the discovery of the superparamagnetic nature of nanostructured ferrites, their applications in biotechnology and biomedical sciences as well as in advanced electronics and microwave devices have gained immense attention. In this review, the historical development of ferrite science and technology, and the synthesis methods for ferrite nanoparticle preparation and their applications have been discussed. Various synthetic methods with typical examples, their advantages as well as limitations have been discussed in details. Traditional industrial applications of various ferrites have also been discussed citing relevant patents. Recent developments on nanoferrite research in terms of synthetic methods as well as advanced applications have been discussed elaborately. PMID:24749468

  1. Preparation and applications of ZnSe nanoparticles

    NASA Astrophysics Data System (ADS)

    Ravindranadh, K.; Shekhawat, M. S.; Rao, M. C.

    2013-06-01

    Semiconductor nanoparticles have been attracting widespread scientific and technological interest due to their unique size-tunable optical and electronic properties. The ZnSe nanoparticles have wide-ranging applications in laser, optical instruments, etc. because it has a wide band gap and transmittance range, high luminescence efficiency, low absorption coefficient, and excellent transparency to infrared. ZnSe nanoparticles have been prepared at room temperature. Zinc chloride 99 mM of 4 mL is added to 2.2g PVA. Volume of the solution is made up to 50 mL by bidistilled water. The Solution is left for 24 h at room temperature to swell. After that the solution is warmed up to 60°C and stirred for 4 h until viscous transparent solution was obtained. One milliliter of Sodium Hydrogen Selenide was dropped into the solution with gentle stirring. Solution is casted on flat glass plate dishes. After the solvent evaporation, a thin film containing ZnSe nanoparticles are obtained. The film is washed with de-ionized water to remove other soluble salts before measurements.

  2. Preparation of uniform nanoparticles of ultra-high purity metal oxides, mixed metal oxides, metals, and metal alloys

    DOEpatents

    Woodfield, Brian F.; Liu, Shengfeng; Boerio-Goates, Juliana; Liu, Qingyuan; Smith, Stacey Janel

    2012-07-03

    In preferred embodiments, metal nanoparticles, mixed-metal (alloy) nanoparticles, metal oxide nanoparticles and mixed-metal oxide nanoparticles are provided. According to embodiments, the nanoparticles may possess narrow size distributions and high purities. In certain preferred embodiments, methods of preparing metal nanoparticles, mixed-metal nanoparticles, metal oxide nanoparticles and mixed-metal nanoparticles are provided. These methods may provide tight control of particle size, size distribution, and oxidation state. Other preferred embodiments relate to a precursor material that may be used to form nanoparticles. In addition, products prepared from such nanoparticles are disclosed.

  3. Nanoparticle preparation of Mefenamic acid by electrospray drying

    SciTech Connect

    Zolkepali, Nurul Karimah Bakar, Noor Fitrah Abu Anuar, Nornizar; Naim, M. Nazli; Bakar, Mohd Rushdi Abu

    2014-02-24

    Nanoparticles preparation of Mefenamic acid (MA) by using an electrospray drying method was conducted in this study. Electrospray drying is a process that uses electrostatic force to disperse a conductive liquid stream into fine charged droplets through the coulomb fission of charges in the liquid and finally dry into fine particles. Electrospray drying modes operation usually in Taylor cone jet, and it was formed by controlling applied voltage and liquid flow rate. A conductive liquid (2.77–8.55μScm{sup −1}) which is MA solution was prepared by using acetone with concentration 0.041 and 0.055 M before pumping at a flow rate of 3–6ml/h. By applying the applied voltage at 1.3–1.5 kV, Taylor cone jet mode was formed prior to the electrospray. During electrospray drying process, solvent evaporation from the droplet was occurring that leads to coulomb disruption and may generate to nanoparticles. The dried nanoparticles were collected on a grounded substrate that was placed at varying distance from the electrospray. MA particle with size range of 100–400 nm were produced by electrospray drying process. Characterization of particles by using X-ray diffractometry (XRD) and differential scanning calorimetry (DSC) show that particles formed into polymorph I.

  4. Preparation and Properties of FeCo Nanoparticles

    SciTech Connect

    Zabransky, K.; David, B.; Pizurova, N.; Schneeweiss, O.; Zboril, R.; Maslan, M.

    2010-07-13

    Fe-Co nanoparticles were prepared from the binary Fe-Co oxalate. The formation of FeCo metallic phase begun at 290 deg. C as determined from the X-ray diffraction patterns recorded during heating of the oxalate sample in hydrogen atmosphere. The reduction finished at 500 deg. C by formation of bcc FeCo phase with a mean particle size of about 50 nm. Analysis of the Moessbauer spectra shows that the ferromagnetic FeCo phase is represented by two sextets corresponding to interiors and surfaces of the nanoparticles. In addition, a weak paramagnetic component, represented by the doublet, was observed which was ascribed to fine particles in a superparamagnetic state. TEM images have shown conglomerates of particles with the composition of about 50 at. % Fe and 50 at. % Co.

  5. The impact of silica encapsulated cobalt zinc ferrite nanoparticles on DNA, lipids and proteins of rat bone marrow mesenchymal stem cells.

    PubMed

    Novotna, Bozena; Turnovcova, Karolina; Veverka, Pavel; Rössner, Pavel; Bagryantseva, Yana; Herynek, Vit; Zvatora, Pavel; Vosmanska, Magda; Klementova, Mariana; Sykova, Eva; Jendelova, Pavla

    2016-08-01

    Nanomaterials are currently the subject of intense research due to their wide variety of potential applications in the biomedical, optical and electronic fields. We prepared and tested cobalt zinc ferrite nanoparticles (Co0.5Zn0.5Fe2O4+γ [CZF-NPs]) encapsulated by amorphous silica in order to find a safe contrast agent and magnetic label for tracking transplanted cells within an organism using magnetic resonance imaging (MRI). Rat mesenchymal stem cells (rMSCs) were labeled for 48 h with a low, medium or high dose of CZF-NPs (0.05; 0.11 or 0.55 mM); silica NPs (Si-NPs; 0.11 mM) served as a positive control. The internalization of NPs into cells was verified by transmission electron microscopy. Biological effects were analyzed at the end of exposure and after an additional 72 h of cell growth without NPs. Compared to untreated cells, Annexin V/Propidium Iodide labeling revealed no significant cytotoxicity for any group of treated cells and only a high dose of CZF-NPs slowed down cell proliferation and induced DNA damage, manifested as a significant increase of DNA-strand breaks and oxidized DNA bases. This was accompanied by high concentrations of 15-F2t-isoprostane and carbonyl groups, demonstrating oxidative injury to lipids and proteins, respectively. No harmful effects were detected in cells exposed to the low dose of CZF-NPs. Nevertheless, the labeled cells still exhibited an adequate relaxation rate for MRI in repeated experiments and ICP-MS confirmed sufficient magnetic label concentrations inside the cells. The results suggest that the silica-coated CZF-NPs, when applied at a non-toxic dose, represent a promising contrast agent for cell labeling. PMID:26581309

  6. Luminol-silver nitrate chemiluminescence enhancement induced by cobalt ferrite nanoparticles.

    PubMed

    Shi, Wenbing; Wang, Hui; Huang, Yuming

    2011-01-01

    CoFe(2)O(4) nanoparticles (NPs) could stimulate the weak chemiluminescence (CL) system of luminol and AgNO(3), resulting in a strong CL emission. The UV-visible spectra, X-ray photoelectron spectra and TEM images of the investigated system revealed that AgNO(3) was reduced by luminol to Ag in the presence of CoFe(2)O(4) NPs and the formed Ag covered the surface of CoFe(2)O(4) NPs, resulting in CoFe(2)O(4)-Ag core-shell nanoparticles. Investigation of the CL reaction kinetics demonstrated that the reaction among luminol, AgNO(3) and CoFe(2)O(4) NPs was fast at the beginning and slowed down later. The CL spectra of the luminol - AgNO(3) - CoFe(2)O(4) NPs system indicated that the luminophor was still an electronically excited 3-aminophthalate anion. A CL mechanism has been postulated. When the CoFe(2)O(4) NPs were injected into the mixture of luminol and AgNO(3), they catalyzed the reduction of AgNO(3) by luminol to produce luminol radicals and Ag, which immediately covered the CoFe(2)O(4) NPs to form CoFe(2)O(4)-Ag core-shell nanoparticles, and the luminol radicals reacted with the dissolved oxygen, leading to a strong CL emission. With the continuous deposition of Ag on the surface of CoFe(2)O(4) NPs, the catalytic activity of the core-shell nanoparticles was inhibited and a decrease in CL intensity was observed and also a slow growth of shell on the nanoparticles. PMID:21400653

  7. Preparation of size-controlled tungsten oxide nanoparticles and evaluation of their adsorption performance

    SciTech Connect

    Hidayat, Darmawan; Purwanto, Agus; Wang, Wei-Ning; Okuyama, Kikuo

    2010-02-15

    The present study investigated the effects of particle size on the adsorption performance of tungsten oxide nanoparticles. Nanoparticles 18-73 nm in diameter were prepared by evaporation of bulk tungsten oxide particles using a flame spray process. Annealing plasma-made tungsten oxide nanoparticles produced particles with diameters of 7-19 nm. The mechanism of nanoparticle formation for each synthetic route was examined. The low-cost, solid-fed flame process readily produced highly crystalline tungsten oxide nanoparticles with controllable size and a remarkably high adsorption capability. These nanoparticles are comparable to those prepared using the more expensive plasma process.

  8. Effects of Mg substitution on the structural and magnetic properties of Co0.5Ni0.5‑x Mg x Fe2O4 nanoparticle ferrites

    NASA Astrophysics Data System (ADS)

    R, M. Rosnan; Z, Othaman; R, Hussin; Ali, A. Ati; Alireza, Samavati; Shadab, Dabagh; Samad, Zare

    2016-04-01

    In this study, nanocrystalline Co–Ni–Mg ferrite powders with composition Co0.5Ni0.5‑x Mg x Fe2O4 are successfully synthesized by the co-precipitation method. A systematic investigation on the structural, morphological and magnetic properties of un-doped and Mg-doped Co–Ni ferrite nanoparticles is carried out. The prepared samples are characterized using x-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), and vibrating sample magnetometry (VSM). The XRD analyses of the synthesized samples confirm the formation of single-phase cubic spinel structures with crystallite sizes in a range of ∼ 32 nm to ∼ 36 nm. The lattice constant increases with increasing Mg content. FESEM images show that the synthesized samples are homogeneous with a uniformly distributed grain. The results of IR spectroscopy analysis indicate the formation of functional groups of spinel ferrite in the co-precipitation process. By increasing Mg2+ substitution, room temperature magnetic measurement shows that maximum magnetization and coercivity increase from ∼ 57.35 emu/g to ∼ 61.49 emu/g and ∼ 603.26 Oe to ∼ 684.11 Oe (1 Oe = 79.5775 A·m‑1), respectively. The higher values of magnetization M s and M r suggest that the optimum composition is Co0.5Ni0.4Mg0.1Fe2O4 that can be applied to high-density recording media and microwave devices. Project supported by the Ibnu Sina Institute for Scientific and Industrial Research, Physics Department of Universiti Teknologi Malaysia and the Ministry of Education Malaysia (Grant Nos. Q.J130000.2526.04H65).

  9. Effect of annealing in a reductive environment on the magnetic properties of barium ferrite nanoparticles doped with Ti4+ and Co2+

    NASA Astrophysics Data System (ADS)

    Petinov, V. I.

    2011-10-01

    It was found experimentally that the annealing of BaFe10.6Co0.7Ti0.7O19 and BaFe10.2Co0.9Ti0.9O19 complex magnetic oxide nanoparticles in paraffin vapor irreversibly increases their coercive force H c and saturation magnetization M s to the H c and M s values for barium ferrite BaFe12O19. The annealing of these nanoparticles, and of particles of magnetic oxides CrO2, γ-Fe2O3, and BaFe12O19 in air and in paraffin vapor, has not been shown to affect their H c and M s values. An explanation in terms of diffusion self-purification of nanoparticles from ion impurities activated by chemical processes on their surface is offered.

  10. Facile preparation of sphere-like copper ferrite nanostructures and their enhanced visible-light-induced photocatalytic conversion of benzene

    SciTech Connect

    Shen, Yu; Wu, Yanbo; Xu, Hongfeng; Fu, Jie; Li, Xinyong; Zhao, Qidong; Hou, Yang

    2013-10-15

    Graphical abstract: - Highlights: • Spinel CuFe{sub 2}O{sub 4} nanospheres were successfully synthesized via a facile method. • CuFe{sub 2}O{sub 4} nanospheres showed high photocatalytic activity toward benzene. • Ethyl acetate, carboxylic acid and aldehyde were the intermediate products. - Abstract: Spinel copper ferrite nanospheres with diameters of about 116 nm were synthesized in high yield via a facile solvothermal route. The prepared nanospheres had cubic spinel structure and exhibited good size uniformity and regularity. The band-gap energy of CuFe{sub 2}O{sub 4} nanospheres was calculated to be about 1.69 eV, indicating their potential visible-light-induced photocatalytic activity. The dramatically enhanced photocatalytic activity of the CuFe{sub 2}O{sub 4} nanospheres was evaluated via the photocatalytic conversion of benzene under Xe lamp irradiation. By using the in situ FTIR technique, ethyl acetate, carboxylic acid and aldehyde could be regarded as the intermediate products, and CO{sub 2} was produced as the final product during the reaction process. This study provided new insight into the design and preparation of functional nanomaterials with sphere structure in high yield, and the as-grown architectures demonstrated an excellent ability to remove organic pollutants in the atmosphere.

  11. Development of oxide dispersion strengthened ferritic steel prepared by chemical reduction and mechanical milling

    NASA Astrophysics Data System (ADS)

    Sun, Q. X.; Fang, Q. F.; Zhou, Y.; Xia, Y. P.; Zhang, T.; Wang, X. P.; Liu, C. S.

    2013-08-01

    The oxide dispersion strengthened ferritic steel with a nominal composition of Fe-14Cr-2W-0.5Ti-0.06Si-0.2V-0.1Mn-0.05Ta-0.03C-0.3Y2O3 (14Cr-ODS) was fabricated by sol-gel method in combination with hydrogen reduction, mechanical alloying (MA) and hot isostatic pressing (HIP) techniques. Pure Fe-1.5Y2O3 precursor was obtained by a sol-gel process and a reduction process at 650 °C for 3 h and pure 14Cr-ODS alloy powders were obtained from this precursor and the alloying metallic powders by mechanical alloying. The microstructure analysis investigated by transmission electron microscopy (TEM) and energy dispersive spectrometry (EDS) reveal that Y-Ti-O complexes and V-Ti-O complexes with a main particle size of 8 nm are formed in the 14Cr-ODS steel matrix. After HIP sintering the weight and the relative density of the compacted ingots are about 0.8 kg and 99.7%. The uniform elongation and ultimate tensile strength of the ODS steel obtained by HIP after annealing at 1100 °C for 5 h are about 13% and 840 MPa, respectively.

  12. Effect of Mo substitution on structural and magnetic properties of Zinc ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Heiba, Zein K.; Mohamed, Mohamed Bakr; Wahba, Adel Maher

    2016-03-01

    Nano ferrite ZnFe2-xMoxO4 (x = 0.0, 0.1, 0.2, and 0.3) samples were synthesized by using citrate method. The phase purity and the structure parameters were studied using X-ray diffraction, FT-IR spectroscopy, and magnetic measurements. Rietveld analysis of X-ray diffraction data revealed that Mo doping ZnFe2O4 changes the degree of inversion of Zn2+ cations. The oxidation state of Mo was studied by using FTIR analysis. Mo doped ZnFe2O4 has a ferromagnetic properties. The magnetization decreases by the replacement of Fe3+ ions by non-magnetic Mo3+ ions. Mo doped ZnFe2O4 samples have a very small coercive field (Hc), which changes depending on the amount of Mo in the sample and reach its maximum value for ZnFe1.7Mo0.3O4. Cation distribution is proposed in an attempt to explain the experimental results of XRD, IR, and VSM data. The direct proportion between the coercive field and the Fe2+ content in the samples was studied in detailed.

  13. Temperature dependent structural and magnetic properties of Cerium substituted Co-Cr ferrite prepared by auto-combustion method

    NASA Astrophysics Data System (ADS)

    Mustafa, Ghulam; Islam, M. U.; Zhang, Wenli; Jamil, Yasir; Asif Iqbal, M.; Hussain, Mudassar; Ahmad, Mukhtar

    2015-03-01

    The effects of heat treatment on a nano-crystalline spinel ferrite with chemical formula CoCr0.04CexFe1.96-xO4 (x=0.06) were investigated in the present work. The sample was prepared by the auto-combustion method and then heat treated at 700-1200 °C for 8 h. The sample heat treated at these temperatures was investigated using thermo-gravimetric analyses and differential scanning calorimetry, X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and vibrating sample magnetometery. The XRD patterns and IR spectra confirmed that the synthesized materials were of single phase at and above 900 °C. The average particle size was found to be in the range of 30.8-63.8 nm estimated by the Scherer formula. IR studies confirm two main absorption bands in the frequency range of 400-800 cm-1 arising due to the tetrahedral (A-site) and octahedral (B-site) stretching vibrations. The average grain size increased with the increase of temperature while distribution of particles became homogeneous as observed by scanning electron microscope. The saturation magnetization was increased gradually from 7.4 to 59.6 emu/g with the increase of temperature. The coercivity lies in the range of 248-811 Oe as a function of temperature. The obtained results suggest that the investigated materials may be potential candidates for high density recording media applications.

  14. Effect of Ti-containing inclusions on the nucleation of acicular ferrite and mechanical properties of multipass weld metals.

    PubMed

    Fattahi, M; Nabhani, N; Hosseini, M; Arabian, N; Rahimi, E

    2013-02-01

    In the present study, the influence of Ti-containing inclusions on the development of acicular ferrite microstructure and mechanical properties in the multipass weld metals has been studied. Shielded metal arc weld deposits were prepared by varying titanium content in the range of 0.003-0.021%. The variation in the titanium content was obtained by the addition of different amounts of titanium oxide nanoparticles to the electrode coating. The dispersion of titanium oxide nanoparticles, composition of inclusions, microstructural analysis, tensile properties and Charpy impact toughness were evaluated. As the amount of Ti-containing inclusions in the weld metal was increased, the microstructure of the weld metal was changed from the grain boundary allotriomorphic ferrite structure to acicular ferrite with the intragranular nucleation of ferrite on the Ti-containing inclusions, and the mechanical properties were improved. This improvement is attributable to the increased percentage of acicular ferrite due to the uniform dispersion of Ti-containing inclusions and the pinning force of oxide nanoparticles against the growth of allotriomorphic ferrite and Widmanstätten ferrite from the austenite grain boundaries. PMID:23238108

  15. Preparation of Eudragit L 100-55 enteric nanoparticles by a novel emulsion diffusion method.

    PubMed

    Hao, Shilei; Wang, Bochu; Wang, Yazhou; Zhu, Liancai; Wang, Bin; Guo, Tingwang

    2013-08-01

    In this study, a novel emulsion diffusion method was used to prepare enteric Eudragit L100-55 nanoparticles by ultrasonic dispersion and diffusion solidification. Omeprazole was selected as the model drug. The prepared nanoparticles were in spherical shape and exhibited negative zeta potential. The Fourier transform infrared spectroscopy results indicated that no molecular interaction occurred between the drug molecule and polymer chain. In addition, the nanoparticles showed a strong pH-sensitive release in vitro. A mild cytotoxicity of nanoparticle was observed in the subsequent studies, and the particle cellular uptake study showed that the nanoparticles could be taken up by Caco-2 cells after 0.5h incubation. Our results indicated that the enteric Eudragit L 100-55 nanoparticle could be synthesized successfully via this ultrasonic solidification method, which also could be applied to prepare other pH-sensitive polymer nanoparticles. PMID:23537830

  16. Effect of retrogradation time on preparation and characterization of proso millet starch nanoparticles.

    PubMed

    Sun, Qingjie; Gong, Min; Li, Ying; Xiong, Liu

    2014-10-13

    Starch nanoparticles were prepared from proso millet starch using a green and facile method combined with enzymolysis and recrystallization. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA) were used to characterize the morphology and crystal structure of the starch nanoparticles prepared with different retrogradation time (0.5, 4, 12, and 24h). The results showed that the sizes of the starch nanoparticles were between 20 nm and 100 nm. The crystal pattern changed from A-type (native starch) to B-type (nanoparticles), and the relative crystallinity of the nanoparticles increased obviously, as compared with the native starch. The nanoparticles prepared with the 12h retrogradation time had the highest degree of crystallinity (47.04%). Compared to conventional acid hydrolysis to make starch nanoparticles, the present approach has the advantage of being quite rapid and presenting a higher yield (about 55%). PMID:25037338

  17. Silver confined within zeolite EMT nanoparticles: preparation and antibacterial properties

    NASA Astrophysics Data System (ADS)

    Dong, B.; Belkhair, S.; Zaarour, M.; Fisher, L.; Verran, J.; Tosheva, L.; Retoux, R.; Gilson, J.-P.; Mintova, S.

    2014-08-01

    The preparation of pure zeolite nanocrystals (EMT-type framework) and their silver ion-exchanged (Ag+-EMT) and reduced silver (Ag0-EMT) forms is reported. The template-free zeolite nanocrystals are stabilized in water suspensions and used directly for silver ion-exchange and subsequent chemical reduction under microwave irradiation. The high porosity, low Si/Al ratio, high concentration of sodium and ultrasmall crystal size of the EMT-type zeolite permitted the introduction of a high amount of silver using short ion-exchange times in the range of 2-6 h. The killing efficacy of pure EMT, Ag+-EMT and Ag0-EMT against Escherichia coli was studied semi-quantitatively. The antibacterial activity increased with increasing Ag content for both types of samples (Ag+-EMT and Ag0-EMT). The Ag0-EMT samples show slightly enhanced antimicrobial efficacy compared to that of Ag+-EMT, however, the differences are not substantial and the preparation of Ag nanoparticles is not viable considering the complexity of preparation steps.The preparation of pure zeolite nanocrystals (EMT-type framework) and their silver ion-exchanged (Ag+-EMT) and reduced silver (Ag0-EMT) forms is reported. The template-free zeolite nanocrystals are stabilized in water suspensions and used directly for silver ion-exchange and subsequent chemical reduction under microwave irradiation. The high porosity, low Si/Al ratio, high concentration of sodium and ultrasmall crystal size of the EMT-type zeolite permitted the introduction of a high amount of silver using short ion-exchange times in the range of 2-6 h. The killing efficacy of pure EMT, Ag+-EMT and Ag0-EMT against Escherichia coli was studied semi-quantitatively. The antibacterial activity increased with increasing Ag content for both types of samples (Ag+-EMT and Ag0-EMT). The Ag0-EMT samples show slightly enhanced antimicrobial efficacy compared to that of Ag+-EMT, however, the differences are not substantial and the preparation of Ag nanoparticles is not viable considering the complexity of preparation steps. Electronic supplementary information (ESI) available: Zeta potential data of Ag-EMT suspensions, pore-size distributions and antibacterial data for Ag-EMT 2 h samples. See DOI: 10.1039/c4nr03169e

  18. Radio-frequency-heating capability of silica-coated manganese ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Qiu, Qing-Wei; Xu, Xiao-Wen; He, Mang; Zhang, Hong-Wang

    2015-06-01

    MnFe2O4 nanoparticles (NPs) with various sizes and tight size-distribution were synthesized by a chemical solution-phase method. The as-synthesized NPs were coated with a silica shell of 4 nm-5 nm in thickness, enabling the water-solubility and biocompatibility of the NPs. The MnFe2O4 NPs with a size of less than 18 nm exhibit superparamagnetic behavior with high saturated magnetization. The capacity of the heat production was enhanced by increasing particle sizes and radio frequency (RF) field strengths. MnFe2O4/SiO2 NPs with 18-nm magnetic cores showed the highest heat-generation ability under an RF field. These MnFe2O4/SiO2 NPs have great potentiality to cancer treatments, controlled drug releases, and remote controls of single cell functions.

  19. Plasmonically enhanced Faraday effect in metal and ferrite nanoparticles composite precipitated inside glass.

    PubMed

    Nakashima, Seisuke; Sugioka, Koji; Tanaka, Katsuhisa; Shimizu, Masahiro; Shimotsuma, Yasuhiko; Miura, Kiyotaka; Midorikawa, Katsumi; Mukai, Kohki

    2012-12-17

    Using femtosecond laser irradiation and subsequent annealing, nanocomposite structures composed of spinel-type ferrimagnetic nanoparticles (NPs) and plasmonic metallic NPs have been formed space-selectively within glass doped with both α-Fe(2)O(3) and Al. The Faraday rotation spectra exhibit a distinct negative peak at around 400 nm, suggesting that the ferrimagnetic Faraday response is enhanced by the localized surface plasmon resonance (LSPR) due to metallic Al NPs. At the interfaces in the nanocomposites, the ferrimagnetism of magnetite NPs is directly coupled with the plasmon in the Al NPs. The control of the resonance wavelength of the magneto-optical peaks, namely, the size of plasmonic NPs has been demonstrated by changing the irradiation or annealing conditions. PMID:23263053

  20. Ligand-induced evolution of intrinsic fluorescence and catalytic activity from cobalt ferrite nanoparticles.

    PubMed

    Pal, Monalisa; Kundu, Anirban; Rakshit, Rupali; Mandal, Kalyan

    2015-06-01

    To develop CoFe(2)O(4) as magneto-fluorescent nanoparticles (NPs) for biomedical applications, it would be advantageous to identify any intrinsic fluorescence of this important magnetic material by simply adjusting the surface chemistry of the NPs themselves. Herein, we demonstrate that intrinsic multicolor fluorescence, covering the whole visible region, can be induced by facile functionalization of CoFe(2)O(4) NPs with Na-tartrate. Moreover, the functionalized CoFe(2)O(4) NPs also show unprecedented catalytic efficiency in the degradation of both biologically and environmentally harmful dyes, pioneering the potential application of these NPs in therapeutics and wastewater treatment. Detailed investigation through various spectroscopic tools unveils the story behind the emergence of this unique optical property of CoFe(2)O(4) NPs upon functionalization with tartrate ligands. We believe our developed multifunctional CoFe(2)O(4) NPs hold great promise for advanced biomedical and technological applications. PMID:25867626

  1. Enrichment of magnetic alignment stimulated by γ-radiation in core-shell type nanoparticle Mn-Zn ferrite

    NASA Astrophysics Data System (ADS)

    Naik, P. P.; Tangsali, R. B.; Sonaye, B.; Sugur, S.

    2013-02-01

    Core shell type nanoparticle MnxZn1-xFe2O4 systems with x=0.55, 0.65 & 0.75 were prepared using autocombustion method. The systems were characterized using tools like XRD and IR for structure confirmation. Magnetic parameter measurements like Saturation magnetization and coercivity were obtained from hysteresis loop which exhibited a symmetry shift due to core shell nature of the nanoparticles. Nanoparticles of particle size between 21.2nm to 25.7nm were found to show 20 percent shrinkage after being radiated by the γ-radiation. This is due to variation in the cation distribution which also affects the cell volume of the cubic cell. Lattice constant reduction observed is reflected in the magnetic properties of the samples. A considerable hike in the saturation magnetization of the samples was observed due to enrichment of magnetic alignment in the magnetic core of the particles. Samples under investigation were irradiated with gamma radiation from Co60 source for different time intervals.

  2. Enrichment of magnetic alignment stimulated by {gamma}-radiation in core-shell type nanoparticle Mn-Zn ferrite

    SciTech Connect

    Naik, P. P.; Tangsali, R. B.; Sonaye, B.; Sugur, S.

    2013-02-05

    Core shell type nanoparticle Mn{sub x}Zn{sub 1-x}Fe{sub 2}O{sub 4} systems with x=0.55, 0.65 and 0.75 were prepared using autocombustion method. The systems were characterized using tools like XRD and IR for structure confirmation. Magnetic parameter measurements like Saturation magnetization and coercivity were obtained from hysteresis loop which exhibited a symmetry shift due to core shell nature of the nanoparticles. Nanoparticles of particle size between 21.2nm to 25.7nm were found to show 20 percent shrinkage after being radiated by the {gamma}-radiation. This is due to variation in the cation distribution which also affects the cell volume of the cubic cell. Lattice constant reduction observed is reflected in the magnetic properties of the samples. A considerable hike in the saturation magnetization of the samples was observed due to enrichment of magnetic alignment in the magnetic core of the particles. Samples under investigation were irradiated with gamma radiation from Co{sup 60} source for different time intervals.

  3. Structural and Magnetic Characterizations of Nano Sized Grain Zinc Ferrite/Hydroxyapatite Ceramic Prepared by Solid State Reaction Route.

    PubMed

    Pankaew, Piyapong; Klumdoung, Pattarinee

    2015-11-01

    A promising composite of bioactive hydroxyapatite (HAp) and zinc ferrite (ZnFe2O4) has potentials for future bone reinforcing formation. In present study, HAp and ZnFe2O4 composite ceramic was prepared by solid state reaction route for easier control of structural and magnetic characteristics and with low cost. HAp powder was synthesized by precipitation method from chicken eggshell. Mixed powders with varying ZnFe2O4/HAp weight ratios from 2-10 wt% were milled together and uniaxially pressed and then sintered at 1200 degrees C for 3 hours. The XRD results showing no other phases of composite ceramics with only HAp and ZnFe2O4 phases were identified, indicating high stability of HAp property. Phase fractions of ZnFe2O4 were found to increase from 10.8 to 18.73 wt% with increasing content of ZnFe2O4. FT-IR results were only revealed vibration bands of standard HAp phase. SEM results revealed primary grains sizes of the prepared ceramics in nano scale. The BET surface area and pore volume increased with increasing content of ZnFe2O4 in composite ceramics. The VSM results of composites with increasing ZnFe2O4 content had been shown with increasing magnetization from 0.05 to 1.85 emu/g while their coercivities were decreased from 44 to 24 Oe. Higher magnetization as well as higher super paramagnetic behavior could be achieved with increasing the studied ZnFe2O4 weight ratios in ZnFe2O4/HAp composite ceramics, which can be tailored for specific applications. PMID:26726683

  4. Synthesis of magnetic cobalt ferrite nanoparticles with controlled morphology, monodispersity and composition: the influence of solvent, surfactant, reductant and synthetic conditions

    NASA Astrophysics Data System (ADS)

    Lu, Le T.; Dung, Ngo T.; Tung, Le D.; Thanh, Cao T.; Quy, Ong K.; Chuc, Nguyen V.; Maenosono, Shinya; Thanh, Nguyen T. K.

    2015-11-01

    In our present work, magnetic cobalt ferrite (CoFe2O4) nanoparticles have been successfully synthesised by thermal decomposition of Fe(iii) and Co(ii) acetylacetonate compounds in organic solvents in the presence of oleic acid (OA)/ oleylamine (OLA) as surfactants and 1,2-hexadecanediol (HDD) or octadecanol (OCD-ol) as an accelerating agent. As a result, CoFe2O4 nanoparticles of different shapes were tightly controlled in size (range of 4-30 nm) and monodispersity (standard deviation only at ca. 5%). Experimental parameters, such as reaction time, temperature, surfactant concentration, solvent, precursor ratio, and accelerating agent, in particular, the role of HDD, OCD-ol, and OA/OLA have been intensively investigated in detail to discover the best conditions for the synthesis of the above magnetic nanoparticles. The obtained nanoparticles have been successfully applied for producing oriented carbon nanotubes (CNTs), and they have potential to be used in biomedical applications.In our present work, magnetic cobalt ferrite (CoFe2O4) nanoparticles have been successfully synthesised by thermal decomposition of Fe(iii) and Co(ii) acetylacetonate compounds in organic solvents in the presence of oleic acid (OA)/ oleylamine (OLA) as surfactants and 1,2-hexadecanediol (HDD) or octadecanol (OCD-ol) as an accelerating agent. As a result, CoFe2O4 nanoparticles of different shapes were tightly controlled in size (range of 4-30 nm) and monodispersity (standard deviation only at ca. 5%). Experimental parameters, such as reaction time, temperature, surfactant concentration, solvent, precursor ratio, and accelerating agent, in particular, the role of HDD, OCD-ol, and OA/OLA have been intensively investigated in detail to discover the best conditions for the synthesis of the above magnetic nanoparticles. The obtained nanoparticles have been successfully applied for producing oriented carbon nanotubes (CNTs), and they have potential to be used in biomedical applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr04266f

  5. CO responses of sensors based on cerium oxide thick films prepared from clustered spherical nanoparticles.

    PubMed

    Izu, Noriya; Matsubara, Ichiro; Itoh, Toshio; Akamatsu, Takafumi; Shin, Woosuck

    2013-01-01

    Various types of CO sensors based on cerium oxide (ceria) have been reported recently. It has also been reported that the response speed of CO sensors fabricated from porous ceria thick films comprising nanoparticles is extremely high. However, the response value of such sensors is not suitably high. In this study, we investigated methods of improving the response values of CO sensors based on ceria and prepared gas sensors from core-shell ceria polymer hybrid nanoparticles. These hybrid nanoparticles have been reported to have a unique structure: The core consists of a cluster of ceria crystallites several nanometers in size. We compared the characteristics of the sensors based on thick films prepared from core-shell nanoparticles with those of sensors based on thick films prepared from conventionally used precipitated nanoparticles. The sensors prepared from the core-shell nanoparticles exhibited a resistance that was ten times greater than that of the sensors prepared from the precipitated nanoparticles. The response values of the gas sensors based on the core-shell nanoparticles also was higher than that of the sensors based on the precipitated nanoparticles. Finally, improvements in sensor response were also noticed after the addition of Au nanoparticles to the thick films used to fabricate the two types of sensors. PMID:23529123

  6. Preparation of bio-compatible boron nanoparticles and novel mesoporous silica nanoparticles for bio-applications

    NASA Astrophysics Data System (ADS)

    Gao, Zhe

    This dissertation presents the synthesis and characterization of several novel inorganic and hybrid nanoparticles, including the bio-compatible boron nanoparticles (BNPs) for boron neutron capture therapy (BNCT), tannic acid-templated mesoporous silica nanoparticles and degradable bridged silsesquioxane silica nanoparticles. Chapter 1 provides background information of BNCT and reviews the development of design and synthesizing silica nanoparticles and the study of silica material degradability. Chapter 2 describes the preparation and characterization of dopamine modified BNPs and the preliminary cell study of them. The BNPs were first produced via ball milling, with fatty acid on the surface to stabilize the combustible boron elements. This chapter will mainly focus on the ligand-exchange strategy, in which the fatty acids were replaced by non-toxic dopamines in a facile one-pot reaction. The dopamine-coated BNPs (DA-BNPs) revealed good water dispersibility and low cytotoxicity. Chapter 3 describes the synthesis of tannic acid template mesoporous silica nanoparticles (TA-TEOS SiNPs) and their application to immobilize proteins. The monodispersed TA SiNPs with uniform pore size up to approximately 13 nm were produced by utilizing tannic acid as a molecular template. We studied the influence of TA concentration and reaction time on the morphology and pore size of the particles. Furthermore, the TA-TEOS particles could subsequently be modified with amine groups allowing them to be capable of incorporating imaging ligands and other guest molecules. The ability of the TA-TEOS particles to store biomolecules was preliminarily assessed with three proteins of different charge characteristics and dimensions. The immobilization of malic dehydrogenase on TA-TEOS enhanced the stability of the enzyme at room temperature. Chapter 4 details the synthesis of several bridged silsesquioxanes and the preparation of degradable hybrid SiNPs via co-condensation of bridged silsesquioxanes with tetraethoxysilane. In vivo studies show that the solid SiNPs accumulate in many organs due to the lack of degradability. The aim of our work is to address this shortcoming by producing novel degradable SiNPs. Bridged silsesquioxanes were used as the precursors of the particles, and upon cleavage of the carbamate groups when brought into contact with aqueous media, the particles degraded into porous structures.

