Science.gov

Sample records for au nanoparticles immobilized

  1. Development of stable pollution free TiO2/Au nanoparticle immobilized green photo catalyst for degradation of methyl orange.

    PubMed

    Murugan, Eagambaram; Rangasamy, Rajmohan

    2011-02-01

    Two types of heterogeneous nanoparticle immobilized photocatalysts viz., PSP4VP-TiO2 and PSP4VP-TiO2-Au were synthesized by immobilization of TiO2 and TiO2-Au nanoparticles individually onto the insoluble cross-linked poly(styrene)-co-poly(4-vinylpyridine) as a common matrix. These two different green photocatalysts were characterized by FT-IR, SEM, HRTEM and EDS analyses and proves that the respective nanoparticles were found to immobilize onto the matrix. The photocatalytic efficiency of these catalysts was examined using degradation of methyl orange as a model reaction and found they are excellent in UV and sunlight. The stability and recycle/reusability of the catalysts were also observed to be good. PMID:21485879

  2. Preparation of Au Nanoparticles Immobilized Cross-Linked Poly(4-vinylpyridine) Nanofibers and Their Catalytic Application for the Reduction of 4-Nitrophenol.

    PubMed

    Qin, Qi-Hu; Na, Hui; Zhang, Chunyu; Yu, Qizhou; Zhang, Xue-Quan; Zhang, He-Xin

    2015-05-01

    Catalytic nanofibers are prepared by the immobilization of Au nanoparticles (AuNPs) onto the surface of cross-linked electrospun poly(4-vinylpyridine) (P4VP) nanofibers. The crosslinking of the P4VP nanofibers by 1,4-diiodobutane via quaternization reaction greatly enhances the stability of the nanofibers against the solvent dissolution, which can then be used as promising platform for the immobilization of catalytic metal nanoparticles. The AuNPs immobilized cross-linked P4VP nanofibers have shown a good catalytic activity for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). PMID:26505022

  3. Synergistic catalysis of metal-organic framework-immobilized Au-Pd nanoparticles in dehydrogenation of formic acid for chemical hydrogen storage.

    PubMed

    Gu, Xiaojun; Lu, Zhang-Hui; Jiang, Hai-Long; Akita, Tomoki; Xu, Qiang

    2011-08-10

    Bimetallic Au-Pd nanoparticles (NPs) were successfully immobilized in the metal-organic frameworks (MOFs) MIL-101 and ethylenediamine (ED)-grafted MIL-101 (ED-MIL-101) using a simple liquid impregnation method. The resulting composites, Au-Pd/MIL-101 and Au-Pd/ED-MIL-101, represent the first highly active MOF-immobilized metal catalysts for the complete conversion of formic acid to high-quality hydrogen at a convenient temperature for chemical hydrogen storage. Au-Pd NPs with strong bimetallic synergistic effects have a much higher catalytic activity and a higher tolerance with respect to CO poisoning than monometallic Au and Pd counterparts. PMID:21761819

  4. Fabrication of quantum dot/silica core-shell particles immobilizing Au nanoparticles and their dual imaging functions

    NASA Astrophysics Data System (ADS)

    Kobayashi, Yoshio; Matsudo, Hiromu; Li, Ting-ting; Shibuya, Kyosuke; Kubota, Yohsuke; Oikawa, Takahiro; Nakagawa, Tomohiko; Gonda, Kohsuke

    2016-03-01

    The present work proposes preparation methods for quantum dot/silica (QD/SiO2) core-shell particles that immobilize Au nanoparticles (QD/SiO2/Au). A colloid solution of QD/SiO2 core-shell particles with an average size of 47.0 ± 6.1 nm was prepared by a sol-gel reaction of tetraethyl orthosilicate in the presence of the QDs with an average size of 10.3 ± 2.1 nm. A colloid solution of Au nanoparticles with an average size of 17.9 ± 1.3 nm was prepared by reducing Au3+ ions with sodium citrate in water at 80 °C. Introduction of amino groups to QD/SiO2 particle surfaces was performed using (3-aminopropyl)-triethoxysilane (QD/SiO2-NH2). The QD/SiO2/Au particles were fabricated by mixing the Au particle colloid solution and the QD/SiO2-NH2 particle colloid solution. Values of radiant efficiency and computed tomography for the QD/SiO2/Au particle colloid solution were 2.23 × 107 (p/s/cm2/sr)/(μW/cm2) at a QD concentration of 8 × 10-7 M and 1180 ± 314 Hounsfield units and an Au concentration of 5.4 × 10-2 M. The QD/SiO2/Au particle colloid solution was injected into a mouse chest wall. Fluorescence emitted from the colloid solution could be detected on the skin covering the chest wall. The colloid solution could also be X-ray-imaged in the chest wall. Consequently, the QD/SiO2/Au particle colloid solution was found to have dual functions, i.e., fluorescence emission and X-ray absorption in vivo, which makes the colloid solution suitable to function as a contrast agent for dual imaging processes.

  5. Immobilization of myoglobin on Au nanoparticle-decorated carbon nanotube/polytyramine composite as a mediator-free H2O2 and nitrite biosensor

    NASA Astrophysics Data System (ADS)

    Vilian, A. T. Ezhil; Veeramani, Vediyappan; Chen, Shen-Ming; Madhu, Rajesh; Kwak, Cheol Hwan; Huh, Yun Suk; Han, Young-Kyu

    2015-12-01

    A novel composite film was designed for use as a highly selective mediator-free amperometric biosensor, and a method was created for accomplishing direct electrochemistry of myoglobin on a multi-walled carbon nanotube and tyramine-modified composite decorated with Au nanoparticles on a glassy carbon electrode. The ultraviolet-visible and electrochemical impedance spectroscopy results showed that myoglobin retained its native conformation in the interaction with Au-PTy-f-MWCNT. The surface coverage of Mb-heme-Fe(II)/(III) immobilized on Au-PTy-f-MWCNT and the heterogeneous electron-transfer rate constant were 2.12 × 10-9 mol cm-2 and 4.86 s-1, respectively, indicating a higher loading capacity of the nanocomposite for direct electron transfer of Mb onto the electrode surface. The proposed Mb/Au-PTy-f-MWCNT biofilm exhibited excellent electrocatalytic behavior toward the reduction of H2O2 and the oxidation of nitrite with linear ranges of 2 to 5000 μM and 1 to 8000 μM and lower detection limits of 0.01 μM and 0.002 μM, respectively. An apparent Michaelis-Menten constant of 0.12 mM indicated that the Mb immobilized on the Au-PTy-f-MWCNT film retained its native activity. This biosensor can be successfully applied to detect H2O2 and nitrite in disinfectant cream, eye drops, pickle juice, and milk samples.

  6. Immobilization of myoglobin on Au nanoparticle-decorated carbon nanotube/polytyramine composite as a mediator-free H2O2 and nitrite biosensor

    PubMed Central

    Vilian, A. T. Ezhil; Veeramani, Vediyappan; Chen, Shen-Ming; Madhu, Rajesh; Kwak, Cheol Hwan; Huh, Yun Suk; Han, Young-Kyu

    2015-01-01

    A novel composite film was designed for use as a highly selective mediator-free amperometric biosensor, and a method was created for accomplishing direct electrochemistry of myoglobin on a multi-walled carbon nanotube and tyramine-modified composite decorated with Au nanoparticles on a glassy carbon electrode. The ultraviolet-visible and electrochemical impedance spectroscopy results showed that myoglobin retained its native conformation in the interaction with Au-PTy-f-MWCNT. The surface coverage of Mb-heme-Fe(II)/(III) immobilized on Au-PTy-f-MWCNT and the heterogeneous electron-transfer rate constant were 2.12 × 10−9 mol cm−2 and 4.86 s−1, respectively, indicating a higher loading capacity of the nanocomposite for direct electron transfer of Mb onto the electrode surface. The proposed Mb/Au-PTy-f-MWCNT biofilm exhibited excellent electrocatalytic behavior toward the reduction of H2O2 and the oxidation of nitrite with linear ranges of 2 to 5000 μM and 1 to 8000 μM and lower detection limits of 0.01 μM and 0.002 μM, respectively. An apparent Michaelis-Menten constant of 0.12 mM indicated that the Mb immobilized on the Au-PTy-f-MWCNT film retained its native activity. This biosensor can be successfully applied to detect H2O2 and nitrite in disinfectant cream, eye drops, pickle juice, and milk samples. PMID:26672985

  7. Flow-injection amperometric determination of glucose using a biosensor based on immobilization of glucose oxidase onto Au seeds decorated on core Fe₃O₄ nanoparticles.

    PubMed

    Samphao, Anchalee; Butmee, Preeyanut; Jitcharoen, Juthamas; Švorc, Ľubomír; Raber, Georg; Kalcher, Kurt

    2015-09-01

    An amperometric biosensor based on chemisorption of glucose oxidase (GOx) on Au seeds decorated on magnetic core Fe3O4 nanoparticles (Fe3O4@Au) and their immobilization on screen-printed carbon electrode bulk-modified with manganese oxide (SPCE{MnO2}) was designed for the determination of glucose. The Fe3O4@Au/GOx modified SPCE{MnO2} was used in a flow-injection analysis (FIA) arrangement. The experimental conditions were investigated in amperometric mode with the following optimized parameters: flow rate 1.7 mL min(-1), applied potential +0.38 V, phosphate buffer solution (PBS; 0.1 mol L(-1), pH 7.0) as carrier and 3.89 unit mm(-2) enzyme glucose oxidase loading on the active surface of the SPCE. The designed biosensor in FIA arrangement yielded a linear dynamic range for glucose from 0.2 to 9.0 mmol L(-1) with a sensitivity of 2.52 µA mM(-1) cm(-2), a detection limit of 0.1 mmol L(-1) and a quantification limit of 0.3 mmol L(-1). Moreover, a good repeatability of 2.8% (number of measurements n=10) and a sufficient reproducibility of 4.0% (number of sensors n=3) were achieved. It was found that the studied system Fe3O4@Au facilitated not only a simpler enzyme immobilization but also provided wider linear range. The practical application of the proposed biosensor for FIA quantification of glucose was tested in glucose sirup samples, honeys and energy drinks with the results in good accordance with those obtained by an optical glucose meter and with the contents declared by the producers. PMID:26003689

  8. Immobilization of bovine catalase onto magnetic nanoparticles.

    PubMed

    Doğaç, Yasemin İspirli; Teke, Mustafa

    2013-01-01

    The scope of this study is to achieve carrier-bound immobilization of catalase onto magnetic particles (Fe₃O₄ and Fe₂O₃NiO₂ · H₂O) to specify the optimum conditions of immobilization. Removal of H2O2 and the properties of immobilized sets were also investigated. To that end, adsorption and then cross-linking methods onto magnetic particles were performed. The optimum immobilization conditions were found for catalase: immobilization time (15 min for Fe₃O₄; 10 min for Fe2O₃NiO₂ · H₂O), the initial enzyme concentration (1 mg/mL), amount of magnetic particles (25 mg), and glutaraldehyde concentration (3%). The activity reaction conditions (optimum temperature, optimum pH, pH stability, thermal stability, operational stability, and reusability) were characterized. Also kinetic parameters were calculated by Lineweaver-Burk plots. The optimum pH values were found to be 7.0, 7.0, and 8.0 for free enzyme, Fe₃O₄-immobilized catalases, and Fe₂O₃NiO₂ · H₂O-immobilized catalases, respectively. All immobilized catalase systems displayed the optimum temperature between 25 and 35°C. Reusability studies showed that Fe₃O₄-immobilized catalase can be used 11 times with 50% loss in original activity, while Fe2O₃NiO₂ · H₂O-immobilized catalase lost 67% of activity after the same number of uses. Furthermore, immobilized catalase systems exhibited improved thermal and pH stability. The results transparently indicate that it is possible to have binding between enzyme and magnetic nanoparticles. PMID:23876136

  9. Self-assembly of thiolated cyanine aggregates on Au(111) and Au nanoparticle surfaces

    NASA Astrophysics Data System (ADS)

    Menéndez, Guillermo O.; Cortés, Emiliano; Grumelli, Doris; Méndez de Leo, Lucila P.; Williams, Federico J.; Tognalli, Nicolás G.; Fainstein, Alejandro; Vela, María Elena; Jares-Erijman, Elizabeth A.; Salvarezza, Roberto C.