  7. Wear-resistant and electromagnetic absorbing behaviors of oleic acid post-modified ferrite-filled epoxy resin composite coating

    NASA Astrophysics Data System (ADS)

    Wang, Wenjie; Zang, Chongguang; Jiao, Qingjie

    2015-03-01

    The post-modified Mn-Zn ferrite was prepared by grafting oleic acid on the surface of Mn-Zn ferrite to inhibit magnetic nanoparticle aggregation. Fourier Transform Infrared (FT-IR) spectroscopy was used to characterize the particle surfaces. The friction and electromagnetic absorbing properties of a thin coating fabricated by dispersing ferrite into epoxy resin (EP) were investigated. The roughness of the coating and water contact angle were measured using the VEECO and water contact angle meter. Friction tests were conducted using a stainless-steel bearing ball and a Rockwell diamond tip, respectively. The complex permittivity and complex permeability of the composite coating were studied in the low frequency (10 MHz-1.5 GHz). Surface modified ferrites are found to improve magnetic particles dispersion in EP resulting in significant compatibility between inorganic and organic materials. Results also indicate that modified ferrite/EP coatings have a lower roughness average value and higher water contact angle than original ferrite/EP coatings. The enhanced tribological properties of the modified ferrite/EP coatings can be seen from the increased coefficient value. The composite coatings with modified ferrite are observed to exhibit better reflection loss compared with the coatings with original ferrite.

  8. A solution for the preparation of hexagonal M-type SrFe12O19 ferrite using egg-white: Structural and magnetic properties

    NASA Astrophysics Data System (ADS)

    Li, Tingting; Li, Yang; Wu, Ruonan; Zhou, Han; Fang, Xiaochen; Su, Shubing; Xia, Ailin; Jin, Chuangui; Liu, Xianguo

    2015-11-01

    A new sol-gel route using egg-white as the binder of metal ions, is developed to prepare hexagonal M-type SrFe12O19 ferrite in this study, and the effects of different atomic ratio of Sr and Fe (Sr/Fe), sintering temperature (Ts) and usage of egg-white (Mew) on the phase formation, morphology and magnetic properties of specimens are studied. It is found that the single-phase SrFe12O19 ferrite only can be obtained under a Sr/Fe of 1:8 and a Ts between 1000 °C and 1300 °C. The magnetic properties of specimens are also obviously affected by the different Sr/Fe and Ts, primarily due to the emergency of impurities. The Mew has an obvious impact on the crystallinity of specimens, which consequently affects their magnetic properties. In our study, the optimum conditions to prepare the single-phase SrFe12O19 ferrite are Sr/Fe=1:8, Mew= 3 g and Ts =1200 °C.

  9. Preparation of anionic polyurethane nanoparticles and blood compatible behaviors.

    PubMed

    Zhu, Qinshu; Wang, Yan; Zhou, Min; Mao, Chun; Huang, Xiaohua; Bao, Jianchun; Shen, Jian

    2012-05-01

    The anionic polyurethane nanoparticles (APU-NPs) were obtained by an emulsion polymerization method. It was found that the average size of the prepared APU-NPs is about 84 nm, and the APU-NPs have zeta-potential of -38.9 mV. The bulk characterization of synthesized APU-NPs was investigated by FTIR. The blood compatibility of APU-NPs was characterized by in vitro for coagulation tests, complement activation, platelet activation, cytotoxicity experiments, and hemolysis assay. The results showed that the APU-NPs synthesized in this paper are blood compatible with low level of cell cytotoxicity, and the results were significant for their potential use in vivo. PMID:22852346

  10. Preparation of silver nanoparticles fabrics against multidrug-resistant bacteria

    NASA Astrophysics Data System (ADS)

    Hanh, Truong Thi; Thu, Nguyen Thi; Hien, Nguyen Quoc; An, Pham Ngoc; Loan, Truong Thi Kieu; Hoa, Phan Thi

    2016-04-01

    The silver nanoparticles (AgNPs)/peco fabrics were prepared by immobilization of AgNPs on fabrics in which AgNPs were synthesized by γ-irradiation of the 10 mM AgNO3 chitosan solution at the dose of 17.6 kGy. The AgNPs size has been estimated to be about 11 nm from TEM image. The AgNPs content onto peco fabrics was of 143±6 mg/kg at the initial AgNPs concentration of 100 ppm. The AgNPs colloidal solution was characterized by UV-vis spectroscopy and TEM image. The antibacterial activity of AgNPs/peco fabrics after 60 washings against Staphylococcus aureus and Klebsiella pneumoniae was found to be over 99%. Effects of AgNPs fabics on multidrug-resistant pathogens from the clinical specimens were also tested.

  11. Preparation and characterization of Fe2O3 nanoparticles

    NASA Astrophysics Data System (ADS)

    Joya, M. R.; Barón-Jaimez, J.; Barba-Ortega, J.

    2013-11-01

    Nano particles hematite (Fe2O3) with good crystallinity were prepared by Pechini method. Hematite (Fe2O3) has emerged as a promising photo-electrode material due to its significant light absorption, chemical stability in aqueous environments, and ample abundance. Photoelectrochemical cells offer the ability to convert electromagnetic energy from our largest renewable source, the Sun, to stored chemical energy through the splitting of water into molecular oxygen and hydrogen. The structure and the size of the Fe2O3 nanoparticles were analyzed by SEM and XRD. The UV-Vis optical absorption of the samples was also investigated. These methods help to define the obstacles that remain to be surmounted in order to fully exploit the potential of this promising material for solar energy conversion.

  12. Preparation and Evaluation of Montelukast Sodium Loaded Solid Lipid Nanoparticles

    PubMed Central

    Priyanka, K; Sathali, A Abdul Hasan

    2012-01-01

    Solid lipid nanoparticles (SLNs) are an alternative carrier system used to load the drug for targeting, to improve the bioavailability by increasing its solubility, and protecting the drug from presystemic metabolism. The avoidance of presystemic metabolism is due to the nano-metric size range, so that the liver cannot uptake the drug from the delivery system and is not metabolized by the liver. Montelukast sodium is an anti-asthmatic drug, because of its poor oral bioavailability, presystemic metabolism, and decreased half-life; it was chosen to formulate as the solid lipid nanoparticle (SLN) system by hot homogenization followed by an ultrasonication method, to overcome the above. Compritol ATO 888, stearic acid, and glyceryl monostearate were used as a lipid matrix and polyvinyl alcohol as a surfactant. The prepared formulations have been evaluated for entrapment efficiency, drug content, in vitro drug release, particle size analysis, scanning electron microscopy, Fourier transform-infrared studies (FT-IR), differential scanning calorimetry (DSC), and stability. Particle size analysis revealed that the SLN prepared from the higher melting point lipid showed a larger particle size and with increased carbon chain length of the fatty acids. Entrapment efficiency (EE) was ranging from 42% to 92%. In vitro release studies showed maximum cumulative drug release was obtained for F 1 (59.1%) containing stearic acid, and the lowest was observed for F 18 (28.1%) containing compritol ATO 888 after 12 h and all the formulations followed first-order release kinetics. FT-IR and DSC studies revealed no interaction between drug and lipids. Studies showed that increase in lipid concentration, increased particle size, EE, and maintained the sustained release of drug. Among all, compritol ATO 888 was chosen as the best lipid for formulating SLN because it had high EE and sustained the drug release. PMID:23112531

  13. Analyses of factors affecting nickel ferrite nanoparticles synthesis in ultrasound-assisted aqueous solution ball milling.

    PubMed

    Yuan, Zhuang; Chen, Zhen-hua; Chen, Ding; Kang, Zhi-tao

    2015-01-01

    Ball milling experiments were conducted with and without ultrasound wave assistance in deionized water using NiCO3·2Ni(OH)2·4H2O as raw materials. In the reaction process of NiFe2O4 prepared by ultrasound-assisted aqueous solution ball milling, some influencing factors including raw materials, ultrasonic frequency, ball to powder ratio and liquid level were changed. Samples were characterized by X-ray diffraction, fluorescence measurements and electroconductivity detections. The results indicate that more hydroxyl radicals and ions can be generated under the coupling effect of ultrasonic and ball milling. The fluorescence measurements and electroconductivity detections also reflect the reaction speed, allowing for optimal parameters to be determined. PMID:25096301

  14. Synthesis of magnetic cobalt ferrite nanoparticles with controlled morphology, monodispersity and composition: the influence of solvent, surfactant, reductant and synthetic conditions.

    PubMed

    Lu, Le T; Dung, Ngo T; Tung, Le D; Thanh, Cao T; Quy, Ong K; Chuc, Nguyen V; Maenosono, Shinya; Thanh, Nguyen T K

    2015-12-14

    In our present work, magnetic cobalt ferrite (CoFe2O4) nanoparticles have been successfully synthesised by thermal decomposition of Fe(III) and Co(II) acetylacetonate compounds in organic solvents in the presence of oleic acid (OA)/ oleylamine (OLA) as surfactants and 1,2-hexadecanediol (HDD) or octadecanol (OCD-ol) as an accelerating agent. As a result, CoFe2O4 nanoparticles of different shapes were tightly controlled in size (range of 4-30 nm) and monodispersity (standard deviation only at ca. 5%). Experimental parameters, such as reaction time, temperature, surfactant concentration, solvent, precursor ratio, and accelerating agent, in particular, the role of HDD, OCD-ol, and OA/OLA have been intensively investigated in detail to discover the best conditions for the synthesis of the above magnetic nanoparticles. The obtained nanoparticles have been successfully applied for producing oriented carbon nanotubes (CNTs), and they have potential to be used in biomedical applications. PMID:26542630

  15. Preparation and Characterization of PEG-albumin-curcumin Nanoparticles Intended to Treat Breast Cancer

    PubMed Central

    Thadakapally, R.; Aafreen, Arshiya; Aukunuru, J.; Habibuddin, M.; Jogala, S.

    2016-01-01

    The aim of present research was to prepare novel serum stable long circulating polymeric nanoparticles for curcumin with a modification to the well known and novel nanoparticle albumin bound technology. polyethylene glycol-albumin-curcumin nanoparticles were prepared using serum albumin and poly ethylene glycol using desolvation technique. Nanoparticles were characterized for encapsulation efficiency, particle size and surface morphology. Drug excipient compatibility was determined using fourier transform infrared spectroscopy. Physical state of the drug in the formulations was known by differential scanning colorimetry. In vitro release and solubility of the drug from nanoparticles were determined. In vivo Drug release, tissue uptake and kupffer cell uptake was determined with optimized nanoformulation in rats after intravenous administration. Cell viability assay was determined using breast cancer cell line MD-MB-231. Entrapment efficiency for prepared nanoparticle was above 95%. The polyethylene glycol-albumin-curcumin nanoparticles exhibited an interesting release profile with small initial burst followed by slower and controlled release. Solubility of the drug from the formulation was increased. A sustained release of drug from nanoparticles was observed for 35 days in both in vitro and in vivo studies with the optimized formulation. Polyethylene glycol-albumin-curcumin nanoparticles showed lesser liver and kupffer cell uptake as compared to that of curcumin-albumin nanoparticles suggesting the bestowment of stealthness to nanoparticles with pegylation. Also, the antiproliferative activity of polyethylene glycol-albumin-curcumin nanoparticle formulation was more as compared to native curcumin. Polyethylene glycol-albumin-curcumin nanoparticles thus developed can be conveniently used in breast cancer with improved efficacy compared to conventional therapies and as an alternate to nanoparticle albumin bound technology which is used in producing Abraxane, albumin based breast cancer targeting nanoparticles of paclitaxel.

  16. Fluorescent nanoparticles from starch: facile preparation, tunable luminescence and bioimaging.

    PubMed

    Liu, Meiying; Zhang, Xiqi; Yang, Bin; Li, Zhan; Deng, Fengjie; Yang, Yang; Zhang, Xiaoyong; Wei, Yen

    2015-05-01

    Fluorescent organic nanoparticles (FONs) based on carbohydrate polymers were prepared through one-pot hydrothermal treatment of starch in the presence of polyethyleneimine. These FONs (named as PEI-Starch FONs) were characterized by a series of techniques including UV-Vis absorption spectroscopy, fluorescent spectroscopy, Fourier transform infrared spectroscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. Results showed that the size of PEI-Starch FONs is 10-30 nm. The PEI-Starch FONs exhibited high water dispersibility because of the existence of hydrophilic functional groups on their surface. After excited with different wavelength, PEI-Starch FONs emitted strong and excitation-dependent fluorescence. To evaluate their potential for biomedical applications, biocompatibility and cell uptake behavior of PEI-Starch FONs were further investigated. We demonstrated that PEI-Starch FONs are biocompatible with cells and can be easily internalized by cells within 3h. Taken together, novel FONs have been prepared via a simple and scalable hydrothermal method using starch and polyethyleneimine as precursors. These PEI-Starch FONs showed excellent fluorescence properties, high water dispersibility and good biocompatibility, making them highly potential for various biomedical applications. PMID:25659670

  17. Z Ferrite Composite

    NASA Astrophysics Data System (ADS)

    Li, Qifan; Feng, Zekun; Yan, Shuoqing; Nie, Yan; Wang, Xian

    2014-09-01

    Fe-Si-Al/Co2Z ferrite composites were prepared by ball-milling. The microstructure, microwave electromagnetic properties, and impedance-matching performance of a series of composites were determined and the results are discussed. Experimental results indicated that, in frequency range 1-18 GHz, the permittivity and permeability of the complexes can be adjusted by changing the Fe-Si-Al-to-Co2Z weight ratio. Calculated reflection losses indicate that the absorption performance of Fe-Si-Al/Co2Z ferrite composites is superior to that of the pure Fe-Si-Al and Co2Z ferrites. It was found that the impedance-matching performance of the materials, which contributes to perfect absorption, can be improved by use of an appropriate weight ratio for the Fe-Si-Al/Co2Z ferrite composite.

  18. Surfactant modification of aggregation-induced emission material as biocompatible nanoparticles: Facile preparation and cell imaging

    NASA Astrophysics Data System (ADS)

    Zhang, Xiqi; Zhang, Xiaoyong; Wang, Shiqi; Liu, Meiying; Tao, Lei; Wei, Yen

    2012-12-01

    Water soluble and biocompatible fluorescent organic nanoparticles based on aggregation-induced emission (AIE) material were facilely prepared by mixing AIE material and surfactant. The utilization of such fluorescent organic nanoparticles for cell imaging applications was further explored.Water soluble and biocompatible fluorescent organic nanoparticles based on aggregation-induced emission (AIE) material were facilely prepared by mixing AIE material and surfactant. The utilization of such fluorescent organic nanoparticles for cell imaging applications was further explored. Electronic supplementary information (ESI) available: Detailed information about 1H NMR spectra of An18 and FT-IR spectra of An18-F127. See DOI: 10.1039/c2nr32698a

  19. Preparation of Chitosan nanoparticles and its effect on detached rice leaves infected with Pyricularia grisea.

    PubMed

    Manikandan, Appu; Sathiyabama, Muthukrishnan

    2016-03-01

    The aim of the present study was to prepare chitosan nanoparticles to evaluate their effect on protection of rice plants from blast fungus. Nanoparticles were prepared using the ionic gelation method by the interaction of Chitosan and sodium tripolyphosphate. The particle size, polydispersity index, zetapotential and structure was confirmed by DLS, FTIR, TEM and XRD. The Chitosan nanoparticle was evaluated for suppression of rice blast fungus (Pyricularia grisea) under the detached leaf condition. It is evident from our results that chitosan nanoparticle have potential in suppressing blast disease of rice which can be used further under field condition to protect rice plants from the devastating fungus. PMID:26656594

  20. In situ preparation of monodispersed Ag/polyaniline/Fe3O4 nanoparticles via heterogeneous nucleation

    PubMed Central

    2013-01-01

    Acrylic acid and styrene were polymerized onto monodispersed Fe3O4 nanoparticles using a grafting copolymerization method. Aniline molecules were then bonded onto the Fe3O4 nanoparticles by electrostatic self-assembly and further polymerized to obtain uniform polyaniline/Fe3O4 (PANI/Fe3O4) nanoparticles (approximately 35 nm). Finally, monodispersed Ag/PANI/Fe3O4 nanoparticles were prepared by an in situ reduction reaction between emeraldine PANI and silver nitrate. Fourier transform infrared and UV-visible spectrometers and a transmission electron microscope were used to characterize both the chemical structure and the morphology of the resulting nanoparticles. PMID:23819820

  1. Sol-Gel-Prepared Nanoparticles of Mixed Praseodymium Cobaltites-Ferrites

    NASA Astrophysics Data System (ADS)

    Pekinchak, Olga; Vasylechko, Leonid; Lutsyuk, Iryna; Vakhula, Yaroslav; Prots, Yuri; Carrillo-Cabrera, Wilder

    2016-02-01

    Two series of nanocrystalline powders of PrCo1 - x Fe x O3 ( x = 0.1, 0.3, 0.5, 0.7 and 0.9) of high purity were obtained by sol-gel citrate method at 700 and 800 °C. The formation of continuous solid solution with an orthorhombic perovskite structure (sp. group Pbnm) was observed. A peculiarity of the PrCo1 - x Fe x O3 solid solution is the lattice parameter crossovers, which occurred at certain compositions and revealed in the pseudo-tetragonal or pseudo-cubic metric. An average crystallite size of the PrCo1 - x Fe x O3 samples estimated from the analysis of the angular dependence of the X-ray diffraction (XRD) line broadening varies between 30 and 155 nm, depending on the composition and synthesis temperature.

  2. Sol-Gel-Prepared Nanoparticles of Mixed Praseodymium Cobaltites-Ferrites.

    PubMed

    Pekinchak, Olga; Vasylechko, Leonid; Lutsyuk, Iryna; Vakhula, Yaroslav; Prots, Yuri; Carrillo-Cabrera, Wilder

    2016-12-01

    Two series of nanocrystalline powders of PrCo1 - x Fe x O3 (x = 0.1, 0.3, 0.5, 0.7 and 0.9) of high purity were obtained by sol-gel citrate method at 700 and 800 °C. The formation of continuous solid solution with an orthorhombic perovskite structure (sp. group Pbnm) was observed. A peculiarity of the PrCo1 - x Fe x O3 solid solution is the lattice parameter crossovers, which occurred at certain compositions and revealed in the pseudo-tetragonal or pseudo-cubic metric. An average crystallite size of the PrCo1 - x Fe x O3 samples estimated from the analysis of the angular dependence of the X-ray diffraction (XRD) line broadening varies between 30 and 155 nm, depending on the composition and synthesis temperature. PMID:26858157

  3. Nanocrystalline spinel ferrite (MFe{sub 2}O{sub 4}, M = Ni, Co, Mn, Mg, Zn) powders prepared by a simple aloe vera plant-extracted solution hydrothermal route

    SciTech Connect

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

    2013-06-01

    Graphical abstract: This figure shows the specific magnetization curves of the as-prepared MFe{sub 2}O{sub 4} (M = Ni, Co, Mn, Mg, Zn) powders obtained from room temperature VSM measurement. These curves are typical for a soft magnetic material and indicate hysteresis ferromagnetism in the field ranges of ±500 Oe, ±1000 Oe, and ±2000 Oe for the CoFe{sub 2}O{sub 4}, MgFe{sub 2}O{sub 4} and MnFe{sub 2}O{sub 4} respectively, whereas the samples of NiFe{sub 2}O{sub 4} and ZnFe{sub 2}O{sub 4} show a superparamagnetic behavior. Highlights: ► Nanocrystalline MFe{sub 2}O{sub 4} powders were synthesized by a novel hydrothermal method. ► Metal acetylacetonates and aloe vera plant-extracted solution are used. ► This biosynthetic route is very simple and provides high-yield oxide nanomaterials. ► XRD and TEM results indicate that the prepared samples have only spinel structure. ► The maximum M{sub s} of 68.9 emu/g at 10 kOe were observed for the samples of MnFe{sub 2}O{sub 4}. - Abstract: Nanocrystalline spinel ferrite MFe{sub 2}O{sub 4} (M = Ni, Co, Mn, Mg, Zn) powders were synthesized by a novel hydrothermal method using Fe(acac){sub 3}, M(acac){sub 3} (M = Ni, Co, Mn, Mg, Zn) and aloe vera plant extracted solution. The X-ray diffraction and selected-area electron diffraction results indicate that the synthesized nanocrystalline have only spinel structure without the presence of other phase impurities. The crystal structure and morphology of the spinel ferrite powders, as revealed by TEM, show that the NiFe{sub 2}O{sub 4} and CoFe{sub 2}O{sub 4} samples contain nanoparticles, whereas the MnFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4} samples consist of many nanoplatelets and nanoparticles. Interestingly, the ZnFe{sub 2}O{sub 4} sample contains plate-like structure of networked nanocrystalline particles. Room temperature magnetization results show a ferromagnetic behavior of the CoFe{sub 2}O{sub 4}, MnFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4} samples, whereas the samples of NiFe{sub 2}O{sub 4} and ZnFe{sub 2}O{sub 4} exhibit a superparamagnetic behavior.

  4. Comparison of Different Crosslinking Methods for Preparation of Docetaxel-loaded Albumin Nanoparticles.

    PubMed

    Niknejad, Hassan; Mahmoudzadeh, Raziyeh

    2015-01-01

    In the last step of desolvation method for preparation of albumin nanoparticles, glutaraldehyde (GA) is added to stabilize the newly formed nanoparticles. Due to undesirable effects of GA, the objective of this study was to evaluate alternative methods of crosslinking including ultraviolet (UV) irradiation, adding of glucose and combination of both methods. The nanoparticles were prepared by desolvation procedure. Final particle size, zeta potential, FTIR, scanning electron micrograph, cellular uptake and cell toxicity of nanoparticles crosslinked with UV and/or glucose were compared with commonly crosslinked nanoparticles with GA. Moreover, drug release and stability parameters of docetaxel-loaded albumin nanoparticles were investigated. Size of all nanoparticles prepared by different methods was in the same range (100-200 nm). Zeta potential showed the same results except for those treated with UV. The results of FTIR assay were the same for all groups. Although crosslinking by UV or glucose alone resulted in cytotoxic effects, combination of UV and glucose had less cytotoxic effects compared to GA. Cellular uptake of nanoparticles crosslinked with UV + glucose and GA showed similar results. The release of docetaxel from UV + glucose and GA crosslinked nanoparticles showed the same biphasic release. These data support the idea that crosslinking with a combination of UV and glucose can be a promising alternative method for production of docetaxel-loaded albumin nanoparticles with the advantage of omitting toxic GA. PMID:25901145

  5. Comparison of Different Crosslinking Methods for Preparation of Docetaxel-loaded Albumin Nanoparticles

    PubMed Central

    Niknejad, Hassan; Mahmoudzadeh, Raziyeh

    2015-01-01

    In the last step of desolvation method for preparation of albumin nanoparticles, glutaraldehyde (GA) is added to stabilize the newly formed nanoparticles. Due to undesirable effects of GA, the objective of this study was to evaluate alternative methods of crosslinking including ultraviolet (UV) irradiation, adding of glucose and combination of both methods. The nanoparticles were prepared by desolvation procedure. Final particle size, zeta potential, FTIR, scanning electron micrograph, cellular uptake and cell toxicity of nanoparticles crosslinked with UV and/or glucose were compared with commonly crosslinked nanoparticles with GA. Moreover, drug release and stability parameters of docetaxel-loaded albumin nanoparticles were investigated. Size of all nanoparticles prepared by different methods was in the same range (100-200 nm). Zeta potential showed the same results except for those treated with UV. The results of FTIR assay were the same for all groups. Although crosslinking by UV or glucose alone resulted in cytotoxic effects, combination of UV and glucose had less cytotoxic effects compared to GA. Cellular uptake of nanoparticles crosslinked with UV + glucose and GA showed similar results. The release of docetaxel from UV + glucose and GA crosslinked nanoparticles showed the same biphasic release. These data support the idea that crosslinking with a combination of UV and glucose can be a promising alternative method for production of docetaxel-loaded albumin nanoparticles with the advantage of omitting toxic GA. PMID:25901145

  6. Ferrous sulfate based low temperature synthesis and magnetic properties of nickel ferrite nanostructures

    SciTech Connect

    Tejabhiram, Y.; Pradeep, R.; Helen, A.T.; Gopalakrishnan, C.; Ramasamy, C.

    2014-12-15

    Highlights: • Novel low temperature synthesis of nickel ferrite nanoparticles. • Comparison with two conventional synthesis techniques including hydrothermal method. • XRD results confirm the formation of crystalline nickel ferrites at 110 °C. • Superparamagnetic particles with applications in drug delivery and hyperthermia. • Magnetic properties superior to conventional methods found in new process. - Abstract: We report a simple, low temperature and surfactant free co-precipitation method for the preparation of nickel ferrite nanostructures using ferrous sulfate as the iron precursor. The products obtained from this method were compared for their physical properties with nickel ferrites produced through conventional co-precipitation and hydrothermal methods which used ferric nitrate as the iron precursor. X-ray diffraction analysis confirmed the synthesis of single phase inverse spinel nanocrystalline nickel ferrites at temperature as low as 110 °C in the low temperature method. Electron microscopy analysis on the samples revealed the formation of nearly spherical nanostructures in the size range of 20–30 nm which are comparable to other conventional methods. Vibrating sample magnetometer measurements showed the formation of superparamagnetic particles with high magnetic saturation 41.3 emu/g which corresponds well with conventional synthesis methods. The spontaneous synthesis of the nickel ferrite nanoparticles by the low temperature synthesis method was attributed to the presence of 0.808 kJ mol{sup −1} of excess Gibbs free energy due to ferrous sulfate precursor.

  7. Investigation of antibacterial properties silver nanoparticles prepared via green method

    PubMed Central

    2012-01-01

    Background This study aims to investigate the influence of different stirring times on antibacterial activity of silver nanoparticles in polyethylene glycol (PEG) suspension. The silver nanoparticles (Ag-NPs) were prepared by green synthesis method using green agents, polyethylene glycol (PEG) under moderate temperature at different stirring times. Silver nitrate (AgNO3) was taken as the metal precursor while PEG was used as the solid support and polymeric stabilizer. The antibacterial activity of different sizes of nanosilver was investigated against Gram–positive [Staphylococcus aureus] and Gram–negative bacteria [Salmonella typhimurium SL1344] by the disk diffusion method using Müeller–Hinton Agar. Results Formation of Ag-NPs was determined by UV–vis spectroscopy where surface plasmon absorption maxima can be observed at 412–437 nm from the UV–vis spectrum. The synthesized nanoparticles were also characterized by X-ray diffraction (XRD). The peaks in the XRD pattern confirmed that the Ag-NPs possessed a face-centered cubic and peaks of contaminated crystalline phases were unable to be located. Transmission electron microscopy (TEM) revealed that Ag-NPs synthesized were in spherical shape. The optimum stirring time to synthesize smallest particle size was 6 hours with mean diameter of 11.23 nm. Zeta potential results indicate that the stability of the Ag-NPs is increases at the 6 h stirring time of reaction. The Fourier transform infrared (FT-IR) spectrum suggested the complexation present between PEG and Ag-NPs. The Ag-NPs in PEG were effective against all bacteria tested. Higher antibacterial activity was observed for Ag-NPs with smaller size. These suggest that Ag-NPs can be employed as an effective bacteria inhibitor and can be applied in medical field. Conclusions Ag-NPs were successfully synthesized in PEG suspension under moderate temperature at different stirring times. The study clearly showed that the Ag-NPs with different stirring times exhibit inhibition towards the tested gram-positive and gram-negative bacteria. PMID:22839208

  8. Thiolated chitosan nanoparticles for enhancing oral absorption of docetaxel: preparation, in vitro and ex vivo evaluation

    PubMed Central

    Saremi, Shahrooz; Atyabi, Fatemeh; Akhlaghi, Seyedeh Parinaz; Ostad, Seyed Nasser; Dinarvand, Rassoul

    2011-01-01

    The aim of this study was to prepare and evaluate mucoadhesive core-shell nanoparticles based on copolymerization of thiolated chitosan coated on poly methyl methacrylate cores as a carrier for oral delivery of docetaxel. Docetaxel-loaded nanoparticles with various concentrations were prepared via a radical emulsion polymerization method using cerium ammonium nitrate as an initiator. The physicochemical properties of the obtained nanoparticles were characterized by: dynamic light-scattering analysis for their mean size, size distribution, and zeta potential; scanning electron microscopy and transmission electron microscopy for surface morphology; and differential scanning calorimetry analysis for confirmation of molecular dispersity of docetaxel in the nanoparticles. Nanoparticles were spherical with mean diameter below 200 nm, polydispersity of below 0.15, and positive zeta potential values. The entrapment efficiency of the nanoparticles was approximately 90%. In vitro release studies showed a sustained release characteristic for 10 days after a burst release at the beginning. Ex vivo studies showed a significant increase in the transportation of docetaxel from intestinal membrane of rat when formulated as nanoparticles. Cellular uptake of nanoparticles was investigated using fluoresceinamine-loaded nanoparticles. Docetaxel nanoparticles showed a high cytotoxicity effect in the Caco-2 and MCF-7 cell lines after 72 hours. It can be concluded that by combining the advantages of both thiolated polymers and colloidal particles, these nanoparticles can be proposed as a drug carrier system for mucosal delivery of hydrophobic drugs. PMID:21289989

  9. Control of Particle Size and Morphology of Cobalt-Ferrite Nanoparticles by Salt-Matrix during Annealing

    NASA Astrophysics Data System (ADS)

    Azizi, A.; Sadrnezhaad, S. K.; Mostafavi, M.

    Salt-matrix annealing of mechanically alloyed Co-ferrite nanopowder was used to modify its particle size and morphology. Efficiency improvement due to suppression of sintering and growth resulted in reduction of average particle size from 100nm for salt-less to 40nm for salt-full annealing procedure. Nanosized single-phase cobalt-ferrite particles were observed after 2h annealing at 750°C in the samples milled for 20 hours both with and without NaCl. NaCl:CoFe2O4 ratio of 10:1 resulted in cabbage-like clusters containing particles smaller than 50 nm.

  10. Synthesis and Optical Properties of Sulfide Nanoparticles Prepared in Dimethylsulfoxide

    SciTech Connect

    Li, Yuebin; Ma, Lun; Zhang, Xing; Joly, Alan G.; Liu, Zuli; Chen, Wei

    2008-11-01

    Many methods have been reported for the formation of sulfide nanoparticles by the reaction of metallic salts with sulfide chemical sources in aqueous solutions or organic solvents. Here, we report the formation of sulfide nanoparticles in dimethylsulfoxide (DMSO) by boiling metallic salts without sulfide sources. The sulfide sources are generated from the boiling of DMSO and react with metallic salts to form sulfide nanoparticles. In this method DMSO functions as a solvent and a sulfide source as well as a stabilizer for the formation of the nanoparticles. The recipe is simple and economical making sulfide nanoparticles formed in this way readily available for many potential applications.