    2012-01-01

    Heptamethinecyanine J-aggregates display sharp, intense fluorescence emission making them attractive candidates for developing a variety of chem-bio-sensing applications. They have been immobilized on planar thiol-covered Au surfaces and thiol-capped Au nanoparticles by weak molecular interactions. In this work the self-assembly of novel thiolated cyanine (CNN) on Au(111) and citrate-capped AuNPs from solutions containing monomers and J-aggregates has been studied by using STM, XPS, PM-IRRAS, electrochemical techniques and Raman spectroscopy. Data show that CNN species adsorb on the Au surfaces by forming thiolate-Au bonds. We found that the J-aggregates are preferentially adsorbed on the Au(111) surface directly from the solution while adsorbed CNN monomers cannot organize into aggregates on the substrate surface. These results indicate that the CNN-Au interaction is not able to disorganize the large J-aggregates stabilized by π-π stacking to optimize the S-Au binding site but it is strong enough to hinder the π-π stacking when CNNs are chemisorbed as monomers. The optical properties of the J-aggregates remain active after adsorption. The possibility of covalently bonding CNN J-aggregates to Au planar surfaces and Au nanoparticles controlling the J-aggregate/Au distance opens a new path regarding their improved stability and the wide range of biological applications of both CNN and AuNP biocompatible systems.Heptamethinecyanine J-aggregates display sharp, intense fluorescence emission making them attractive candidates for developing a variety of chem-bio-sensing applications. They have been immobilized on planar thiol-covered Au surfaces and thiol-capped Au nanoparticles by weak molecular interactions. In this work the self-assembly of novel thiolated cyanine (CNN) on Au(111) and citrate-capped AuNPs from solutions containing monomers and J-aggregates has been studied by using STM, XPS, PM-IRRAS, electrochemical techniques and Raman spectroscopy. Data show

  10. Immobilization of Polymeric Luminophor on Nanoparticles Surface

    NASA Astrophysics Data System (ADS)

    Bolbukh, Yuliia; Podkoscielna, Beata; Lipke, Agnieszka; Bartnicki, Andrzej; Gawdzik, Barbara; Tertykh, Valentin

    2016-04-01

    Polymeric luminophors with reduced toxicity are of the priorities in the production of lighting devices, sensors, detectors, bioassays or diagnostic systems. The aim of this study was to develop a method of immobilization of the new luminophor on a surface of nanoparticles and investigation of the structure of the grafted layer. Monomer 2,7-(2-hydroxy-3-methacryloyloxypropoxy)naphthalene (2,7-NAF.DM) with luminophoric properties was immobilized on silica and carbon nanotubes in two ways: mechanical mixing with previously obtained polymer and by in situ oligomerization with chemisorption after carrier's modification with vinyl groups. The attached polymeric (or oligomeric) surface layer was studied using thermal and spectral techniques. Obtained results confirm the chemisorption of luminophor on the nanotubes and silica nanoparticles at the elaborated synthesis techniques. The microstructure of 2,7-NAF.DM molecules after chemisorption was found to be not changed. The elaborated modification approach allows one to obtain nanoparticles uniformly covered with polymeric luminophor.

  11. Using supported Au nanoparticles as starting material for preparing uniform Au/Pd bimetallic catalysts

    SciTech Connect

    Villa, Alberto; Prati, Laura; Su, Dangshen; Wang, Di; Veith, Gabriel M

    2010-01-01

    One of the best methods for producing bulk homogeneous (composition) supported bimetallic AuPd clusters involves the immobilization of a protected Au seed followed by the addition of Pd. This paper investigates the importance of this gold seed in controlling the resulting bimetallic AuPd clusters structures, sizes and catalytic activities by investigating three different gold seeds. Uniform Au-Pd alloy were obtained when a steric/electrostatic protecting group, poly(vinyl alcohol) (PVA), was used to form the gold clusters on activated carbon (AC). In contrast Au/AC precursors prepared using Au nanoparticles with only electrostatic stabilization (tetrakis(hydroxypropyl)phosphonium chloride (THPC)), or no stabilization (magnetron sputtering) produced inhomogeneous alloys and segregation of the gold and palladium. The uniform alloyed catalyst (Pd{at}Au{sub PVA}/AC) is the most active and selective catalyst, while the inhomogenous catalysts are less active and selective. Further study of the PVA protected Au clusters revealed that the amount of PVA used is also critical for the preparation of uniform alloyed catalyst, their stability, and their catalytic activity.

  12. Immobilization of Polymeric Luminophor on Nanoparticles Surface.

    PubMed

    Bolbukh, Yuliia; Podkoscielna, Beata; Lipke, Agnieszka; Bartnicki, Andrzej; Gawdzik, Barbara; Tertykh, Valentin

    2016-12-01

    Polymeric luminophors with reduced toxicity are of the priorities in the production of lighting devices, sensors, detectors, bioassays or diagnostic systems. The aim of this study was to develop a method of immobilization of the new luminophor on a surface of nanoparticles and investigation of the structure of the grafted layer. Monomer 2,7-(2-hydroxy-3-methacryloyloxypropoxy)naphthalene (2,7-NAF.DM) with luminophoric properties was immobilized on silica and carbon nanotubes in two ways: mechanical mixing with previously obtained polymer and by in situ oligomerization with chemisorption after carrier's modification with vinyl groups. The attached polymeric (or oligomeric) surface layer was studied using thermal and spectral techniques. Obtained results confirm the chemisorption of luminophor on the nanotubes and silica nanoparticles at the elaborated synthesis techniques. The microstructure of 2,7-NAF.DM molecules after chemisorption was found to be not changed. The elaborated modification approach allows one to obtain nanoparticles uniformly covered with polymeric luminophor. PMID:27090657

  13. Collision-spike Sputtering of Au Nanoparticles.

    PubMed

    Sandoval, Luis; Urbassek, Herbert M

    2015-12-01

    Ion irradiation of nanoparticles leads to enhanced sputter yields if the nanoparticle size is of the order of the ion penetration depth. While this feature is reasonably well understood for collision-cascade sputtering, we explore it in the regime of collision-spike sputtering using molecular-dynamics simulation. For the particular case of 200-keV Xe bombardment of Au particles, we show that collision spikes lead to abundant sputtering with an average yield of 397 ± 121 atoms compared to only 116 ± 48 atoms for a bulk Au target. Only around 31 % of the impact energy remains in the nanoparticles after impact; the remainder is transported away by the transmitted projectile and the ejecta. The sputter yield of supported nanoparticles is estimated to be around 80 % of that of free nanoparticles due to the suppression of forward sputtering. PMID:26245857

  14. Collision-spike sputtering of Au nanoparticles

    SciTech Connect

    Sandoval, Luis; Urbassek, Herbert M.

    2015-08-06

    Ion irradiation of nanoparticles leads to enhanced sputter yields if the nanoparticle size is of the order of the ion penetration depth. While this feature is reasonably well understood for collision-cascade sputtering, we explore it in the regime of collision-spike sputtering using molecular-dynamics simulation. For this specific case of 200-keV Xe bombardment of Au particles, we show that collision spikes lead to abundant sputtering with an average yield of 397 ± 121 atoms compared to only 116 ± 48 atoms for a bulk Au target. Only around 31% of the impact energy remains in the nanoparticles after impact; the remainder is transported away by the transmitted projectile and the ejecta. The sputter yield of supported nanoparticles is estimated to be around 80% of that of free nanoparticles due to the suppression of forward sputtering.

  15. Collision-spike sputtering of Au nanoparticles

    DOE PAGESBeta

    Sandoval, Luis; Urbassek, Herbert M.

    2015-08-06

    Ion irradiation of nanoparticles leads to enhanced sputter yields if the nanoparticle size is of the order of the ion penetration depth. While this feature is reasonably well understood for collision-cascade sputtering, we explore it in the regime of collision-spike sputtering using molecular-dynamics simulation. For this specific case of 200-keV Xe bombardment of Au particles, we show that collision spikes lead to abundant sputtering with an average yield of 397 ± 121 atoms compared to only 116 ± 48 atoms for a bulk Au target. Only around 31% of the impact energy remains in the nanoparticles after impact; the remaindermore » is transported away by the transmitted projectile and the ejecta. The sputter yield of supported nanoparticles is estimated to be around 80% of that of free nanoparticles due to the suppression of forward sputtering.« less

  16. Mimetic biomembrane-AuNPs-graphene hybrid as matrix for enzyme immobilization and bioelectrocatalysis study.

    PubMed

    Wang, Tianshu; Liu, Jiyang; Ren, Jiangtao; Wang, Jin; Wang, Erkang

    2015-10-01

    A hybrid composite constructed of phospholipids bilayer membrane, gold nanoparticles and graphene was prepared and used as matrices for microperoxidase-11 (MP11) immobilization. The direct electrochemistry and corresponding bioelectrocatalysis of the enzyme electrode was further investigated. Phospholipid bilayer membrane protected gold nanoparticles (AuNPs) were assembled on polyelectrolyte functionalized graphene sheets through electrostatic attraction to form a hybrid bionanocomposite. Owing to the biocompatible microenvironment provided by the mimetic biomembrane, microperoxidase-11 entrapped in this matrix well retained its native structure and exhibited high bioactivity. Moreover, the AuNPs-graphene assemblies could efficiently promote the direct electron transfer between the immobilized MP11 and the substrate electrode. The as-prepared enzyme electrode presented good direct electrochemistry and electrocatalytic responses to the reduction of hydrogen peroxide (H2O2). The resulting H2O2 biosensor showed a wide linear range (2.0×10(-5)-2.8×10(-4) M), a low detection limit (2.6×10(-6) M), good reproducibility and stability. Furthermore, this sensor was used for real-time detection of H2O2 dynamically released from the tumor cells MCF-7 in response to a pro-inflammatory stimulant. PMID:26078181

  17. Conjugating folate on superparamagnetic Fe3O4@Au nanoparticles using click chemistry

    NASA Astrophysics Data System (ADS)

    Shen, Xiaofang; Ge, Zhaoqiang; Pang, Yuehong

    2015-02-01

    Gold-coated magnetic core@shell nanoparticles, which exhibit magneto-optical properties, not only enhance the chemical stability of core and biocompatibility of surface, but also provide a combination of multimodal imaging and therapeutics. The conjugation of these tiny nanoparticles with specific biomolecules allows researchers to target the desired location. In this paper, superparamagnetic Fe3O4@Au nanoparticles were synthesized and functionalized with the azide group on the surface by formation of self-assembled monolayers. Folate (FA) molecules, non-immunogenic target ligands for cancer cells, are conjugated with alkyne and then immobilized on the azide-terminated Fe3O4@Au nanoparticles through copper(I)-catalyzed azide-alkyne cycloaddition (click reaction). Myelogenous leukemia K562 cells were used as a folate receptor (FR) model, which can be targeted and extracted by magnetic field after interaction with the Fe3O4@Au-FA nanoparticles.

  18. Application of magnetic nanoparticles in smart enzyme immobilization.

    PubMed

    Vaghari, Hamideh; Jafarizadeh-Malmiri, Hoda; Mohammadlou, Mojgan; Berenjian, Aydin; Anarjan, Navideh; Jafari, Nahideh; Nasiri, Shahin

    2016-02-01

    Immobilization of enzymes enhances their properties for efficient utilization in industrial processes. Magnetic nanoparticles, due to their high surface area, large surface-to-volume ratio and easy separation under external magnetic fields, are highly valued. Significant progress has been made to develop new catalytic systems that are immobilized onto magnetic nanocarriers. This review provides an overview of recent developments in enzyme immobilization and stabilization protocols using this technology. The current applications of immobilized enzymes based on magnetic nanoparticles are summarized and future growth prospects are discussed. Recommendations are also given for areas of future research. PMID:26472272

  19. Acetylcholinesterase immobilized onto PEI-coated silica nanoparticles.

    PubMed

    Tumturk, Hayrettin; Yüksekdag, Hazer

    2016-01-01

    Polyethyleneimine (PEI) coated-silica nanoparticles were prepared by the Stöber method. The formation and the structure of the nanoparticles were characterized by ATR-FT-IR spectroscopy and transmission electron microscopy (TEM). TEM images of the silica and PEI-coated nanoparticles revealed that they were well dispersed and that there was no agglomeration. The acetylcholineesterase enzyme was immobilized onto these nanoparticles. The effects of pH and temperature on the storage stability of the free and immobilized enzyme were investigated. The optimum pHs for free and immobilized enzymes were determined as 7.0 and 8.0, respectively. The optimum temperatures for free and immobilized enzymes were found to be 30.0 and 35.0°C, respectively. The maximum reaction rate (Vmax) and the Michaelis-Menten constant (Km) were investigated for the free and immobilized enzyme. The storage stability of acetylcholinesterase was increased when immobilized onto the novel PEI-coated silica nanoparticles. The reuse numbers of immobilized enzyme were also studied. These hybrid nanoparticles are desirable as carriers for biomedical applications. PMID:25365355

  20. Influence of Surfactant Bilayers and Substrate Immobilization on the Refractive Index Sensitivity of Anisotropic Gold Nanoparticles

    NASA Astrophysics Data System (ADS)

    Shahjamali, Mohammad; Large, Nicolas; Martinsson, Erik; Zaraee, Negin; Schatz, George; Aili, Daniel; Mirkin, Chad

    2015-03-01

    Shape-controlled synthesis of gold nanoparticles (AuNPs) generally involves the use of surfactants to regulate the nucleation growth process and to obtain colloidally stable AuNPs. The surfactants adsorb on the NP surface making further functionalization difficult and therefore limit their practical use in many applications such as bio- and molecular sensing, surface-enhanced spectrosopies, and NP assembly. Herein, we report on how cetyltrimethylammonium (CTAX, X =Cl-, Br-) , a common surfactant used in anisotropic AuNPs synthesis, affectsthe nanoparticle sensitivity to local dielectric environment changes and limitsrefractometric plasmonic sensing. We experimentally and theoretically show that the CTAX bilayer significantly reduces the refractive index (RI) sensitivity of anisotropic AuNPs such as flat and concave nanocubes, nanorods, and nanoprisms. We show that the RI sensitivity can be improvedby up to 40% by removing the CTAXfrom immobilized AuNPs using oxygen plasma treatment. The substrate effect on the RI sensitivity caused by NP immobilization isalso investigated. The strategy presented herein is a simple andeffective method to improvethe RI sensitivity of CTAX-stabilized AuNPs, thus increasing their potential in nanoplasmonic sensingand in biomedical applications.

  1. Au nanoparticles films used in biological sensing

    NASA Astrophysics Data System (ADS)

    Rosales Pérez, M.; Delgado Macuil, R.; Rojas López, M.; Gayou, V. L.; Sánchez Ramírez, J. F.

    2009-05-01

    Lactobacillus para paracasei are used commonly as functional food and probiotic substances. In this work Au nanoparticles self-assembled films were used for Lactobacillus para paracasei determination at five different concentrations. Functionalized substrates were immersed in a colloidal solution for one and a half hour at room temperature and dried at room temperature during four hours. After that, drops of Lactobacillus para paracasei in aqueous solution were put into the Au nanoparticles film and let dry at room temperature for another two hours. Infrared spectroscopy in attenuated total reflectance sampling mode was used to observe generation peaks due to substrate silanization, enhancement of Si-O band intensity due to the Au colloids added to silanized substrate and also to observe the enhancement of Lactobacillus para paracasei infrared intensity of the characteristic frequencies at 1650, 1534 and 1450 cm-1 due to surface enhancement infrared absorption.

  2. Immobilized Polymer Layers on Spherical Nanoparticles

    SciTech Connect

    Harton, S.; Kumar, S; Yang, H; Koga, T; Hicks, K; Lee, H; Mijovic, J; Liu, M; Vallery, R; Gidley, D

    2010-01-01

    Polymer properties, such as their mechanical strength, barrier properties, and dielectric response, can be dramatically improved by the addition of nanoparticles. This improvement is thought to be because the surface area per unit mass of particles increases with decreasing particle size, R, as 1/R. This favorable effect has to be reconciled with the expectation that at small enough R the nanoparticles must behave akin to a solvent and cause a deterioration of properties. How does this transition in behavior from large solutes to the solvent limit occur? We conjecture that for small enough particles the layer of polymer affected by the particles ('bound' polymer layer) must be much smaller than that for large particles: the favorable effect of increasing particle surface area can thus be overcome and lead to the small solvent limit with unfavorable mechanical properties, for example. To substantiate this picture requires that we measure and compare the 'bound polymer layer' formed on nanoparticles with those near large particles with equivalent chemistry. We have implemented a novel strategy to obtain uniform nanoparticle dispersion in polymers, a problem for many previous works. Then, by combining theory and a suite of experimental techniques, including differential scanning calorimetry and positron annihilation lifetime spectroscopy, we show that the immobilized poly(2-vinylpyridine) layer near 15 nm diameter silica particles ({approx}1 nm) is considerably thinner than that at flat silica surfaces ({approx}4 to 5 nm), which is the limit of an infinitely large particle. We have also determined that the changes in the polymer's glass-transition temperature due to the presence of this strongly interacting surface are very small in both well-dispersed nanocomposites and thin films (<100 nm). Similarly, the polymer's fragility, as determined by dielectric spectroscopy, is also found to be little affected in the nanocomposites relative to the pure polymer. While a

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

    PubMed

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

    2013-06-12

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

  4. Purification, immobilization, and characterization of nattokinase on PHB nanoparticles.

    PubMed

    Deepak, Venkataraman; Pandian, Suresh babu Ram Kumar; Kalishwaralal, Kalimuthu; Gurunathan, Sangiliyandi

    2009-12-01

    In this study, nattokinase was purified from Bacillus subtilis using ion exchange chromatography and immobilized upon polyhydroxybutyrate (PHB) nanoparticles. A novel strain isolated from industrial dairy waste was found to synthesize polyhydroxyalkanoates (PHA) and the strain was identified as Brevibacterium casei SRKP2. PHA granules were extracted from 48 h culture and the FT-IR analysis characterized them as PHB, a natural biopolymer from B. casei. Nanoprecipitation by solvent displacement technique was used to synthesize PHB nanoparticles. PHB nanoparticles were characterized using transmission electron microscopy and particle size ranged from 100-125 nm. Immobilization of nattokinase upon PHB nanoparticles resulted in a 20% increase in the enzyme activity. Immobilization also contributed to the enhanced stability of the enzyme. Moreover, the activity was completely retained on storage at 4 degrees C for 25 days. The method has proven to be highly simple and can be implemented to other enzymes also. PMID:19608412

  5. Click Chemistry Immobilization of Antibodies on Polymer Coated Gold Nanoparticles.

    PubMed

    Finetti, Chiara; Sola, Laura; Pezzullo, Margherita; Prosperi, Davide; Colombo, Miriam; Riva, Benedetta; Avvakumova, Svetlana; Morasso, Carlo; Picciolini, Silvia; Chiari, Marcella

    2016-07-26

    The goal of this work is to develop an innovative approach for the coating of gold nanoparticles (AuNPs) with a synthetic functional copolymer. This stable coating with a thickness of few nanometers provides, at the same time, stabilization and functionalization of the particles. The polymeric coating consists of a backbone of polydimethylacrylamide (DMA) functionalized with an alkyne monomer that allows the binding of azido modified molecules by Cu(I)-catalyzed azide/alkyne 1,3-dipolar cycloaddition (CuAAC, click chemistry). The thin polymer layer on the surface stabilizes the colloidal suspension whereas the alkyne functions pending from the backbone are available for the reaction with azido-modified proteins. The reactivity of the coating is demonstrated by immobilizing an azido modified anti-mouse IgG antibody on the particle surface. This approach for the covalent binding of antibody to a gold-NPs is applied to the development of gold labels in biosensing techniques. PMID:27367748

  6. Characterization of protein-immobilized polystyrene nanoparticles using impedance spectroscopy.

    PubMed

    Park, Soo-In; Lee, Sang-Yup

    2014-10-01

    A novel approach for characterization of non-conductive protein-immobilized nanoparticles using AC impedance spectroscopy combined with conductive atomic force microscopy was examined. As AC impedance spectroscopy can provide information on diverse electrical properties such as capacitance and inductance, it is applicable to the characterization of non-conductive substances. Several non-conductive protein-immobilized polystyrene nanoparticles were analyzed using AC impedance spectroscopy, and their impedance spectra were used as markers for nanoparticle identification. Analyses of impedance signals using an electrical circuit model established that the capacitance and inductance of each nanoparticle changed with the adsorbed protein and that impedance spectral differences were characteristic properties of the proteins. From this study, AC impedance spectroscopy was shown to be a useful tool for characterization of non-conductive nanoparticles and is expected to be applicable to the development of sensors for nanomaterials. PMID:25942903

  7. (Au/PANA/PVAc) nanofibers as a novel composite matrix for albumin and streptavidin immobilization.

    PubMed

    Golshaei, Rana; Guler, Zeliha; Sarac, Sezai A

    2016-03-01

    A novel electrospun nanofiber mat (Au/PANA/PVAc) consists of (Gold/Poly Anthranilic acid) (Au/PANA) core/shell nanostructures as a support material for protein immobilization that was developed and characterized by electrochemical impedance spectroscopy. In the core/shells, PANA served carboxyl groups (-COOH) for covalent protein immobilization and Au enhanced the electrochemical properties by acting as tiny conduction centers to facilitate electron transfer. Covalent immobilization of albumin and streptavidin as model proteins onto the (Au/PANA/PVAc) nanofibers was carried out by using 1-ethyl-3-(dimethyl-aminopropyl) carbodiimide hydrochloride (EDC)/N-hydroxyl succinimide (NHS) activation. PVAc nanofibers were compared with Au/PANA/PVAc nanofibers before and after protein immobilization. The successful covalent binding of both albumin and streptavidin onto (Au/PANA/PVAc) nanofibers was confirmed by FTIR-ATR, Electron Microscopy/Energy-Dispersive X-ray Spectroscopy SEM/EDX and Electrochemical impedance spectroscopy (EIS). The nanofibers became resistive due to protein immobilization and the higher charge transfer resistance was observed after higher amount of protein was immobilized. PMID:26706530

  8. Photosynthetic electron transport system promotes synthesis of Au-nanoparticles.

    PubMed

    Shabnam, Nisha; Pardha-Saradhi, P

    2013-01-01

    In this communication, a novel, green, efficient and economically viable light mediated protocol for generation of Au-nanoparticles using most vital organelle, chloroplasts, of the plant system is portrayed. Thylakoids/chloroplasts isolated from Potamogeton nodosus (an aquatic plant) and Spinacia oleracea (a terrestrial plant) turned Au³⁺ solutions purple in presence of light of 600 µmol m⁻² s⁻¹ photon flux density (PFD) and the purple coloration intensified with time. UV-Vis spectra of these purple colored solutions showed absorption peak at ∼545 nm which is known to arise due to surface plasmon oscillations specific to Au-nanoparticles. However, thylakoids/chloroplasts did not alter color of Au³⁺ solutions in dark. These results clearly demonstrated that photosynthetic electron transport can reduce Au³⁺ to Au⁰ which nucleate to form Au-nanoparticles in presence of light. Transmission electron microscopic studies revealed that Au-nanoparticles generated by light driven photosynthetic electron transport system of thylakoids/chloroplasts were in range of 5-20 nm. Selected area electron diffraction and powder X-ray diffraction indicated crystalline nature of these nanoparticles. Energy dispersive X-ray confirmed that these nanoparticles were composed of Au. To confirm the potential of light driven photosynthetic electron transport in generation of Au-nanoparticles, thylakoids/chloroplasts were tested for their efficacy to generate Au-nanoparticles in presence of light of PFD ranging from 60 to 600 µmol m⁻² s⁻¹. The capacity of thylakoids/chloroplasts to generate Au-nanoparticles increased remarkably with increase in PFD, which further clearly demonstrated potential of light driven photosynthetic electron transport in reduction of Au³⁺ to Au⁰ to form nanoparticles. The light driven donation of electrons to metal ions by thylakoids/chloroplasts can be exploited for large scale production of nanoparticles. PMID:23976990

  9. Au-nanoparticles grafted on plasma treated PE

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Chaloupka, A.; Řezanka, P.; Slepička, P.; Kolská, Z.; Kasálková, N.; Hubáček, T.; Siegel, J.