  11. Chitosan graft copolymer nanoparticles for oral protein drug delivery: preparation and characterization.

    PubMed

    Qian, Feng; Cui, Fuying; Ding, Jieying; Tang, Cui; Yin, Chunhua

    2006-10-01

    Several novel functionalized graft copolymer nanoparticles consisting of chitosan (CS) and the monomer methyl methacrylate (MMA), N-dimethylaminoethyl methacrylate hydrochloride (DMAEMC), and N-trimethylaminoethyl methacrylate chloride (TMAEMC), which show a higher solubility than chitosan in a broader pH range, have been prepared by free radical polymerization. The nanoparticles were characterized in terms of particle size, zeta potential, TEM, and FT-IR. These nanoparticles were 150-280 nm in size and carried obvious positive surface charges. Protein-loaded nanoparticles were prepared, and their maximal encapsulation efficiency was up to 100%. In vitro release showed that these nanoparticles provided an initial burst release followed by a slowly sustained release for more than 24 h. These graft copolymer nanoparticles enhanced the absorption and improved the bioavailability of insulin via the gastrointestinal (GI) tract of normal male Sprague-Dawley (SD) strain rats to a greater extent than that of the phosphate buffer solution (PBS) of insulin. PMID:17025345

  12. Preparation and characterization of PEG-Mentha oil nanoparticles for housefly control.

    PubMed

    Kumar, Peeyush; Mishra, Sapna; Malik, Anushree; Satya, Santosh

    2014-04-01

    Nanoparticles of Mentha × piperita essential oil were prepared by melt-dispersion method. The nanoparticles prepared at varying oil doses (5-10%, w/v) showed an encapsulation efficiency of 78.2-83.4%, while the oil load was observed to range between 3.64 and 7.46%. The average particle size of the nanoparticles varied between 226 and 331 nm, while polydispersity index showed variation between 0.547 and 1.000. DSC analysis indicated endothermic reaction during formation of nanoparticles, while a 2-term exponential kinetic model was followed during oil release. Nanoparticles showed considerable mortality against housefly larvae in lab (100%) as well as simulated field condition after first week (93%) and 6th week (57%) of application. This was the first study utilizing controlled release property of nanoparticles to formulate a cost effective product for breeding site application against housefly. PMID:24287110

  13. Magnetic properties of Co1-xZnxFe2O4 spinel ferrite nanoparticles synthesized by starch-assisted sol-gel autocombustion method and its ball milling

    NASA Astrophysics Data System (ADS)

    Yadav, Raghvendra Singh; Havlica, Jaromir; Hnatko, Miroslav; Šajgalík, Pavol; Alexander, Cigáň; Palou, Martin; Bartoníčková, Eva; Boháč, Martin; Frajkorová, Františka; Masilko, Jiri; Zmrzlý, Martin; Kalina, Lukas; Hajdúchová, Miroslava; Enev, Vojtěch

    2015-03-01

    In this article, Co1-xZnxFe2O4 (x=0.0 and 0.5) spinel ferrite nanoparticles were achieved at 800 °C by starch-assisted sol-gel autocombustion method. To further reduce the particle size, these synthesized ferrite nanoparticles were ball-milled for 2 h. X-ray diffraction patterns demonstrated single phase formation of Co1-xZnxFe2O4 (x=0.0 and 0.5) spinel ferrite nanoparticles. FE-SEM analysis indicated the nanosized spherical particles formation with spherical morphology. The change in Raman modes and relative intensity were observed due to ball milling and consequently decrease of particle size and cationic redistribution. An X-ray Photoelectron Spectroscopy (XPS) result indicated that Co2+, Zn2+ and Fe3+ exist in octahedral and tetrahedral sites. The cationic redistribution of Zn2+ and consequently Fe3+ occurred between octahedral and tetrahedral sites after ball-milling. The change in saturation magnetization (Ms) and coercivity (Hc) with decrease of nanocrystalline size and distribution of cations in spinel ferrite were observed.

  14. Cation distribution and enhanced surface effects on the temperature-dependent magnetization of as-prepared NiFe2O4 nanoparticles

    NASA Astrophysics Data System (ADS)

    Atif, M.; Nadeem, M.; Siddique, M.

    2015-08-01

    Nickel ferrite, i.e., NiFe2O4, nanoparticles are synthesized by sol-gel method using urea as a neutralizing agent. The formation of spinel phase and crystal structure of the as-prepared sample is analyzed by X-ray diffraction and transmission electron microscope. In order to confirm phase formation and cation arrangement, room temperature 57Fe Mössbauer spectroscopy is employed. The degree of inversion ( i) estimated from the relative peak area is found to be 0.6, which confirms a mixed spinel structure of the as-prepared sample. Zero-field-cooled/field-cooled measurements showed evidence of superparamagnetic behavior associated with the nanosized particles. Hysteresis loop measurements revealed temperature-dependent magnetic properties: The coercive field ( H C) decreases with increasing temperature and deviates from the Kneller's law for ferromagnetic nanostructures; and the saturation magnetization ( M s) follows modified Bloch's law in the temperature range between 25 and 400 K. However, below 25 K, an abrupt increase in magnetization of nanoparticles is observed. In order to understand this behavior, an additional contribution has to be added to the core magnetization to properly fit the data. Hence, a surface correction term to the Bloch's law is found to describe the temperature dependence of magnetization in the core-shell NiFe2O4 nanoparticles.

  15. Preparation and characterization of silver chloride nanoparticles as an antibacterial agent

    NASA Astrophysics Data System (ADS)

    Duong Trinh, Ngoc; Thanh Binh Nguyen, Thi; Hai Nguyen, Thanh

    2015-12-01

    Silver chloride nanoparticles were prepared by the precipitation reaction between silver nitrate and sodium chloride in an aqueous solution containing poly(vinyl alcohol) as a stabilizing agent. Different characteristics of the nanoparticles in suspension and in lyophilized powder such as size, morphology, chemical nature, interaction with stabilizing agent and photo-stability were investigated. Biological tests showed that the obtained silver chloride nanoparticles displayed antibacterial activities against Escherichia coli and Staphylococcus aureus.

  16. Fluorescence of silicon nanoparticles prepared by nanosecond pulsed laser

    SciTech Connect

    Liu, Chunyang Sui, Xin; Yang, Fang; Ma, Wei; Li, Jishun; Xue, Yujun; Fu, Xing

    2014-03-15

    A pulsed laser fabrication method is used to prepare fluorescent microstructures on silicon substrates in this paper. A 355 nm nanosecond pulsed laser micromachining system was designed, and the performance was verified and optimized. Fluorescence microscopy was used to analyze the photoluminescence of the microstructures which were formed using the pulsed laser processing technique. Photoluminescence spectra of the microstructure reveal a peak emission around 500 nm, from 370 nm laser irradiation. The light intensity also shows an exponential decay with irradiation time, which is similar to attenuation processes seen in porous silicon. The surface morphology and chemical composition of the microstructure in the fabricated region was also analyzed with multifunction scanning electron microscopy. Spherical particles are produced with diameters around 100 nm. The structure is compared with porous silicon. It is likely that these nanoparticles act as luminescence recombination centers on the silicon surface. The small diameter of the particles modifies the band gap of silicon by quantum confinement effects. Electron-hole pairs recombine and the fluorescence emission shifts into the visible range. The chemical elements of the processed region are also changed during the interaction between laser and silicon. Oxidation and carbonization play an important role in the enhancement of fluorescence emission.

  17. Metal nanoparticle deposited inorganic nanostructure hybrids, uses thereof and processes for their preparation

    DOEpatents

    Tenne, Reshef; Tsverin, Yulia; Burghaus, Uwe; Komarneni, Mallikharjuna Rao

    2016-01-26

    This invention relates to a hybrid component comprising at least one nanoparticle of inorganic layered compound (in the form of fullerene-like structure or nanotube), and at least one metal nanoparticle, uses thereof as a catalyst, (e.g. photocatalysis) and processes for its preparation.

  18. Temperature Dependence of Saturation Magnetization and Coercivity in Mn0.5Zn0.5Gd0.02Fe1.98O4 Ferrite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Obaidat, I. M.; Issa, B.; Albiss, B. A.; Haik, Y.

    2015-10-01

    The influence of temperature on coercivity, Hc and saturation magnetization, Ms were investigated experimentally in Mn0.5Zn0.5Gd0.02Fe1.98O4 ferrite nanoparticles (average size 35 nm). Isothermal magnetization curves M (H) were obtained in the field range from -5 kOe to +5 kOe at different temperatures after the zero field cooling (ZFC) process. The temperature dependence of the coercivity, Hc(T) deviated slightly from the classical Kneller's law. The temperature dependence of saturation magnetization, Ms(T) was found to have an excellent agreement with the Bloch's law. These results are discussed in terms of several factors such as the size and size distribution of the particles, inter-particle interactions and the surface spin.

  19. Experimental demonstration of all-optical weak magnetic field detection using beam-deflection of single-mode fiber coated with cobalt-doped nickel ferrite nanoparticles.

    PubMed

    Pradhan, Somarpita; Chaudhuri, Partha Roy

    2015-07-10

    We experimentally demonstrate single-mode optical-fiber-beam-deflection configuration for weak magnetic-field-detection using an optimized (low coercive-field) composition of cobalt-doped nickel ferrite nanoparticles. Devising a fiber-double-slit type experiment, we measure the surrounding magnetic field through precisely measuring interference-fringe yielding a minimum detectable field ∼100  mT and we procure magnetization data of the sample that fairly predicts SQUID measurement. To improve sensitivity, we incorporate etched single-mode fiber in double-slit arrangement and recorded a minimum detectable field, ∼30  mT. To further improve, we redefine the experiment as modulating fiber-to-fiber light-transmission and demonstrate the minimum field as 2.0 mT. The device will be uniquely suited for electrical or otherwise hazardous environments. PMID:26193403

  20. Preparation and In Vitro Evaluation of Hydrophilic Fenretinide Nanoparticles

    PubMed Central

    Ledet, Grace A.; Graves, Richard A.; Glotser, Elena Y.; Mandal, Tarun K.; Bostanian, Levon A.

    2015-01-01

    Fenretinide is an effective anti-cancer drug with high in vitro cytotoxicity and low in vivo systemic toxicity. In clinical trials, fenretinide has shown poor therapeutic efficacy following oral administration – attributed to its low bioavailability and solubility. The long term goal of this project is to develop a formulation for the oral delivery of fenretinide. The purpose of this part of the study wasto prepare and characterize hydrophilic nanoparticle formulations of fenretinide. Three different ratios of polyvinyl pyrrolidone (PVP) to fenretinide were used, namely, 3:1, 4:1, and 5:1. Both drug and polymer were dissolved in a mixture of methanol and dichloromethane (2:23 v/v). Rotary evaporation was used to remove the solvents, and, following reconstitution with water, a high pressure homogenizer was used to form nanoparticles. The particle size and polydispersity index were measured before and after lyophilization. The formulations were studied by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and x-ray powder diffraction (XRPD). The effectiveness of the formulations was assessed by releasestudies and Caco-2 cell permeability assays. As the PVP content increased, the recovered particle size following lyophilization became more consistent with the pre-lyophilization particle size, especially for those formulations with less lactose. The DSC scans of the formulations did not show any fenretinide melting endotherms, indicating that the drug was either present in an amorphous form in the formulation or that a solid solution of the drug in PVP had formed. For the release studies, the highest drug release among the formulations was 249.2 ± 35.5 ng/mL for the formulation with 4:1 polymer-to-drug. When the permeability of the formulations was evaluated in a Caco-2 cell model, the mean normalized flux for each treatment group was significantly higher (p<0.05) from the fenretinide control. The formulation containing 4:1 polymer-to-drug ratio and 6:5 lactose-to-formulation ratio emerged as the optimal choice for further evaluation as a potential oral delivery formulation for fenretinide. PMID:25542987

  1. Aqueous Solution Preparation, Structure, and Magnetic Properties of Nano-Granular ZnxFe3?xO4 Ferrite Films

    PubMed Central

    2010-01-01

    This paper reports a simple and novel process for preparing nano-granular ZnxFe3?xO4 ferrite films (0 ? x ? 0.99) on Ag-coated glass substrates in DMAB-Fe(NO3)3-Zn(NO3)2 solutions. The deposition process may be applied in preparing other cations-doped spinel ferrite films. The Zn content x in the ZnxFe3?xO4 films depends linearly on the Zn2+ ion concentration ranging from 0.0 to 1.0 mM in the aqueous solutions. With x increasing from 0 to 0.99, the lattice constant increases from 0.8399 to 0.8464 nm; and the microstructure of the films changes from the non-uniform nano-granules to the fine and uniform nano-granules of 5060 nm in size. The saturation magnetization of the films first increases from 75 emu/g to the maximum 108 emu/g with x increasing from 0 to 0.33 and then decreases monotonously to 5 emu/g with x increasing from 0.33 to 0.99. Meanwhile, the coercive force decreases monotonously from 116 to 13 Oe. PMID:20730079

  2. Magnetic and Structural Properties of Nanosized Magnesium Doped Zinc Ferrite Synthesized by Citrate Precursor Method

    NASA Astrophysics Data System (ADS)

    Srivastava, A. K.; Bansal, Shweta Dikshu; Singh, Simranjit

    2011-12-01

    Nanoparticles of MgxZn1-xFe2O4 ferrite (where x = 0.2, 0.4, 0.5,) are synthesized via citrate precursor method and then all the samples are sintered at 600 °C for 1 hour. The prepared samples are characterized through XRD (X-ray diffraction), FTIR (Fourier transform infrared spectroscopy), TEM (transmission electron microscope) and VSM (vibrating sample magnetometer). The M-H curves show evidence of a superparamagnetic (SPM) regime in the synthesized ferrites.

  3. Controlling of optical energy gap of Co-ferrite quantum dots in poly (methyl methacrylate) matrix

    NASA Astrophysics Data System (ADS)

    El-Sayed, H. M.; Agami, W. R.

    2015-07-01

    Different crystallite sizes of Co-ferrite nanoparticles were prepared and dispersed in the matrix of poly (methyl methacrylate) (PMMA) polymer. The effect of crystallite size on the structure and optical energy gap of Co-nanoferrite/PMMA composite has been studied. The optical energy gap of Co-ferrite was greatly affected by the crystallite size. This result was discussed in terms of the formation of electron-hole exciton using particle in a box model. The effective mass and the Bohr radius of the formed exciton have been calculated from the spectroscopic measurements.

  4. Facile synthesis of cobalt ferrite nanotubes using bacterial nanocellulose as template.

    PubMed

    Menchaca-Nal, S; Londoño-Calderón, C L; Cerrutti, P; Foresti, M L; Pampillo, L; Bilovol, V; Candal, R; Martínez-García, R

    2016-02-10

    A facile method for the preparation of cobalt ferrite nanotubes by use of bacterial cellulose nanoribbons as a template is described. The proposed method relays on a simple coprecipitation operation, which is a technique extensively used for the synthesis of nanoparticles (either isolated or as aggregates) but not for the synthesis of nanotubes. The precursors employed in the synthesis are chlorides, and the procedure is carried out at low temperature (90 °C). By the method proposed a homogeneous distribution of cobalt ferrite nanotubes with an average diameter of 217 nm in the bacterial nanocellulose (BC) aerogel (3%) was obtained. The obtained nanotubes are formed by 26-102 nm cobalt ferrite clusters of cobalt ferrite nanoparticles with diameters in the 9-13 nm interval. The nanoparticles that form the nanotubes showed to have a certain crystalline disorder, which could be attributed in a greater extent to the small crystallite size, and, in a lesser extent, to microstrains existing in the crystalline lattice. The BC-templated-CoFe2O4 nanotubes exhibited magnetic behavior at room temperature. The magnetic properties showed to be influenced by a fraction of nanoparticles in superparamagnetic state. PMID:26686185

  5. Antimicrobial Lemongrass Essential Oil-Copper Ferrite Cellulose Acetate Nanocapsules.

    PubMed

    Liakos, Ioannis L; Abdellatif, Mohamed H; Innocenti, Claudia; Scarpellini, Alice; Carzino, Riccardo; Brunetti, Virgilio; Marras, Sergio; Brescia, Rosaria; Drago, Filippo; Pompa, Pier Paolo

    2016-01-01

    Cellulose acetate (CA) nanoparticles were combined with two antimicrobial agents, namely lemongrass (LG) essential oil and Cu-ferrite nanoparticles. The preparation method of CA nanocapsules (NCs), with the two antimicrobial agents, was based on the nanoprecipitation method using the solvent/anti-solvent technique. Several physical and chemical analyses were performed to characterize the resulting NCs and to study their formation mechanism. The size of the combined antimicrobial NCs was found to be ca. 220 nm. The presence of Cu-ferrites enhanced the attachment of LG essential oil into the CA matrix. The magnetic properties of the combined construct were weak, due to the shielding of Cu-ferrites from the polymeric matrix, making them available for drug delivery applications where spontaneous magnetization effects should be avoided. The antimicrobial properties of the NCs were significantly enhanced with respect to CA/LG only. This work opens novel routes for the development of organic/inorganic nanoparticles with exceptional antimicrobial activities. PMID:27104514

  6. SERS active systems of water-soluble polythiophene and plasmonic nanoparticles: preparation and optical properties

    NASA Astrophysics Data System (ADS)

    Kazim, S.; Pfleger, J.; Halašová, K.; Procházka, M.; Bondarev, D.; Vohlídal, J.

    2011-08-01

    Aggregated systems of silver (Ag) and gold (Au) nanoparticles coated with cationic polythiophene were prepared, which showed optical properties typical for strongly coupled plasmonic excitations. The procedure allowed tune up the three-dimensional arrangement of nanoparticles assembly for achieving strong SERS effect at the excitation wavelength depending on the polymer concentration. By combination with an anionic derivative of polythiophene thin multilayer films composed of alternating anionic and cationic polythiophene with mutually interacting plasmonic Au nanoparticles were successfully prepared using layer-by-layer deposition.

  7. Preparation and luminescent properties of GdOF:Ce, Tb nanoparticles and their transparent PMMA nanocomposites

    NASA Astrophysics Data System (ADS)

    Cai, Wen; Wang, Aiwu; Fu, Li; Hu, Jie; Rao, Tingke; Wang, Junqing; Zhong, Jiasong; Xiang, Weidong

    2015-05-01

    GdOF:Ce, Tb nanoparticles and their poly (methyl methacrylate) (PMMA) nanocomposites have been successfully prepared by a thermolysis route and thermal polymerization of methyl methacrylate (MMA) monomer, respectively. The obtained nanoparticles and nanocomposites are characterized by XRD, EDS, TEM, FTIR, TGA, UV-Vis and PL spectrum. The as-synthesized transparent GdOF:Ce, Tb/PMMA nanocomposites exhibit green photoluminescence under the irradiation of 254 nm UV lamp due to the incorporation of luminescent GdOF:Ce, Tb nanoparticles into the PMMA matrix. The present route would provide a general strategy to prepare other functional nanocomposites.

  8. Preparation and properties of bio-compatible magnetic Fe 3O 4 nanoparticles

    NASA Astrophysics Data System (ADS)

    Chan, H. T.; Do, Y. Y.; Huang, P. L.; Chien, P. L.; Chan, T. S.; Liu, R. S.; Huang, C. Y.; Yang, S. Y.; Horng, H. E.

    2006-09-01

    In this work, we study the preparation and properties of bio-compatible magnetic nanoparticles for immunoassay and DNA detection. The magnetite (Fe 3O 4) nanoparticles were prepared by a chemical co-precipitation method and dextran was selected as the surfactant to suspend the nanoparticles. Suspended particles associated with avidin followed by biotin were qualitatively analyzed by enzyme-linked immunosorbent assay (ELISA) method. We found further the ethylenediamine blocked activated residual groups efficiently, hence enhancing the attachment of biotin for probing the avidin.

  9. Green preparation and spectroscopic characterization of plasmonic silver nanoparticles using fruits as reducing agents.

    PubMed

    Ærøe Hyllested, Jes; Espina Palanco, Marta; Hagen, Nicolai; Mogensen, Klaus Bo; Kneipp, Katrin

    2015-01-01

    Chemicals typically available in plants have the capability to reduce silver and gold salts and to create silver and gold nanoparticles. We report the preparation of silver nanoparticles with sizes between 10 and 300 nm from silver nitrate using fruit extract collected from pineapples and oranges as reducing agents. The evolvement of a characteristic surface plasmon extinction spectrum in the range of 420 nm to 480 nm indicates the formation of silver nanoparticles after mixing silver nitrate solution and fruit extract. Shifts in plasmon peaks over time indicate the growth of nanoparticles. Electron microscopy shows that the shapes of the nanoparticles are different depending on the fruit used for preparation. The green preparation process can result in individual nanoparticles with a very poor tendency to form aggregates with narrow gaps even when aggregation is forced by the addition of NaCl. This explains only modest enhancement factors for near-infrared-excited surface enhanced Raman scattering. In addition to the surface plasmon band, UV-visible absorption spectra show features in the UV range which indicates also the presence of small silver clusters, such as Ag4 (2+). The increase of the plasmon absorption correlates with the decrease of absorption band in the UV. This confirms the evolution of silver nanoparticles from silver clusters. The presence of various silver clusters on the surface of the "green" plasmonic silver nanoparticles is also supported by a strong multicolor luminesce signal emitted by the plasmonic particles during 473 nm excitation. PMID:25821667

  10. Noncrystalline structure of Ni-P nanoparticles prepared by liquid pulse discharge.

    PubMed

    Tan, Yuanyuan; Yu, Hongying; Wu, Zhonghua; Yang, Bin; Gong, Yu; Yan, Shi; Du, Rong; Chen, Zhongjun; Sun, Dongbai

    2015-03-01

    Noncrystalline nickel phosphide (Ni-P) nanoparticles have drawn great attention due to their high potential as catalysts. However, the structure of noncrystalline Ni-P nanoparticles is still unknown, which may shed light on explaining the catalysis mechanism of the Ni-P nanoparticles. In this paper, noncrystalline Ni-P nanoparticles were synthesized. Their morphology, particle size, element contents, local atomic structures, as well as the catalysis in the thermal decomposition of ammonium perchlorate were studied. The results demonstrate that the as-prepared Ni-P nanoparticles are spherical with an average diameter of about 13.5 nm. The Ni and P contents are, respectively, 78.15% and 21.85%. The noncrystalline nature of the as-prepared Ni-P nanoparticles can be attributed to cross-linkage between P-doping f.c.c.-like Ni centers and Ni3P-like P centers. The locally ordered Ni centers and P centers are the nuclei sites, which can explain well the origin of initial nuclei to form the crystalline phases after high-temperature annealing. The starting temperature of high-temperature decomposition of ammonium perchlorate was found having a significant decrease in the presence of the noncrystalline Ni-P nanoparticles. Therefore, the as-prepared noncrystalline Ni-P nanoparticles can be used as a potential catalyst in the thermal decomposition of ammonium perchlorate. PMID:25723939

  11. Optical investigations on indium oxide nano-particles prepared through precipitation method

    SciTech Connect

    Seetha, M.; Bharathi, S.; Dhayal Raj, A.; Mangalaraj, D.; Nataraj, D.

    2009-12-15

    Visible light emitting indium oxide nanoparticles were synthesized by precipitation method. Sodium hydroxide dissolved in ethanol was used as a precipitating agent to obtain indium hydroxide precipitates. Precipitates, thus formed were calcined at 600 deg. C for 1 h to obtain indium oxide nanoparticles. The structure of the particles as determined from the X-Ray diffraction pattern was found to be body centered cubic. The phase transformation of the prepared nanoparticles was analyzed using thermogravimetry. Surface morphology of the prepared nanoparticles was analyzed using high resolution-scanning electron microscopy and transmission electron microscopy. The results of the analysis show cube-like aggregates of size around 50 nm. It was found that the nanoparticles have a strong emission at 427 nm and a weak emission at 530 nm. These emissions were due to the presence of singly ionized oxygen vacancies and the nature of the defect was confirmed through Electron paramagnetic resonance analysis.

  12. Preparation of Pt-Ru-Ni ternary nanoparticles by microemulsion and electrocatalytic activity for methanol oxidation

    SciTech Connect

    Zhang Xin . E-mail: xzhang@stu.edu.cn; Zhang Feng; Guan Renfeng; Chan, K.-Y.

    2007-02-15

    Ternary platinum-ruthenium-nickel nanoparticles are prepared by water-in-oil reverse microemulsions of water/Triton X-100/propanol-2/cyclohexane. Nanoparticles formed in the microemulsions are characterized by transmission electron microscopy (TEM), electron diffraction (ED), X-ray diffractometry (XRD), energy dispersive X-ray analysis (EDX). These resulting materials showed a homogenous alloy structure, the mono-dispersion and an average diameter of 2.6 {+-} 0.3 nm with a narrow particle size distribution. The composition and particle size of ternary Pt-Ru-Ni nanoparticles can be controlled by adjusting the initial metal salt solution and preparation conditions. Pt-Ru-Ni ternary metallic nanoparticles showed an enhanced catalytic activity towards methanol oxidation compared to Pt-Ru bimetallic nanoparticles.

  13. Polymeric nanoparticles containing diazepam: preparation, optimization, characterization, in-vitro drug release and release kinetic study

    NASA Astrophysics Data System (ADS)

    Bohrey, Sarvesh; Chourasiya, Vibha; Pandey, Archna

    2016-03-01

    Nanoparticles formulated from biodegradable polymers like poly(lactic-co-glycolic acid) (PLGA) are being extensively investigated as drug delivery systems due to their two important properties such as biocompatibility and controlled drug release characteristics. The aim of this work to formulated diazepam loaded PLGA nanoparticles by using emulsion solvent evaporation technique. Polyvinyl alcohol (PVA) is used as stabilizing agent. Diazepam is a benzodiazepine derivative drug, and widely used as an anticonvulsant in the treatment of various types of epilepsy, insomnia and anxiety. This work investigates the effects of some preparation variables on the size and shape of nanoparticles prepared by emulsion solvent evaporation method. These nanoparticles were characterized by photon correlation spectroscopy (PCS), transmission electron microscopy (TEM). Zeta potential study was also performed to understand the surface charge of nanoparticles. The drug release from drug loaded nanoparticles was studied by dialysis bag method and the in vitro drug release data was also studied by various kinetic models. The results show that sonication time, polymer content, surfactant concentration, ratio of organic to aqueous phase volume, and the amount of drug have an important effect on the size of nanoparticles. Hopefully we produced spherical shape Diazepam loaded PLGA nanoparticles with a size range under 250 nm with zeta potential -23.3 mV. The in vitro drug release analysis shows sustained release of drug from nanoparticles and follow Korsmeyer-Peppas model.

  14. [Preparation, characterization and surface-enhanced Raman properties of agarose gel/gold nanoparticles hybrid].

    PubMed

    Ma, Xiao-yuan; Liu, Ying; Wang, Zhou-ping

    2014-08-01

    Agarose gel/gold nanoparticles hybrid was prepared by adding gold nanoparticles to preformed agarose gel. Naniocomposite structures and properties were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and UV-Vis-NIR absorption spectroscopy. Experimental data indicated a uniform distribution of gold nanoparticles adsorbed on agarose gel network And the excellent optical absorption properties were shown. Based on the swelling-contraction characteristics of agarose gel and the adjustable localized surface plasmon resonance (LSPR) of the gold nanoparticles, the nano-composites were used as surface enhanced Raman scattering (SERS) substrate to detect the Raman signal molecules Nile blue A. Results revealed that the porous structure of the agarose gel provided a good carrier for the enrichment of the gold nanoparticles. The gold nanoparticles dynamic hot-spot effect arising from the agarose gel contraction loss of water in the air greatly enhanced the Raman signal. PMID:25508727

  15. [Preparation, characterization and surface-enhanced Raman properties of agarose gel/gold nanoparticles hybrid].

    PubMed

    Ma, Xiao-yuan; Liu, Ying; Wang, Zhou-ping

    2014-08-01

    Agarose gel/gold nanoparticles hybrid was prepared by adding gold nanoparticles to preformed agarose gel. Naniocomposite structures and properties were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and UV-Vis-NIR absorption spectroscopy. Experimental data indicated a uniform distribution of gold nanoparticles adsorbed on agarose gel network And the excellent optical absorption properties were shown. Based on the swelling-contraction characteristics of agarose gel and the adjustable localized surface plasmon resonance (LSPR) of the gold nanoparticles, the nano-composites were used as surface enhanced Raman scattering (SERS) substrate to detect the Raman signal molecules Nile blue A. Results revealed that the porous structure of the agarose gel provided a good carrier for the enrichment of the gold nanoparticles. The gold nanoparticles dynamic hot-spot effect arising from the agarose gel contraction loss of water in the air greatly enhanced the Raman signal. PMID:25474948

  16. Core/shell structured ZnO/SiO2 nanoparticles: Preparation, characterization and photocatalytic property

    NASA Astrophysics Data System (ADS)

    Zhai, Jing; Tao, Xia; Pu, Yuan; Zeng, Xiao-Fei; Chen, Jian-Feng

    2010-11-01

    ZnO nanoparticles were prepared by a simple chemical synthesis route. Subsequently, SiO2 layers were successfully coated onto the surface of ZnO nanoparticles to modify the photocatalytic activity in acidic or alkaline solutions. The obtained particles were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectrometry (EDS) and zeta potential. It was found that ultrafine core/shell structured ZnO/SiO2 nanoparticles were successfully obtained. The photocatalytic performance of ZnO/SiO2 core/shell structured nanoparticles in Rhodamine B aqueous solution at varied pH value were also investigated. Compared with uncoated ZnO nanoparticles, core/shell structured ZnO/SiO2 nanoparticles with thinner SiO2 shell possess improved stability and relatively better photocatalytic activity in acidic or alkaline solutions, which would broaden its potential application in pollutant treatment.

  17. Non-linear optical properties of silver nanoparticles prepared by hydrogen reduction method

    NASA Astrophysics Data System (ADS)

    Majles Ara, M. H.; Dehghani, Z.; Sahraei, R.; Nabiyouni, G.

    2010-04-01

    Silver nanoparticles have been prepared using hydrogen gas as the reducing agent for silver nitrate and poly(vinyl pyrrolidone) as the capping agent; the reaction was carried out at 70 °C for 3 h. The size of the nanoparticles was found to be about 20 nm as analyzed using transmission electron micrographs. The X-ray diffraction pattern revealed the face-centered cubic (fcc) structure of silver nanoparticles. The linear absorption of Ag nanoparticles, α, is obtained about 3.71 cm -1. The non-linear refractive indices of silver nanoparticles were defined by the z-scan technique using CW He-Ne laser ( λ = 632.8 nm) at different incident intensities. The magnitude of non-linear refractive index ( n2) was measured to be in the order of 10 -7 (cm 2/W) with a negative sign. Therefore self-defocusing phenomena is taking placed for Ag nanoparticles.

  18. Preparation, characterization, and manipulation of iron platinum, barium titanate, and vanadium oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Morris, William Homer, III

    2008-12-01

    New synthesis strategies for preparation of FePt, BaTiO 3, VO2, V2O3, V2O5 , and V6O13 nanoparticles are presented in this thesis. Electron microscopy, diffraction, elemental analysis, and physical property measurement studies confirm the composition and structure of the synthesized material. Also reported is size-selection of ferromagnetic nanoparticles by binding PEG (2000 MW) ligand to particle surfaces and fractionally precipitating more narrowed size cuts. Large (30--100 nm) ferromagnetic nanoparticles are prepared by employing vesicle templates. Barium titanate nanoparticles with an average diameter of 3.8 nm have been synthesized within inverse micelles. A variety of vanadium oxide compositions within the nanometer size regime have been prepared using sol-gel chemistry.

  19. Preparation of highly dispersed core/shell-type titania nanocapsules containing a single Ag nanoparticle.

    PubMed

    Sakai, Hideki; Kanda, Takashi; Shibata, Hirobumi; Ohkubo, Takahiro; Abe, Masahiko

    2006-04-19

    Core/shell-type titania nanocapsules containing a single Ag nanoparticle were prepared. Ag nanoparticles were prepared using the reduction of silver nitrate with hydrazine in the presence of cetyltrimethylammonium bromide (CTAB) as protective agent. The sol-gel reaction of titanium tetraisopropoxide (TTIP) was used to prepare core/shell-type titania nanocapsules with CTAB-coated Ag nanoparticles as the core. TEM observations revealed that the size of the core (Ag particle) and the thickness of the shell (titania) of the core/shell particles obtained are about 10 nm and 5-10 nm, respectively. In addition, the nanocapsules were found to be dispersed in the medium as individual particles without aggregation. Moreover, titania coating caused the surface plasmon absorption of Ag nanoparticles to shift toward the longer wavelength side. PMID:16608315

  20. Load partitioning between ferrite/martensite and dispersed nanoparticles of a 9Cr ferritic/martensitic (F/M) ODS steel at high temperatures

    SciTech Connect

    Zhang, Guangming; Mo, Kun; Miao, Yinbin; Liu, Xiang; Almer, Jonathan; Zhou, Zhangjian; Stubbins, James F.

    2015-06-18

    In thisstudy,ahigh-energysynchrotronradiationX-raytechniquewasusedtoinvestigatethetensile deformation processesofa9Cr-ODSferritic/martensitic(F/M)steelatdifferenttemperatures.Twominor phases withinthe9Cr-ODSF/Msteelmatrixwereidentified asY2Ti2O7 and TiNbythehigh-energyX-ray diffraction, andconfirmed bytheanalysisusingenergydispersiveX-rayspectroscopy(EDS)ofscanning transmission electronmicroscope(STEM).Thelatticestrainsofthematrixandparticlesweremeasured through theentiretensiledeformationprocess.Duringthetensiletests,thelatticestrainsoftheferrite/ martensiteandtheparticles(TiNandY2Ti2O7) showedastrongtemperaturedependence,decreasing with increasingtemperature.Analysisoftheinternalstressatthreetemperaturesshowedthattheload partitioning betweentheferrite/martensiteandtheparticles(TiNandY2Ti2O7) wasinitiatedduring sample yieldingandreachedtoapeakduringsamplenecking.Atthreestudiedtemperatures,the internal stressofminorphases(Y2Ti2O7 and TiN)wasabout2timesthatofF/Mmatrixatyielding position, whiletheinternalstressofY2Ti2O7 and TiNreachedabout4.5–6 timesand3–3.5 timesthatof the F/Mmatrixatneckingposition,respectively.Itindicatesthatthestrengtheningofthematrixisdueto minor phases(Y2Ti2O7 and TiN),especiallyY2Ti2O7 particles. Althoughtheinternalstressesofallphases decreased withincreasingtemperaturefromRTto600 °C, theratioofinternalstressesofeachphaseat necking positionstayedinastablerange(internalstressesofY2Ti2O7 and TiNwereabout4.5–6 times and 3–3.5 timesofthatofF/Mmatrix,respectively).ThedifferencebetweeninternalstressoftheF/M matrix andtheappliedstressat600 °C isslightlylowerthanthoseatRTand300 °C, indicatingthatthe nanoparticles stillhavegoodstrengtheningeffectat600 °C.

  1. Characterization of soy protein nanoparticles prepared by high shear microfluidization

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soy protein nanoparticles were produced with a microfluidizer and characterized in terms of particle size, size distribution, morphology, rheological properties, and aggregate structure. Three stages of structure breakdown were observed when the soy protein dispersion was passed through the microflu...

  2. Preparation and anti-bacterial properties of a temperature sensitive gel containing silver nanoparticles

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The purpose of this study was to prepare a novel temperature-sensitive spray gel containing silver nanoparticles and investigate its anti-bacterial properties in vitro. Methods: The aqueous complex gel was prepared by Pluronic F127 (18-22%) and Pluronic F68 (3-9%) through a cold method to obtain a p...