    2010-03-01

    Polyethylene (PE) surface was treated with Ar plasma. Activated surface was grafted from methanol solution of 1,2-ethanedithiol. Then the sample was immersed into freshly prepared colloid solution of Au-nanoparticles. Finally Au layer was sputtered on the samples. Properties of the modified PE were studied using various methods: AFM, EPR, RBS and nanoindentation. It was shown that the plasma treatment results in degradation of polymer chain (AFM) and creation of free radicals by EPR. After grafting with dithiol, the concentration of free radicals declines. The presence of Au and S in the surface layer after the coating with Au-nanoparticles was proved by RBS. Plasma treatment changes PE surface morphology and increases surface roughness, too. Another significant change in surface morphology and roughness was observed after deposition of Au-nanoparticles. Nanoindentation measurements show that the grafting with Au-nanoparticles increases adhesion of subsequently sputtered Au layer.

  10. Magnetic nanoparticles coated with polyaniline to stabilize immobilized trypsin

    NASA Astrophysics Data System (ADS)

    Maciel, J. C.; D. Mercês, A. A.; Cabrera, M.; Shigeyosi, W. T.; de Souza, S. D.; Olzon-Dionysio, M.; Fabris, J. D.; Cardoso, C. A.; Neri, D. F. M.; C. Silva, M. P.; Carvalho, L. B.

    2016-12-01

    It is reported the synthesis of magnetic nanoparticles via the chemical co-precipitation of Fe 3+ ions and their preparation by coating them with polyaniline. The electronic micrograph analysis showed that the mean diameter for the nanoparticles is ˜15 nm. FTIR, powder X-ray diffraction and Mössbauer spectroscopy were used to understand the chemical, crystallographic and 57Fe hyperfine structures for the two samples. The nanoparticles, which exhibited magnetic behavior with relatively high spontaneous magnetization at room temperature, were identified as being mainly formed by maghemite ( γFe2O3). The coated magnetic nanoparticles (sample labeled "mPANI") presented a real ability to bind biological molecules such as trypsin, forming the magnetic enzyme derivative (sample "mPANIG-Trypsin"). The amount of protein and specific activity of the immobilized trypsin were found to be 13±5 μg of protein/mg of mPANI (49.3 % of immobilized protein) and 24.1±0.7 U/mg of immobilized protein, respectively. After 48 days of storage at 4 ∘C, the activity of the immobilized trypsin was found to be 89 % of its initial activity. This simple, fast and low-cost procedure was revealed to be a promising way to prepare mPANI nanoparticles if technological applications addressed to covalently link biomolecules are envisaged. This route yields chemically stable derivatives, which can be easily recovered from the reaction mixture with a magnetic field and recyclable reused.

  11. Optimizing immobilization of avidin on surface-modified magnetic nanoparticles: characterization and application of protein-immobilized nanoparticles.

    PubMed

    Yang, Tao; Sun, Shuguo; Ma, Meihu; Lin, Qinlu; Zhang, Lin; Li, Yan; Luo, Feijun

    2015-10-01

    A simple optimization method of immobilization of avidin on magnetic nanoparticles (MNPs)' surface was proposed in this study. The avidin-immobilized MNPs were then developed and used to immobilize a model enzyme [Horseradish peroxidase (HRP)]. The loading capacity (LC) and activity of avidin-immobilized MNPs were optimized through selecting the most appropriate nanoparticle's size and shape, glutaraldehyde concentration, cross-linking reaction time, ultrasonic processing time, and initial concentration of avidin. The LC under optimized conditions was 63.37 ± 1.29 mg avidin/g MNPs, and the immobilized protein was still able to maintain its high biological activity of 10.86 ± 0.13 U/mg (biotin-binding activity of nature avidin was 14.1 U/mg) and better thermal stability compared to free avidin. A highly reusable, stable, and easily recovered immobilized HRP was obtained using MNPs as carriers. The immobilized HRP was reused repeatedly more than 9 times and retained more than 65 % of its original activity. PMID:26224655

  12. Prolonged reorganization of thiol-capped Au nanoparticles layered structures

    NASA Astrophysics Data System (ADS)

    Kundu, Sarathi; Das, Kaushik; Konovalov, Oleg

    2013-09-01

    Prolonged reorganization behaviour of mono-, di-, tri- and multi-layer films of Au nanoparticles prepared by Langmuir-Blodgett method on hydrophobic Si(001) substrates have been studied by using X-ray scattering techniques. Out-of-plane study shows that although at the initial stage the reorganization occurs through the compaction of the films keeping the layered structure unchanged but finally all layered structures modify to monolayer structure. Due to this reorganization the Au density increases within the nanometer thick films. In-plane study shows that inside the reorganized films Au nanoparticles are distributed randomly and the particle size modifies as the metallic core of Au nanoparticles coalesces.

  13. Enzyme-controlled sensing-actuating nanomachine based on Janus Au-mesoporous silica nanoparticles.

    PubMed

    Villalonga, Reynaldo; Díez, Paula; Sánchez, Alfredo; Aznar, Elena; Martínez-Máñez, Ramón; Pingarrón, José M

    2013-06-10

    Novel Janus nanoparticles with Au and mesoporous silica faces on opposite sides were prepared using a Pickering emulsion template with paraffin wax as the oil phase. These anisotropic colloids were employed as integrated sensing-actuating nanomachines for enzyme-controlled stimuli-responsive cargo delivery. As a proof of concept, we demonstrated the successful use of the Janus colloids for controlled delivery of tris(2,2'-bipyridyl) ruthenium(II) chloride from the mesoporous silica face, which was grafted with pH-sensitive gatelike scaffoldings. The release was mediated by the on-demand catalytic decomposition of urea by urease, which was covalently immobilized on the Au face. PMID:23649789

  14. Novel functionalized fluorescent polymeric nanoparticles for immobilization of biomolecules

    NASA Astrophysics Data System (ADS)

    Jain, Swati; Chattopadhyay, Sruti; Jackeray, Richa; Abid, C. K. V. Zainul; Singh, Harpal

    2013-07-01

    Novel, size controlled fluorescent polymeric nanoparticles (FPNP) were synthesized having acetoacetoxy functionality on the surface for immobilization of biomolecules which can be utilized as biomarkers and labels in fluoroimmunoassays. Core-shell nanoparticles of poly(styrene, St-methyl methacrylate, MMA-acetoacetoxy ethyl methacrylate, AAEM), stabilized by various concentrations of surfactant, sodium lauryl sulphate (SLS), were obtained by facile miniemulsion co-polymerization encapsulated with pyrene molecules in their hydrophobic core. Analytical, spectroscopic and imaging characterization techniques revealed the formation of stable, monodisperse, spherical nano sized particles exhibiting high luminescence properties. Particles with 1% SLS (S1) showed good dispersion stability and fluorescence intensity and were chosen as ideal candidates for further immobilization studies. Steady state fluorescence studies showed 10 times higher fluorescence intensity of S1 nanoparticles than that of pyrene solution in solvent-toluene at the same concentration. Environmental factors such as pH, ionic strength and time were found to have no effect on fluorescence intensity of FPNPs. Surface β-di-ketone groups were utilized for the covalent immobilization of enzyme conjugated antibodies without any activation or pre-treatment of nanoparticles.Novel, size controlled fluorescent polymeric nanoparticles (FPNP) were synthesized having acetoacetoxy functionality on the surface for immobilization of biomolecules which can be utilized as biomarkers and labels in fluoroimmunoassays. Core-shell nanoparticles of poly(styrene, St-methyl methacrylate, MMA-acetoacetoxy ethyl methacrylate, AAEM), stabilized by various concentrations of surfactant, sodium lauryl sulphate (SLS), were obtained by facile miniemulsion co-polymerization encapsulated with pyrene molecules in their hydrophobic core. Analytical, spectroscopic and imaging characterization techniques revealed the formation of stable

  15. Kinetic analysis of the reduction of 4-nitrophenol catalyzed by Au/Pd nanoalloys immobilized in spherical polyelectrolyte brushes.

    PubMed

    Gu, Sasa; Lu, Yan; Kaiser, Julian; Albrecht, Martin; Ballauff, Matthias

    2015-11-14

    We present a detailed study of the catalytic activity of Au/Pd nanoalloys with Au : Pd molar ratio 75 : 25 synthesized using spherical polyelectrolyte brushes (SPB) as carrier system. The reduction of 4-nitrophenol (Nip) by sodium borohydride (BH4(-)) has been used as a model reaction. This reaction proceeds in two steps: 4-nitrophenol is first reduced to 4-hydroxylaminophenol which in a second step is reduced to the final product 4-aminophenol. Both steps of the reaction proceed on the surface of the nanoparticles (Langmuir-Hinshelwood-mechanism). We use this model to analyze the experimental data obtained by catalysis with the Au/Pd-nanoalloys. Good agreements between theory and experiments were found up to 30% conversion of Nip. The kinetic parameters were compared with the data derived from neat Au and Pd nanoparticles immobilized in the same SPB carrier system. The addition of 25% molar ratio of Pd to the nanoalloys increases the reaction rate of the first step nearly 10 times compared with that of SPB-Au and 60 times compared with that of SPB-Pd. Analysis of the nanoalloy by high-resolution transmission electron microscopy suggests that the surface defects of the nanoalloys play an important role for the enhanced catalytic activity. PMID:25790094

  16. Affinity-Driven Immobilization of Proteins to Hematite Nanoparticles.

    PubMed

    Zare-Eelanjegh, Elaheh; Bora, Debajeet K; Rupper, Patrick; Schrantz, Krisztina; Thöny-Meyer, Linda; Maniura-Weber, Katharina; Richter, Michael; Faccio, Greta

    2016-08-10

    Functional nanoparticles are valuable materials for energy production, bioelectronics, and diagnostic devices. The combination of biomolecules with nanosized material produces a new hybrid material with properties that can exceed the ones of the single components. Hematite is a widely available material that has found application in various sectors such as in sensing and solar energy production. We report a single-step immobilization process based on affinity and achieved by genetically engineering the protein of interest to carry a hematite-binding peptide. Fabricated hematite nanoparticles were then investigated for the immobilization of the two biomolecules C-phycocyanin (CPC) and laccase from Bacillus pumilus (LACC) under mild conditions. Genetic engineering of biomolecules with a hematite-affinity peptide led to a higher extent of protein immobilization and enhanced the catalytic activity of the enzyme. PMID:27429157

  17. Covalent immobilization of molecularly imprinted polymer nanoparticles on a gold surface using carbodiimide coupling for chemical sensing.

    PubMed

    Kamra, Tripta; Chaudhary, Shilpi; Xu, Changgang; Montelius, Lars; Schnadt, Joachim; Ye, Lei

    2016-01-01

    One challenging task in building (bio)chemical sensors is the efficient and stable immobilization of receptor on a suitable transducer. Herein, we report a method for covalent immobilization of molecularly imprinted core-shell nanoparticles for construction of robust chemical sensors. The imprinted nanoparticles with a core-shell structure have selective molecular binding sites in the core and multiple amino groups in the shell. The model Au transducer surface is first functionalized with a self-assembled monolayer of 11-mercaptoundecanoic acid. The 11-mercaptoundecanoic acid is activated by treatment with carbodiimide/N-hydroxysuccinimide and then reacted with the core-shell nanoparticles to form amide bonds. We have characterized the process by studying the treated surfaces after each preparation step using atomic force microscopy, scanning electron microscopy, fluorescence microscopy, contact angle measurements and X-ray photoelectron spectroscopy. The microscopy results show the successful immobilization of the imprinted nanoparticles on the surface. The photoelectron spectroscopy results further confirm the success of each functionalization step. Further, the amino groups on the MIP surface were activated by electrostatically adsorbing negatively charged Au colloids. The functionalized surface was shown to be active for surface enhanced Raman scattering detection of propranolol. The particle immobilization and surface enhanced Raman scattering approach described here has a general applicability for constructing chemical sensors in different formats. PMID:26397901

  18. Polymer-assisted iron oxide magnetic nanoparticle immobilized keratinase

    NASA Astrophysics Data System (ADS)

    Konwarh, Rocktotpal; Karak, Niranjan; Rai, Sudhir Kumar; Mukherjee, Ashis Kumar

    2009-06-01

    Nanotechnology holds the prospect for avant-garde changes to improve the performance of materials in various sectors. The domain of enzyme biotechnology is no exception. Immobilization of industrially important enzymes onto nanomaterials, with improved performance, would pave the way to myriad application-based commercialization. Keratinase produced by Bacillus subtilis was immobilized onto poly(ethylene glycol)-supported Fe3O4 superparamagnetic nanoparticles. The optimization process showed that the highest enzyme activity was noted when immobilized onto cyanamide-activated PEG-assisted MNP prepared under conditions of 25 °C and pH 7.2 of the reaction mixture before addition of H2O2 (3% w/w), 2% (w/v) PEG6000 and 0.062:1 molar ratio of PEG to FeCl2·4H2O. Further statistical optimization using response surface methodology yielded an R2 value that could explain more than 94% of the sample variations. Along with the magnetization studies, the immobilization of the enzyme onto the PEG-assisted MNP was characterized by UV, XRD, FTIR and TEM. The immobilization process had resulted in an almost fourfold increase in the enzyme activity over the free enzyme. Furthermore, the immobilized enzyme exhibited a significant thermostability, storage stability and recyclability. The leather-industry-oriented application of the immobilized enzyme was tested for the dehairing of goat-skin.