  3. Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process

    PubMed Central

    Kim, Min-Soo; Kim, Jeong-Soo; Park, Hee Jun; Cho, Won Kyung; Cha, Kwang-Ho; Hwang, Sung-Joo

    2011-01-01

    Background The aim of this study was to improve the physicochemical properties and bioavailability of poorly water-soluble sirolimus via preparation of a solid dispersion of nanoparticles using a supercritical antisolvent (SAS) process. Methods First, excipients for enhancing the stability and solubility of sirolimus were screened. Second, using the SAS process, solid dispersions of sirolimus-polyvinylpyrrolidone (PVP) K30 nanoparticles were prepared with or without surfactants such as sodium lauryl sulfate (SLS), tocopheryl propylene glycol succinate, Sucroester 15, Gelucire 50/13, and Myrj 52. A mean particle size of approximately 250 nm was obtained for PVP K30-sirolimus nanoparticles. Solid state characterization, kinetic solubility, powder dissolution, stability, and pharmacokinetics were analyzed in rats. Results X-ray diffraction, differential scanning calorimetry, and high-pressure liquid chromatography indicated that sirolimus existed in an anhydrous amorphous form within a solid dispersion of nanoparticles and that no degradation occurred after SAS processing. The improved supersaturation and dissolution of sirolimus as a solid dispersion of nanoparticles appeared to be well correlated with enhanced bioavailability of oral sirolimus in rats. With oral administration of a solid dispersion of PVP K30-SLS-sirolimus nanoparticles, the peak concentration and AUC0→12h of sirolimus were increased by approximately 18.3-fold and 15.2-fold, respectively. Conclusion The results of this study suggest that preparation of PVP K30-sirolimus-surfactant nanoparticles using the SAS process may be a promising approach for improving the bioavailability of sirolimus. PMID:22162657

  4. Stability, size and optical properties of colloidal silver nanoparticles prepared by electrical arc discharge in water

    NASA Astrophysics Data System (ADS)

    Ashkarran, A. A.; Iraji Zad, A.; Ahadian, M. M.; Hormozi Nezhad, M. R.

    2009-10-01

    We have fabricated and characterised colloidal silver nanoparticles by the electrical arc discharge method in DI water. Size and optical properties of the silver nanoparticles were studied versus different arc currents. Optical absorption indicates a plasmonic peak at 392 nm for 10 A which increases to 398 nm for 20 A arc current. This reveals that by raising the arc current the size of the nanoparticles increases. Optical absorption of silver nanoparticles after 3 weeks shows precipitation of them in a water medium. The effect of different surfactant and stabilizer concentrations such as cethyl trimethylammonium bromide (CTAB), polyvinyl pyrrolidone (PVP), sodium citrate, sodium dodecyl sulfate (SDS), sodium di-2-ethylsulfosuccinate (AOT) and carboxymethyl cellulose (CMC) on the stability of silver nanoparticles was investigated. The colloidal silver nanoparticles with 100 μM concentration were stable for more than 3 months at 50 μM CTAB and 6 months at 10 μM sodium citrate concentration, respectively. SEM images of the sample prepared at 50 μM CTAB concentration reveal uniform and fine nanoparticles. The mean size from TEM images is about 14 nm. TEM images of the sample prepared at 10 μM sodium citrate concentration show a shell of citrate that covers the silver nanoparticles.

  5. Preparation and characterization of carvacrol loaded polyhydroxybutyrate nanoparticles by nanoprecipitation and dialysis methods.

    PubMed

    Shakeri, Fatemeh; Shakeri, Shahryar; Hojjatoleslami, Mohammad

    2014-04-01

    In this investigation, preparation of carvacrol loaded polyhydroxybutyrate (PHB) nanoparticles was performed by nanoprecipitation and dialysis methods. PHB particles were obtained by nanoprecipitation method without and with low concentration of Tween 80 or pluronic as surfactant. Nano- and micro-sized particles were formed with trimodal distribution and large aggregates. Size and distribution of nanoparticles were decreased when concentration of Tween 80 was increased to 1% (v/v) in water as polar phase. PHB nanoparticles had narrow size (157 nm) with monomodal distribution. Nanoparticles, which were prepared by dialysis method had 140 nm in diameter with monomodal distribution. Carvacrol was used as a lipophilic drug and entrapped in optimized nanoparticles formulation by nanoprecipitation and dialysis methods. Entrapment efficacy was 21% and 11%, respectively. Morphology of PHB nanoparticles was spherical. The results of kinetic release study showed that carvacrol was released for at least 3 days. Release kinetic parameters showed a simple Fickian diffusion behavior for both formulations. Carvacrol loaded PHB nanoparticles had good dispersion into the agar medium and antimicrobial activity against Escherichia coli. This study describes the 1st work on loading of carvacrol into the PHB nanoparticles by nanoprecipitation and dialysis methods. PMID:24621231

  6. Microbial mediated preparation, characterization and optimization of gold nanoparticles

    PubMed Central

    Barabadi, Hamed; Honary, Soheila; Ebrahimi, Pouneh; Mohammadi, Milad Ali; Alizadeh, Ahad; Naghibi, Farzaneh

    2014-01-01

    The need for eco-friendly and cost effective methods for nanoparticles synthesis is developing interest in biological approaches which are free from the use of toxic chemicals as byproducts. This study aimed to biosynthesize and optimize the size of gold nanoparticles which produced by biotechnological method using Penicillium crustosum isolated from soil. Initially, Penicillium crustosum was grown in fluid czapek dox broth on shaker at 28 °C and 200 rpm for ten days and then the supernatant was separated from the mycelia to convert AuCl4 solution into gold nanoparticles. The synthesized nanoparticles in the optimum conditions were formed with fairly well-defined dimensions and good monodispersity. The characterizations were done by using different methods (UV-Visible Spectroscopy, Fluorescence, FT-IR, AFM (Atomic Force Microscopy) and DLS (Dynamic Light Scattering). The bioconversion was optimized by Box-Behnken experimental design. The results show that the effective factors in this process were concentration of AuCl4, pH of medium and temperature of shaker incubator. The R2 value was calculated to be 0.9999 indicating the accuracy and ability of the polynomial model. It can be concluded that the use of multivariate analysis facilitated to find out the optimum conditions for the biosynthesis of gold nanoparticles induced by Penicillium crustosum in a time and cost effective process. The current approach suggested that rapid synthesis of gold nanoparticles would be suitable for developing a biological process for mass scale production of formulations. PMID:25763059

  7. Preparation and characterization of magnetic Fe3O4-chitosan nanoparticles loaded with isoniazid

    NASA Astrophysics Data System (ADS)

    Qin, H.; Wang, C. M.; Dong, Q. Q.; Zhang, L.; Zhang, X.; Ma, Z. Y.; Han, Q. R.

    2015-05-01

    A novel and simple method has been proposed to prepare magnetic Fe3O4-chitosan nanoparticles loaded with isoniazid (Fe3O4/CS/INH nanocomposites). Efforts have been made to develop isoniazid (INH) loaded chitosan (CS) nanoparticles by ionic gelation of chitosan with tripolyphosphate (TPP). The factors that influence the preparation of chitosan nanoparticles, including the TPP concentration, the chitosan/TPP weight ratio and the chitosan concentration on loading capacity and encapsulation efficiency of chitosan nanoparticles were studied. The magnetic Fe3O4 nanoparticles were prepared by co-precipitation method of Fe2+ and Fe3+. Then the magnetic Fe3O4/CS/INH nanocomposites were prepared by ionic gelation method. The magnetic Fe3O4 nanoparticles and magnetic Fe3O4/CS/INH nanocomposites were characterized by XRD, TEM, FTIR and SQUID magnetometry. The in vitro release of Fe3O4/CS/INH nanocomposites showed an initial burst release in the first 10 h, followed by a more gradual and sustained release for 48 h. It is suggested that the magnetic Fe3O4/CS/INH nanocomposites may be exploited as potential drug carriers for controlled-release applications in magnetic targeted drugs delivery system.

  8. Preparation and Characterization of Silver Nanoparticles from the Super-Heated Water Degraded Keratin Solutions.

    PubMed

    Zhang, Qianjie; Hu, Chunyan; Yan, Kelu

    2015-09-01

    This research demonstrates that silver nanoparticles can be prepared from the chicken feathers keratin solution obtained by superheated water treatment. Feathers are inexpensive and renewable resources but have limited applications. In this study, a facile method was described for synthesis of silver nanoparticles by the super-heated water degradation of chicken feathers keratin without using any additional chemicals. Stable and well-dispersed silver nanoparticles of about 3.24 nm were biosynthesized. The prepared nanoparticles were characterized using UV-Vis spectroscopy, transmission electron microscopy, FTIR-ATR spectroscopy and X-ray diffract. Prepared silver nanoparticles were stable on keeping at room temperature for more than 6 months and also stable in the presence of NaCl. The agglomerates caused by the decrease of pH value can easily be re-dispersed in alkaline aqueous media with no obvious change in their optical properties. The as-prepared silver nanoparticles have excellent antibacterial property reducing the bacterial population with more than 99.99%. PMID:26716245

  9. Preparation of compact nanoparticle clusters from polyethylene glycol-coated gold nanoparticles by fine-tuning colloidal interactions.

    PubMed

    Zmb, Dniel; Radnczi, Gyrgy Z; Dek, Andrs

    2015-03-10

    Low-molecular weight polyethylene glycol (PEG) has a lower critical solution temperature well outside the boiling point of water at ambient pressure, but it can be reduced at high ionic strengths. We extend this concept to trigger the clustering of gold nanoparticles through the control of colloidal interactions. At high ionic strengths, low-molecular weight (<2000 Da) mPEG-SH-modified gold nanoparticles show clustering with an increase in the solution temperature. The clustering temperature decreases with an increasing ionic strength. The clustering is attributed to the delicate interplay between the high ionic strength and elevated temperature and is interpreted in terms of chain collapse of the surface-grafted PEG molecules. The chain collapse results in a change in the steric interaction term, whereas the high ionic strength eliminates the double-layer repulsion between the particles. The observations are backed by nanoparticle interaction model calculations. We found that the intermediate attractive potential on the order of a few kT allows the experimental fabrication of compact nanoparticle clusters in agreement with theoretical predictions. The approach presented here has the potential to be extended on the externally triggered preparation of nanoparticle clusters with different types of nanoparticles. PMID:25686160

  10. Development of alpha-tocopherol acetate nanoparticles: influence of preparative processes.

    PubMed

    Anais, J P; Razzouq, N; Carvalho, M; Fernandez, C; Astier, A; Paul, M; Astier, A; Fessi, H; Lorino, A M

    2009-02-01

    We studied different methods of preparing alpha-tocopherol acetate (ATA) nanoparticles, which are to be used in targeting the lungs as aerosols in order to prevent cigarette smoke toxicity. Poly-(lactide) nanoparticles were prepared using nanoprecipitation and solvent evaporation techniques, which produced, respectively, too small and too large nanoparticles to be aerosolized. The emulsification-diffusion method produced 2 months stable nanoparticles with a size between (500-700 nm). Increasing ATA concentration (1-7 mg/mL) induced a decrease in the association rate (97-93%) and in the adsorbed ATA rate (7-4.5%), which was associated with variations of Zeta potentials (-27.5 to -24.3 mV) and decrease in polymeric wall thickness and density. PMID:19169943

  11. Preparation and characterization of ketoprofen loaded eudragit RS polymeric nanoparticles for controlled release

    NASA Astrophysics Data System (ADS)

    Anh, Nguyen Tuan; Chi, Nguyen T.; Khai Tran, T.; Tuyen Dao, T. P.; Nhan Le, N. T.; Mau Chien, Dang; Hoai, Nguyen To

    2012-12-01

    Nanospheres containing ketoprofen (Keto) and polymer eudragit RS were prepared using an emulsion solvent evaporation method. The ultrasonic probe (VCX500, vibracell) was used as a tool to disperse oil phase into aqueous phase leading to water/oil emulsion. Nanoparticles were successfully prepared and their morphologies and diameters were confirmed by transmission electron microscope (TEM) and dynamic light scattering (DLS), respectively. The result showed that particles were spherical with submicron size. The particle size was dependent on the RS concentration, emulsification tools and the types of organic solvents. For the encapsulation ability, Keto-loaded RS nanoparticle showed 9.8% of Keto in nanoparticle, which was evaluated by high-performance liquid chromatography (HPLC). Moreover, the drug release behavior of Keto-loaded eudragit RS nanoparticle was also investigated in vitro at pH 7.4 and compared to referential profenid.

  12. Preparation of cobalt nanoparticles from polymorphic bacterial templates: A novel platform for biocatalysis.

    PubMed

    Jang, Eunjin; Shim, Hyun-Woo; Ryu, Bum Han; An, Deu Rae; Yoo, Wan Ki; Kim, Kyeong Kyu; Kim, Dong-Wan; Kim, T Doohun

    2015-11-01

    Nanoparticles have gathered significant research attention as materials for enzyme immobilization due to their advantageous properties such as low diffusion rates, ease of manipulation, and large surface areas. Here, polymorphic cobalt nanoparticles of varied sizes and shapes were prepared using Micrococcus lylae, Bacillus subtilis, Escherichia coli, Paracoccus sp., and Haloarcula vallismortis as bacterial templates. Furthermore, nine lipases/carboxylesterases were successfully immobilized on these cobalt nanoparticles. Especially, immobilized forms of Est-Y29, LmH, and Sm23 were characterized in more detail for potential industrial applications. Immobilization of enzymes onto cobalt oxide nanoparticles prepared from polymorphic bacterial templates may have potential for efficient hydrolysis on an industrial-scale, with several advantages such as high retention of enzymatic activity, increased stability, and strong reusability. PMID:26358553

  13. Preparation of lisinopril-capped gold nanoparticles for molecular imaging of angiotensin-converting enzyme

    NASA Astrophysics Data System (ADS)

    Li, Yuan; Baeta, Cesar; Aras, Omer; Daniel, Marie-Christine

    2009-05-01

    Overexpression of angiotensin-converting enzyme (ACE) has been associated with the pathophysiology of cardiac and pulmonary fibrosis. Moreover, the prescription of ACE inhibitors, such as lisinopril, has shown a favorable effect on patient outcome for patients with heart failure or systemic hypertension. Thus targeted imaging of the ACE would be of crucial importance for monitoring tissue ACE activity as well as the treatment efficacy in heart failure. In this respect, lisinopril-coated gold nanoparticles were prepared to provide a new type of probe for targeted molecular imaging of ACE by tuned K-edge computed tomography (CT) imaging. The preparation involved non-modified lisinopril, using its primary amine group as the anchoring function on the gold nanoparticles surface. The stable lisinopril-coated gold nanoparticles obtained were characterized by UV-vis spectroscopy, dynamic light scattering (DLS), transmission electron microscopy (TEM). Their zeta potential was also measured in order to assess the charge density on the modified gold nanoparticles (GNPs).

  14. Sample preparation and EFTEM of Meat Samples for Nanoparticle Analysis in Food

    NASA Astrophysics Data System (ADS)

    Lari, L.; Dudkiewicz, A.

    2014-06-01

    Nanoparticles are used in industry for personal care products and the preparation of food. In the latter application, their functions include the prevention of microbes' growth, increase of the foods nutritional value and sensory quality. EU regulations require a risk assessment of the nanoparticles used in foods and food contact materials before the products can reach the market. However, availability of validated analytical methodologies for detection and characterisation of the nanoparticles in food hampers appropriate risk assessment. As part of a research on the evaluation of the methods for screening and quantification of Ag nanoparticles in meat we have tested a new TEM sample preparation alternative to resin embedding and cryo-sectioning. Energy filtered TEM analysis was applied to evaluate thickness and the uniformity of thin meat layers acquired at increasing input of the sample demonstrating that the protocols used ensured good stability under the electron beam, reliable sample concentration and reproducibility.

  15. Preparation and biomedical applications of core-shell silica/magnetic nanoparticle composites.

    PubMed

    Li, Chuanyan; Ma, Chao; Wang, Fang; Xil, Zhijiang; Wang, Zhifei; Deng, Yan; Hel, Nongyue

    2012-04-01

    Core-shell structured silica/magnetic nanoparticle composites have recently been subjected to extensive research since the shells could offer protection to the cores and introduce new properties to the hybrid structures, which endue them with great application potentials in various fields. Several approaches have been studied for the synthesis of SiO2 coated on magnetic nanoparticles. These approaches include Stöber process, microemulsion, sodium silicate and tetraethoxysilane hydrolysis, aerosol pyrolysis, layer-by-layer strategy, polymer-templating and sonochemical deposition. This review is focused on describing state-of-the-art synthetic routes and methods for the preparation of silica/magnetic nanoparticle composites. Furthermore, we also introduce main applications of these nanoparticle composites in biomedical scopes and address some challenges in the synthesis of high-quality magnetic nanoparticles. PMID:22849053

  16. Synthesis and characterization of nickel nanoparticles prepared using the aquolif approach.

    PubMed

    Menezes, J C A; Ferreira, N S; Abraçado, L G; Macêdo, M A

    2014-08-01

    We report on the synthesis of nickel nanoparticles using a combination of chemical reduction and freezing-drying processes that we named the aquolif approach. The X-ray diffraction (XRD) patterns reveal that the synthesized nanoparticles were composed of a single metallic nickel phase. The average crystallite sizes of the nickel nanoparticles were determined using the Scherrer method. The average crystallite sizes increased from 8±3 to 16±3 nm as the annealing temperature increased, which is consistent with the XRD and transmission electron microscopy results. The zero-field-cooling and field-cooling (ZFC-FC) magnetization curves reveal that the nickel nanoparticles exhibited superparamagnetic behavior with a high blocking temperature and a surface effect at lower temperatures. Our experimental results demonstrate that the aquolif approach can be successfully scaled up to industrially prepare other types of metallic nanoparticles. PMID:25936025

  17. Solid Lipid Nanoparticles and Nanostructured Lipid Carriers: Structure, Preparation and Application

    PubMed Central

    Naseri, Neda; Valizadeh, Hadi; Zakeri-Milani, Parvin

    2015-01-01

    Lipid nanoparticles (LNPs) have attracted special interest during last few decades. Solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) are two major types of Lipid-based nanoparticles. SLNs were developed to overcome the limitations of other colloidal carriers, such as emulsions, liposomes and polymeric nanoparticles because they have advantages like good release profile and targeted drug delivery with excellent physical stability. In the next generation of the lipid nanoparticle, NLCs are modified SLNs which improve the stability and capacity loading. Three structural models of NLCs have been proposed. These LNPs have potential applications in drug delivery field, research, cosmetics, clinical medicine, etc. This article focuses on features, structure and innovation of LNPs and presents a wide discussion about preparation methods, advantages, disadvantages and applications of LNPs by focusing on SLNs and NLCs. PMID:26504751

  18. Structural, magnetic and electrical characterization of Mg-Ni nano-crystalline ferrites prepared through egg-white precursor

    NASA Astrophysics Data System (ADS)

    Gabal, M. A.; Al Angari, Y. M.; Zaki, H. M.

    2014-08-01

    Soft Ni-Mg nano-crystalline ferrites with the general formula Ni1-xMgxFe2O4 (0≤x≤1) were synthesized through egg-white method. The precursor decomposition was followed by thermal analysis techniques. The obtained ferrites were characterized by X-ray diffraction, Fourier transform infrared and transmission electron microscopy measurements. X-ray diffraction showed the cubic spinel structure with crystallite size variation within the range 20-45 nm. The different structural data obtained were discussed in the view of ionic radii of the entire ions and their distribution within the lattice. The appropriate suggested cation distribution was then confirmed through Fourier transform infrared as well as electrical and magnetic properties measurements. Transmission electron microscopy exhibited a nano-crystal aggregation phenomenon. The observed size of the spherical particles agrees well with that obtained by X-ray diffraction. Hysteresis loop measurements revealed dilution in the obtained magnetic parameters by Mg-substitution due to the preferential occupancy of Mg2+ ions by the octahedral sites. Ac-electrical conductivity as a function of temperature and frequency exhibited a semi-conducting behavior with conductivity decreases by increasing Mg-content. The change in the slope of the curve indicates the changing in the conduction mechanism from electron hopping to polaron mechanism by increasing temperature. The obtained structural, electrical and magnetic properties were explained based on the cation distribution among tetrahedral and octahedral sites.

  19. Preparation and characterization of polymeric nanoparticles from Gadong starch

    SciTech Connect

    Sisika, Regina; Ahmad, Wan Yaacob Wan; Lazim, Azwan Mat; Fazry, Shazrul

    2015-09-25

    Dioscorea hispida (Gadong tuber) was seldom used and forgotten as a food source due to their toxicity. In contrast to that, the Gadong tuber can be a source of polysaccharides which can be manipulated as an alternative source for industrial applications. This research reported on how to synthesize starch nanoparticles from Gadong tuber by using a simple acid hydrolysis process. The yield of starch nanoparticles obtained from seven days of acid hydrolysis was reduced to 13%. The X-ray diffraction measurements showed that the native Gadong starch particle is of the C-crystalline type, and that the synthesized nanoparticles showed an increase in crystallinity compared to the native particles. Transmission electron microscopy results demonstrated that the starch particle morphologies were either round or irregular shape, with diameters ranging from 96-110 nm.

  20. Preparation and characterization of polymeric nanoparticles from Gadong starch

    NASA Astrophysics Data System (ADS)

    Sisika, Regina; Ahmad, Wan Yaacob Wan; Fazry, Shazrul; Lazim, Azwan Mat

    2015-09-01

    Dioscorea hispida (Gadong tuber) was seldom used and forgotten as a food source due to their toxicity. In contrast to that, the Gadong tuber can be a source of polysaccharides which can be manipulated as an alternative source for industrial applications. This research reported on how to synthesize starch nanoparticles from Gadong tuber by using a simple acid hydrolysis process. The yield of starch nanoparticles obtained from seven days of acid hydrolysis was reduced to 13%. The X-ray diffraction measurements showed that the native Gadong starch particle is of the C-crystalline type, and that the synthesized nanoparticles showed an increase in crystallinity compared to the native particles. Transmission electron microscopy results demonstrated that the starch particle morphologies were either round or irregular shape, with diameters ranging from 96-110 nm.

  1. Electromagnetic properties of low-temperature-sintered Ba 3Co 2- xZn xFe 24O 41 ferrites prepared by solid state reaction method

    NASA Astrophysics Data System (ADS)

    Wang, Xiaohui; Li, Longtu; Su, Shuiyuan; Yue, Zhenxing

    2004-09-01

    Hexagonal ferrites Ba 3Co 2- xZn xFe 24O 41 ( X=0-2.0) were prepared by a solid state reaction method. The influences of Zn content ( X) on the Z-type phase formation temperature and specific saturation magnetization were investigated. With a small amount of sintering aids, highly dense hexaferrite ceramics with fine-grained microstructure were obtained after sintering at a relatively low temperature below 900°C. The hexaferrite ceramics show excellent high-frequency properties such as high initial permeability up to 10, high cut-off frequency over 1.1 GHz and good DC resistivity more than 10 9 Ω cm .

  2. Influence of PVP in magnetic properties of NiSn nanoparticles prepared by polyol method

    NASA Astrophysics Data System (ADS)

    Bobadilla, L. F.; García, C.; Delgado, J. J.; Sanz, O.; Romero-Sarria, F.; Centeno, M. A.; Odriozola, J. A.

    2012-11-01

    The influence of PVP on the magnetic properties of NiSn nanoparticles prepared by polyol method has been studied. NiSn nanoparticles exhibit superparamagnetic behavior although there is a ferromagnetic contribution due to particles agglomerated below the blocking temperature. The particle size is controlled by the addiction of PVP in varying amounts. The addition of PVP also favours the particles isolation, narrow the particle size distribution and decrease the interparticle interaction strength increasing the superparamagnetic contribution.

  3. Effects of Microemulsion Preparation Conditions on Drug Encapsulation Efficiency of PLGA Nanoparticles

    NASA Astrophysics Data System (ADS)

    Ng, Set Hui; Ooi, Ing Hong

    2011-12-01

    Emulsion solvent evaporation technique is widely used to prepare nanoparticles of many organic polymer drug carriers. The mechanism of nanoparticle generation by this technique involves oil-in-water (O/W) microemulsion formation followed by solvent evaporation. Various microemulsion preparation conditions can affect the encapsulation efficiency of drug in the nanoparticulate carrier. In this study, emulsifying speed, emulsifying temperature, and organic-to-aqueous phase ratio were varied and the resulting encapsulation efficiency of a model drug in Poly(Lactide-co-Glycolide) (PLGA) nanoparticles was determined. The organic phase containing PLGA and a model drug dissolved in chloroform was first dispersed in an aqueous solution containing 0.5 %(w/v) Poly(vinyl alcohol) (PVA), which was then homogenized at high speeds. The resulting O/W microemulsion was subsequently subjected to stirring at room temperature for four hours during which the solvent diffused and evaporated gradually. The fine white suspension was centrifuged and freeze-dried. The model drug loading in the PLGA nanoparticles was determined using UV spectrophotometry. Results showed that the encapsulation efficiency of a model drug, salicylic acid, ranged from 8.5% to 17% depending on the microemulsion preparation conditions. Under the same temperature (15 °C) and homogenization speed (19000 rpm) conditions studied, a relatively high organic-to-aqueous phase ratio (1:5) provided salicylic acid loaded PLGA nanoparticles with significantly higher drug encapsulation efficiency. In addition, under all microemulsion preparation conditions, PLGA nanoparticles obtained after solvent evaporation and freeze drying were spherical and aggregation between the nanoparticles was not observed under a high power microscope. This indicates that PLGA nanoparticles with desirable amount of drug and with anticipated size and shape can be realized by controlling emulsification process conditions.

  4. Preparation and properties of superparamagnetic nanoparticles with narrow size distribution and biocompatible

    NASA Astrophysics Data System (ADS)

    Jiang, Wanquan; Yang, H. C.; Yang, S. Y.; Horng, H. E.; Hung, J. C.; Chen, Y. C.; Hong, Chin-Yih

    2004-12-01

    A chemical co-precipitation method capable of controlling the average size and size distribution of magnetic Fe3O4 nano-particles was developed. It was found that the homogeneous variation of the pH value in the solution plays a role in the size distribution of the synthesized Fe3O4 particles. In this work, we added urea to the ferrite solution, followed by heating the solution to decompose the urea before titrating a base solution into the ferrite solution. Thus, the variation in pH value in the solution can become uniform, and the uniformity in the particles size can be greatly enhanced. In addition, the average particle size is adjustable via control of the amount of urea decomposing at one time. To be biocompatible, dextran is selected as the surfactant for the Fe3O4 particles, because of its non-toxicity and high bio-affinity. The desired bio-probes can be coated on the dextran layer through adequate chemical reactions.

  5. Multiplexed TEM Specimen Preparation and Analysis of Plasmonic Nanoparticles

    PubMed Central

    Cheng, Anchi; Crum, John; Jain, Tilak; Duggan, Erika; Liu, Er; Nolan, John P.; Carragher, Bridget; Potter, Clinton S.

    2015-01-01

    We describe a system for rapidly screening hundreds of nanoparticle samples using transmission electron microscopy (TEM). The system uses a liquid handling robot to place up to 96 individual samples onto a single standard TEM grid at separate locations. The grid is then transferred into the TEM and automated software is used to acquire multi-scale images of each sample. The images are then analyzed to extract metrics on the size, shape, and morphology of the nanoparticles. The system has been used to characterize plasmonically-active nanomaterials. PMID:26223550

  6. Magnetic properties of isolated Co nanoparticles in SiO 2 capsule prepared with reversed micelle

    NASA Astrophysics Data System (ADS)

    Haeiwa, Tetsuji; Segawa, Kazuhiro; Konishi, Kenji

    Magnetic properties and thermal stability of cobalt nanoparticles encapsulated in SiO 2 prepared with the reversed micelle technique with various w were investigated. The average diameters of the Co nanoparticles and SiO 2 capsules were about 2.9 and about 5.2 nm. The magnetization curves of Co nanoparticles exhibit superparamagnetic nature. After annealing up to 673 K in vacuum, the magnetization increases by a factor of 2.4 and the average diameter of the Co particles increases by a factor of 1.3, although shape and size of the SiO 2 capsules were kept.

  7. Surface-modified superparamagnetic nanoparticles for drug delivery: preparation, characterization, and cytotoxicity studies.

    PubMed

    Gupta, Ajay Kumar; Wells, Stephen

    2004-03-01

    Superparamagnetic iron oxide nanoparticles have been used for many years as magnetic resonance imaging (MRI) contrast agents or in drug delivery applications. In this study, a novel approach to prepare magnetic polymeric nanoparticles with magnetic core and polymeric shell using inverse microemulsion polymerization process is reported. Poly(ethyleneglycol) (PEG)-modified superparamagnetic iron oxide nanoparticles with specific shape and size have been prepared inside the aqueous cores of AOT/n-Hexane reverse micelles and characterized by various physicochemical means such as transmission electron microscopy (TEM), infrared spectroscopy, atomic force microscopy (AFM), vibrating sample magnetometry (VSM), and ultraviolet/visible spectroscopy. The inverse microemulsion polymerization of a polymerizable derivative of PEG and a cross-linking agent resulted in a stable hydrophilic polymeric shell of the nanoparticles. The results taken together from TEM and AFM studies showed that the particles are spherical in shape with core-shell structure. The average size of the PEG-modified nanoparticles was found to be around 40-50 nm with narrow size distribution. The magnetic measurement studies revealed the superparamagnetic behavior of the nanoparticles with saturation magnetization values between 45-50 electromagnetic units per gram. The cytotoxicity profile of the nanoparticles on human dermal fibroblasts as measured by standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay showed that the particles are nontoxic and may be useful for various in vivo and in vitro biomedical applications. PMID:15382647

  8. Preparation of magnetic Fe3O4@SiO2 nanoparticles for immobilization of lipase.

    PubMed

    Liu, Wei; Zhou, Fang; Zhang, Xiao-Yun; Li, Yue; Wang, Xiang-Yu; Xu, Xi-Ming; Zhang, Ye-Wang

    2014-04-01

    Magnetic Fe3O4 nanoparticles were prepared with coprecipitatation method and covered with SiO2 to form the core-shell Fe3O4@SiO2 nanoparticles. Then the nanoparticles were modified with glutaradehyde for functionalization of the surface to aldehyde groups. The transmission electron microscopy confirmed the core-shell structure and revealed that the size of the nanoparticles was around 10 nm. It was observed that the lipase was immobilized on the nanoparticles successfully from the Fourier transform infrared spectra. The immobilized lipase on Fe3O4@SiO2 nanoparticles was characterized and compared to free enzyme. There are no significant differences observed in the optimal pH, temperature and Km before and after immobilization. However, the immobilized lipase displayed higher relative activity in the range of pH from 7.0 to 9.5. Compare with the free enzyme, the immobilized one showed higher thermal stability at temperature range from 30 to 70 degrees C, especially at high temperature. The relative activity of immobilized enzyme was 5.8 fold of the free lipase at 70 degrees C after 10 h incubation. Thus, the prepared lipase was proved to have the advantages like higher relative activity, better stability, broader pH range and easy to recovery. These results suggest that immobilization of lipase on Fe3O4@SiO2 nanoparticles has the potential industrial applications. PMID:24734736

  9. Organic colloid method to prepare ultrafine cobalt nanoparticles with the size of 2 nm

    NASA Astrophysics Data System (ADS)

    Li, Hao; Liao, Shijun

    2008-01-01

    Ultrafine Co nanoparticles with the size of ca. 2 nm were prepared by an organic colloid method, in which sodium formate acted as reducing agent, ethylene glycol acted as solvent, sodium citrate acted as both complexing agent and stabilizing agent, respectively. X-ray diffraction (XRD) analysis indicated that the as-prepared Co nanoparticles were in hexagonal close-packed phase, and transmission electron microscope (TEM) images revealed that the size of the well-dispersed Co nanoparticles was as small as 2 nm, and the sizes were distributed in a very narrow region. The hysteresis loop of the as-prepared Co sample measured at room temperature showed a superparamagnetic behavior due to the extremely small size of the products. It was revealed that sodium citrate played a crucial role in decreasing the particle size and narrowing the size distribution.

  10. Preparation and characterization of platinum-ruthenium bimetallic nanoparticles using reverse microemulsions for fuel cell catalyst.

    PubMed

    Kim, Taeyoon; Kobayashi, Koichi; Nagai, Masayuki

    2007-01-01

    Platinum-ruthenium bimetallic nanoparticles are prepared by chemical reduction using sodium borohydride in reverse microemulsions of water/isooctane/Igepal CA-630/2-propanol for fuel cell catalysts. The prepared nanoparticles are characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and energy-dispersive X-ray analysis. The average size and morphology of nanoparticles are dependent on the water volume fraction in reverse microemulsion system in the range of ca. 2-4 nm. The morphology of particles is related with the percolation behavior of water droplets in reverse microemulsions. By the pretreatment of water phase using a hydrochloric acid, the particles of a homogeneous solid solution state can be obtained. The CO stripping cyclovoltammetry and the electrochemical measurements compared with commercial catalyst show that the prepared particles have a high electrochemically active surface area and a stable and high catalytic activity for reformate gas oxidation. PMID:17898462

  11. Anomalous magnetic behaviour of zinc and chromium ferrites without any hyperfine splitting

    NASA Astrophysics Data System (ADS)

    Pandey, B.; Verma, H. C.

    2008-04-01

    Two groups of ferrite namely zinc ferrite and chromium ferrite were synthesized by citrate precursor route in the size range of 8 to 35 nm. We have studied the structural and magnetic behaviour of these ferrites using X-ray diffraction (XRD), vibrating sample magnetometer (VSM) and Mössbauer spectroscopic techniques. Our studies show that the nanocrystalline ferrites interact with the hand magnet strongly and give large magnetization in the VSM measurement. The maximum magnetization in the samples sensitively depends on the particle size of synthesized ferrites. We observed as large as 28 Am2/kg of magnetization in the zinc ferrite nanoparticles while that in chromium ferrite is around 11 Am2/kg. In spite of the large magnetization in the zinc ferrite nanoparticles we did not observe any hyperfine splitting even down to 12 K of temperature. Similar behaviour is also observed for chromium ferrite down to 16 K.

  12. Preparation of Gold Nanoparticles Using Tea: A Green Chemistry Experiment

    ERIC Educational Resources Information Center

    Sharma, R. K.; Gulati, Shikha; Mehta, Shilpa

    2012-01-01

    Assimilating green chemistry principles in nanotechnology is a developing area of nanoscience research nowadays. Thus, there is a growing demand to develop environmentally friendly and sustainable methods for the synthesis of nanoparticles that utilize nontoxic chemicals, environmentally benign solvents, and renewable materials to avoid their…

  13. Preparation of Gold Nanoparticles Using Tea: A Green Chemistry Experiment

    ERIC Educational Resources Information Center

    Sharma, R. K.; Gulati, Shikha; Mehta, Shilpa

    2012-01-01

    Assimilating green chemistry principles in nanotechnology is a developing area of nanoscience research nowadays. Thus, there is a growing demand to develop environmentally friendly and sustainable methods for the synthesis of nanoparticles that utilize nontoxic chemicals, environmentally benign solvents, and renewable materials to avoid their

  14. Streptomycin-loaded PLGA-alginate nanoparticles: preparation, characterization, and assessment

    NASA Astrophysics Data System (ADS)

    Asadi, Asadollah

    2013-04-01

    The aim of this study was to formulate and characterize streptomycin-loaded PLGA-alginate nanoparticles for their potential therapeutic use in Salmonella subsp. enterica ATCC 14028 infections. The streptomycin nanoparticle was prepared by solvent diffusion method, and the other properties such as size, zeta potential, loading efficacy, release kinetics, and antimicrobial strength were evaluated. The survey shows that nanoparticles may serve as a carrier of streptomycin and may provide localized antibacterial activity in the treatment of Salmonellosis. Electron microscopy showed spherical particles with indentations. The average size of the nanoparticles was 90 nm. At pH 7.2, the release kinetics of streptomycin from the nanoparticles was successfully illustrated as an initial burst defined by a first order equation that after this stage, it has a drastic tendency to obtain steady state. Nevertheless, nanoparticles showed loading efficacy nearly about 70-75 %. In addition, the tendency of concentration of streptomycin released from nanoparticles to reach antibacterial activity was similar to that of free streptomycin against PLGA-alginate, but it had threefold more antimicrobial strength in comparison with free streptomycin. This work shows the potential use of streptomycin-loaded PLGA-alginate nanoparticles and its capability.

  15. Streptomycin-loaded PLGA-alginate nanoparticles: preparation, characterization, and assessment

    NASA Astrophysics Data System (ADS)

    Asadi, Asadollah

    2014-04-01

    The aim of this study was to formulate and characterize streptomycin-loaded PLGA-alginate nanoparticles for their potential therapeutic use in Salmonella subsp. enterica ATCC 14028 infections. The streptomycin nanoparticle was prepared by solvent diffusion method, and the other properties such as size, zeta potential, loading efficacy, release kinetics, and antimicrobial strength were evaluated. The survey shows that nanoparticles may serve as a carrier of streptomycin and may provide localized antibacterial activity in the treatment of Salmonellosis. Electron microscopy showed spherical particles with indentations. The average size of the nanoparticles was 90 nm. At pH 7.2, the release kinetics of streptomycin from the nanoparticles was successfully illustrated as an initial burst defined by a first order equation that after this stage, it has a drastic tendency to obtain steady state. Nevertheless, nanoparticles showed loading efficacy nearly about 70-75 %. In addition, the tendency of concentration of streptomycin released from nanoparticles to reach antibacterial activity was similar to that of free streptomycin against PLGA-alginate, but it had threefold more antimicrobial strength in comparison with free streptomycin. This work shows the potential use of streptomycin-loaded PLGA-alginate nanoparticles and its capability.

  16. Preparation and Antibacterial Activity Evaluation of 18-β-glycyrrhetinic Acid Loaded PLGA Nanoparticles

    PubMed Central

    Darvishi, Behrad; Manoochehri, Saeed; Kamalinia, Golnaz; Samadi, Nasrin; Amini, Mohsen; Mostafavi, Seyyed Hossein; Maghazei, Shahab; Atyabi, Fatemeh; Dinarvand, Rassoul

    2015-01-01

    The aim of the present study was to formulate poly (lactide-co-glycolide) (PLGA) nanoparticles loaded with 18-β-glycyrrhetinic acid (GLA) with appropriate physicochemical properties and antimicrobial activity. GLA loaded PLGA nanoparticles were prepared with different drug to polymer ratios, acetone contents and sonication times and the antibacterial activity of the developed nanoparticles was examined against different gram-negative and gram-positive bacteria. The antibacterial effect was studied using serial dilution technique to determine the minimum inhibitory concentration of nanoparticles. Results demonstrated that physicochemical properties of nanoparticles were affected by the above mentioned parameters where nanoscale size particles ranging from 175 to 212 nm were achieved. The highest encapsulation efficiency (53.2 ± 2.4%) was obtained when the ratio of drug to polymer was 1:4. Zeta potential of the developed nanoparticles was fairly negative (-11±1.5). In-vitro release profile of nanoparticles showed two phases: an initial phase of burst release for 10 h followed by a slow release pattern up to the end. The antimicrobial results revealed that the nanoparticles were more effective than pure GLA against P. aeuroginosa, S. aureus and S. epidermidis. This improvement in antibacterial activity of GLA loaded nanoparticles when compared to pure GLA may be related to higher nanoparticles penetration into infected cells and a higher amount of GLA delivery in its site of action. Herein, it was shown that GLA loaded PLGA nanoparticles displayed appropriate physicochemical properties as well as an improved antimicrobial effect. PMID:25901144

  17. Preparation and Antibacterial Activity Evaluation of 18-β-glycyrrhetinic Acid Loaded PLGA Nanoparticles.

    PubMed

    Darvishi, Behrad; Manoochehri, Saeed; Kamalinia, Golnaz; Samadi, Nasrin; Amini, Mohsen; Mostafavi, Seyyed Hossein; Maghazei, Shahab; Atyabi, Fatemeh; Dinarvand, Rassoul

    2015-01-01

    The aim of the present study was to formulate poly (lactide-co-glycolide) (PLGA) nanoparticles loaded with 18-β-glycyrrhetinic acid (GLA) with appropriate physicochemical properties and antimicrobial activity. GLA loaded PLGA nanoparticles were prepared with different drug to polymer ratios, acetone contents and sonication times and the antibacterial activity of the developed nanoparticles was examined against different gram-negative and gram-positive bacteria. The antibacterial effect was studied using serial dilution technique to determine the minimum inhibitory concentration of nanoparticles. Results demonstrated that physicochemical properties of nanoparticles were affected by the above mentioned parameters where nanoscale size particles ranging from 175 to 212 nm were achieved. The highest encapsulation efficiency (53.2 ± 2.4%) was obtained when the ratio of drug to polymer was 1:4. Zeta potential of the developed nanoparticles was fairly negative (-11±1.5). In-vitro release profile of nanoparticles showed two phases: an initial phase of burst release for 10 h followed by a slow release pattern up to the end. The antimicrobial results revealed that the nanoparticles were more effective than pure GLA against P. aeuroginosa, S. aureus and S. epidermidis. This improvement in antibacterial activity of GLA loaded nanoparticles when compared to pure GLA may be related to higher nanoparticles penetration into infected cells and a higher amount of GLA delivery in its site of action. Herein, it was shown that GLA loaded PLGA nanoparticles displayed appropriate physicochemical properties as well as an improved antimicrobial effect. PMID:25901144

  18. Electromagnetic properties of samarium-substituted NiCuZn ferrite prepared by auto-combustion method

    NASA Astrophysics Data System (ADS)

    Roy, P. K.; Bera, J.

    2009-02-01

    Ni 0.25Cu 0.2Zn 0.55Sm xFe 2-xO 4 ferrite with x=0.00, 0.025, 0.05 and 0.075 compositions were synthesized through the nitrate-citrate auto-combustion method. These powders were calcined, compacted and sintered at 900 °C for 4 h. Effect of Sm substitution on phase composition, microstructure and relative density were studied. Permeability, magnetic loss and AC resistivity were measured in the frequency range of 1 kHz-10 MHz. Permeability and AC resistivity were found to increase and loss decreased with Sm substitution up to x=0.05. Saturation magnetization also increased up to that substitution limit. Observed variations in electromagnetic properties have been explained.

  19. Characterization of perovskite film prepared by pulsed laser deposition on ferritic stainless steel using microscopic and optical methods

    NASA Astrophysics Data System (ADS)

    Durda, E.; Jaglarz, J.; Kąc, S.; Przybylski, K.; El Kouari, Y.

    2016-06-01

    The perovskite La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF48) film was deposited on Crofer 22 APU ferritic stainless steel by pulsed laser deposition (PLD). Morphological studies of the sample were performed using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Information about film thickness and surface topography of the film and the steel substrate were obtained using following optical methods: spectroscopic ellipsometry (SE), bidirectional reflection distribution function (BRDF) and total integrated reflectometry (TIS). In particular, the BRDF study, being complementary to atomic force microscopy, yielded information about surface topography. Using the previously mentioned methods, the following statistic surface parameters were determined: root-mean square (rms) roughness and autocorrelation length by determining the power spectral density (PSD) function of surface irregularities.

  20. Effect of PVP on the low temperature bonding process using polyol prepared Ag nanoparticle paste for electronic packaging application

    NASA Astrophysics Data System (ADS)

    Yan, Jianfeng; Zou, Guisheng; Wu, Aiping; Ren, Jialie; Yan, Jiuchun; Hu, Anming; Liu, Lei; Zhou, Y. Norman

    2012-08-01

    There has been an increasing interest in developing low temperature interconnection process using metal nanoparticles. In this study the Ag nanoparticles (NPs) for this low temperature bonding process applications were prepared based on the polyol method using polyvinylpyrrolidone (PVP) as the protecting agent. The effect of PVP on the Ag nanoparticle size, nanoparticle solution viscosity and the bondability of the Ag nanoparticle paste were studied. The silver nanoparticle with diameter of 90 nm, 40 nm and 20 nm were synthesized by adjusting PVP concentration. The bonding processes using different kind of Ag nanoparticle paste were conducted. The joint with shear strength of 50 MPa were formed using Ag nanoparticle (NP) paste prepared with appropriate PVP concentration.

  1. NMR-D study of the local spin dynamics and magnetic anisotropy in different nearly monodispersed ferrite nanoparticles.

    PubMed

    Bordonali, L; Kalaivani, T; Sabareesh, K P V; Innocenti, C; Fantechi, E; Sangregorio, C; Casula, M F; Lartigue, L; Larionova, J; Guari, Y; Corti, M; Arosio, P; Lascialfari, A

    2013-02-13

    We present a systematic experimental comparison of the superparamagnetic relaxation time constants obtained by means of dynamic magnetic measurements and (1)H-NMR relaxometry, on ferrite-based nanosystems with different composition, various core sizes and dispersed in different solvents. The application of a heuristic model for the relaxivity allowed a comparison between the reversal time of magnetization as seen by NMR and the results from the AC susceptibility experiments, and an estimation of fundamental microscopic properties. A good agreement between the NMR and AC results was found when fitting the AC data to a Vogel-Fulcher law. Key parameters obtained from the model have been exploited to evaluate the impact of the contribution from magnetic anisotropy to the relaxivity curves and estimate the minimum approach distance of the bulk solvent. PMID:23315450

  2. Size dependence of magnetorheological properties of cobalt ferrite ferrofluid

    NASA Astrophysics Data System (ADS)

    Radhika, B.; Sahoo, Rasmita; Srinath, S.

    2015-06-01

    Cobalt Ferrite nanoparticles were synthesized using co-precipitation method at reaction temperatures of 40°C and 80°C. X-Ray diffraction studies confirm cubic phase formation. The average crystallite sizes were found to be ˜30nm and ˜48nm for 40°C sample and 80°C sample respectively. Magnetic properties measured using vibrating sample magnetometer show higher coercivety and magnetization for sample prepared at 80°C. Magnetorheological properties of CoFe2O4 ferrofluids were measured and studied.

  3. Epigallocatechin-3-gallate-capped Ag nanoparticles: preparation and characterization.

    PubMed

    Hussain, Shokit; Khan, Zaheer

    2014-07-01

    We used an aqueous leaf extract of Camellia sinensis to synthesize Ag nanoparticles (AgNPs). A layer of ca. 6 nm around a group of the AgNPs in which the inner layer is bound to the AgNPs surface via the hydroxyl groups of catechin has been observed. TEM analysis of AgNPs showed the formation of truncated triangular nanoplates and/or nanodisks and spherical with some irregular-shaped polydispersed nanoparticles in absence and presence of shape-directing cetyltrimethylammonium bromide. The polyphenolic groups of epigallocatechin-3-gallate (EGCG) are responsible for the rapid reduction of Ag(+) ions into metallic Ag(0). The free -OH groups are able to stabilize AgNPs by the interaction between the surface Ag atoms of AgNPs and oxygen atoms of EGCG molecules. PMID:24297160

  4. Role of interparticle interactions on the magnetic behavior of Mg0.95Mn0.05Fe2O4 ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Sharma, S. K.; Kumar, Ravi; Kumar, Shalendra; Knobel, M.; Meneses, C. T.; Siva Kumar, V. V.; Reddy, V. R.; Singh, M.; Lee, C. G.

    2008-06-01

    We present here a detailed investigation of the static and dynamic magnetic behavior of a Mg0.95Mn0.05Fe2O4 spinel ferrite nanoparticle system synthesized by high-energy ball milling of almost identical particle size distributions (\\langle D\\rangle=4.7 , 5.1 and 6.0 ± 0.6 nm). The samples were characterized by using x-ray diffraction, Mössbauer spectroscopy, dc magnetization and frequency dependent real χ'(T) and imaginary χ''(T) parts of ac susceptibility measurements. The zero-field-cooled (ZFC) and field-cooled (FC) magnetization have been recorded in a low field and show a behavior typical of superparamagnetic particles above a temperature of 185 ± 5 K, which is further supported from the temperature dependent Mössbauer measurements. The fact that the blocking temperature calculated from the ZFC magnetization and Mössbauer data are almost similar gives a clear indication of the interparticle interactions among these nanoparticle systems. This is further supported from the FC magnetization curves, which are almost flat below a certain temperature (less than the blocking temperature), as compared with the monotonically increasing behavior characteristics of non-interacting superparamagnetic particles. A shift of the blocking temperature with increasing frequency was observed in the real χ'(T) and imaginary χ''(T) parts of the ac susceptibility measurements. The analysis of the results shows that the data fit well with the Vogel-Fulcher law, whereas trials using the Neel-Brown and power law are unproductive. The role of magnetic interparticle interactions on the magnetic behavior, namely superparamagnetic relaxation time and magnetic anisotropy, are discussed.

  5. Preparation and characterization of solid lipid nanoparticles-a review.

    PubMed

    Parhi, Rabinarayan; Suresh, Padilama

    2012-03-01

    In the present scenario, most of the developed and new discovered drugs are posing real challenge to the formulation scientists due to their poor aqueous solubility which in turn is responsible for poor bioavailability. One of the approach to overcome above problem is the packaging of the drug in to particulate carrier system. Among various carriers, lipid emerged as very attractive candidate because of its unique property of enhancing the bioavailability of poorly water soluble drugs. Solid lipid, one of the physical forms of lipid, is used to formulate nanoparticles, popularly known as Solid lipid nanoparticles (SLNs), as an alternative carrier system to emulsions, liposomes and polymeric micro- and nano-particles. SLNs combine advantages of the traditional systems but avoid some of their major disadvantages. This paper reviews numerous production techniques for SLNs along with their advantages and disadvantages. Special attention is paid to the characterization of the SLNs by using various analytical tools. It also emphasizes on physical state of lipid (supercooled melts, different lipid modifications). PMID:22235925

  6. 2-Amino-2-deoxy-glucose conjugated cobalt ferrite magnetic nanoparticle (2DG-MNP) as a targeting agent for breast cancer cells.

    PubMed

    Aşık, Elif; Aslan, Tuğba Nur; Volkan, Mürvet; Güray, N Tülin

    2016-01-01

    In this study, 2-amino-2-deoxy-glucose (2DG) was conjugated to COOH modified cobalt ferrite magnetic nanoparticles (COOH-MNPs), which were designed to target tumor cells as a potential targetable drug/gene delivery agent for cancer treatment. According to our results, it is apparent that, 2DG labeled MNPs were internalized more efficiently than COOH-MNPs under the same conditions in all cell types (MDA-MB-231 and MCF-7 cancer and MCF-10A normal breast cells) (p<0.001). Moreover, the highest amount of uptake was observed in MDA-MB-231, followed by MCF-7 and normal MCF-10A cells for both MNPs. The apoptotic effects of 2DG-MNPs were further evaluated, and it was found that apoptosis was not induced at low concentrations of 2DG-MNPs in all cell types, whereas dramatic cell death was observed at higher concentrations. In addition, the gene expression levels of four drug-metabolizing enzymes, two Phase I (CYP1A1, CYP1B1) and two Phase II (GSTM3, GSTZ1) were also increased with the high concentrations of 2DG-MNPs. PMID:26761626

  7. Dextrin-coated zinc substituted cobalt-ferrite nanoparticles as an MRI contrast agent: In vitro and in vivo imaging studies.

    PubMed

    Sattarahmady, N; Zare, T; Mehdizadeh, A R; Azarpira, N; Heidari, M; Lotfi, M; Heli, H

    2015-05-01

    Application of superparamagnetic iron oxide nanoparticles (NPs) as a negative contrast agent in magnetic resonance imaging (MRI) has been of widespread interest. These particles can enhance contrast of images by altering the relaxation times of the water protons. In this study, dextrin-coated zinc substituted cobalt-ferrite (Zn0.5Co0.5Fe2O4) NPs were synthesized by a co-precipitation method, and the morphology, size, structure and magnetic properties of the NPs were investigated. These NPs had superparamagnetic behavior with an average size of 3.9 (±0.9, n=200)nm measured by transmission electron microscopy. Measurements on the relaxivities (r2 and r2(*)) of the NPs were performed in vitro by agarose phantom. In addition, after subcutaneous injection of the NPs into C540 cell line in C-57 inbred mice, the relaxivities were measured in vivo by a 1.5T MRI system. These NPs could effectively increase the image contrast in both T2-and T2(*)-weighted samples. PMID:25819361

  8. Investigation of structural and magnetic properties of co-precipitated Mn-Ni ferrite nanoparticles in the presence of α-Fe2O3 phase

    NASA Astrophysics Data System (ADS)

    Tirupanyam, B. V.; Srinivas, Ch.; Meena, S. S.; Yusuf, S. M.; Satish Kumar, A.; Sastry, D. L.; Seshubai, V.

    2015-10-01

    A systematic study on structural and magnetic properties of co-precipitated MnxNi1-xFe2O4 (x=0.5, 0.6, 0.7) ferrite nanoparticles annealed at 800 °C was carried out using XRD, FE-SEM, VSM and MÖSSBAUER techniques. Anti-ferromagnetic α-Fe2O3 phase was observed along with the magnetic spinel phase in the XRD patterns. It is observed that both lattice parameter and crystallite size of spinel phase increase with increase in concentration of Mn2+ along with the amount of α-Fe2O3 phase. The saturation magnetization (Ms) decreases while coercivity (Hc) increases with increase of Mn2+ ion concentration. Mössbauer spectra indicate that iron ions present in A and B sites are in the Fe3+ state and Fe2+ is absent. The results are interpreted in terms of observed anti-ferromagnetic α-Fe2O3 phase, core-shell interactions and cation redistribution.

  9. Silk fibroin nanoparticles prepared by electrospray as controlled release carriers of cisplatin.

    PubMed

    Qu, Jing; Liu, Yu; Yu, Yanni; Li, Jing; Luo, Jingwan; Li, Mingzhong

    2014-11-01

    To maintain the anti-tumor activity of cis-dichlorodiamminoplatinum (CDDP) while avoiding its cytotoxicity and negative influence on normal tissue, CDDP-loaded silk fibroin nanoparticles approximately 59 nm in diameter were successfully prepared by electrospray without using organic solvent. CDDP was incorporated into nanoparticles through metal-polymer coordination bond exchange. In vitro release tests showed that the cisplatin in the nanoparticles could be slowly and sustainably released for more than 15 days. In vitro anti-cancer experiments and intracellular Pt content testing indicated that CDDP-loaded silk fibroin nanoparticles were easily internalized by A549 lung cancer cells, transferring CDDP into cancer cells and then triggering their apoptosis. In contrast, the particles were not easily internalized by L929 mouse fibroblast cells and hence showed weaker cell growth inhibition. The CDDP-loaded silk fibroin nanoparticles showed sustained and efficient killing of tumor cells but weaker inhibition of normal cells. In general, this study provides not only a novel method for preparing CDDP-loaded silk fibroin nanoparticles but also a new carrier system for clinical therapeutic drugs against lung cancers and other tumors. PMID:25280693

  10. Preparation and Evaluation of Contact Lenses Embedded with Polycaprolactone-Based Nanoparticles for Ocular Drug Delivery.

    PubMed

    Nasr, Farzaneh Hashemi; Khoee, Sepideh; Dehghan, Mohammad Mehdi; Chaleshtori, Sirous Sadeghian; Shafiee, Abbas

    2016-02-01

    To improve the efficiency of topical ocular drug administration, we focused on development of a nanoparticles loaded contact lens to deliver the hydrophobic drug over a prolonged period of time. The cross-linked nanoparticles based on PCL (poly ε-caprolactone), 2-hydroxy ethyl methacrylate (HEMA), and poly ethylene glycol diacrylate (PEG-DA) were prepared by surfactant-free miniemulsion polymerization. The lens material was prepared through photopolymerization of HEMA and N-vinylpyrrolidone (NVP) using PEG-DA as the cross-linker. Effects of nanoparticles loading on critical contact lens properties such as transparency, water content, modulus and ion and oxygen permeabilities were studied. Nanoparticles and hydrogel showed high viability, indicating the absence of cytotoxicity and stimulatory effect. Drug release studies revealed that the hydrogel embedded with nanoparticles released the drug for a period of 12 days. The results of this study provide evidence that nanoparticles loaded hydrogels could be used for extended delivery of loteprednol etabonate and perhaps other drugs. PMID:26652301

  11. Preparation and Characterization of Cationic PLA-PEG Nanoparticles for Delivery of Plasmid DNA

    NASA Astrophysics Data System (ADS)

    Zou, Weiwei; Liu, Chunxi; Chen, Zhijin; Zhang, Na

    2009-09-01

    The purpose of the present work was to formulate and evaluate cationic poly(lactic acid)-poly(ethylene glycol) (PLA-PEG) nanoparticles as novel non-viral gene delivery nano-device. Cationic PLA-PEG nanoparticles were prepared by nanoprecipitation method. The gene loaded nanoparticles were obtained by incubating the report gene pEGFP with cationic PLA-PEG nanoparticles. The physicochemical properties (e.g., morphology, particle size, surface charge, DNA binding efficiency) and biological properties (e.g., integrity of the released DNA, protection from nuclease degradation, plasma stability, in vitro cytotoxicity, and in vitro transfection ability in Hela cells) of the gene loaded PLA-PEG nanoparticles were evaluated, respectively. The obtained cationic PLA-PEG nanoparticles and gene loaded nanoparticles were both spherical in shape with average particle size of 89.7 and 128.9 nm, polydispersity index of 0.185 and 0.161, zeta potentials of +28.9 and +16.8 mV, respectively. The obtained cationic PLA-PEG nanoparticles with high binding efficiency (>95%) could protect the loaded DNA from the degradation by nuclease and plasma. The nanoparticles displayed sustained-release properties in vitro and the released DNA maintained its structural and functional integrity. It also showed lower cytotoxicity than Lipofectamine 2000 and could successfully transfect gene into Hela cells even in presence of serum. It could be concluded that the established gene loaded cationic PLA-PEG nanoparticles with excellent properties were promising non-viral nano-device, which had potential to make cancer gene therapy achievable.

  12. Preparation and characterization of polymeric and lipid nanoparticles of pilocarpine HCl for ocular application.

    PubMed

    Lütfi, Genç; Müzeyyen, Demirel

    2013-01-01

    Pilocarpine is used topically in the treatment of glaucoma. Various studies were performed to improve the bioavailability and prolong the residence time of drugs in ocular drug delivery. Drug loaded polymeric and lipid nanoparticles offer several favourable biological properties, such as biodegradability, nontoxicity, biocompatibility and mucoadhesiveness. Therefore, preparing positively-charged pilocarpine HCl-loaded polymeric and lipid nanoparticles was the purpose of this study. Nanoparticles were prepared by quasi-emulsion solvent evaporation technique. The non-biodegradable positively-charged polymer Eudragit(®) RS 100 and semi-solid lipid excipient Gelucire(®) 44/14 were used as a vehicle, the cationic lipid octadecylamine was used as a cationic agent. The formulations were evaluated in terms of particle size, size distribution, zeta potential measurement, thermal behavior (Differential Scanning Calorimetry DSC), entrapment efficacy and pH. Characterizations of nanoparticles were analyzed during the storage period of 6 months for stability tests. Polymeric and lipid nanoparticles could be prepared successfully promising their use for ophthalmic delivery. PMID:22813238

  13. Green preparation and characterisation of waxy maize starch nanoparticles through enzymolysis and recrystallisation.

    PubMed

    Sun, Qingjie; Li, Guanghua; Dai, Lei; Ji, Na; Xiong, Liu

    2014-11-01

    Waxy maize starch was treated by a facile and green enzymolysis procedure to fabricate starch nanoparticles (StNPs). The yield of StNPs was raised to 85% by pullulanase treatment, and the preparation duration was two days. Morphology (SEM, TEM), crystalline structure (XRD), thermal gravimetry analysis (TGA), and the group changing (FTIR) of StNPs prepared with different starch concentrations (10%, 15%, 20% and 25%,w/v) were investigated. Compared with native starch, the topography of all StNPs exhibited irregularly-shaped fragments, the particle diameters decreased from several μm to about 60-120 nm, and the crystal pattern changed from A-type to B+V-type. The StNPs prepared with 15% starch slurry had the highest degree of crystallinity at 55.41%. The eco-friendly prepared nanoparticles could be widely used in biomedical applications and development of new materials. PMID:24874379

  14. Microwave Absorption Properties of Iron Nanoparticles Prepared by Ball-Milling

    NASA Astrophysics Data System (ADS)

    Chu, Xuan T. A.; Ta, Bach N.; Ngo, Le T. H.; Do, Manh H.; Nguyen, Phuc X.; Nam, Dao N. H.

    2015-12-01

    A nanopowder of iron was prepared using a high-energy ball milling method, which is capable of producing nanoparticles at a reasonably larger scale compared to conventional chemical methods. Analyses using x-ray diffraction and magnetic measurements indicate that the iron nanoparticles are a single phase of a body-centered cubic structure and have quite stable magnetic characteristics in the air. The iron nanoparticles were then mixed with paraffin and pressed into flat square plates for free-space microwave transmission and reflection measurements in the 4-8 GHz range. Without an Al backing plate, the Fe nanoparticles seem to only weakly absorb microwave radiation. The reflected signal S 11 drops to zero and a very large negative value of reflection loss (RL) are observed for Al-backed samples, suggesting the existence of a phase matching resonance near frequency f ˜ 6 GHz.

  15. Preparation and characterization of poly (ethylene glycol)-coated Stoeber silica nanoparticles for biomedical applications

    NASA Astrophysics Data System (ADS)

    Kopelman, Raoul; Xu, Hao; Yan, Fei; Monson, Eric E.; Tang, Wei; Schneider, Randy; Philbert, Martin A.

    2002-06-01

    Monodisperse, spherical, polyethylene glycol (PEG)-coated silica nanoparticles have been prepared in the size range of 50-350 nm, and their size distribution were characterized by SEM and multi-angle static light scattering experiments. The chemical binding of PEG to the silica nanoparticles was confirmed by IR spectroscopy. The biocompatibility of these PEGylated nanoparticles was also studied by non-specific protein binding tests and in-vivo toxicology studies in live animals. These silica nanoparticles, as a matrix for encapsulation of certain reagents, have been used for the fabrication of intracellular sensors and have potential for applications to in vivo diagnosis, analysis and measurements, due to their small physical size and their biocompatibility, both stemming from the specialized PEG coating.

  16. Preparation of tourmaline nano-particles through a hydrothermal process and its infrared emission properties.

    PubMed

    Xue, Gang; Han, Chao; Liang, Jinsheng; Wang, Saifei; Zhao, Chaoyue

    2014-05-01

    Tourmaline nano-particles were successfully prepared via a hydrothermal process using HCl as an additive. The reaction temperature (T) and the concentration of HCI (C(HCl)) had effects on the size and morphology of the tourmaline nano-particles. The optimum reaction condition was that: T = 180 degrees C and C(HCl) = 0.1 mol/l. The obtained nano-particles were spherical with the diameter of 48 nm. The far-infrared emissivity of the product was 0.923. The formation mechnism of the tourmaline nano-particles might come from the corrosion of grain boundary between the tourmaline crystals in acidic hydrothermal conditions and then the asymmetric contraction of the crystals. PMID:24734669

  17. Highly magnetic silica-coated iron nanoparticles prepared by the arc-discharge method

    NASA Astrophysics Data System (ADS)

    Fernández-Pacheco, Rodrigo; Arruebo, Manuel; Marquina, Clara; Ibarra, Ricardo; Arbiol, Jordi; Santamaría, Jesús

    2006-03-01

    In spite of encouraging progress in recent years, the development of magnetic nanoparticles that can be used as drug delivery vectors remains a significant challenge for materials scientists. Among the multiple hurdles that must be overcome are the provision of a sufficiently high magnetic response, a high loading capacity for therapeutic or diagnosis materials and a sufficient degree of biocompatibility. In this work we describe the preparation of encapsulated magnetic nanoparticles consisting of a metallic iron core and an amorphous silica shell by using a modification of the arc-discharge method. This is a simple and inexpensive way to produce well-coated iron nanoparticles. The particles thus obtained present a much stronger magnetic response than any composite material produced up to now involving magnetic nanoparticles encapsulated in inorganic matrices, and the rich chemistry and easy functionalization of the silica outer surface make them promising materials for their application as magnetic carriers.

  18. Preparation of silver nanoparticles in virgin coconut oil using laser ablation

    PubMed Central

    Zamiri, Reza; Azmi, B Z; Sadrolhosseini, Amir Reza; Ahangar, Hossein Abbastabar; Zaidan, A W; Mahdi, M A

    2011-01-01

    Laser ablation of a silver plate immersed in virgin coconut oil was carried out for fabrication of silver nanoparticles. A Nd:YAG laser at wavelengths of 1064 nm was used for ablation of the plate at different times. The virgin coconut oil allowed formation of nanoparticles with well-dispersed, uniform particle diameters that were stable for a reasonable length of time. The particle sizes and volume fraction of nanoparticles inside the solutions obtained at 15, 30, 45 min ablation times were 4.84, 5.18, 6.33 nm and 1.0 × 10−8, 1.6 × 10−8, 2.4 × 10−8, respectively. The presented method for preparation of silver nanoparticles in virgin coconut oil is environmentally friendly and may be considered a green method. PMID:21289983

  19. Role of electrolytes in the preparation of nanoparticles via the emulsion polymerization of vinyl pivalate.

    PubMed

    Kikuchi, Kenji; Kitawaki, Mayuka; Suzuki, Atsushi; Oku, Takeo

    2009-10-15

    By controlling both the kind of ion and the ionic strength of electrolytes in an emulsion polymerization system of vinyl pivalate containing about 1% sodium lauryl sulfate as a surfactant, nanoparticles of polyvinylpivalate having a diameter of about 25 nm were successfully prepared. The use of high concentrations of lithium chloride and lithium sulfate (approximately 1.0 mol L(-1)) prevented the nanoparticles from aggregating and produced nanoparticles sizes of 25-50 nm. Ammonium acetate and sodium acetate, on the other hand, accelerated the aggregate of the nanoparticles. These phenomena were examined in detail and found to be similar to the Hofmeister phenomena and the combination rule proposed by Craig et al. PMID:19647265

  20. Microwave Absorption Properties of Iron Nanoparticles Prepared by Ball-Milling

    NASA Astrophysics Data System (ADS)

    Chu, Xuan T. A.; Ta, Bach N.; Ngo, Le T. H.; Do, Manh H.; Nguyen, Phuc X.; Nam, Dao N. H.

    2016-05-01

    A nanopowder of iron was prepared using a high-energy ball milling method, which is capable of producing nanoparticles at a reasonably larger scale compared to conventional chemical methods. Analyses using x-ray diffraction and magnetic measurements indicate that the iron nanoparticles are a single phase of a body-centered cubic structure and have quite stable magnetic characteristics in the air. The iron nanoparticles were then mixed with paraffin and pressed into flat square plates for free-space microwave transmission and reflection measurements in the 4-8 GHz range. Without an Al backing plate, the Fe nanoparticles seem to only weakly absorb microwave radiation. The reflected signal S 11 drops to zero and a very large negative value of reflection loss ( RL) are observed for Al-backed samples, suggesting the existence of a phase matching resonance near frequency f ˜ 6 GHz.

  1. Preparation and characterization of surface-coated ZnS nanoparticles

    SciTech Connect

    Chen, S.; Liu, W.

    1999-11-09

    ZnS nanoparticles coated with di-n-hexadecyldithiophosphate (DDP) were chemically synthesized. The structure of the prepared ZnS nanoparticles was investigated by means of transmission electron microscopy, electron diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The thermal stability of DDP coated on nanoparticles was compared with that of pyridinium di-n-hexadecyldithiophosphate (PyDDP) using a thermogravimetric analyzer. The tribiological properties of ZnS nanoparticles as an additive in tetradecane were investigated by a SRV tester in a ball-on-disk configuration. DDP-coated ZnS nanoparticles, with an average diameter of about 4 nm, are able to prevent water adsorption, and oxidation and are capable of being dispersed stably in organic solvents or mineral oil. Thermal stability of DDP coating on ZnS nanoparticles was superior to that of PyDDP. Wear tests show that DDP-coated ZnS nanoparticles as additive in tetradecane are capable of reducing friction and wear of steel.