  19. Site-specific immobilization of gold binding polypeptide on gold nanoparticle-coated graphene sheet for biosensor application

    NASA Astrophysics Data System (ADS)

    Yang, Minho; Choi, Bong Gill; Park, Tae Jung; Heo, Nam Su; Hong, Won Hi; Lee, Sang Yup

    2011-07-01

    The effective and strong immobilization of enzymes on solid surfaces is required for current biological applications, such as microchips, biofuel cells, and biosensors. Gold-binding polypeptide (GBP), a genetically designed peptide, possesses unique and specific interactions with a gold surface, resulting in improved enzyme stability and activity. Herein we demonstrated an immobilization method for biosensor applications through site-specific interactions between GBP-fused organophosphorus hydrolase (GBP-OPH) and gold nanoparticle-coated chemically modified graphene (Au-CMG), showing enhanced sensing capability. A flow injection biosensor was fabricated by using GBP-OPH/Au-CMG to detect paraoxons, a model pesticide, showing higher sensitivity, lower detection limit and better operating stability compared that of OPH/Au-CMG. This strategy, which integrates biotic and abiotic moieties through site-specific interactions, has a great potential for use in biosensing and bioconversion process.The effective and strong immobilization of enzymes on solid surfaces is required for current biological applications, such as microchips, biofuel cells, and biosensors. Gold-binding polypeptide (GBP), a genetically designed peptide, possesses unique and specific interactions with a gold surface, resulting in improved enzyme stability and activity. Herein we demonstrated an immobilization method for biosensor applications through site-specific interactions between GBP-fused organophosphorus hydrolase (GBP-OPH) and gold nanoparticle-coated chemically modified graphene (Au-CMG), showing enhanced sensing capability. A flow injection biosensor was fabricated by using GBP-OPH/Au-CMG to detect paraoxons, a model pesticide, showing higher sensitivity, lower detection limit and better operating stability compared that of OPH/Au-CMG. This strategy, which integrates biotic and abiotic moieties through site-specific interactions, has a great potential for use in biosensing and bioconversion

  20. Using light to covalently immobilize and pattern nanoparticles onto surfaces.

    PubMed

    Park, Ellane J; Wagenaar, Tina; Zhang, Siyan; Link, A James; Prud'homme, Robert K; Koberstein, Jeffrey T; Turro, Nicholas J

    2012-07-24

    There is considerable current interest in developing methods to integrate nanoparticles into optical, electronic, and biological systems due to their unique size-dependent properties and controllable shape. We report herein a versatile new approach for covalent immobilization of nanoparticles onto substrates modified with photoactive, phthalimide-functional, self-assembled monolayers. Upon illumination with UV radiation, the phthalimide group abstracts a hydrogen atom from a neighboring organic molecule, leading to radical-based photografting reactions. The approach is potentially "universal" since virtually any polymeric or organic-inorganic hybrid nanoparticle can be covalently immobilized in this fashion. Because grafting is confined to illuminated regions that undergo photoexcitation, masking provides a simple and direct method for nanoparticle patterning. To illustrate the technique, nanoparticles formed from diblock copolymers of poly(styrene-b-polyethylene oxide) and laden with Hostasol Red dye are photografted and patterned onto glass and silicon substrates modified with photoactive phthalimide-silane self-assembled monolayers. Atomic force microscopy and X-ray photoelectron spectroscopy are applied to characterize the grafted nanoparticle films while confocal fluorescence microscopy is used to image patterned nanoparticle deposition. PMID:22746532

  1. Adsorptive recovery of Au3+ from aqueous solutions using bayberry tannin-immobilized mesoporous silica.

    PubMed

    Huang, Xin; Wang, Yanpin; Liao, Xuepin; Shi, Bi

    2010-11-15

    Tannin is well known to be an inexpensive and ubiquitous natural biomass, which has high chelating affinity towards many metal ions. In this study, bayberry tannin (BT) was immobilized on mesoporous silica matrix to prepare a novel adsorbent, which was subsequently used for the adsorptive recovery of Au(3+) from aqueous solutions. It was found that bayberry tannin-immobilized mesoporous silica (BT-SiO(2)) was able to effectively recover Au(3+) from acidic solutions (pH 2.0). The equilibrium adsorption capacity of Au(3+) on BT-SiO(2) was high up to 642.0 mg/g at 323 K. Due to its mesoporous structure, BT-SiO(2) exhibited an extremely fast adsorption rate to Au(3+) as compared with other tannin gel adsorbent. The presence of other coexisting metal ions, such as Pb(2+), Ni(2+), Cu(2+) and Zn(2+), did not decrease the adsorption capacity of Au(3+) on BT-SiO(2), and BT-SiO(2) had almost no adsorption capacity to these coexisting metal ions, which suggested the high adsorption selectivity of BT-SiO(2) to Au(3+). Additionally, about 73% of adsorbed Au(3+) can be desorbed using aqua regia, and the Au(3+) solution was concentrated about 18.0 times as compared with the original solution. Consequently, the outstanding characteristics of BT-SiO(2) provide the possibility of effective recovery and concentration of Au(3+) from diluted solutions. PMID:20728986

  2. Core-shell of FePt@SiO2-Au magnetic nanoparticles for rapid SERS detection.

    PubMed

    Hardiansyah, Andri; Chen, An-Yu; Liao, Hung-Liang; Yang, Ming-Chien; Liu, Ting-Yu; Chan, Tzu-Yi; Tsou, Hui-Ming; Kuo, Chih-Yu; Wang, Juen-Kai; Wang, Yuh-Lin

    2015-12-01

    In this study, multifunctional hybrid nanoparticles composed of iron platinum (FePt), silica (SiO2), and gold nanoparticles (AuNPs) had been developed for surface-enhanced Raman scattering (SERS) application. Core-shell structure of SiO2 and FePt nanoparticles (FePt@SiO2) was fabricated through sol-gel process and then immobilized gold nanoparticles onto the surface of FePt@SiO2, which displays huge Raman enhancement effect and magnetic separation capability. The resulting core-shell nanoparticles were subject to evaluation by transmission electron microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDX), zeta potential measurement, and X-ray photoelectron spectroscopy (XPS). TEM observation revealed that the particle size of resultant nanoparticles displayed spherical structure with the size ~30 nm and further proved the successful immobilization of Au onto the surface of FePt@SiO2. Zeta potential measurement exhibited the successful reaction between FePt@SiO2 and AuNPs. The rapid SERS detection and identification of small biomolecules (adenine) and microorganisms (gram-positive bacteria, Staphylococcus aureus) was conducted through Raman spectroscopy. In summary, the novel core-shell magnetic nanoparticles could be anticipated to apply in the rapid magnetic separation under the external magnetic field due to the core of the FePt superparamagnetic nanoparticles and label-free SERS bio-sensing of biomolecules and bacteria. PMID:26489855

  3. Core-shell of FePt@SiO2-Au magnetic nanoparticles for rapid SERS detection

    NASA Astrophysics Data System (ADS)

    Hardiansyah, Andri; Chen, An-Yu; Liao, Hung-Liang; Yang, Ming-Chien; Liu, Ting-Yu; Chan, Tzu-Yi; Tsou, Hui-Ming; Kuo, Chih-Yu; Wang, Juen-Kai; Wang, Yuh-Lin

    2015-10-01

    In this study, multifunctional hybrid nanoparticles composed of iron platinum (FePt), silica (SiO2), and gold nanoparticles (AuNPs) had been developed for surface-enhanced Raman scattering (SERS) application. Core-shell structure of SiO2 and FePt nanoparticles (FePt@SiO2) was fabricated through sol-gel process and then immobilized gold nanoparticles onto the surface of FePt@SiO2, which displays huge Raman enhancement effect and magnetic separation capability. The resulting core-shell nanoparticles were subject to evaluation by transmission electron microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDX), zeta potential measurement, and X-ray photoelectron spectroscopy (XPS). TEM observation revealed that the particle size of resultant nanoparticles displayed spherical structure with the size ~30 nm and further proved the successful immobilization of Au onto the surface of FePt@SiO2. Zeta potential measurement exhibited the successful reaction between FePt@SiO2 and AuNPs. The rapid SERS detection and identification of small biomolecules (adenine) and microorganisms (gram-positive bacteria, Staphylococcus aureus) was conducted through Raman spectroscopy. In summary, the novel core-shell magnetic nanoparticles could be anticipated to apply in the rapid magnetic separation under the external magnetic field due to the core of the FePt superparamagnetic nanoparticles and label-free SERS bio-sensing of biomolecules and bacteria.

  4. Graphene quantum dots/Au hybrid nanoparticles as electrocatalyst for hydrogen evolution reaction

    NASA Astrophysics Data System (ADS)

    Luo, Peihui; Jiang, Linqin; Zhang, Weilong; Guan, Xiangfeng

    2015-11-01

    Graphene quantum dots/Au hybrid nanoparticles (denoted as GQDs-Au) were prepared by heating HAuCl4 with GQDs, and they showed higher electrocatalytic activity for hydrogen evolution reaction than that of pure Au nanoparticles.

  5. Immobilization of Ag-deposited Au nanoprisms by thiol-coupling and oil-coating methods

    NASA Astrophysics Data System (ADS)

    Noda, Yuta; Hayakawa, Tomokatsu

    2016-01-01

    We have demonstrated the immobilization of Ag-deposited Au (Au@Ag) nanoprisms on glass substrates by two different methods: self-assembly on a thiol-modified glass (thiol-coupling method) and evaporation of the Au@Ag nanoprism colloidal solution in silicone oil (oil-coating method). In the thiol-coupling method, the Au@Ag nanoprisms were well dispersed and accumulated on the substrates as single or stacked layers. On the other hand, the oil-coating method allowed Au@Ag nanoprisms to accumulate as multilayers without excessive agglomeration. The multilayers of Au@Ag nanoprisms were subjected to surface-enhanced Raman scattering (SERS), and a very low concentration (2.1 × 10-5 M) of rhodamine 6G molecules was sensitively detected.

  6. Nanoshells made easy: improving Au layer growth on nanoparticle surfaces.

    PubMed

    Brinson, Bruce E; Lassiter, J Britt; Levin, Carly S; Bardhan, Rizia; Mirin, Nikolay; Halas, Naomi J

    2008-12-16

    The growth of a continuous, uniform Au layer on a dielectric nanoparticle is the critical step in the synthesis of nanoparticles such as nanoshells or nanorice, giving rise to their unique geometry-dependent plasmon resonant properties. Here, we report a novel, streamlined method for Au layer metallization on prepared nanoparticle surfaces using carbon monoxide as the reducing agent. This approach consistently yields plasmonic nanoparticles with highly regular shell layers and is immune to variations in precursor or reagent preparation. Single particle spectroscopy combined with scanning electron microscopy reveal that thinner, more uniform shell layers with correspondingly red-shifted optical resonances are achievable with this approach. PMID:19360963

  7. Immobilizing metal nanoparticles to metal-organic frameworks with size and location control for optimizing catalytic performance.