  2. Zeolite LTA Nanoparticles Prepared by Laser-Induced Fracture of Zeolite Microcrystals.

    PubMed

    Nichols, William T; Kodaira, Tetsuya; Sasaki, Yukichi; Shimizu, Yoshiki; Sasaki, Takeshi; Koshizaki, Naoto

    2006-01-12

    Zeolite LTA nanoparticles are prepared by laser-induced fragmentation of zeolite LTA microparticles using a pulsed laser. Zeolite nanoparticle formation is attributed to absorption of the laser at impurities or defects within the zeolite microcrystal generating thermoelastic stress that mechanically fractures the microparticle into smaller nanoparticle fragments. Experimentally, it is found that nanoparticles have a wide size and morphology distribution. Large nanoparticles (>200 nm) are typically irregularly shaped crystals of zeolite LTA, whereas small nanoparticles (<50 nm) tend to be spherical, dense, and amorphous, indicative of destruction of the original LTA crystal structure. Results of the fragmentation versus laser parameters show that shorter laser wavelengths are more efficient at producing zeolite nanoparticles, which is explained based on a larger cross section for optical absorption in the zeolite crystal. Increasing the laser energy density irradiating the sample was found to be a trade-off between increasing the amount of fragmentation and increasing the amount of structural damage to the zeolite crystal. It is suggested that in the presence of strongly absorbing defects, plasma formation is induced resulting in dramatically higher temperatures. On the basis of these results it is suggested the optimal laser processing conditions are 355 nm and 10 mJ/pulse laser energy for our LTA samples. PMID:16471503

  3. Schisandra lignans-loaded enteric nanoparticles: preparation, characterization, and in vitro-in vivo evaluation.

    PubMed

    Pei, Jin; Lv, Qingyuan; Han, Jin; Li, Xianyi; Jin, Shiying; Huang, Yajie; Jin, Shixiao; Yuan, Hailong

    2013-02-01

    Schisandrae lignans (SL) have been well proven to possess hepatoprotective effect against the hepatic dysfunction induced by various chemical hepatotoxins. Deoxyschisandrin (DA) and schisantherin A (SA) are both considered as the major active components in SL. The objective of the study was to prepare and evaluate Schisandra lignans (composed of DA and SA)-loaded enteric nanoparticles produced by a novel toxic solvent-free modified spontaneous emulsification solvent diffusion (SESD) method. An organic Schisandra lignans/Eudragit(®) S100 solution was injected into an aqueous poloxamer 188 solution under a agitation. The nanoparticles were characterized with respect to particle size distribution, morphology, encapsulation efficiency (EE) and physical stability of the drug, wettability, in vitro release and in vivo bioavailability. Nanoparticles with a smooth surface and dense structure were obtained with high EE (EE(DA) >90%; EE(SA) >85%). The drug was in a noncrystalline state in the matrix and physically stable for 120 days at room temperature. In vitro drug release study, the drug dissolution rate from the nanoparticles was significantly enhanced compared to the physical mixture and to the pure drug; the release profile of the nanoparticles was stable after 120 days. The appropriate size of nanoparticles (~93 nm), the solubilization of the surfactant, the noncrystalline state of the drug in the matrix and the fast dissolution rate contributed to a significantly enhanced oral bioavailability from the nanoparticles when compared to pure drug suspension. PMID:23373544

  4. Preparation and antibacterial activity of Fe3O4@Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Gong, Ping; Li, Huimin; He, Xiaoxiao; Wang, Kemin; Hu, Jianbing; Tan, Weihong; Zhang, Shouchun; Yang, Xiaohai

    2007-07-01

    Bifunctional Fe3O4@Ag nanoparticles with both superparamagnetic and antibacterial properties were prepared by reducing silver nitrate on the surface of Fe3O4 nanoparticles using the water-in-oil microemulsion method. Formation of well-dispersed nanoparticles with sizes of 60 ± 20 nm was confirmed by transmission electron microscopy and dynamic light scattering. X-ray diffraction patterns and UV-visible spectroscopy indicated that both Fe3O4 and silver are present in the same particle. The superparamagnetism of Fe3O4@Ag nanoparticles was confirmed with a vibrating sample magnetometer. Their antibacterial activity was evaluated by means of minimum inhibitory concentration value, flow cytometry, and antibacterial rate assays. The results showed that Fe3O4@Ag nanoparticles presented good antibacterial performance against Escherichia coli (gram-negative bacteria), Staphylococcus epidermidis (gram-positive bacteria) and Bacillus subtilis (spore bacteria). Furthermore, Fe3O4@Ag nanoparticles can be easily removed from water by using a magnetic field to avoid contamination of surroundings. Reclaimed Fe3O4@Ag nanoparticles can still have antibacterial capability and can be reused.

  5. Green preparation of Au nanoparticles for electrochemical detection of H2O2

    NASA Astrophysics Data System (ADS)

    Wenchao, Wang; Ye, Ji; Yong, Zhang; Ziying, Wang; Tong, Zhang

    2016-01-01

    A simple and green method for preparation of Au nanoparticles by reduction of HAuCl4 using carbon nanodots as the reducing agent is reported. The carbon nanodots were prepared by a green method as well, using hydrothermal treatment of grass. It is observed that Au nanoparticles show obvious electrochemical catalytic ability for reduction of hydrogen peroxide, leading to its application of a high-performance non-enzymatic hydrogen peroxide sensor. The hydrogen peroxide sensor based on Au nanoparticles was made, with the detection limit at 23 μM and linear range between 0.1-160 mM. Project supported by the National Natural Science Foundation of China (No. 51202085), and the Open Project from State Key Laboratory of Transducer Technology (No. SKT1402).

  6. Structural and spectroscopic characterization of prepared Ag2S nanoparticles with a novel sulfuring agent

    NASA Astrophysics Data System (ADS)

    Shakouri-Arani, Maryam; Salavati-Niasari, Masoud

    2014-12-01

    Ag2S nanoparticles were prepared by a solvothermal process via reaction of Ag(NO3) and a new sulfuring agent from class of thio Schiff-base (2-(benzylidene amino) benzenethiol (C13H11NS)) in presence of various solvents. Spectra such as X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SEAD), ultraviolet-visible (UV-Vis) spectroscopy, thermo gravimetric-differential thermal analysis (TG-DTA), and Fourier transform Infrared (FT-IR) employed to characterize the synthesized products. Results of this paper indicate that shape and size of the silver sulfide can be controlled by means of setting certain reaction parameters such as the reaction temperature, presence of surfactant, and type of solvent. Silver sulfide nanoparticles with different morphology and size successfully prepared. In addition, the growth mechanisms of the Ag2S nanoparticles discussed preliminarily.

  7. 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 tissue. PMID:24106420

  8. Synthesis and characterization of magnetic nanoparticles for use as sensors

    NASA Astrophysics Data System (ADS)

    Calero Diaz Del Castillo, Victoria L.

    A comprehensive study of physical and magnetic properties of cobalt substituted ferrite and magnetite nanoparticles synthesized by thermal-decomposition was carried out. Initially, a systematic study of the effect of synthesis conditions on final size, crystalline structure, and composition of cobalt substituted ferrite nanoparticles synthesized by thermal-decomposition was carried out. Using a statistical design of experiments, the impact of the temperature and time during nucleation and growth stages on final particle size, lattice parameter, and Fe/Co ratio was determined. Based on DC and AC susceptibility measurements, the effect of sample preparation on determination of the anisotropy constant of magnetite nanoparticles was studied. Magnetite nanoparticles synthesized by the thermal-decomposition method were fixed in a poly(styrene-divinylbenzene) matrix at 0.1%, 1%, and 6%(w/w). ZFC curves and the out-of-phase component of the dynamic susceptibility were obtained for each of sample and using Neel and Vogel-Fulcher models, the anisotropy constant was determined. The effect of particle size on the anisotropy constant of magnetite nanoparticles was also studied. In this case, magnetite with different diameter were synthesized by vary the synthesis conditions during thermal-decomposition method. Magnetite nanoparticles were fixed in poly(styrene-divinylbenzene) at 0.1% (w/w) and ZFC curves and AC susceptibility measurements were carried out. Finally, cobalt ferrite nanoparticles synthesized by the thermal-decomposition method were tested as possible sensors. Cobalt ferrite nanoparticles were functionalized with biotin using a COO--silane coupling agent. Using AC measurements, avidin molecules at a concentration of 1 microM in aqueous solution could be detected by monitoring the change in Brownian relaxation time after the attachment of avidin molecule to biotinylized cobalt ferrite nanoparticle. This analysis required a sample volume of 100 microl and on 8 microg of the protein to be detected.

  9. Preparation of magnetic polymer particles with nanoparticles of Fe(0).

    PubMed

    Buendía, S; Cabañas, G; Alvarez-Lucio, G; Montiel-Sánchez, H; Navarro-Clemente, M E; Corea, M

    2011-02-01

    Iron nanoparticles (Fe(0)), were encapsulated into polymethyl methacrylate (PMMA), by means of emulsion polymerization techniques in a semicontinuous process. The final average diameter of the composite particle was calculated until three times of average particle of iron particles and were stabilized with a non-ionic surfactant. They were then characterized by scanning electron microscopy and dynamic light scattering. Their magnetic properties were determined by parallel field vibrating-sample magnetometry method. The results indicated that the magnetic properties are a function of polymer concentration in the nanocomposite particle. PMID:21051044

  10. Preparation of Y2O3:Er,Yb nanoparticles by laser ablation in liquid

    NASA Astrophysics Data System (ADS)

    Nunokawa, Takashi; Onodera, Yuji; Hara, Masahiko; Kitamoto, Yoshitaka; Odawara, Osamu; Wada, Hiroyuki

    2012-11-01

    We prepared a Y2O3:Er,Yb nanoparticles by laser ablation in liquid. The laser used the second harmonic generation Nd:YAG (532 nm). A preparation process and measurement of upconversion properties were performed by varying the range of the energy density of the laser. Images from scanning electron microscopy (SEM) indicated that two types of nanoparticles existed in the product of laser ablation in liquid. We concluded the following: one type of nanoparticles was prepared from the nucleation of materials in a plume and the other was prepared by fragmentation. In the photoluminescence spectra, green (2H11/2, 4S3/2 ? 4I15/2) and red (4F9/2 ? 4I15/2) fluorescence were observed using a 980 nm laser diode (LD) as the excitation source. We confirmed that the fluorescence intensity increased with increasing energy density of the laser. Thus, we concluded that the number of the nanoparticles increased as the energy density of the laser was increased.

  11. Preparation of starch-stabilized silver nanoparticles from amylose-sodium palmitate inclusion complexes

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Starch-stabilized silver nanoparticles were prepared from amylose-sodium palmitate complexes by first converting sodium palmitate to silver palmitate by reaction with silver nitrate and then reducing the silver ion to metallic silver. This process produced water solutions that could be dried and the...

  12. A method for top down preparation of chitosan nanoparticles and nanofibers.

    PubMed

    Wijesena, Ruchira N; Tissera, Nadeeka; Kannangara, Yasun Y; Lin, Yuan; Amaratunga, Gehan A J; de Silva, K M Nalin

    2015-03-01

    A method of top down preparation of chitosan nanoparticles and nanofibers is proposed. Chitin nanofibrils (chitin NFs) were prepared using ultrasonic assisted method from crab shells with an average diameter of 5 nm and the length less than 3 μm as analyzed by atomic force microscopy and transmission electron microscopy. These chitin nanofibers were used as the precursor material for the preparation of chitosan nanoparticles and nanofibers. The degree of deacetylation of these prepared chitosan nanostructures were found to be approximately 98%. In addition these chitosan nanostructures showed amorphous crystallinity. Transmission electron microscopic studies revealed that chitosan nanoparticles were roughly spherical in nature and had diameters less than 300 nm. These larger particles formed through self-assembly of much smaller 25 nm particles as evidenced by the TEM imaging. The diameter and the length of the chitosan nanofibers were found to be less than 100 nm and 3 μm respectively. It is envisaged that due to the cavitation effect, the deacetylated chitin nanofibers were broken down to small pieces to form seed particles. These seed particles can then be self-assembled to form larger chitosan nanoparticles. PMID:25498694

  13. Structural and magnetic properties of NiZn-ferrite thin films prepared by radio frequency magnetron sputtering

    SciTech Connect

    Liu Yingli; Li Yuanxun; Zhang Huaiwu; Chen Daming; Mu Chunhong

    2011-04-01

    Polycrystalline NiZn-ferrite thin films were deposited on Si(100) substrate by rf magnetron sputtering, using targets with a nominal composition of Ni{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4}. The effects of substrate condition, sputtering pressure, and postannealing on the structure and magnetic properties of thin films have been investigated. Our results show that the preferred orientation of the NiZn spinel film changed from (311) to (400) with increasing the Ar pressure from 0.8 to 1.6 Pa, meanwhile, the grain size also increased. Atomic force microscopy analysis indicates that perfect surface morphology of the film can be obtained at a relatively lower sputtering pressure of 1.0 Pa. The relative percentage of residual oxygen increases significantly on a condition of lower sputtering pressure, and plays an important role in film structure due to the strong molecular adsorption tendency of oxygen on the film surface during the deposition process. A thin film with a typical thickness of 1 {mu}m, a saturation magnetization of 150 emu/cm{sup 3}, and a coercivity of 8.8 kA/m has been obtained after annealing at 800 deg. C, which has the potential application in magnetic integrated circuits.

  14. Fabrication and integrity test preparation of HIP-joined W and ferritic-martensitic steel mockups for fusion reactor development

    NASA Astrophysics Data System (ADS)

    Lee, Dong Won; Shin, Kyu In; Kim, Suk Kwon; Jin, Hyung Gon; Lee, Eo Hwak; Yoon, Jae Sung; Choi, Bo Guen; Moon, Se Youn; Hong, Bong Guen

    2014-10-01

    Tungsten (W) and ferritic-martensitic steel (FMS) as armor and structural materials, respectively, are the major candidates for plasma-facing components (PFCs) such as the blanket first wall (BFW) and the divertor, in a fusion reactor. In the present study, three W/FMS mockups were successfully fabricated using a hot isostatic pressing (HIP, 900 °C, 100 MPa, 1.5 hrs) with a following post-HIP heat treatment (PHHT, tempering, 750 °C, 70 MPa, 2 hrs), and the W/FMS joining method was developed based on the ITER BFW and the test blanket module (TBM) development project from 2004 to the present. Using a 10-MHz-frequency flat-type probe to ultrasonically test of the joint, we found no defects in the fabricated mockups. For confirmation of the joint integrity, a high heat flux test will be performed up to the thermal lifetime of the mockup under the proper test conditions. These conditions were determined through a preliminary analysis with conventional codes such as ANSYS-CFX for thermal-hydraulic conditions considering the test facility, the Korea heat load test facility with an electron beam (KoHLT-EB), and its water coolant system at the Korea Atomic Energy Research Institute (KAERI).

  15. Dispersoid Distribution and Microstructure in Fe-Cr-Al Ferritic Oxide Dispersion-Strengthened Alloy Prepared by Friction Consolidation

    SciTech Connect

    Catalini, David; Kaoumi, Djamel; Reynolds, Anthony; Grant, Glenn J.

    2015-07-09

    INCOLOY® MA956 is a ferritic Oxide Dispersion Strengthened (ODS) alloy. Three different oxides, Y4Al2O9, YAlO3 and Y3Al5O12, have been observed in this alloy. The oxide particle sizes range from just a few up to hundreds of nm and these particles are responsible of the high temperature mechanical strength of this alloy. Mechanically alloyed MA956 powder was consolidated via Friction Consolidation using three different processing conditions. As a result, three small compacts of low porosity were produced. The compacts exhibited a refined equiaxed grain structure with grain sizes smaller than 10 µm and the desired oxide dispersion.YAlO3 and Y3Al5O12 were identified in the compacts by Scanning Electron Microscopy (SEM), Electron Dispersive Spectroscopy (EDS) and X-ray diffraction (XRD). The size distribution of precipitates above 50 nm showed a direct proportionality between average precipitate size and grain size. The total energy input during processing was correlated with the relative amount of each of the oxides in the disks: the higher the total processing energy input, the higher the relative amount of Y3Al5O12 precipitates. The elemental composition of the oxide precipitates was also probed individually by EDS showing an aluminum enrichment trend as precipitates grow in size.

  16. Effect of cobalt ferrite (CoFe2O4) nanoparticles on the growth and development of Lycopersicon lycopersicum (tomato plants).

    PubMed

    López-Moreno, Martha L; Avilés, Leany Lugo; Pérez, Nitza Guzmán; Irizarry, Bianca Álamo; Perales, Oscar; Cedeno-Mattei, Yarilyn; Román, Félix

    2016-04-15

    Nanoparticles (NPs) have been synthetized and studied to be incorporated in many industrial and medical applications in recent decades. Due to their different physical and chemical properties compared with bulk materials, researchers are focused to understand their interactions with the surroundings. Living organisms such as plants are exposed to these materials and they are able to tolerate different concentrations and types of NPs. Cobalt ferrite (CoFe2O4) NPs are being studied for their application in medical sciences because of their high coercivity, anisotropy, and large magnetostriction. These properties are desirable in magnetic resonance imaging, drug delivery, and cell labeling. This study is aimed to explore the tolerance of Solanum lycopersicum L. (tomato) plants to CoFe2O4 NPs. Tomato plants were grown in hydroponic media amended with CoFe2O4 nanoparticles in a range from 0 to 1000mgL(-1). Exposure to CoFe2O4 NPs did not affect germination and growth of plants. Uptake of Fe and Co inside plant tissues increased as CoFe2O4 nanoparticle concentration was increased in the media. Mg uptake in plant leaves reached its maximum level of 4.9mgg(-1) DW (dry weight) at 125mgL(-1) of CoFe2O4 NPs exposure and decreased at high CoFe2O4 NPs concentrations. Similar pattern was observed for Ca uptake in leaves where the maximum concentration found was 10mgg(-1) DW at 125mgL(-1) of CoFe2O4 NPs exposure. Mn uptake in plant leaves was higher at 62.5mgL(-1) of CoFe2O4 NPs compared with 125 and 250mgL(-1) treatments. Catalase activity in tomato roots and leaves decreased in plants exposed to CoFe2O4 NPs. Tomato plants were able to tolerate CoFe2O4 NPs concentrations up to 1000mgL(-1) without visible toxicity symptoms. Macronutrient uptake in plants was affected when plants were exposed to 250, 500 and 1000mgL(-1) of CoFe2O4 NPs. PMID:26803683

  17. PEGylated human serum albumin (HSA) nanoparticles: preparation, characterization and quantification of the PEGylation extent

    NASA Astrophysics Data System (ADS)

    Fahrländer, E.; Schelhaas, S.; Jacobs, A. H.; Langer, K.

    2015-04-01

    Modification with poly(ethylene glycol) (PEG) is a widely used method for the prolongation of plasma half-life of colloidal carrier systems such as nanoparticles prepared from human serum albumin (HSA). However, the quantification of the PEGylation extent is still challenging. Moreover, the influence of different PEG derivatives, which are commonly used for nanoparticle conjugation, has not been investigated so far. The objective of the present study is to develop a method for the quantification of PEG and to monitor the influence of diverse PEG reagents on the amount of PEG linked to the surface of HSA nanoparticles. A size exclusion chromatography method with refractive index detection was established which enabled the quantification of unreacted PEG in the supernatant. The achieved results were confirmed using a fluorescent PEG derivative, which was detected by photometry and fluorimetry. Additionally, PEGylated HSA nanoparticles were enzymatically digested and the linked amount of fluorescently active PEG was directly determined. All the analytical methods confirmed that under optimized PEGylation conditions a PEGylation efficiency of up to 0.5 mg PEG per mg nanoparticle could be achieved. Model calculations made a ‘brush’ conformation of the PEG chains on the particle surface very likely. By incubating the nanoparticles with fetal bovine serum the reduced adsorption of serum proteins on PEGylated HSA nanoparticles compared to non-PEGylated HSA nanoparticles was demonstrated using sodium dodecylsulfate polyacrylamide gel electrophoresis. Finally, the positive effect of PEGylation on plasma half-life was demonstrated in an in vivo study in mice. Compared to unmodified nanoparticles the PEGylation led to a four times larger plasma half-life.

  18. Preparation and characterization of insulin nanoparticles employing chitosan and poly(methylmethacrylate/methylmethacrylic acid) copolymer.

    PubMed

    Li, Ming-Guang; Lu, Wan-Liang; Wang, Jian-Cheng; Zhang, Xuan; Zhang, Hua; Wang, Xue-Qing; Wu, Cui-Shuan; Zhang, Qiang

    2006-01-01

    As most of polypeptides are marginally stable, a mild formulation procedure would be beneficial for the activities of these drugs. The objective of the present study was to develop a novel pH-sensitive nanoparticle system that was suitable for entrapment of hydrophilic insulin but without affecting its conformation. Chitosan was incorporated as a positively charged material, and one of the three poly(methylmethacrylate/methylmethacrylic acid) copolymers, consisting of Eudragit L100-55, L100, and S100, was used as a negatively charged polymer for preparation of three insulin nanoparticles, respectively. Three nanoparticles obtained were spherical. The mean diameters were in the range from 200 nm to 250 nm, and the entrapment efficiencies, from 50% to 70%. The surface analysis indicated that insulin was evenly distributed in the nanoparticles. Polymer ratio of chitosan to Eudragit was the factor which influenced the nanoparticles significantly. Characterization results showed that the electrostatic interactions existed, thus providing a mild formulation procedure which did not affect the chemical integrity and the conformation of insulin. In vitro release studies revealed that all three types of the nanoparticles exhibited a pH-dependant characteristic. The modeling data indicated that the release kinetics of insulin was nonlinear, and during the release process, the nanoparticles showed a polynomial swelling. On overall estimation, the insulin chitosan-Eudragit L100-55 nanoparticles may be better for the oral delivery. This new pH-sensitive nanoparticle formulation using chitosan and Eudragit L100-55 polymer may provide a useful approach for entrapment of hydrophilic polypeptides without affecting their conformation. PMID:17048494

  19. PEGylated human serum albumin (HSA) nanoparticles: preparation, characterization and quantification of the PEGylation extent.

    PubMed

    Fahrländer, E; Schelhaas, S; Jacobs, A H; Langer, K

    2015-04-10

    Modification with poly(ethylene glycol) (PEG) is a widely used method for the prolongation of plasma half-life of colloidal carrier systems such as nanoparticles prepared from human serum albumin (HSA). However, the quantification of the PEGylation extent is still challenging. Moreover, the influence of different PEG derivatives, which are commonly used for nanoparticle conjugation, has not been investigated so far. The objective of the present study is to develop a method for the quantification of PEG and to monitor the influence of diverse PEG reagents on the amount of PEG linked to the surface of HSA nanoparticles. A size exclusion chromatography method with refractive index detection was established which enabled the quantification of unreacted PEG in the supernatant. The achieved results were confirmed using a fluorescent PEG derivative, which was detected by photometry and fluorimetry. Additionally, PEGylated HSA nanoparticles were enzymatically digested and the linked amount of fluorescently active PEG was directly determined. All the analytical methods confirmed that under optimized PEGylation conditions a PEGylation efficiency of up to 0.5 mg PEG per mg nanoparticle could be achieved. Model calculations made a 'brush' conformation of the PEG chains on the particle surface very likely. By incubating the nanoparticles with fetal bovine serum the reduced adsorption of serum proteins on PEGylated HSA nanoparticles compared to non-PEGylated HSA nanoparticles was demonstrated using sodium dodecylsulfate polyacrylamide gel electrophoresis. Finally, the positive effect of PEGylation on plasma half-life was demonstrated in an in vivo study in mice. Compared to unmodified nanoparticles the PEGylation led to a four times larger plasma half-life. PMID:25789544

  20. Role of copper on structural, magnetic and dielectric properties of nickel ferrite nano particles

    NASA Astrophysics Data System (ADS)

    Balavijayalakshmi, J.; Suriyanarayanan, N.; Jayaprakash, R.

    2015-07-01

    Copper doped nickel ferrites Ni(1-x)CuxFe2O4 (where x=0.2, 0.4, 0.6) nanoparticles are prepared by co-precipitation method and sintered at 600 °C. The XRD study confirms the formation of single-phase cubic spinel Ni-Cu ferrites. The particle size increases with Cu substitution. FT-IR spectra confirm the absorption bands around 554-547 cm-1 for the tetrahedral sites and around 448-450 cm-1 for the octahedral sites. The inclusion of copper shifts the tetrahedral band to lower values. The saturation magnetization (Ms) and remanent magnetization (Mr) decrease with increase in copper concentration and the coercivity (Hc) is found to increase for all the compositions sintered at 600 °C. The dielectric constant decreases drastically for all the compositions and reaches a constant value. These nanoparticles can be tested for humidity sensing applications.

  1. Facile synthetic route to nanosized ferrites by using mesoporous silica as a hard template

    NASA Astrophysics Data System (ADS)

    Valds-Sols, T.; Tartaj, P.; Marbn, G.; Fuertes, A. B.

    2007-04-01

    Spinel ferrite nanoparticles (AFe2O4; A = Mn, Ni, Cu, Co) of around 10-20 nm have been successfully synthesized via a simple nanocasting route using metal nitrates as precursors and mesoporous silica gel as a hard template. Spinel nanoparticles were formed under a nitrogen atmosphere by the high-temperature decomposition of a mixture of metal nitrates that fill the silica pores. The decomposition reactions occurred in the confined space provided by the mesopores of the silica template. Under these conditions, the silica walls restricted the growth of the oxide particles formed and so nanosized particles were obtained. The incorporation of different cations into the spinel ferrite enabled us to easily modulate the magnetic properties of the nanomaterials prepared by the template method. Depending on the chemical composition and temperature, we were able to obtain samples that display reversible magnetic behaviour (zero coercivity field) and samples with coercivity values as high as 1.3 T (13 000 Oe).

  2. Comparison study of the magnetic permeability and dc conductivity of Co-Ni-Li ferrite nanoparticles and their bulk counterparts

    NASA Astrophysics Data System (ADS)

    Assar, S. T.; Abosheiasha, H. F.; El Nimr, M. K.

    2014-03-01

    The temperature dependence of relative permeability and dc electrical conductivity of nanosamples and their bulk counterparts of Co0.5Ni0.5-2xLixFe2+xO4 (from x=0.00 to 0.25 in step of 0.05) was investigated. The values of the relative permeability of the nano-samples are lower than their bulk counterparts as a result of porous and nano-grained structure besides the effect of the larger volume of grain boundaries in the nanosamples. Moreover, the dc conductivity of the nanosamples is higher than their bulk counterparts. This is probable explained according to the shorter metal-oxygen bonding length and higher lattice vibrations of the nanosamples. Also, the values of the relative permeability of both nano and bulk samples exhibit stability over a considerable range of temperatures. This may make them useful in practical applications that require stability. All the nanosamples show high rising Curie temperature values with increasing the Li content up to the sample of x=0.15 thereafter a decrease of the Curie temperature occurs while the inverse behavior was observed in their bulk counterparts. The interpretation of these findings is explained in the discussion. Moreover, in general doping Co-Ni ferrites with Li ions improves their electrical and magnetic properties and this is clearly observed in the nanosample of x=0.15 which can be regarded as the most promising sample for microwave applications.

  3. Cobalt ferrite nanoparticles decorated on exfoliated graphene oxide, application for amperometric determination of NADH and H2O2.

    PubMed

    Ensafi, Ali A; Alinajafi, Hossein A; Jafari-Asl, M; Rezaei, B; Ghazaei, F

    2016-03-01

    Here, cobalt ferrite nanohybrid decorated on exfoliated graphene oxide (CoFe2O4/EGO) was synthesized. The nanohybrid was characterized by different methods such as X-ray diffraction spectroscopy, scanning electron microscopy, energy dispersive X-ray diffraction microanalysis, transmission electron microscopy, FT-IR, Raman spectroscopy and electrochemical methods. The CoFe2O4/EGO nanohybrid was used to modify glassy carbon electrode (GCE). The voltammetric investigations showed that CoFe2O4/EGO nanohybrid has synergetic effect towards the electro-reduction of H2O2 and electro-oxidation of nicotinamide adenine dinucleotide (NADH). Rotating disk chronoamperometry was used for their quantitative analysis. The calibration curves were observed in the range of 0.50 to 100.0 μmol L(-1) NADH and 0.9 to 900.0 μmol L(-1) H2O2 with detections limit of 0.38 and 0.54 μmol L(-1), respectively. The repeatability, reproducibility and selectivity of the electrochemical sensor for analysis of the analytes were studied. The new electrochemical sensor was successfully applied for the determination of NADH and H2O2 in real samples with satisfactory results. PMID:26706531

  4. Laser ablation of gadolinium targets in liquids for nanoparticle preparation

    NASA Astrophysics Data System (ADS)

    Tarasenko, N. V.; Butsen, A. V.; Nevar, A. A.

    2008-12-01

    Synthesis and preliminary characterization of gadolinium colloids prepared by pulsed laser ablation in different solutions was performed to clarify the capabilities of the laser ablation technique for preparation of stable nanoscale particles suitable for further bio(chemical) functionalization. Experiments were made by using a 10 Hz pulsed Nd:YAG laser, operating at 1064 nm. The formed colloids were examined by UV/VIS absorption spectroscopy, TEM and XRD. The developed technique was shown to be suitable for the preparation of particles of various compositions (oxides and carbides) with sizes in the nanometric range (of 5-12 nm diameters) by proper selection of both laser experimental parameters and the type of the liquid used (distilled water, ethanol and acetone).

  5. Preparation and characterization of polymer nanocomposites coated magnetic nanoparticles for drug delivery applications

    NASA Astrophysics Data System (ADS)

    Prabha, G.; Raj, V.

    2016-06-01

    In the present research work, the anticancer drug 'curcumin' is loaded with Chitosan (CS)-polyethylene glycol (PEG)-polyvinylpyrrolidone (PVP) (CS-PEG-PVP) polymer nanocomposites coated with superparamagnetic iron oxide (Fe3O4) nanoparticles. The system can be used for targeted and controlled drug delivery of anticancer drugs with reduced side effects and greater efficiency. The prepared nanoparticles were characterized by Fourier transmission infrared spectroscopy (FTIR), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Curcumin drug loaded Fe3O4-CS, Fe3O4-CS-PEG and Fe3O4-CS-PEG-PVP nanoparticles exhibited the mean particle size in the range of 183-390 nm with a zeta potential value of 26-41 mV as measured using Malvern Zetasizer. The encapsulation efficiency, loading capacity and in-vitro drug release behavior of curcumin drug loaded Fe3O4-CS, Fe3O4-CS-PEG and Fe3O4-CS-PEG-PVP nanoparticles were studied using UV spectrophotometer. Besides, the cytotoxicity of the prepared nanoparticles using MTT assay was also studied. The curcumin drug release was examined at different pH medium and it was proved that the drug release depends upon the pH medium in addition to the nature of matrix.

  6. Novel combustion method to prepare octahedral NiO nanoparticles and its photocatalytic activity

    SciTech Connect

    Jegatha Christy, A.; Umadevi, M.

    2013-10-15

    Graphical abstract: - Highlights: • NiO nanoparticles were synthesized by solution combustion method. • Prepared NiO nanoparticles are fcc structure. • Synthesized NiO nanoparticles are octahedral shape. • Shows good photocatalytic activity. - Abstract: Nickel oxide nanoparticles (NiO NPs) were synthesized by solution combustion method using glycine and citric acid as fuels. The X-ray diffraction (XRD) result confirms the face centered cubic (fcc) structure of NiO. The octahedral shape of NiO NPs was confirmed by field emission scanning electron microscope (FESEM) and high resolution transmission electron microscopy (HRTEM). It is possible to suggest that the organic fuel (citric acid/glycine) is responsible for the formation of the octahedral shape due to the easier complex formation. Photocatalytic activity of NiO NPs also evaluated and found that the prepared NiO NPs have high photocatalytic degradation. In the present study, the crystalline nature and shape of the NiO nanoparticles plays a vital role in determining the photocatalytic activity.

  7. Enhanced Oral Delivery of Docetaxel Using Thiolated Chitosan Nanoparticles: Preparation, In Vitro and In Vivo Studies

    PubMed Central

    Saremi, Shahrooz; Kebriaeezadeh, Abbas; Ostad, Seyed Nasser; Atyabi, Fatemeh

    2013-01-01

    The aim of this study was to evaluate a nanoparticulate system with mucoadhesion properties composed of a core of polymethyl methacrylate surrounded by a shell of thiolated chitosan (Ch-GSH-pMMA) for enhancing oral bioavailability of docetaxel (DTX), an anticancer drug. DTX-loaded nanoparticles were prepared by emulsion polymerization method using cerium ammonium nitrate as an initiator. Physicochemical properties of the nanoparticles such as particle size, size distribution, morphology, drug loading, and entrapment efficiency were characterized. The pharmacokinetic study was carried out in vivo using wistar rats. The half-life of DTX-loaded NPs was about 9 times longer than oral DTX used as positive control. The oral bioavailability of DTX was increased to 68.9% for DTX-loaded nanoparticles compared to 6.5% for positive control. The nanoparticles showed stronger effect on the reduction of the transepithelial electrical resistance (TEER) of Caco-2 cell monolayer by opening the tight junctions. According to apparent permeability coefficient (Papp) results, the DTX-loaded NPs showed more specific permeation across the Caco-2 cell monolayer in comparison to the DTX. In conclusion, the nanoparticles prepared in this study showed promising results for the development of an oral drug delivery system for anticancer drugs. PMID:23971023

  8. Preparation of starch nanoparticles in water in oil microemulsion system and their drug delivery properties.

    PubMed

    Wang, Xinge; Chen, Haiming; Luo, Zhigang; Fu, Xiong

    2016-03-15

    In this research, 1-hexadecyl-3-methylimidazolium bromide C16mimBr/butan-1-ol/cyclohexane/water ionic liquid microemulsion was prepared. The effects of n-alkyl alcohols, alkanes, water content and temperature on the properties of microemulsion were studied by dilution experiment. The microregion of microemulsion was identified by pseudo-ternary phase diagram and conductivity measurement. Then starch nanoparticles were prepared by water in oil (W/O) microemulsion-cross-linking methods with C16mimBr as surfactant. Starch nanoparticles with a mean diameter of 94.3nm and narrow size distribution (SD=3.3) were confirmed by dynamic light scattering (DLS). Scanning electron microscope (SEM) data revealed that starch nanoparticles were spherical granules with the size about 60nm. Moreover the results of Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) demonstrated the formation of cross-linking bonds in starch molecules. Finally, the drug loading and releasing properties of starch nanoparticles were investigated with methylene blue (MB) as drug model. This work may provide an efficient pathway to synthesis starch nanoparticles. PMID:26794752

  9. [Preparation of nanoparticles-modified silica monolith for on-column surface enhanced Raman spectroscopy].