    PubMed

    Zhu, Qi-Long; Li, Jun; Xu, Qiang

    2013-07-17

    AuNi alloy nanoparticles were successfully immobilized to MIL-101 with size and location control for the first time by double solvents method (DSM) combined with a liquid-phase concentration-controlled reduction strategy. When an overwhelming reduction approach was employed, the uniform 3D distribution of the ultrafine AuNi nanoparticles (NPs) encapsulated in the pores of MIL-101 was achieved, as demonstrated by TEM and electron tomographic measurements, which brings light to new opportunities in the fabrication of ultrafine non-noble metal-based NPs throughout the interior pores of MOFs. The ultrafine AuNi alloy NPs inside the mesoporous MIL-101 exerted exceedingly high activity for hydrogen generation from the catalytic hydrolysis of ammonia borane. PMID:23805877

  8. Au, Ge and AuGe Nanoparticles Fabricated by Laser Ablation

    SciTech Connect

    Musaev, O.R.; Sutter, E.; Wrobel, J.M.; Kruger, M.B.

    2012-02-01

    A eutectic AuGe target immersed in distilled water was ablated by pulsed ultraviolet laser light. The structure of the ablated material was investigated by high-resolution transmission electron microscopy (HRTEM). The images show formation of nanowire structures of AuGe up to 100 nm in length, with widths of 5-10 nm. These nanostructures have Ge content significantly lower than the target material. Electron diffraction demonstrates that they crystallize in the {alpha}-AuGe structure. For comparison, laser ablation of pure Au and pure Ge targets was also performed under the same conditions. HRTEM shows that Ge forms spherical nanoparticles with a characteristic size of {approx}30 nm. Au forms spherical nanoparticles with diameters of {approx}10 nm. Similar to AuGe, it also forms chainlike structures with substantially lower aspect ratio.

  9. The effect of Au amount on size uniformity of self-assembled Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Chen, S.-H.; Wang, D.-C.; Chen, G.-Y.; Chen, K.-Y.

    2008-03-01

    The self-assembled fabrication of nanostructure, a dreaming approach in the area of fabrication engineering, is the ultimate goal of this research. A finding was proved through previous research that the size of the self-assembled gold nanoparticles could be controlled with the mole ratio between AuCl4- and thiol. In this study, the moles of Au were fixed, only the moles of thiol were adjusted. Five different mole ratios of Au/S with their effect on size uniformity were investigated. The mole ratios were 1:1/16, 1:1/8, 1:1, 1:8, 1:16, respectively. The size distributions of the gold nanoparticles were analyzed by Mac-View analysis software. HR-TEM was used to derive images of self-assembled gold nanoparticles. The result reached was also the higher the mole ratio between AuCl4- and thiol the bigger the self-assembled gold nanoparticles. Under the condition of moles of Au fixed, the most homogeneous nanoparticles in size distribution derived with the mole ratio of 1:1/8 between AuCl4- and thiol. The obtained nanoparticles could be used, for example, in uniform surface nanofabrication, leading to the fabrication of ordered array of quantum dots.

  10. Thermal and photoinduced reduction of ionic Au(III) to elemental Au nanoparticles by dissolved organic matter in water: possible source of naturally occurring Au nanoparticles.

    PubMed

    Yin, Yongguang; Yu, Sujuan; Liu, Jingfu; Jiang, Guibin

    2014-01-01

    Naturally occurring Au nanoparticles (AuNPs) have been widely observed in ore deposits, coal, soil, and environmental water. Identifying the source of these naturally occurring AuNPs could be helpful for not only the discovery of Au deposits through advanced exploration methods, but also the elucidation of the biogeochemical cycle and environmental toxicity of ionic Au and engineered AuNPs. Here, we investigated the effect of natural/simulated sunlight and heating on the reduction of ionic Au by ubiquitous dissolved organic matter (DOM) in river water. The reductive process probed by X-ray photoelectron spectroscopy revealed that phenolic, alcoholic, and aldehyde groups in DOM act as reductive sites. Long-time exposure with thermal and photoirradiation induced the further fusion and growth of AuNPs to branched Au nanostructure as precipitation. The formation processes and kinetics of AuNPs were further investigated using humic acid (HA) as the DOM model, with comprehensive characterizing methods. We have observed that HA can reduce ionic Au(III) complex (as chloride or hydroxyl complex) to elemental Au nanoparticles under sunlight or heating. In this process, nearly all of the Au(III) could be reduced to AuNPs, in which HA serves as not only the reductive agent, but also the coating agent to stabilize and disperse AuNPs. The size and stability of AuNPs were highly dependent on the concentration ratio of Au(III) to HA. These results imply that, besides biological processes, this thermal or photochemical reduction process is another possible source of naturally occurring AuNPs in natural environments, which possibly has critical impacts on the transport and transformation of Au and engineered AuNPs. PMID:24471802

  11. Enzymatic deposition of Au nanoparticles on the designed electrode surface and its application in glucose detection.

    PubMed

    Zhang, Hongfang; Liu, Ruixiao; Sheng, Qinglin; Zheng, Jianbin

    2011-02-01

    This paper reported the enzymatic deposition of Au nanoparticles (AuNPs) on the designed 3-mercapto-propionic acid/glucose oxidase/chitosan (MPA/GOD/Chit) modified glassy carbon electrode and its application in glucose detection. Chit served as GOD immobilization matrix and interacted with MPA through electrostatic attraction. AuNPs, without nano-seeds presented on the electrode surface, was produced through the glucose oxidase catalyzed oxidation of glucose. The mechanism of production of AuNPs was confirmed to be that enzymatic reaction products H(2)O(2) in the solution reduce gold complex to AuNPs. The characterizations of the electrode modified after each assembly step was investigated by cyclic voltammetry and electrochemical impedance spectroscopy. Scanning electron microscopy showed the average particle size of the AuNPs is 40nm with a narrow particle size distribution. The content of AuNPs on the electrode surfaces was measured by differential pulse stripping voltammetry. The electrochemical signals on voltammogram showed a linear increase with the glucose concentration in the range of 0.010-0.12mM with a detection limit of 4μM. This provided a method to the determination of glucose. PMID:21115279

  12. a High-Performance Glucose Biosensor Based on Zno Nanorod Arrays Modified with AU Nanoparticles

    NASA Astrophysics Data System (ADS)

    Zhang, Gong; Lei, Yang; Yan, Xiaoqin

    2012-08-01

    An amperometric glucose biosensor based on vertically aligned ZnO nanorod (NR) arrays modified with Au nanoparticles (NPs) was constructed in a channel-limited way. Au NPs with diameters in the range of 8-10 nm have been successfully synthesized by photoreduction method and were uniformly loaded onto the surface of ZnO NRs that was hydrothermally deposited on the Fluorine doped SnO2 conductive glass (FTO) via electrostatic self-assembly technique. The morphology and structure of Au/ZnO NR arrays were characterized by field-emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectrum analyzer (XPS). The electrocatalytic properties of glucose oxidase (GOD)- immobilized Au/ZnO NR arrays were evaluated by amperometry. Compared with the biosensor based on ZnO NR arrays, the resulting Au/ZnO NR arrays modified biosensor exhibited an expanded linear range from 3 μM to 3 mM with the detection limit of 30 nM and a smaller Michaelis-Menten constant of 0.7836 mM. All these results suggest that the Au NPs can greatly improve the biosensing properties of ZnO NR arrays and therefore Au/ZnO NR arrays provide a promising material for the biosensor designs and other biological applications.

  13. Synthesis and biosensor application of Ag@Au bimetallic nanoparticles based on localized surface plasmon resonance

    NASA Astrophysics Data System (ADS)

    Ghodselahi, T.; Arsalani, S.; Neishaboorynejad, T.

    2014-05-01

    This work demonstrates a simple method for synthesizing gold-silver bimetallic nanoparticles (Ag@Au BNPs). Ag@Au BNPs on the carbon thin film are prepared by co-deposition of RF-sputtering and RF-PECVD using acetylene gas and gold-silver target. X-ray diffraction analysis indicates that Au and Ag NPs with FCC crystal structure are formed in our samples. From AFM image and data, average particles size of gold and silver are estimated to be about 5 and 8 nm, respectively. XRD profile and localized surface plasmon resonance (LSPR) spectroscopy indicate that Ag NPs in Ag@Au BNPs composite have a more chemical activity with respect to bare Ag NPs. Biosensor application of Ag@Au BNPs without probe immobilization is introduced too. The change in LSPR absorption peak of Ag@Au BNPs in presence of DNA primer decamer (ten-deoxycytosine) at fM concentrations is investigated. The LSPR absorption peak of Au NPs has a blue shift and the LSPR absorption peak of Ag NPs has a red shift by addition of DNA primer and under DNA exposure up to 1 h. Our sample shows a good response to low concentration of DNA and has a short response time. Both of these are prerequisite for applying this sample as LSPR biosensor chip.

  14. Co-immobilization of gold nanoparticles with glucose oxidase to improve bioelectrocatalytic glucose oxidation

    NASA Astrophysics Data System (ADS)

    Aquino Neto, Sidney; Milton, Ross D.; Crepaldi, Laís B.; Hickey, David P.; de Andrade, Adalgisa R.; Minteer, Shelley D.

    2015-07-01

    Recently, there has been much effort in developing metal nanoparticle catalysts for fuel oxidation, as well as the development of enzymatic bioelectrocatalysts for fuel oxidation. However, there has been little study of the synergy of hybrid electrocatalytic systems. We report the preparation of hybrid bioanodes based on Au nanoparticles supported on multi-walled carbon nanotubes (MWCNTs) co-immobilized with glucose oxidase (GOx). Mediated electron transfer was achieved by two strategies: ferrocene entrapped within polypyrrole and a ferrocene-modified linear poly(ethylenimine) (Fc-LPEI) redox polymer. Electrochemical characterization of the Au nanoparticles supported on MWCNTs indicate that this catalyst exhibits an electrocatalytic response for glucose even in acidic conditions. Using the redox polymer Fc-LPEI as the mediator, voltammetric and amperometric data demonstrated that these bioanodes can efficiently achieve mediated electron transfer and also indicated higher catalytic currents with the hybrid bioelectrode. From the amperometry, the maximum current density (Jmax) achieved with the hybrid bioelectrode was 615 ± 39 μA cm-2, whereas the bioanode employing GOx only achieved a Jmax of 409 ± 26 μA cm-2. Biofuel cell tests are consistent with the electrochemical characterization, thus confirming that the addition of the metallic species into the bioanode structure can improve fuel oxidation and consequently, improve the power generated by the system.