    PubMed

    Liu, Chan; Chen, Lei; Ren, Hua-Hua; Zhou, Ji

    2014-05-01

    A novel silica monolith modified with Ag/Au nanoparticles was prepared for the on-column surface enhanced Raman spectroscopy (SERS). The bare monolithic silica column was prepared from in-situ co-condensation of tetraethoxysilane (TMOS) and methyl trimethoxysilane (MTMS) in the presence of polyethylene glycol (PEG) via a sol-gel process in the capillary, and was chemically modified with (3-mercaptopropyl) trimethoxysilane (MTPMS), followed by immobilization of Ag/Au nanoparticles. Transmission electron microscopy (TEM) and UV-Vis spectrometer were used to collect the TEM images and the extinction spectra of the nanoparticles colloid, respectively. Scanning electron microscope (SEM) was utilized to record the morphology of the silica monolith The authros used p-aminothiophenol (PATP) as a probing molecule, and the SERS effect was investigated on Au/Ag nanoparticle-modified silica monolith under the excitation line of 633 and 532 nm, respectively. It is concluded that nanoparticle-modified silica monoliths will have broad application to the on-site detection of food and water contaminants in the field. PMID:25095424

  10. A facile and general approach for preparation of glycoprotein-imprinted magnetic nanoparticles with synergistic selectivity.

    PubMed

    Hao, Yi; Gao, Ruixia; Liu, Dechun; He, Gaiyan; Tang, Yuhai; Guo, Zengjun

    2016-06-01

    In light of the significance of glycoprotein biomarkers for early clinical diagnostics and treatments of diseases, it is essential to develop efficient and selective enrichment platforms for glycoproteins. In this study, we present a facile and general strategy to prepare the boronate affinity-based magnetic imprinted nanoparticles. Boronic acid ligands were first grafted on the directly aldehyde-functionalized magnetic nanoparticles through amidation reaction. Then, template glycoproteins were immobilized on the boronic acid-modified magnetic nanoparticles via boronate affinity binding. Subsequently, a thin layer of dopamine was formed to coat the surface of magnetic nanoparticles through self-polymerization. After the template glycoproteins were removed, the cavities that can specific bind the template glycoproteins were fabricated. Adopting horseradish peroxidase as model template, the effects of imprinting conditions as well as the properties and performance of the obtained products were investigated. The resultant imprinted materials exhibit highly favorable features, including uniform surface morphology with thin imprinted shell of about 8nm, super-paramagnetic property, fast kinetics of 40min, high adsorption capacity of 60.3mgg(-1), and satisfactory reusability for at least five cycles of adsorption-desorption without obvious deterioration. Meanwhile, the obtained magnetic imprinted nanoparticles could capture target glycoprotein from nonglycoproteins, but also from other glycoproteins because the synergistic selectivity of boronate affinity and imprinting effect. In addition, the facile preparation method shows feasibility in the imprinting of different glycoproteins. PMID:27130111

  11. Comparison and functionalization study of microemulsion-prepared magnetic iron oxide nanoparticles.

    PubMed

    Okoli, Chuka; Sanchez-Dominguez, Margarita; Boutonnet, Magali; Järås, Sven; Civera, Concepción; Solans, Conxita; Kuttuva, Gunaratna Rajarao

    2012-06-01

    Magnetic iron oxide nanoparticles (MION) for protein binding and separation were obtained from water-in-oil (w/o) and oil-in-water (o/w) microemulsions. Characterization of the prepared nanoparticles have been performed by TEM, XRD, SQUID magnetometry, and BET. Microemulsion-prepared magnetic iron oxide nanoparticles (ME-MION) with sizes ranging from 2 to 10 nm were obtained. Study on the magnetic properties at 300 K shows a large increase of the magnetization ~35 emu/g for w/o-ME-MION with superparamagnetic behavior and nanoscale dimensions in comparison with o/w-ME-MION (10 emu/g) due to larger particle size and anisotropic property. Moringa oleifera coagulation protein (MOCP) bound w/o- and o/w-ME-MION showed an enhanced performance in terms of coagulation activity. A significant interaction between the magnetic nanoparticles and the protein can be described by changes in fluorescence emission spectra. Adsorbed protein from MOCP is still retaining its functionality even after binding to the nanoparticles, thus implying the extension of this technique for various applications. PMID:22578053

  12. Preparation of polylysine-modified superparamagnetic iron oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Yang, Gao; Zhang, Baolin; Wang, Jun; Xie, Songbo; Li, Xuan

    2015-01-01

    Polylysine (PLL) coated iron oxide nanoparticles (SPIONs) have potential in biomedical application. In the present work PEG coated SPIONs (PEG-SPIONs) with the particle size of 9.4±1.4 nm were synthesized by thermal decomposition of Fe(acac)3 in PEG, and then coated with PLL (PLL/PEG-SPIONs). The PEG-SPIONs and PLL/PEG-SPIONs were superparamagnetic with the saturation magnetization of 53 and 44 emu/g, respectively. The hydrodynamic diameter of PEG-SPIONs in deionized water was 18.8 nm, which increased to 21.3-28.2 nm after mixing with different amount of PLL. The zeta potentials of PLL/PEG-SPIONs were -8.9 - -3.4 mV which were changing with time. Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) analyses indicated that PLL was attached to the PEG-SPIONs.

  13. Solvothermal synthesis of CZTS nanoparticles in ethanol: Preparation and characterization

    NASA Astrophysics Data System (ADS)

    Yan, Xinlong; Hu, Xiaoyan; Komarneni, Sridhar

    2015-05-01

    In this work, a low-cost, non-toxic and convenient one-pot solvothermal route to synthesize Cu2ZnSnS4 (CZTS) nanoparticles is reported. The effects of solvothermal temperature and reaction time on the structure, morphology and optical properties of the as-synthesized product were investigated by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX) measurements and X-ray photoelectron spectroscopy (XPS). The results showed that the crystallinity of the CZTS powders was influenced by the solvothermal temperature and reaction time. The band gap of selected CZTS samples was near the optimum value for photovoltaic solar conversion in a single-band-gap device.

  14. Dispersoid Distribution and Microstructure in Fe-Cr-Al Ferritic Oxide Dispersion-Strengthened Alloy Prepared by Friction Consolidation

    NASA Astrophysics Data System (ADS)

    Catalini, David; Kaoumi, Djamel; Reynolds, Anthony P.; Grant, Glenn J.

    2015-10-01

    INCOLOY® MA956 is a ferritic oxide dispersion-strengthened alloy manufactured by mechanical alloying followed by hot extrusion in vacuum-sealed cans or by degassing and hot isostatic pressing. This could be followed by a tailored heat treatment sequence in order to obtain a desired microstructure and to allow the oxide dispersion to precipitate. Three different oxides, responsible for the high-temperature mechanical strength, have been observed in this alloy: Y4Al2O9, YAlO3, and Y3Al5O12. Their sizes range from just a few to hundreds of nanometers. In this work, mechanically alloyed MA956 powder was consolidated via friction consolidation, a single-step and potentially cheaper processing alternative. Three fully dense compacts were produced. The compacts exhibited a refined, equiaxed grain structure with grain sizes smaller than 10 µm and the desired oxide dispersion. YAlO3 and Y3Al5O12 were identified by scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction. The size distribution of precipitates above 50 nm showed a direct proportionality between average precipitate size and grain size. The total energy input during processing was correlated with the relative amount of each of the oxides in the disks: the higher the total processing energy input, the higher the relative amount of Y3Al5O12 precipitates. The elemental composition of the oxide precipitates was also probed individually by EDS, showing an aluminum enrichment trend as precipitates grew in size.

  15. Preparation of Iron Nanoparticles from Iron Pentacarbonyl Using an Atmospheric Microwave Plasma

    NASA Astrophysics Data System (ADS)

    Zhang, Boya; Wang, Qiang; Zhang, Guixin; Liao, Shanshan; Wang, Zhong; Li, Guobin

    2015-10-01

    A novel method is introduced for preparing iron nanoparticles from iron pentacarbonyl using an atmospheric microwave plasma. The prepared iron nanoparticles were characterized by transmission electron microscopy and X-ray diffraction. The results show that the size of the particles can be controlled by adjusting the microwave power and the flow rate of the carrier gas. The magnetic properties of the synthesized iron particles were studied and a saturation magnetization of ∼95 emu/g was obtained. The convenient preparation process and considerable production rate were also found to be satisfactory for industrial applications. supported by National Natural Science Foundation of China (No. 51177085), the State Key Laboratory Foundation of Power System of China (No. SKLD10M07) and China Postdoctoral Science Foundation (No. 2013M540942)

  16. Preparation and Characterization of Large Area Monolayer Films of Pt Nanoparticles

    NASA Astrophysics Data System (ADS)

    Kelly, Brian; Cichocki, Ronald; Ren, Jie; Schmidt, Robert; Theopold, Klaus; Unruh, Karl

    Highly uniform monolayer thick coatings of Pt nanoparticles with areas as large as 20 cm2 have been prepared by first self-assembling the desired Pt film at the interface between two immiscible liquids and then transferring the film to a glass substrate. The controlled addition of ethyl alcohol to a phase separated mixture of an aqueous colloidal solution of Pt nanoparticles and hexane allowed both monolayer and multilayer films to be prepared. Optical microscopy and UV-vis spectrophotometry measurements have been used to verify the large scale uniformity of the coatings while transmission electron and atomic force microscopy measurements confirmed that single and multilayer films can be prepared. This material is based upon work supported by the National Science Foundation under Grant No. 1410076.

  17. Effect of nanoparticle stabilization and physicochemical properties on exposure outcome: acute toxicity of silver nanoparticle preparations in zebrafish (Danio rerio).

    PubMed

    Cunningham, Stephen; Brennan-Fournet, Margaret E; Ledwith, Deirdre; Byrnes, Lucy; Joshi, Lokesh

    2013-04-16

    Nanotechnology has vast potential for expanded development and novel application in numerous sectors of society. With growing use and applications, substantial production volumes and associated environmental release can be anticipated. Exposure effect of nanoparticles (NP) on biological systems may be intrinsic to their physicochemical properties introducing unknown associated risk. Herein, we expand the knowledge of health and environmental impact of silver nanoparticles (AgNPs), testing the acute toxicity of 14 AgNP preparations on developing zebrafish embryos (Danio rerio). Toxicological end points, including mortality, hatching rate, and heart rate were recorded. Concentration, stabilization agent and physicochemical properties were monitored as contributing outcome factors. Our findings indicate wide ranging LC50 24 h postfertilization values (0.487 ppm (0.315, 0.744 95% CI) to 47.89 ppm (18.45, 203.49 95% CI)), and indicate surface charge and ionic dissolution as key contributory factors in AgNP exposure outcome. PMID:23458316

  18. Nickel nanoparticles with hcp structure: Preparation, deposition as thin films and application as electrochemical sensor.

    PubMed

    Neiva, Eduardo G C; Oliveira, Marcela M; Marcolino, Luiz H; Zarbin, Aldo J G

    2016-04-15

    Hexagonal close packed (hcp) nickel nanoparticles stabilized by polyvinylpyrrolidone (PVP) were synthesized through the thermal treatment of face centered cubic (fcc) nickel nanoparticles. Controlling both the temperature of the heat treatment and the amount of PVP was possible the control of the hcp/fcc rate in the samples, where the higher Ni/PVP ratio produces only the hcp-nickel phase (average size of 8.9nm) highly stable in air. The crystalline structure, the presence of PVP, the size of the nanoparticles and the stability of the hcp-nickel were confirmed using X-ray diffractometry, Fourier transform infrared spectroscopy, transmission electron microscopy, Raman spectroscopy, scanning electron microscopy and thermogravimetric analysis. Thin films of hcp and fcc nickel nanoparticles were prepared through a biphasic system and deposited over indium-doped tin oxide (ITO) substrates, which were electrochemically characterized and applied as glycerol amperometric sensors in NaOH medium. Parameters as the number of cycles applied and the scan rate were evaluated and indicate that hcp nickel nanoparticles are more reactive to form Ni(OH)2 and lead to more electroactive Ni(OH)2 structure. The hcp nickel nanoparticles-modified electrode showed the best sensitivity (0.258μALμmol(-1)) and detection limit (2.4μmolL(-1)) toward glycerol. PMID:26821149

  19. Application of a new coordination compound for the preparation of AgI nanoparticles

    SciTech Connect

    Mohandes, Fatemeh; Salavati-Niasari, Masoud

    2013-10-15

    Graphical abstract: Silver iodide nanoparticles have been sonochemically synthesized by using silver salicylate complex, [Ag(HSal)], as silver precursor. A series of control experiments were carried out to investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures. - Highlights: • Silver salicylate as a new precursor was applied to fabricate γ-AgI nanoparticles. • To further decrease the particle size of AgI, SDS was used as surfactant. • The effect of preparation parameters on the particle size of AgI was investigated. - Abstract: AgI nanoparticles have been sonochemically synthesized by using silver salicylate, [Ag(HSal)], as silver precursor. To investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures, several experiments were carried out. The products were characterized by SEM, TEM, XRD, TGA/DTA, UV–vis, and FT-IR. Based on the experimental findings in this research, it was found that the size of AgI nanoparticles was dramatically dependent on the silver precursor, sonochemical irradiation, and surfactant concentration. Sodium dodecyl sulfate (SDS) was applied as surfactant. When the concentration of SDS was 0.055 mM, very uniform sphere-like AgI nanoparticles with grain size of about 25–30 nm were obtained. These results indicated that the high concentration of SDS could prevent the aggregation between colloidal nanoparticles due to its steric hindrance effect.

  20. Preparation and characterization of a thermostable enzyme (Mn-SOD) immobilized on supermagnetic nanoparticles.

    PubMed

    Song, Chongfu; Sheng, Liangquan; Zhang, Xiaobo

    2012-10-01

    Superoxide dismutase (SOD) has been widely applied in medical treatments, cosmetic, food, agriculture, and chemical industries. In industry, the immobilization of enzymes can offer better stability, feasible continuous operations, easy separation and reusing, and significant decrease of the operation costs. However, little attention has focused on the immobilization of the SOD, as well as the immobilization of thermostable enzymes. In this study, the recombinant thermostable manganese superoxide dismutase (Mn-SOD) of Thermus thermophilus wl was purified and covalently immobilized onto supermagnetic 3-APTES-modified Fe(3)O(4)@SiO(2) nanoparticles using glutaraldehyde method to prepare the Mn-SOD bound magnetic nanoparticles. The Mn-SOD nanoparticles were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, X-ray diffraction, transmission electron microscopy, and vibrating sample magnetometer analysis. The results indicated that the diameter of Mn-SOD nanoparticles was 40 (± 5) nm, and its saturation magnetization value was 27.9 emu/g without remanence or coercivity. By comparison with the free Mn-SOD, it was found that the immobilized Mn-SOD on nanoparticles exhibited better resistance to temperature, pH, metal ions, enzyme inhibitors, and detergents. The results showed that the immobilized Mn-SOD on nanoparticles could be reused ten times without significant decrease of enzymatic activity. Therefore, our study presented a novel strategy for the immobilization of thermostable Mn-SOD and for the application of thermostable enzymes. PMID:22237672

  1. Preparation and in vitro-in vivo evaluation of salmon calcitonin-loaded polymeric nanoparticles.

    PubMed

    Glowka, Eliza; Sapin-Minet, Anne; Leroy, Pierre; Lulek, Janina; Maincent, Philippe

    2010-01-01

    The aim of the study was to develop and characterize polymeric nanoparticles as a sustained release system for salmon calcitonin (sCT). Nanoparticles were prepared by a double emulsion solvent evaporation method using Eudragit RS and two types of a biodegradable poly(lactic-co-glycolic) copolymer (PLGA). It was demonstrated that sCT was incorporated into nanoparticles with encapsulation efficiencies in the range 69-83%. In vitro release studies, unconventionally conducted in 5% acetic acid, showed great differences in sCT release time profiles. Nanoparticles with fast release profile (Eudragit RS, PLGA/Eudragit RS) released 80-100% of the encapsulated drug within a few hours. In contrast, the sCT release from pure PLGA nanoparticles was very slow, incomplete and reached only 20% after 4 weeks. In vivo study, conducted in Wistar rats, proved that elevated serum sCT levels could be sustained for 3 days after subcutaneous administration of PLGA nanoparticles and the achieved bioavailability was increased compared to sCT solution. PMID:19229671

  2. Synthesis and optical properties of copper nanoparticles prepared by a chemical reduction method

    NASA Astrophysics Data System (ADS)

    Dung Dang, Thi My; Tuyet Thu Le, Thi; Fribourg-Blanc, Eric; Chien Dang, Mau

    2011-03-01

    Copper nanoparticles, due to their interesting properties, low cost preparation and many potential applications in catalysis, cooling fluid or conductive inks, have attracted a lot of interest in recent years. In this study, copper nanoparticles were synthesized through the chemical reduction of copper sulfate with sodium borohydride in water without inert gas protection. In our synthesis route, ascorbic acid (natural vitamin C) was employed as a protective agent to prevent the nascent Cu nanoparticles from oxidation during the synthesis process and in storage. Polyethylene glycol (PEG) was added and worked both as a size controller and as a capping agent. Cu nanoparticles were characterized by Fourier transform infrared (FT-IR) spectroscopy to investigate the coordination between Cu nanoparticles and PEG. Transmission electron microscopy (TEM) and UV–vis spectrometry contributed to the analysis of size and optical properties of the nanoparticles, respectively. The average crystal sizes of the particles at room temperature were less than 10 nm. It was observed that the surface plasmon resonance phenomenon can be controlled during synthesis by varying the reaction time, pH, and relative ratio of copper sulfate to the surfactant. The surface plasmon resonance peak shifts from 561 to 572 nm, while the apparent color changes from red to black, which is partly related to the change in particle size. Upon oxidation, the color of the solution changes from red to violet and ultimately a blue solution appears.

  3. Preparation of spherical ceria coated silica nanoparticle abrasives for CMP application

    NASA Astrophysics Data System (ADS)

    Peedikakkandy, Lekha; Kalita, Laksheswar; Kavle, Pravin; Kadam, Ankur; Gujar, Vikas; Arcot, Mahesh; Bhargava, Parag

    2015-12-01

    This paper describes synthesis of spherical and highly mono-dispersed ceria coated silica nanoparticles of size ∼70-80 nm for application as abrasive particles in Chemical Mechanical Planarization (CMP) process. Core silica nanoparticles were initially synthesized using micro-emulsion method. Ceria coating on these ultrafine and spherical silica nanoparticles was achieved using controlled chemical precipitation method. Study of various parameters influencing the formation of ceria coated silica nanoparticles of size less than 100 nm has been undertaken and reported. Ceria coating over silica nanoparticles was varied by controlling the reaction temperature, pH and precursor concentrations. Characterization studies using X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Energy Dispersive X-ray analysis show formation of crystalline CeO2 coating of ∼10 nm thickness over silica with spherical morphology and particle size <100 nm. Aqueous slurry of ceria coated silica abrasive was prepared and employed for polishing of oxide and nitride films on silicon substrates. Polished films were studied using ellipsometry and an improvement in SiO2:SiN selective removal rates up to 12 was observed using 1 wt% ceria coated silica nanoparticles slurry.

  4. Titanium dioxide nanoparticles prepared by laser pyrolysis: Synthesis and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Figgemeier, E.; Kylberg, W.; Constable, E.; Scarisoreanu, M.; Alexandrescu, R.; Morjan, I.; Soare, I.; Birjega, R.; Popovici, E.; Fleaca, C.; Gavrila-Florescu, L.; Prodan, G.

    2007-12-01

    TiO 2 nanoparticles were synthesized via the laser pyrolysis of titanium tetrachloride-based gas-phase mixtures. In the obtained nanopowders, a mixture of anatase and rutile phases with mean particle size of about 14 nm was identified. Using the thermal heated laser nanopowders, mechanically stable films were produced by immobilizing titania nanopowders on glass substrates (the doctor blading method followed by compression). The photocatalytic activity of the prepared films was tested by the degradation of 4-chlorophenol in an aqueous solution under UV-illumination. By referring to known commercial samples (Degussa P25) similarly prepared, higher photocatalytic efficiency was found for the laser-prepared samples.

  5. Sonochemical Process for the Preparation of Novel Calcium Zinc Molybdate Nanoparticles

    NASA Astrophysics Data System (ADS)

    Bhanvase, B. A.; Kadam, V. B.; Rode, T. D.; Jadhao, P. R.

    2015-06-01

    The present work deals with the use of sonochemical and conventional mixing process for the preparation of calcium zinc molybdate (CZM) nanoparticles using calcium chloride and sodium zinc molybdate as a precursor material without addition of any emulsifying agent. This new process is useful to control the size and shape of the CZM nanoparticles. The formed product was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The formation of CZM was confirmed through XRD, FTIR and elemental analysis. The pH and conductivity results show that sonochemical process takes less time compared to conventional process for the preparation of CZM nanoparticles. The use of sonochemical process during the preparation of CZM nanoparticles results in reduction of the size and nearly the cubic shape is obtained due to the improved solute transfer rate, rapid nucleation, and formation of a large number of nuclei in the presence of cavitation.

  6. Preparation and characterization of Ga2O3 and GaN nanoparticles

    NASA Astrophysics Data System (ADS)

    Rusu, E.; Ursaki, V.; Raevschi, S.; Vlazan, P.

    2015-02-01

    In this communication, we present results on preparation of GaN nanoparticles by conversion of Ga2O3 nanocrystals in a flow of NH3 and H2. The monoclinic Ga2O3 nanoparticles have been prepared by hydrothermal method with gallium nitrate and sodium hydroxide as precursors. Ga2O3 nanowires are produced with increasing the duration of the hydrothermal process up to 24 hours. The production of β-phase Ga2O3 has been confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. According to XRD, Raman and FTIR spectra, wurtzite type GaN nanocrystals with an average size of 28.6 nm are obtained by nitridation of Ga2O3 nanoparticles. Doping of Ga2O3 nanomaterial with Eu3+ ions in the hydrothermal process is demonstrated, and the emission spectra of this Eu-doped nanomaterial are compared with those of Eu-doped nanoparticles prepared previously by solid state reactions.

  7. Preparation and characterization of resistant starch type IV nanoparticles through ultrasonication and miniemulsion cross-linking.

    PubMed

    Ding, Yongbo; Zheng, Jiong; Xia, Xuejuan; Ren, Tingyuan; Kan, Jianquan

    2016-05-01

    This study aimed to assess the properties of resistant starch type IV (chemically modified starch, RS4) prepared from a new and convenient synthesis route by using ultrasonication combined with water-in-oil miniemulsion cross-linking technique. A three-factor Box-Behnken design and optimization was used to minimize particle size through the developed RS4 nanoparticles. The predicted minimized Z-Avel (576.1nm) under the optimum conditions of the process variables (ultrasonic power, 214.57W; sonication time, 114.73min; and oil/water ratio, 10.54:1) was very close to the experimental value (651.0nm) determined in a batch experiment. After preparing the RS4 nanoparticles, morphological, physical, chemical, and functional properties were assessed. Results revealed that RS4 nanoparticle size reached about 600nm. Scanning electron microscopy images showed that ultrasonication induced notches and grooves on the surface. Under polarized light, the polarized cross was impaired. X-ray diffraction results revealed that the crystalline structure was disrupted. Smaller or no endotherms were exhibited in DSC analysis. In the FTIR graph, new peaks at 1532.91 and 1451.50cm(-1) were observed, and pasting properties were reduced. Amylose content, solubility, and SP increased, but RS content decreased. Anti-digestibility remained after ultrasonication. The prepared RS4 nanoparticles could be extensively used in biomedical applications and in the development of new medical materials. PMID:26877007

  8. Preparation of albumin based nanoparticles for delivery of fisetin and evaluation of its cytotoxic activity.

    PubMed

    Ghosh, Pooja; Singha Roy, Atanu; Chaudhury, Susmitnarayan; Jana, Saikat Kumar; Chaudhury, Koel; Dasgupta, Swagata

    2016-05-01

    Fisetin is a well known flavonoid that shows several properties such as antioxidant, antiviral and anticancer activities. Its use in the pharmaceutical field is limited due to its poor aqueous solubility which results in poor bioavailability and poor permeability. The aim of our present study is to prepare fisetin loaded human serum albumin nanoparticles to improve its bioavailability. The nanoparticles were prepared by a desolvation method and characterized by spectroscopic and microscopic techniques. The particles were smooth and spherical in nature with an average size of 220±8nm. The encapsulation efficiency was found to be 84%. The in vitro release profile showed a biphasic pattern and the release rate increases with increase in ionic strength of solution. We have also confirmed the antioxidant activity of the prepared nanoparticles by a DPPH (2,2-diphenyl-1-picrylhydrazyl) assay. Further its anticancer activity was evaluated using MCF-7 breast cancer cell lines. Our findings suggest that fisetin loaded HSA nanoparticles could be used to transfer fisetin to target areas under specific conditions and thus may find use as a delivery vehicle for the flavonoid. PMID:26820351

  9. Holmium Nanoparticles: Preparation and In Vitro Characterization of a New Device for Radioablation of Solid Malignancies

    PubMed Central

    Bult, Wouter; Varkevisser, Rosanne; Soulimani, Fouad; Seevinck, Peter R.; de Leeuw, Hendrik; Bakker, Chris J. G.; Luijten, Peter R.; van het Schip, Alfred D.; Hennink, Wim E.

    2010-01-01

    ABSTRACT Purpose The present study introduces the preparation and in vitro characterization of a nanoparticle device comprising holmium acetylacetonate for radioablation of unresectable solid malignancies. Methods HoAcAc nanoparticles were prepared by dissolving holmium acetylacetonate in chloroform, followed by emulsification in an aqueous solution of a surfactant and evaporation of the solvent. The diameter, surface morphology, holmium content, and zeta potential were measured, and thermal behavior of the resulting particles was investigated. The stability of the particles was tested in HEPES buffer. The r2* relaxivity of protons and mass attenuation coefficient of the nanoparticles were determined. The particle diameter and surface morphology were studied after neutron activation. Results Spherical particles with a smooth surface and diameter of 78 ± 10 nm were obtained, and the particles were stable in buffer. Neutron irradiation did not damage the particles, and adequate amounts of activity were produced for nuclear imaging and radioablation of malignancies through intratumoral injections. Conclusions The present study demonstrates that HoAcAc nanoparticles were prepared using a solvent evaporation process. The particle diameter can easily be adapted and can be optimized for specific therapeutic applications and tumor types. PMID:20680667

  10. Hydrothermal preparation of one-dimensional assemblies of PbS nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, Debao; Yu, Dabin; Mo, Maosong; Liu, Xianming; Qian, Yitai

    2003-03-01

    The preparation of one-dimensional assemblies of PbS nanoparticles is described. By treating the suspension of PbCl2 powders in aqueous thioacetamide solution at 120 °C for 18 h, PbS nanoparticles were synthesized in regular chain-like patterns. The particles were less than 100 nm in sizes, and were organized into micron-length assemblies. The starting agents have much influence on the morphology of the products. The possible growth mechanism is also discussed.

  11. Preparation of linoleic acid-capped silver nanoparticles and their antimicrobial effect.

    PubMed

    Das, R; Gang, S; Nath, S S; Bhattacharjee, R

    2012-06-01

    Silver nanoparticles have been prepared through the chemical reduction of silver ions by ethanol using linoleic acid as a stabilising agent. This colloidal solution shows an absorption band in the visible range with an absorption peak at 421 nm. The peaks in the X-ray diffraction (XRD) pattern matches well with the standard values of the face-centred-cubic form of metallic silver. Transmission Electron Microscope (TEM) micrograph shows a nearly uniform distribution of the particles with an average size of 8 nm. This linoleic acid-capped silver nanoparticles show antimicrobial activity against Escherichia coli and Staphylococcus aureus. PMID:22559712

  12. Preparation and application of polymer-grafted magnetic nanoparticles for lipase immobilization

    NASA Astrophysics Data System (ADS)

    Yong, Yang; Bai, Yongxiao; Li, Yanfeng; Lin, Lei; Cui, Yanjun; Xia, Chungu

    Functionalized superparamagnetic particles were prepared by graft polymerization of glycidyl methacrylate and methacryloxyethyl trimethyl ammonium chloride onto the surface of modified-Fe 3O 4 nanoparticles. The resultant particles were characterized by X-ray powder diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and vibrating sample magnetometry. The results indicate that the polymer chains had been effectively grafted onto the surface of Fe 3O 4 nanoparticles. The functionalized particles remained dispersive and superparamagnetic. Lipase was immobilized on the magnetic particles under mild conditions by electrostatic adsorption and covalent binding with the activity recovery up to 70.4%. The immobilized lipase had better thermal stability compared to free lipase.

  13. Preparation and properties of amorphous titania-coated zinc oxide nanoparticles

    SciTech Connect

    Liao Minhung . E-mail: liaomh@mail.tit.edu.tw; Hsu, C.-H.; Chen, D.-H. . E-mail: chendh@mail.ncku.edu.tw

    2006-07-15

    Amorphous TiO{sub 2}-coated ZnO nanoparticles were prepared by the solvothermal synthesis of ZnO nanoparticles in ethanol and the followed by sol-gel coating of TiO{sub 2} nanolayer. The analyses of X-ray diffraction (XRD) and transmission electron microscopy (TEM) revealed that the resultant ZnO nanoparticles were hexagonal with a wurtzite structure and a mean diameter of about 60 nm. Also, after TiO{sub 2} coating, the TEM images clearly indicated the darker ZnO nanoparticles being surrounded by the lighter amorphous TiO{sub 2} layers. The zeta potential analysis revealed the pH dependence of zeta potentials for ZnO nanoparticles shifted completely to that for TiO{sub 2} nanoparticles after TiO{sub 2} coating, confirming the formation of core-shell structure and suggesting the coating of TiO{sub 2} was achieved via the adhesion of the hydrolyzed species Ti-O{sup -} to the positively charged surface of ZnO nanoparticles. Furthermore, the analyses of Fourier transform infrared (FTIR) and Raman spectra were also conducted to confirm that amorphous TiO{sub 2} were indeed coated on the surface of ZnO nanoparticles. In addition, the analyses of ultraviolet-visible (UV-VIS) and photoluminescence (PL) spectra revealed that the absorbance of amorphous TiO{sub 2}-coated ZnO nanoparticles at 375 nm gradually decreased with an increase in the Ti/Zn molar ratio and the time for TiO{sub 2} coating, and the emission intensity of ZnO cores could be significantly enhanced by the amorphous TiO{sub 2} shell. - Graphical abstract: Amorphous titania-coated ZnO nanoparticles with a core-shell structure were prepared. It was found that the emission intensity of ZnO cores could be significantly enhanced by the amorphous TiO{sub 2} shell.

  14. An investigation of structural, magnetic and microwave properties of strontium hexaferrite nanoparticles prepared by a sol-gel process with doping SN and Tb

    NASA Astrophysics Data System (ADS)

    Jamalian, Majid

    2015-03-01

    The goal of this study was to investigate the structural, magnetic and microwave properties of Sn4+-Tb4+ substituted strontium ferrite with chemical formula of SrFe12-x(SnTb)x/2O19(x=0-2)(in the step of 0.5) nanoparticles prepared by the sol-gel method. In order to study the formation of hexaferrite phase, X-ray diffraction analysis was carried out and it was discovered that a single magnetoplumbite was formed. A field emission scanning microscopy was hired to explore the morphology and particle size of nanopowders. Fourier-transform infrared was employed to confirm different bond modes which were structured. A vibrating-sample magnetometer was used to investigate the magnetic characteristics of the prepared samples. The results showed that with an increase in substitutions, Sn-Tb, magnetization and remanence were increased along with a decrease in coercivity. A vector network analyzer was utilized to scrutinize the microwave properties. The resultant data showed a striking achievement with high reflection loss value and a wide bandwidth in the range of 20-26 GHz.

  15. Chitosan-poly (lactide-co-glycolide) (CS-PLGA) nanoparticles containing metformin HCl: preparation and in vitro evaluation.

    PubMed

    Gundogdu, Nuran; Cetin, Meltem

    2014-11-01

    In this study, the preparation and in vitro characterisation of metformin HCl-loaded CS-PLGA nanoparticles (NPs) were aimed. The prepared nanoparticles (blank nanoparticles (C-1), 50 mg of metformin HCl loaded nanoparticles (C-2) and 75 mg of metformin HCl loaded nanoparticles (C-3) ranged in size from 506.67±13.61 to 516.33±16.85 nm and had surface charges of 22.57±1.21 to 32.37±0.57 mV. Low encapsulation efficiency was observed for both nanoparticle formulations due to the leakage of metformin HCl to the external medium during preparation of nanoparticles. Nanoparticle formulations showed highly reproducible drug release profiles. ~20% of metformin HCl was released within 30 minutes and approximately 98% of the loaded metformin HCl was released at 144 hours in a phosphate buffer (PB; pH 6.8). No statistically significant difference was noted between the in vitro release profiles of the nanoparticles (C-2 and C-3) containing metformin HCl. Also, nanoparticles were characterised using FT-IR and DSC. PMID:25362616

  16. Au nanoparticle micropatterns prepared from self-assembled films.

    PubMed

    Lu, Conghua; Wei, Fang; Wu, Nianzu; Huang, Lan; Zhao, Xinsheng; Jiao, Xiaoming; Luo, Chuanqiou; Cao, Weixiao

    2004-02-01

    A kind of hybrid multilayer film based on mercaptobenzoic acid-capped Au nanoparticles (MBA-Au-NPs) and photoreactive nitrodiazoresin (NDR) has been fabricated via electrostatic self-assembly. Upon exposure to UV light, the initial ionic bonds between the layers of the film convert into covalent bonds and the film stability toward polar solvents, salt, or surfactant solutions increases significantly. The micropatterned NDR/MBA-Au-NP film with the covalently linked architecture was formed by selecting exposure of the film through a photomask and later developed in sodium dodecyl sulfate (SDS) aqueous solution. The metallic Au-NP micropatterns, furthermore, are produced by sintering the micropatterned NDR/MBA-Au-NP film at 550 degrees C, at which the organic components are removed completely. The well-defined micropatterns were characterized with atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM), microscope with a charge-coupled device (CCD) camera, and X-ray photoelectron spectroscopy (XPS). PMID:15773132

  17. Preparation and Characterization of Gelatin Nanofibers Containing Silver Nanoparticles

    PubMed Central

    Jeong, Lim; Park, Won Ho

    2014-01-01

    Ag nanoparticles (NPs) were synthesized in formic acid aqueous solutions through chemical reduction. Formic acid was used for a reducing agent of Ag precursor and solvent of gelatin. Silver acetate, silver tetrafluoroborate, silver nitrate, and silver phosphate were used as Ag precursors. Ag+ ions were reduced into Ag NPs by formic acid. The formation of Ag NPs was characterized by a UV-Vis spectrophotometer. Ag NPs were quickly generated within a few minutes in silver nitrate (AgNO3)/formic acid solution. As the water content of formic acid aqueous solution increased, more Ag NPs were generated, at a higher rate and with greater size. When gelatin was added to the AgNO3/formic acid solution, the Ag NPs were stabilized, resulting in smaller particles. Moreover, gelatin limits further aggregation of Ag NPs, which were effectively dispersed in solution. The amount of Ag NPs formed increased with increasing concentration of AgNO3 and aging time. Gelatin nanofibers containing Ag NPs were fabricated by electrospinning. The average diameters of gelatin nanofibers were 166.52 ± 32.72 nm, but these decreased with the addition of AgNO3. The average diameters of the Ag NPs in gelatin nanofibers ranged between 13 and 25 nm, which was confirmed by transmission electron microscopy (TEM). PMID:24758929

  18. Oleate-based hydrothermal preparation of CoFe2O4 nanoparticles, and their magnetic properties with respect to particle size and surface coating

    NASA Astrophysics Data System (ADS)

    Repko, Anton; Vejpravová, Jana; Vacková, Taťana; Zákutná, Dominika; Nižňanský, Daniel

    2015-09-01

    We present a facile and high-yield synthesis of cobalt ferrite nanoparticles by hydrothermal hydrolysis of Co-Fe oleate in the presence of pentanol/octanol/toluene and water at 180 or 220 °C. The particle size (6-10 nm) was controlled by the composition of the organic solvent and temperature. Magnetic properties were then investigated with respect to the particle size and surface modification with citric acid or titanium dioxide (leading to hydrophilic particles). The as-prepared hydrophobic nanoparticles (coated by oleic acid) had a minimum inter-particle distance of 2.5 nm. Their apparent blocking temperature (estimated as a maximum of the zero-field-cooled magnetization) was 180 K, 280 K and 330 K for the particles with size of 6, 9 and 10.5 nm, respectively. Replacement of oleic acid on the surface by citric acid decreased inter-particle distance to less than 1 nm, and increased blocking temperature by ca. 10 K. On the other hand, coating with titanium dioxide, supported by nitrilotri(methylphosphonic acid), caused increase of the particle spacing, and lowering of the blocking temperature by ca. 20 K. The CoFe2O4@TiO2 nanoparticles were sufficiently stable in water, methanol and ethanol. The particles were also investigated by Mössbauer spectroscopy and alternating-current (AC) susceptibility measurements, and their analysis with Vögel-Fulcher and power law. Effect of different particle coating and dipolar interactions on the magnetic properties is discussed.

  19. Formulation/Preparation of Functionalized Nanoparticles for In Vivo Targeted Drug Delivery

    PubMed Central

    Gu, Frank; Langer, Robert; Farokhzad, Omid C.

    2014-01-01

    Summary Targeted cancer therapy allows the delivery of therapeutic agents to cancer cells without incurring undesirable side effects on the neighboring healthy tissues. Over the past decade, there has been an increasing interest in the development of advanced cancer therapeutics using targeted nanoparticles. Here we describe the preparation of drug-encapsulated nanoparticles formulated with biocompatible and biodegradable poly(D,L-lactic-co-glycolic acid)-block-poly(ethylene glycol) (PLGA-b-PEG) copolymer and surface functionalized with the A10 2-fluoropyrimidine ribonucleic acid aptamers that recognize the extracellular domain of prostate-specific membrane antigen (PSMA), a well-characterized antigen expressed on the surface of prostate cancer cells. We show that the self-assembled nanoparticles can selectively bind to PSMA-targeted prostate cancer cells in vitro and in vivo. This formulation method may contribute to the development of highly selective and effective cancer therapeutic and diagnostic devices. PMID:19488725

  20. Preparation of gold nanoparticles using Salicornia brachiata plant extract and evaluation of catalytic and antibacterial activity.

    PubMed

    Ayaz Ahmed, Khan Behlol; Subramanian, Swetha; Sivasubramanian, Aravind; Veerappan, Ganapathy; Veerappan, Anbazhagan

    2014-09-15

    The current study deals with the synthesis of gold nanoparticles (AuNPs) using Salicornia brachiata (Sb) and evaluation of their antibacterial and catalytic activity. The SbAuNPs showed purple color with a characteristic surface plasmon resonance peak at 532 nm. Scanning electron microscopy and transmission electron microscopy revealed polydispersed AuNPs with the size range from 22 to 35 nm. Energy dispersive X-ray and thin layer X-ray diffraction analysis clearly shows that SbAuNPs was pure and crystalline in nature. As prepared gold nanoparticles was used as a catalyst for the sodium borohydride reduction of 4-nitro phenol to 4-amino phenol and methylene blue to leucomethylene blue. The green synthesized nanoparticles exhibited potent antibacterial activity against the pathogenic bacteria, as evidenced by their zone of inhibition. In addition, we showed that the SbAuNPs in combination with the regular antibiotic, ofloxacin, exhibit superior antibacterial activity than the individual. PMID:24762573

  1. Preparation of gold nanoparticles using Salicornia brachiata plant extract and evaluation of catalytic and antibacterial activity

    NASA Astrophysics Data System (ADS)

    Ayaz Ahmed, Khan Behlol; Subramanian, Swetha; Sivasubramanian, Aravind; Veerappan, Ganapathy; Veerappan, Anbazhagan

    2014-09-01

    The current study deals with the synthesis of gold nanoparticles (AuNPs) using Salicornia brachiata (Sb) and evaluation of their antibacterial and catalytic activity. The SbAuNPs showed purple color with a characteristic surface plasmon resonance peak at 532 nm. Scanning electron microscopy and transmission electron microscopy revealed polydispersed AuNPs with the size range from 22 to 35 nm. Energy dispersive X-ray and thin layer X-ray diffraction analysis clearly shows that SbAuNPs was pure and crystalline in nature. As prepared gold nanoparticles was used as a catalyst for the sodium borohydride reduction of 4-nitro phenol to 4-amino phenol and methylene blue to leucomethylene blue. The green synthesized nanoparticles exhibited potent antibacterial activity against the pathogenic bacteria, as evidenced by their zone of inhibition. In addition, we showed that the SbAuNPs in combination with the regular antibiotic, ofloxacin, exhibit superior antibacterial activity than the individual.

  2. Formulation/Preparation of Functionalized Nanoparticles for In Vivo Targeted Drug Delivery

    NASA Astrophysics Data System (ADS)

    Gu, Frank; Langer, Robert; Farokhzad, Omid C.

    Targeted cancer therapy allows the delivery of therapeutic agents to cancer cells without incurring undesirable side effects on the neighboring healthy tissues. Over the past decade, there has been an increasing interest in the development of advanced cancer therapeutics using targeted nanoparticles. Here we describe the preparation of drug-encapsulated nanoparticles formulated with biocompatible and biodegradable poly( d, l-lactic-co-glycolic acid)-block-poly(ethylene glycol) (PLGA-b-PEG) copolymer and surface functionalized with the A10 2-fluoropyrimidine ribonucleic acid aptamers that recognize the extracellular domain of prostate-specific membrane antigen (PSMA), a well-characterized antigen expressed on the surface of prostate cancer cells. We show that the self-assembled nanoparticles can selectively bind to PSMA-targeted prostate cancer cells in vitro and in vivo. This formulation method may contribute to the development of highly selective and effective cancer therapeutic and diagnostic devices.

  3. Effect of various formulation parameters on the properties of polymeric nanoparticles prepared by multiple emulsion method.

    PubMed

    Rizkalla, Nevine; Range, Charlotte; Lacasse, François-Xavier; Hildgen, Patrice

    2006-02-01

    This work evaluates and interprets underlying mechanisms behind various aspects related to preparation and physical characteristics of polymeric nanoparticles (NP). These were prepared from different biodegradable polymers according to a water-in-oil-in-water emulsion solvent evaporation method. Polymers used were poly(lactic-co-glycolic) acid (PLGA), poly (lactic acid) (PLA), (PLA-PEG-PLA) triblock and (PLA-PEG-PLA)n multi-block co-polymers. A model DNA, as an example of a hydrophilic drug, was encapsulated in the internal aqueous phase. The primary emulsion was prepared using a high shear turbine mixer. The secondary emulsion was prepared by high-pressure homogenization. Surface morphology and internal structure were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Influence of process variables on the physical properties of NP has been studied. Release of DNA was evaluated. In addition, changes occurring to NP porosity and surface area during degradation were followed. Nanoparticle size was ranging between 200-700 nm, according to the preparation conditions. Homogenizing pressure, concentration of the emulsifying agent used, polymer concentration and type and the concentration of a cryoprotectant had variable effects on NP size, surface area and porosity. Batches of NP where no emulsifying agent was added were obtained successfully. The release rate of the DNA from NP was mainly dependent on porosity, which varied significantly among used polymers. The preparation technique was efficient in encapsulating the model DNA and will be used for plasmid encapsulation in a future work. PMID:16830976

  4. Preparation and in vitro investigation of antigastric cancer activities of carvacrol-loaded human serum albumin nanoparticles.

    PubMed

    Maryam, Keshavarzi; Shakeri, Shahryar; Kiani, Keyhaneh

    2015-10-01

    In this study, carvacrol-loaded human serum albumin (HSA) nanoparticles were developed and characterised. Nanoparticles were prepared by desolvation and emulsion/desolvation methods. Encapsulation efficiency (EE%) and loading capacity (LC%) of nanoparticles prepared by desolvation method were 48.4 and 45.1%, respectively. Carvacrol-loaded nanoparticles had 132±42 nm in diameter with monomodal distribution. Carvacrol-loaded nanoparticles which is prepared by emulsion/desolvation method had EE% and LC% of 32 and 32.3%, respectively, and 230±38 nm in size. The release of carvacrol from nanoparticles was monitored in phosphate-buffered saline (pH=7.4), 100 rpm at 37°C for 10 days. About 21.4% of carvacrol was released after 3 h from nanoparticles that were prepared by desolvation method. In emulsion/desolvation method, 26.8% of total carvacrol was released during 3 h of incubation. Cytotoxicity effect of loaded carvacrol was assessed by 3-[4, 5 dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) test on gastric cancer cells line (AGS). Cell line was exposed to the free carvacrol, unloaded and carvacrol-loaded nanoparticles for 48 h. The half maximal inhibitory concentration (IC50) for free carvacrol, unloaded and carvacrol-loaded HSA nanoparticles were 30, 1070 and 120 µg/ml, respectively. In conclusion, the results of this study showed applications of HSA nanoparticles for entrapment of carvacrol and antigastric cancer activity. Moreover, loading of carvacrol in combination with chemotherapy agents into the HSA nanoparticles may treat cancer cells better than single drug loaded nanoparticles. PMID:26435283

  5. Preparation and optimization of N-trimethyl-O-carboxymethyl chitosan nanoparticles for delivery of low-molecular-weight heparin.

    PubMed

    Mahjub, Reza; Heidari Shayesteh, Tavakol; Radmehr, Moojan; Vafaei, Seyed Yaser; Amini, Mohsen; Dinarvand, Rasoul; Dorkoosh, Farid Abedin

    2016-02-01

    The aim of this study was preparation, optimization and in vitro characterization of nanoparticles composed of 6-[O-carboxymethyl]-[N,N,N-trimethyl] (TMCMC) for oral delivery of low-molecular-weight heparin. The chitosan derivative was synthesized. Nanoparticles were prepared using the polyelectrolyte complexation method. Box-Behnken response surface experimental design methodology was used for optimization of nanoparticles. The morphology of nanoparticles was studied using transmission electron microscopy. In vitro release of enoxaparin from nanoparticles was determined under simulated intestinal fluid. The cytotoxicity of nanoparticles on a Caco-2 cell line was determined, and finally the transport of prepared nanoparticles across Caco-2 cell monolayer was defined. Optimized nanoparticles with proper physico-chemical properties were obtained. The size, zeta potential, poly-dispersity index, entrapment efficiency and loading efficiency of nanoparticles were reported as 235 ± 24.3 nm, +18.6 ± 2.57 mV, 0.230 ± 0.03, 76.4 ± 5.43% and 12.6 ± 1.37%, respectively. Morphological studies revealed spherical nanoparticles with no sign of aggregation. In vitro release studies demonstrated that 93.6 ± 1.17% of enoxaparin released from nanoparticles after 600 min of incubation. MTT cell cytotoxicity studies showed no cytotoxicity at 3 h post-incubation, while the study demonstrated concentration-dependent cytotoxicity after 24 h of exposure. The obtained data had shown that the nanoparticles prepared from trimethylcarboxymethyl chitosan may be considered as a good candidate for oral delivery of enoxaparin. PMID:25255172

  6. Heat generation ability in AC magnetic field of nano MgFe2O4-based ferrite powder prepared by bead milling

    NASA Astrophysics Data System (ADS)

    Hirazawa, Hideyuki; Aono, Hiromichi; Naohara, Takashi; Maehara, Tsunehiro; Sato, Mitsunori; Watanabe, Yuji

    2011-03-01

    Nanosized MgFe2O4-based ferrite powder having heat generation ability in an AC magnetic field was prepared by bead milling and studied for thermal coagulation therapy applications. The crystal size and the particle size significantly decreased by bead milling. The heat generation ability in an AC magnetic field improved with the milling time, i.e. a decrease in crystal size. However, the heat generation ability decreased for excessively milled samples with crystal sizes of less than 5.5 nm. The highest heat ability (ΔT=34 °C) in the AC magnetic field (370 kHz, 1.77 kA/m) was obtained for fine MgFe2O4 powder having a ca. 6 nm crystal size (the samples were milled for 6-8 h using 0.1 mm ϕ beads). The heat generation of the samples was closely related to hysteresis loss, a B-H magnetic property. The reason for the high heat generation properties of the samples milled for 6-8 h using 0.1 mm ϕ beads was ascribed to the increase in hysteresis loss by the formation of a single domain. Moreover, the improvement in heating ability was obtained by calcination of the bead-milled sample at low temperature. In this case, the maximum heat generation (ΔT=41 °C) ability was obtained for a ca. 11 nm crystal size sample was prepared by crystal growth during the sample calcination. On the other hand, the ΔT value for Mg0.5Ca0.5Fe2O4 was synthesized using a reverse precipitation method decreased by bead milling.

  7. Facile preparation of magnetic carbonaceous nanoparticles for Pb2+ ions removal.

    PubMed

    Nata, Iryanti Fatyasari; Salim, Giyanto Wijaya; Lee, Cheng-Kang

    2010-11-15

    Magnetic carbonaceous nanoparticles were prepared by a facile two-step solution phase thermal synthesis. Magnetic nanoparticles (MNPs) with size less than 100 nm were first generated from FeCl(3) in a solvothermal reaction. The size could be significantly reduced to approximately 30 nm when 1,6-hexanediamine was employed in the reaction solution to functionalize the surface of MNPs with amine. Both the plain and amine-functionalized MNPs (MH) were effectively encapsulated in the carbonaceous shell by hydrothermal treatment in 0.5 M glucose solution. The saturation magnetization of MH decreased significantly from 70 to 25 emu/g after carbonaceous shell was formed. The as-prepared magnetic carbonaceous nanoparticles (MH@C) carries a negative surface charge (-30 mV) at neutral pH and has a point of zero charge (PZC) at pH 2. The carbonaceous shell not only can protect the magnetic nanoparticles (MNP) from the corrosive environment but also possesses a high adsorption capacity towards Pb(II). The adsorption isotherm at room temperature can be well-fitted by Langmuir model with a maximum adsorption capacity of 123 mg/g. PMID:20800347

  8. Film electrode prepared from oppositely charged silicate submicroparticles and carbon nanoparticles for selective dopamine sensing.

    PubMed

    Celebanska, Anna; Tomaszewska, Dorota; Lesniewski, Adam; Opallo, Marcin

    2011-07-15

    Film electrodes prepared from oppositely charged silicate submicroparticles and carbon nanoparticles was applied for selective dopamine sensing. Mesoporous silicate submicroparticles with tetraalkylammonium functionalities were prepared by sol-gel method. They were immobilised on an indium tin oxide film surface together with phenylsulphonated carbon nanoparticles by layer-by-layer method: alternative immersion into their suspensions. As it is shown by scanning electron microscopy the obtained film is composed of silicate submicroparticles covered by carbon nanoparticles. The nanoparticulate film is stable and its electroactive surface is significantly larger than substrate. Accumulation of redox active cations indicates that only fraction charged functionalities of carbon nanoparticles are employed in film formation. The obtained electrode exhibits catalytic properties towards dopamine oxidation and its interferences as ascorbic acid, uric acid and acetaminophen. This allows for selective determination of tenth micromolar concentration of dopamine in the presence of these interferences at milimolar level. The detection limit and linear range were determined to 0.1 × 10⁻⁶ mol dm⁻³ and 0.3-18 × 10⁻⁶ mol dm⁻³ respectively. PMID:21641787

  9. Preparation and quality control of silver nanoparticle-antibody conjugate for use in electrochemical immunoassays.

    PubMed

    Szymanski, Mateusz S; Porter, Robert A

    2013-01-31

    Metal nanoparticle-antibody conjugates are often used as optical or electrochemical markers in applications like immunohistochemistry, lateral flow tests, biosensors and immunoassays. In order to serve that role, an antibody needs to be immobilized on the surface of the nanoparticle. This is easily done, as proteins bind to gold and silver nanoparticles spontaneously. However, this immobilization process might result in nanoparticle aggregation or the loss of the bioactivity of the conjugated antibodies. In this work the optimization of antibody immobilization on silver colloid in order to obtain conjugates with the best possible activity is investigated. The parameters investigated were the type of immobilization buffer, its molarity and pH, the nanoparticle/antibody ratio and also blocking and washing protocols to reduce non-specific binding. The functionality of the obtained conjugates was tested with electrochemical immunoassay. It was found out that the optimum environment for immobilization of an anti-myoglobin antibody on silver nanoparticles was 0.2M boric acid pH 6.5 with 10 μg of antibody loading per 1 mL of silver colloid. For an anti-troponin antibody it was 0.1M boric acid pH 7.5 also with 10 μg/mL of antibody loading. The main problem for silver conjugation was the tendency of silver nanoparticles to aggregate during the immobilization process, but by choosing the optimum conditions the aggregation problem was completely removed. Here it is demonstrated that by using the conjugates prepared with an optimized protocol an increase in the sensitivity of the assay 10 times can be achieved. The electrochemical immunoassay described here can be used as a test for quality control of conjugates and for the estimation of batch-to-batch variability. PMID:23153725

  10. Tamoxifen citrate loaded solid lipid nanoparticles (SLN): preparation, characterization, in vitro drug release, and pharmacokinetic evaluation.

    PubMed

    Reddy, L Harivardhan; Vivek, K; Bakshi, Nishant; Murthy, R S R

    2006-01-01

    Solid lipid nanoparticles (SLN) were prepared by emulsification and high pressure homogenization technique and characterized by size analysis and differential scanning calorimetry. The influence of experimental factors such as homogenization pressure, time, and surfactant concentration on the nanoparticle size and distribution were investigated to optimize the formulation. Homogenization at 15,000 psi for 3 cycles was found to be optimum and resulted in smaller sized nanoparticles. In case of tristearin SLN (TSSLN), tripalmitin SLN (TPSLN), and glycerol behenate SLN (GBSLN), the relatively smaller sized nanoparticles were obtained with 3% sodium tauroglycocholate. The SLN were loaded with an anticancer agent, tamoxifen citrate (TC). The TC-loaded TSSLN shown lower entrapment efficiency (78.78%) compared to the TPSLN (86.75%) and GBSLN (98.64%). Short term stability studies indicated a significant increase in size of nanoparticles when stored at 500C, compared to those stored at 30 degrees C and 4 degrees C. The particle destabilization upon storage in case of all the types of nanoparticles studied was in the order of day light > artificial light > dark. An ultraviolet (UV) spectrophotometric method of estimation of tamoxifen in rat plasma was developed and validated. The TC-loaded TSSLN was administered to the rats intravenously and the pharmacokinetic parameters in the plasma were determined. The t(1/2) and mean residence time of TC-loaded TSSLN in plasma was about 3.5-fold (p < 0.001) and 3-fold (p < 0.001) higher, respectively, than the free tamoxifen, indicating the potential of TC-loaded TSSLN as a long circulating system in blood. Thus the above mentioned solid lipid nanoparticles can be a beneficial system to deliver tamoxifen to cancer tissues through enhanced permeability and retention (EPR) effect. PMID:16749527

  11. Preparation of multi-functionalized Fe3O4/Au nanoparticles for medical purposes.

    PubMed

    del Mar Ramos-Tejada, María; Viota, Julian L; Rudzka, Katarzyna; Delgado, Angel V

    2015-04-01

    In this work, we investigate a route towards the synthesis of multi-functionalized nanoparticles for medical purposes. The aim is to produce magnetite/gold (Fe3O4/Au) nanoparticles combining several complementary properties, specifically, being able to carry simultaneously an antitumor drug and a selected antibody chosen so as to improve specificity of the drug vehicle. The procedure included, firstly, the preparation of Fe3O4 cores coated with Au nanoparticles: this was achieved by using initially the layer-by-layer technique in order to coat the magnetite particles with a three polyelectrolyte (cationic-anionic-cationic) layer. With this, the particles became a good substrate for the growth of the gold layer in a well-defined core-shell structure. The resulting nanoparticles benefit from the magnetic properties of the magnetite and the robust chemistry and the biostability of gold surfaces. Subsequently, the Fe3O4/Au nanoparticles were functionalized with a humanized monoclonal antibody, bevacizumab, and a chemotherapy drug, doxorubicin. Taken together, bevacizumab enhances the therapeutic effect of chemotherapy agents on some kinds of tumors. In this work we first discuss the morphology of the particles and the electrical characteristics of their surface in the successive synthesis stages. Special attention is paid to the chemical stability of the final coating, and the physical stability of the suspensions of the nanoparticles in aqueous solutions and phosphate buffer. We describe how optical absorbance and electrokinetic data provide a follow up of the progress of the nanostructure formation. Additionally, the same techniques are employed to demonstrate that the composite nanoparticles are capable of loading/releasing doxorubicin and/or bevacizumab. PMID:25710633

  12. Preparation of Fe3O4 magnetic nanoparticles coated with gallic acid for drug delivery

    PubMed Central

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

    2012-01-01

    Background and methods Magnetic iron oxide nanoparticles were prepared using a sonochemical method under atmospheric conditions at a Fe2+ to Fe3+ molar ratio of 1:2. The iron oxide nanoparticles were subsequently coated with chitosan and gallic acid to produce a core-shell structure. Results X-ray diffraction demonstrated that the magnetic nanoparticles were pure Fe3O4 with a cubic inverse spinel structure. Transmission electron microscopy showed that the Fe3O4 nanoparticles were of spherical shape with a mean diameter of 11 nm, compared with 13 nm for the iron oxide-chitosan-gallic acid (FCG) nanocarriers. Conclusion The magnetic nanocarrier enhanced the thermal stability of the drug, gallic acid. Release of the active drug from the FCG nanocarrier was found to occur in a controlled manner. The gallic acid and FCG nanoparticles were not toxic in a normal human fibroblast (3T3) line, and anticancer activity was higher in HT29 than MCF7 cell lines. PMID:23166439

  13. Silk sericin loaded alginate nanoparticles: Preparation and anti-inflammatory efficacy.

    PubMed

    Khampieng, Thitikan; Aramwit, Pornanong; Supaphol, Pitt

    2015-09-01

    In this study, silk sericin loaded alginate nanoparticles were prepared by the emulsification method followed by internal crosslinking. The effects of various silk sericin loading concentration on particle size, shape, thermal properties, and release characteristics were investigated. The initial silk sericin loadings of 20, 40, and 80% w/w to polymer were incorporated into these alginate nanoparticles. SEM images showed a spherical shape and small particles of about 71.30-89.50 nm. TGA analysis showed that thermal stability slightly increased with increasing silk sericin loadings. FTIR analysis suggested interactions between alginate and silk sericin in the nanoparticles. The release study was performed in acetate buffer at normal skin conditions (pH 5.5; 32 °C). The release profiles of silk sericin exhibited initial rapid release, consequently with sustained release. These silk sericin loaded alginate nanoparticles were further incorporated into topical hydrogel and their anti-inflammatory properties were studied using carrageenan-induced paw edema assay. The current study confirms the hypothesis that the application of silk sericin loaded alginate nanoparticle gel can inhibit inflammation induced by carrageenan. PMID:26188300

  14. Chitosan-lignosulfonates sono-chemically prepared nanoparticles: characterisation and potential applications.

    PubMed

    Kim, Suyeon; Fernandes, Margarida M; Matamá, Teresa; Loureiro, Ana; Gomes, Andreia C; Cavaco-Paulo, Artur

    2013-03-01

    Due to their recognised properties of biocompatibility, biodegradability and sustainability, chitosan nanocarriers have been successfully used as new delivery systems. In this work, nanoparticles combining chitosan and lignosulfonates were developed for the first time for cosmetic and biomedical applications. The ability of lignosulfonates to act as a counter polyion for stabilisation of chitosan particles, generated using high intensity ultrasound, was investigated. Several conditions for particles preparation were tested and optimised and the resulting nanoparticles were comprehensively characterised by measuring particle size, zeta potential and polydispersity index. The pH of chitosan solution, sonication time and the presence of an adequate surfactant, poloxamer 407, were determinant factors on the development of smaller particles with low polydispersity index (an average particle size of 230 nm was obtained at pH 5 after 8 min of sonication). The beneficial effects of lignosulfonates complex on chitosan nanoparticles were further characterised. Greater stability to lysozyme degradation, biocompatibility with human cells and antimicrobial activity was found upon lignosulfonates incorporation into chitosan nanoparticles. Furthermore, these particles were able to incorporate a hydrophilic model protein - RNase A. A burst release was observed when nanoparticles were loaded with low amount of protein while with high protein content, a sustained release was found, suggesting that the protein cargo maybe loaded both at the surface as in the bulk of the particle, depending on the concentration of drug incorporated. PMID:23178385

  15. Preparation and Characterizations of Dispersible Fluorinated Hydroxyapatite Nanoparticles with Weak Antibacterial Activity.

    PubMed

    Furuzono, Tsutomu; Azuma, Yoshinao; Niigawa, Yuichi; Kogai, Yasumichi; Sawa, Yoshiki

    2016-01-01

    To develop a nanoscaled coating material for medical devices possessing weak antibacterial activity, dispersible and crystalline fluorinated hydroxyapatite (F-HAp) nanoparticles were prepared using antisintering agent to avoid calcination-induced sintering. The product was identical to fluorapatite, as determined by X-ray diffraction and Fourier transform infrared spectroscopy. The primary particles generally showed rod-shaped morphology with a length of 367 ± 67 nm and a width of 223 ± 21 nm measured by scanning electron microscopy (SEM). The dispersed average particle size (313 ± 51 nm) in ethanol analyzed by dynamic light scattering was almost the same as that obtained from the SEM images. In the evaluation of solubility in acidic aqueous solution, F-HAp and original hydroxyapatite (HAp) nanoparticles started to dissolve at around pH 3.4 and 4.2, respectively. Thus, the stability of F-HAp in a living body increased compared with original HAp. The antibacterial activity of F-HAp nanoparticles was higher than that of fluoride in sodium fluoride alone or the original HAp nanoparticles. However, it was estimated that the effect of F-HAp was much lower compared with that of silver, one of the popular antibacterial materials. Thus, the dispersed F-HAp nanoparticles possessing weak antimicrobial activity can be useful without severe damage to the living tissue. PMID:26720738

  16. Identification of Dewetting Stages and Preparation of Single Chain Gold Nanoparticle Rings by Colloidal Lithography.

    PubMed

    Nagy, Norbert; Zámbó, Dániel; Pothorszky, Szilárd; Gergely-Fülöp, Eszter; Deák, András

    2016-02-01

    Massively parallel nanoparticle assembly was carried out by means of colloidal lithographic experiments over a silicon substrate supported (sub)microparticle Langmuir-Blodgett monolayer, using high purity aqueous solution of PEGylated gold nanoparticles. The size of the polystyrene template particles in the monolayer was varied between 608 nm and 2.48 μm, while gold nanoparticles with diameters between 18 and 65 nm were used. Thanks to the PEGylation of the gold nanoparticles, they could be used as tracer objects to follow the drying process. In this way, different dewetting stages could be identified in the confined space between and underneath the template polystyrene spheres. Depending on the concentration of the nanoparticles, the presented approach allows the preparation of single-particle width necklace structures composed of gold particles. At the same time, the high purity of the substrate as well as of the evolved particle rings is preserved and unwanted particle deposition on the substrate surface is minimized. PMID:26751906

  17. Preparation, characterisation and antibacterial activity of a florfenicol-loaded solid lipid nanoparticle suspension.

    PubMed

    Wang, Ting; Chen, Xiaojin; Lu, Mengmeng; Li, Xihe; Zhou, WenZhong

    2015-12-01

    A florfenicol-loaded solid lipid nanoparticle (FFC-SLN) suspension was prepared by hot homogenisation and ultrasonic technique. The suspension was characterised for its release profile, stability, toxicity, and the physicochemical properties of the nanoparticles. Antibacterial activity of the suspension was evaluated in vitro and in vivo. The results showed that the mean diameter, polydispersity index and zeta potential of the nanoparticles were 253 ± 3 nm, 0.409 ± 0.022 and 47.5 ± 0.21 mV, respectively. In vitro release profile showed the FFC-SLN suspension had sustained release effect. The minimum inhibition concentration values of the FFC-SLN suspension were 6 and 3 µg/mL against Staphylococcus aureus and Escherichia coli respectively, compared with 3.5 and 2 µg/mL of native florfenicol. The suspension was relatively stable at 4°C and less stable at room temperature during 9 months storage. Although the nanoparticle carriers exhibited cytotoxicity in cell cultures, the LD50 of the lyophilised dry power of the suspension was higher than 5 g/kg body weight. Mortality protection against E. coli lethal infection in mice showed that the nanoparticle suspension had much better efficacy (6/10) than native drug (1/10). These results indicate that FFC-SLN suspension could be a promising formulation in veterinary medicine. PMID:26647811

  18. Formation and Cytotoxicity of Nanoparticles and Nanocubes Prepared from Gold and Silver Salts

    NASA Astrophysics Data System (ADS)

    Banker, Daniel; Dorrell, Skyler; Ivey, Prescott; Scurti, Joseph; Dobbins, Tabbetha

    Photothermal therapy is the use of electromagnetic radiation as the treatment for medical conditions such as cancer. Noble metal nanoparticles and nanocubes are brought to an excited state with laser light and as a result they release vibrational energy in the form of heat, which can be used to kill targeted cancer cells. Wet chemistry gives the basics for the preparation of nanoparticles and nanocubes. Using HAuCl4, AgNO3, tri-sodium citrate and other chemicals, we were able to successfully create gold and silver nanoparticles and nanocubes. The goal is to make sure that 3T3 cells can survive in a nanoparticle or nanocube doped medium so that we can then observe their reaction to photothermal effects. Cell culture techniques were done to 3T3 cells to keep them alive before the testing of cytotoxicity. Photothermal effect refers to the way that our nanoparticles or nanocubes can be photoexcited to release enough heat to kill the cells. We used a UV-Vis spectrophotometer to ensure that the correct wavelength laser. Assuming that the cells will survive living in the doped medium, a medium that has had nanomaterials introduced into it, we will use a high powered laser to observe what the excitation does to the cells since the photothermal effect should result in dead cells.

  19. Preparation, characterization, and in vivo evaluation of tanshinone IIA solid dispersions with silica nanoparticles

    PubMed Central

    Jiang, Yan-rong; Zhang, Zhen-hai; Liu, Qi-yuan; Hu, Shao-ying; Chen, Xiao-yun; Jia, Xiao-bin

    2013-01-01

    We prepared solid dispersions (SDs) of tanshinone IIA (TSIIA) with silica nanoparticles, which function as dispersing carriers, using a spray-drying method and evaluated their in vitro dissolution and in vivo performance. The extent of TSIIA dissolution in the silica nanoparticles/TSIIA system (weight ratio, 5:1) was approximately 92% higher than that of the pure drug after 60 minutes. However, increasing the content of silica nanoparticles from 5:1 to 7:1 in this system did not significantly increase the rate or extent of TSIIA dissolution. The physicochemical properties of SDs were investigated using scanning electron microscopy, differential scanning calorimetry, X-ray powder diffraction, and Fourier transforms infrared spectroscopy. Studying the stability of the SDs of TSIIA revealed that the drug content of the formulation and dissolution behavior was unchanged under the applied storage conditions. In vivo tests showed that SDs of the silica nanoparticles/TSIIA had a significantly larger area under the concentration-time curve, which was 1.27 times more than that of TSIIA (P < 0.01). Additionally, the values of maximum plasma concentration and the time to reach maximum plasma concentration of the SDs were higher than those of TSIIA and the physical mixing system. Based on these results, we conclude that the silica nanoparticle based SDs achieved complete dissolution, increased absorption rate, maintained drug stability, and showed improved oral bioavailability compared to TSIIA alone. PMID:23836971

  20. Electrochemical preparation and characterization of polypyrrole/stainless steel electrodes decorated with gold nanoparticles.

    PubMed

    Gutirrez Pineda, Eduart; Alcaide, Francisco; Rodrguez Presa, Mara J; Bolzn, Agustn E; Gervasi, Claudio A

    2015-02-01

    The electrosynthesis and characterization of polypyrrole(PPy)/stainless steel electrodes decorated with gold nanoparticles and the performance of the composite electrode for sensing applications is described. PPy films were grown in potassium perchlorate and sodium salicylate solutions under comparable electropolymerization conditions. Polymer films prepared in the presence of perchlorate ions exhibited worm-like structures, whereas columnar structures were obtained in salicylate-containing solutions. Voltammetric response of PPy films prepared in salicylate solutions was more reversible. PPy films were decorated with gold nanoparticles obtained by a double step potentiostatic electrodeposition routine that allowed fine control of deposit characteristics. Analysis of deposits was performed by means of SEM and confocal Raman spectroscopy. The electrocatalytic activity of the Au/PPy electrodes was assessed for the electro-oxidation of hydrazine and hydroxylamine. Results showed a successful optimization of the route of synthesis that rendered nanocomposite electrode materials with promising applications in electrochemical sensing. PMID:25569325