  15. Biosynthesis of Au, Ag and Au-Ag nanoparticles using edible mushroom extract.

    PubMed

    Philip, Daizy

    2009-07-15

    Integration of green chemistry principles to nanotechnology is one of the key issues in nanoscience research. There is growing need to develop environmentally benign metal nanoparticle synthesis process that do not use toxic chemicals in the synthesis protocols to avoid adverse effects in medical applications. Here, it is a report on extracellular synthesis method for the preparation of Au, Ag and Au-Ag nanoparticles in water, using the extract of Volvariella volvacea, a naturally occurring edible mushroom, as reducing and protecting agents. Gold nanoparticles of different sizes (20-150 nm) and shapes from triangular nanoprisms to nearly spherical and hexagonal are obtained by this novel method. The size and shape of gold nanoparticles are also found to depend on temperature of the extract. The silver nanoparticles are spherical with size approximately 15 nm. There is increased productivity of nanoparticles as shown by sharp and intense surface plasmon resonance bands for the nanoparticles prepared using an excess of the extract. The Au-Ag nanoparticles prepared by co-reduction has only one plasmon band due to alloying of the constituents. All the synthesized nanoparticles are found to be photoluminescent and are highly crystalline as shown by SAED and XRD patterns with fcc phase oriented along the (111) plane. FTIR measurements were carried out to identify the possible biomolecules responsible for capping and efficient stabilization of the nanoparticles. It is found that Au nanoparticles are bound to proteins through free amino groups and silver nanoparticles through the carboxylate group of the amino acid residues. The position and intensity of the emission band is found to depend on composition of the nanoparticles indicating the possible use in therapeutic applications. PMID:19324587

  16. Biosynthesis of Au, Ag and Au-Ag nanoparticles using edible mushroom extract

    NASA Astrophysics Data System (ADS)

    Philip, Daizy

    2009-07-01

    Integration of green chemistry principles to nanotechnology is one of the key issues in nanoscience research. There is growing need to develop environmentally benign metal nanoparticle synthesis process that do not use toxic chemicals in the synthesis protocols to avoid adverse effects in medical applications. Here, it is a report on extracellular synthesis method for the preparation of Au, Ag and Au-Ag nanoparticles in water, using the extract of Volvariella volvacea, a naturally occurring edible mushroom, as reducing and protecting agents. Gold nanoparticles of different sizes (20-150 nm) and shapes from triangular nanoprisms to nearly spherical and hexagonal are obtained by this novel method. The size and shape of gold nanoparticles are also found to depend on temperature of the extract. The silver nanoparticles are spherical with size ˜15 nm. There is increased productivity of nanoparticles as shown by sharp and intense surface plasmon resonance bands for the nanoparticles prepared using an excess of the extract. The Au-Ag nanoparticles prepared by co-reduction has only one plasmon band due to alloying of the constituents. All the synthesized nanoparticles are found to be photoluminescent and are highly crystalline as shown by SAED and XRD patterns with fcc phase oriented along the (1 1 1) plane. FTIR measurements were carried out to identify the possible biomolecules responsible for capping and efficient stabilization of the nanoparticles. It is found that Au nanoparticles are bound to proteins through free amino groups and silver nanoparticles through the carboxylate group of the amino acid residues. The position and intensity of the emission band is found to depend on composition of the nanoparticles indicating the possible use in therapeutic applications.

  17. Fully Crystalline Faceted Fe-Au Core-Shell Nanoparticles.

    PubMed

    Langlois, C; Benzo, P; Arenal, R; Benoit, M; Nicolai, J; Combe, N; Ponchet, A; Casanove, M J

    2015-08-12

    Fe-Au core-shell nanoparticles displaying an original polyhedral morphology have been successfully synthesized through a physical route. Analyses using transmission electron microscopy show that the Au shell forms truncated pyramids epitaxially grown on the (100) facets of the iron cubic core. The evolution of the elastic energy and strain field in the nanoparticles as a function of their geometry and composition is calculated using the finite-element method. The stability of the remarkable centered core-shell morphology experimentally observed is attributed to the weak elastic energy resulting from the low misfit at the Fe/Au (100) interface compared to the surface energy contribution. PMID:26146846

  18. Spin Polarization and Quantum Spins in Au Nanoparticles

    PubMed Central

    Li, Chi-Yen; Karna, Sunil K.; Wang, Chin-Wei; Li, Wen-Hsien

    2013-01-01

    The present study focuses on investigating the magnetic properties and the critical particle size for developing sizable spontaneous magnetic moment of bare Au nanoparticles. Seven sets of bare Au nanoparticle assemblies, with diameters from 3.5 to 17.5 nm, were fabricated with the gas condensation method. Line profiles of the X-ray diffraction peaks were used to determine the mean particle diameters and size distributions of the nanoparticle assemblies. The magnetization curves M(Ha) reveal Langevin field profiles. Magnetic hysteresis was clearly revealed in the low field regime even at 300 K. Contributions to the magnetization from different size particles in the nanoparticle assemblies were considered when analyzing the M(Ha) curves. The results show that the maximum particle moment will appear in 2.4 nm Au particles. A similar result of the maximum saturation magnetization appearing in 2.3 nm Au particles is also concluded through analysis of the dependency of the saturation magnetization MP on particle size. The MP(d) curve departs significantly from the 1/d dependence, but can be described by a log-normal function. Magnetization can be barely detected for Au particles larger than 27 nm. Magnetic field induced Zeeman magnetization from the quantum confined Kubo gap opening appears in Au nanoparticles smaller than 9.5 nm in diameter. PMID:23989607

  19. Immobilization of recombinant vault nanoparticles on solid substrates.

    PubMed

    Xia, Yun; Ramgopal, Yamini; Li, Hai; Shang, Lei; Srinivas, Parisa; Kickhoefer, Valerie A; Rome, Leonard H; Preiser, Peter R; Boey, Freddy; Zhang, Hua; Venkatraman, Subbu S

    2010-03-23

    Native vaults are nanoscale particles found abundantly in the cytoplasm of most eukaryotic cells. They have a capsule-like structure with a thin shell surrounding a "hollow" interior compartment. Recombinant vault particles were found to self-assemble following expression of the major vault protein (MVP) in a baculovirus expression system, and these particles are virtually identical to native vaults. Such particles have been recently studied as potential delivery vehicles. In this study, we focus on immobilization of vault particles on a solid substrate, such as glass, as a first step to study their interactions with cells. To this end, we first engineered the recombinant vaults by fusing two different tags to the C-terminus of MVP, a 3 amino acid RGD peptide and a 12 amino acid RGD-strep-tag peptide. We have demonstrated two strategies for immobilizing vaults on solid substrates. The barrel-and-cap structure of vault particles was observed for the first time, by atomic force microscopy (AFM), in a dry condition. This work proved the feasibility of immobilizing vault nanoparticles on a material surface, and the possibility of using vault nanoparticles as localized and sustainable drug carriers as well as a biocompatible surface moiety. PMID:20146454

  20. Electronic and chemical properties of supported Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Lim, Dong Chan; Lopez-Salido, Ignacio; Dietsche, Rainer; Bubek, Moritz; Kim, Young Dok

    2006-11-01

    Oxidation and reduction behaviors of Au nanoparticles with different sizes on highly ordered pyrolytic graphite (HOPG) and silica were studied using X-ray photoelectron spectroscopy (XPS). For Au nanoparticles smaller than ˜6 nm in diameter, we found a novel oxygen species formed in Au nanoparticles, which is absent in larger particles and Au bulk crystals. This new oxygen species is attributed to the subsurface oxygen: for a complete understanding of the structures of catalytically active Au, the new oxygen species should be taken into account. In this context, it is worth mentioning that the subsurface oxygen species has been suggested to play an important role in heterogeneous catalysis. With decreasing Au particle size, a positive core level shift can be observed, which can be mostly attributed to the final state effects. Increase of the number of undercoordinated atoms with decreasing particle size is evidenced by a reduced splitting between 5d 3/2 and 5d 5/2 states and a band narrowing. Our results on electronic structures of Au nanoparticles on silica are compared to those on other substrates such as zirconia and titania to shed light onto the metal-support interactions.

  1. Magnetic order of Au nanoparticle with clean surface

    NASA Astrophysics Data System (ADS)

    Sato, Ryuju; Ishikawa, Soichiro; Sato, Hiroyuki; Sato, Tetsuya

    2015-11-01

    Au nanoparticles, which are kept in vacuum after the preparation by gas evaporation method, show ferromagnetism even in 1.7 nm in diameter. The intrinsic magnetism is examined by detecting the disappearance of spontaneous magnetization in Au bulk prepared by heating the nanoparticles without exposure to the air. The temperature dependence of spontaneous magnetization is not monotonic and the increase in magnetization is observed after Au nanoparticles are exposed to the air. The magnetic behavior can be interpreted by the ferrimagnetic-like core-shell structure with shell thickness of 0.16±0.01 nm and magnetic moment of (1.5±0.1)×10-2 μB/Au atom, respectively.

  2. Reliable methods for silica coating of Au nanoparticles.

    PubMed

    Pastoriza-Santos, Isabel; Liz-Marzán, Luis M

    2013-01-01

    The inherent properties of silica, such as optical transparency, high biocompatibility, chemical and colloidal stability, controllable porosity, and easy surface modification, provide silica materials with a tremendous potential in biomedicine. Therefore, the coating of Au nanoparticles with silica largely contributes to enhance the important applications of metal nanoparticles in biomedicine. We describe in this chapter a number of reliable strategies that have been reported for silica coating of different types of Au nanoparticles. All descriptions are based on tested protocols and are expected to provide a reference for scientists with an interest in this field. PMID:23918330

  3. Designed synthesis of aptamer-immobilized magnetic mesoporous silica/Au nanocomposites for highly selective enrichment and detection of insulin.

    PubMed

    Xiong, Ya; Deng, Chunhui; Zhang, Xiangmin; Yang, Pengyuan

    2015-04-29

    We designed and synthesized aptamer-immobilized magnetic mesoporous silica/Au nanocomposites (MMANs) for highly selective detection of unlabeled insulin in complex biological media using MALDI-TOF MS. The aptamer was easily anchored onto the gold nanoparticles in the mesochannels of MMANs with high capacity for highly efficient and specific enrichment of insulin. With the benefit from the size-exclusion effect of the mesoporous silica shell with a narrow pore size distribution (∼2.9 nm), insulin could be selectively detected despite interference from seven untargeted proteins with different size dimensions. This method exhibited an excellent response for insulin in the range 2-1000 ng mL(-1). Moreover, good recoveries in the detection of insulin in 20-fold diluted human serum were achieved. We anticipate that this novel method could be extended to other biomarkers of interest and potentially applied in disease diagnostics. PMID:25854412

  4. Detection of glucose using immobilized bienzyme on cyclic bisureas-gold nanoparticle conjugate.

    PubMed

    Mathew, Manjusha; Sandhyarani, N

    2014-08-15

    A highly sensitive electrochemical glucose sensor has been developed by the co-immobilization of glucose oxidase (GOx) and horseradish peroxidase (HRP) onto a gold electrode modified with biocompatible cyclic bisureas-gold nanoparticle conjugate (CBU-AuNP). A self-assembled monolayer of mercaptopropionic acid (MPA) and CBU-AuNP was formed on the gold electrode through a layer-by-layer assembly. This modified electrode was used for immobilization of the enzymes GOx and HRP. Both the HRP and GOx retained their catalytic activity for an extended time, as indicated by the low value of Michaelis-Menten constant. Analytical performance of the sensor was examined in terms of sensitivity, selectivity, reproducibility, lower detection limit, and stability. The developed sensor surface exhibited a limit of detection of 100nM with a linear range of 100nM to 1mM. A high sensitivity of 217.5μAmM(-1)cm(-2) at a low potential of -0.3V was obtained in this sensor design. Various kinetic parameters were calculated. The sensor was examined for its practical clinical application by estimating glucose in human blood sample. PMID:24835425

  5. Rational Design of Nanoparticle Platforms for "Cutting-the-Fat": Covalent Immobilization of Lipase, Glycerol Kinase, and Glycerol-3-Phosphate Oxidase on Metal Nanoparticles.

    PubMed

    Aggarwal, V; Pundir, C S

    2016-01-01

    The aggregates of nanoparticles (NPs) are considered better supports for the immobilization of enzymes, as these promote enzyme kinetics, due to their unusual but favorable properties such as larger surface area to volume ratio, high catalytic efficiency of certain immobilized enzymes, non-toxicity of some of the nanoparticle matrices, high stability, strong adsorption of the enzyme of interest by a number of different approaches, and faster electron transportability. Co-immobilization of multiple enzymes required for a multistep reaction cascade on a single support is more efficient than separately immobilizing the corresponding enzymes and mixing them physically, since products of one enzyme could serve as reactants for another. These products can diffuse much more easily between enzymes on the same particle than diffusion from one particle to the next, in the reaction medium. Thus, co-immobilization of enzymes onto NP aggregates is expected to produce faster kinetics than their individual immobilizations on separate matrices. Lipase, glycerol kinase, and glycerol-3-phosphate oxidase are required for lipid analysis in a cascade reaction, and we describe the co-immobilization of these three enzymes on nanocomposites of zinc oxide nanoparticles (ZnONPs)-chitosan (CHIT) and gold nanoparticles-polypyrrole-polyindole carboxylic acid (AuPPy-Pin5COOH) which are electrodeposited on Pt and Au electrodes, respectively. The kinetic properties and analytes used for amperometric determination of TG are fully described for others to practice in a trained laboratory. Cyclic voltammetry, scanning electron microscopy, Fourier transform infra-red spectra, and electrochemical impedance spectra confirmed their covalent co-immobilization onto electrode surfaces through glutaraldehyde coupling on CHIT-ZnONPs and amide bonding on AuPPy/Pin5COOH. The combined activities of co-immobilized enzymes was tested amperometrically, and these composite nanobiocatalysts showed optimum activity

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

    PubMed

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

    2014-09-01

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

  7. Counterion-Mediated Assembly of Spherical Nucleic Acid-Au Nanoparticle Conjugates (SNA-AuNPs)

    NASA Astrophysics Data System (ADS)

    Kewalramani, Sumit; Moreau, Liane; Guerrero-García, Guillermo; Mirkin, Chad; Olvera de La Cruz, Monica; Bedzyk, Michael; Afosr Muri Team

    2015-03-01

    Controlled crystallization of colloids from solution has been a goal of material scientists for decades. Recently, nucleic acid functionalized spherical Au nanoparticles (SNA-AuNPs) have been programmed to assemble in a wide variety of crystal structures. In this approach, the assembly is driven by Watson-Crick hybridization between DNAs coating the AuNPs. Here, we show that counterions can induce ordered assembly of SNA-AuNPs in bulk solutions, even in the absence of base pairing interactions. The electrostatics-driven assembly of spherical nucleic acid-Au nanoparticle conjugates (SNA-AuNPs) is probed as a function of counterion concentration and counterion valency [ +1 (Na+) or +2 (Ca2+) ] by in situ solution X-ray scattering. Assemblies of AuNPs capped with single-stranded (ss-) or double-stranded (ds-) DNA are examined. SAXS reveals disordered (gas-like) --> face-centered-cubic (FCC) --> glass-like phase transitions with increasing solution ionic strength. These studies demonstrate how non-base-pairing interactions can be tuned to create crystalline assemblies of SNA-AuNPs. The dependence of the inter-SNA-AuNP interactions on counterion valency and stiffness of the DNA corona will be discussed.

  8. Gold nanoparticles supported on mesoporous silica: origin of high activity and role of Au NPs in selective oxidation of cyclohexane.

    PubMed

    Wu, Pingping; Bai, Peng; Yan, Zifeng; Zhao, George X S

    2016-01-01

    Homogeneous immobilization of gold nanoparticles (Au NPs) on mesoporous silica has been achieved by using a one-pot synthesis method in the presence of organosilane mercapto-propyl-trimethoxysilane (MPTMS). The resultant Au NPs exhibited an excellent catalytic activity in the solvent-free selective oxidation of cyclohexane using molecular oxygen. By establishing the structure-performance relationship, the origin of the high activity of mesoporous supported Au catalyst was identified to be due to the presence of low-coordinated Au (0) sites with high dispersion. Au NPs were confirmed to play a critical role in the catalytic oxidation of cyclohexane by promoting the activation of O2 molecules and accelerating the formation of surface-active oxygen species. PMID:26729288

  9. Gold nanoparticles supported on mesoporous silica: origin of high activity and role of Au NPs in selective oxidation of cyclohexane

    PubMed Central

    Wu, Pingping; Bai, Peng; Yan, Zifeng; Zhao, George X. S.

    2016-01-01

    Homogeneous immobilization of gold nanoparticles (Au NPs) on mesoporous silica has been achieved by using a one-pot synthesis method in the presence of organosilane mercapto-propyl-trimethoxysilane (MPTMS). The resultant Au NPs exhibited an excellent catalytic activity in the solvent-free selective oxidation of cyclohexane using molecular oxygen. By establishing the structure-performance relationship, the origin of the high activity of mesoporous supported Au catalyst was identified to be due to the presence of low-coordinated Au (0) sites with high dispersion. Au NPs were confirmed to play a critical role in the catalytic oxidation of cyclohexane by promoting the activation of O2 molecules and accelerating the formation of surface-active oxygen species. PMID:26729288

  10. Fe/Au Core-Shell Nanoparticles for Biomedical Applications

    NASA Astrophysics Data System (ADS)

    Sra, Amandeep; Leslie-Pelecky, Diandra

    2009-10-01

    The physical properties of nanoparticles, including size, composition and surface chemistry, greatly influence biological and pharmacological properties and, ultimately, their clinical applications. Superparamagnetic iron oxide nanoparticles are widely used for applications such as MRI contrast agents, drug delivery via magnetic targeting and hyperthermia due to their chemical stability and biocompatibility; however, enhancing the saturation magnetization (Ms) of nanoparticles would produce greater sensitivity. Our design strategy involves a bottom-up wet chemistry approach to the synthesis of Fe nanoparticles. Specific advantages of Fe are the high value of Ms (210 emu/g in bulk) coupled with low toxicity; however, Fe nanoparticles must be protected from oxidation, which causes a dramatic reduction in Ms. To circumvent oxidation, Fe nanoparticles are coated with a Au shell that prevents the oxidation of the magnetic core and also provides the nanoparticles with plasmonic properties for optical stimulation. Ligands of various functionalities can be introduced through the well established Au-thiol surface chemistry for different biomedical applications while maintaining the magnetic functionality of the Fe core. In this presentation, we will discuss the physical, chemical and magnetic properties of our Fe/Au nanoparticles and their resistance to oxidation.

  11. Au nanoparticles improve amorphous carbon to be gas sensors

    NASA Astrophysics Data System (ADS)

    Liu, Keng-Wen; Lee, Jian-Heng; Chou, Hsiung; Lin, Tzu-Ching; Lin, Si-Ting; Shih-Jye Sun Collaboration

    In order to make the amorphous carbon possess the gas sensing capability transferring some sp3 orbits to sp2 is necessary. It is proposed that the metallic materials having a large charge exchange with sp3 carbon orbits are being catalysts to transfer the carbon orbits. We found embedding gold nanoparticles to the amorphous carbon will induce many compact sp2 orbits around the nanoparticles, which make the amorphous carbon be the candidate material for the gas sensors. The orbits of amorphous carbon near the interface of Au nanoparticles can be changed from sp3 to compact sp2 to reduce the surface energy of Au nanoparticles. Meanwhile, our molecular dynamics simulation has confirmed the fact, when an Au nanoparticle is embedded in the amorphous carbon system the ratio of sp2 orbits increases dramatically. Similar results also have been confirmed from the Raman spectrum measurements. We controlled the carrier transport by changing the hopping barriers formed by amorphous carbon matrix between the Au nanoparticles to modify the resistance. These nanocomposites exhibit a superior sensitivity to NH3 at room temperature as well as good reproducibility and short response/recovery times, which could have potential applications in gas sensors. Dept. of Applied Physics,NUK, Kaohsiung, Taiwan.

  12. Gold nanoparticles-immobilized, hierarchically ordered, porous TiO2 nanotubes for biosensing of glutathione

    PubMed Central

    Mers, SV Sheen; Kumar, Elumalai Thambuswamy Deva; Ganesh, V

    2015-01-01

    Glutathione (GSH) is vital for several functions of our human body such as neutralization of free radicals and reactive oxygen compounds, maintaining the active forms of vitamin C and E, regulation of nitric oxide cycle, iron metabolism, etc. It is also an endogenous antioxidant in most of the biological reactions. Given the importance of GSH, a simple strategy is proposed in this work to develop a biosensor for quantitative detection of GSH. This particular biosensor comprises of gold nanoparticles (Au NPs)-immobilized, hierarchically ordered titanium dioxide (TiO2) porous nanotubes. Hexagonally arranged, honeycomb-like nanoporous tubular TiO2 electrodes are prepared by using a simple electrochemical anodization process by applying a constant potential of 30 V for 24 hours using ethylene glycol consisting of ammonium fluoride as an electrolytic medium. Structural morphology and crystalline nature of such TiO2 nanotubes are analyzed using field emission scanning electron microscope (FESEM) and X-ray diffraction (XRD). Interestingly, nanocomposites of TiO2 with Au NPs is prepared in an effort to alter the intrinsic properties of TiO2, especially tuning of its band gap. Au NPs are prepared by a well-known Brust and Schiffrin method and are immobilized onto TiO2 electrodes which act as a perfect electrochemical sensing platform for GSH detection. Structural characterization and analysis of these modified electrodes are performed using FESEM, XRD, and UV-visible spectroscopic studies. GSH binding events on Au NPs-immobilized porous TiO2 electrodes are monitored by electrochemical techniques, namely, cyclic voltammetry (CV) and chronoamperometry (CA). Several parameters such as sensitivity, selectivity, stability, limit of detection, etc are investigated. In addition, Au NPs dispersed in aqueous medium are also explored for naked-eye detection of GSH using UV-visible spectroscopy in order to compare the performance of the proposed sensor. Our studies clearly indicate

  13. Gold nanoparticles-immobilized, hierarchically ordered, porous TiO2 nanotubes for biosensing of glutathione.

    PubMed

    Mers, Sv Sheen; Kumar, Elumalai Thambuswamy Deva; Ganesh, V

    2015-01-01

    Glutathione (GSH) is vital for several functions of our human body such as neutralization of free radicals and reactive oxygen compounds, maintaining the active forms of vitamin C and E, regulation of nitric oxide cycle, iron metabolism, etc. It is also an endogenous antioxidant in most of the biological reactions. Given the importance of GSH, a simple strategy is proposed in this work to develop a biosensor for quantitative detection of GSH. This particular biosensor comprises of gold nanoparticles (Au NPs)-immobilized, hierarchically ordered titanium dioxide (TiO2) porous nanotubes. Hexagonally arranged, honeycomb-like nanoporous tubular TiO2 electrodes are prepared by using a simple electrochemical anodization process by applying a constant potential of 30 V for 24 hours using ethylene glycol consisting of ammonium fluoride as an electrolytic medium. Structural morphology and crystalline nature of such TiO2 nanotubes are analyzed using field emission scanning electron microscope (FESEM) and X-ray diffraction (XRD). Interestingly, nanocomposites of TiO2 with Au NPs is prepared in an effort to alter the intrinsic properties of TiO2, especially tuning of its band gap. Au NPs are prepared by a well-known Brust and Schiffrin method and are immobilized onto TiO2 electrodes which act as a perfect electrochemical sensing platform for GSH detection. Structural characterization and analysis of these modified electrodes are performed using FESEM, XRD, and UV-visible spectroscopic studies. GSH binding events on Au NPs-immobilized porous TiO2 electrodes are monitored by electrochemical techniques, namely, cyclic voltammetry (CV) and chronoamperometry (CA). Several parameters such as sensitivity, selectivity, stability, limit of detection, etc are investigated. In addition, Au NPs dispersed in aqueous medium are also explored for naked-eye detection of GSH using UV-visible spectroscopy in order to compare the performance of the proposed sensor. Our studies clearly indicate

  14. A new strategy for the controlled deposition of gold nanoparticle aggregates on two-dimensional polystyrene arrays and its application in glucose oxidase immobilization.

    PubMed

    Xia, Yuetong; Li, Jinru; Jiang, Long

    2012-07-01

    Nano/microstructures play an important role in nanoparticle applications. This paper describes an innovative strategy to fabricate a variety of gold nanoparticle aggregates (AuNPs) on large-scale arrays of up to ∼1 cm(2) made from polystyrene (PS). A dendritic surfactant, C18N3, has multi-amine head groups that can control the thickness of a double layer adsorbed on the PS sphere surface in a pH-dependent manner. Controlling the pH and immersion time in the C18N3 solution allows the morphology of AuNPs deposited on the PS spheres (PS@AuNP) to be regulated. The influence of nano/microstructures on the activity enhancement of glucose oxidase (GOD) was investigated. The results indicated that well-ordered PS@AuNP arrays performed much better in the specific activity enhancement of GOD compared with free GOD and GOD immobilized on PS arrays. Furthermore, it was observed that the immobilized GOD on 2D PS@AuNP arrays maintained a highly improved operational stability compared to free GOD. The mechanism behind this effect is discussed. For practical applications, prepared PS@AuNP arrays can be used as an effective chip for GOD immobilization and application. PMID:22498366

  15. Immobilization of human carbonic anhydrase on gold nanoparticles assembled onto amine/thiol-functionalized mesoporous SBA-15 for biomimetic sequestration of CO2.

    PubMed

    Vinoba, Mari; Lim, Kyoung Soo; Lee, Si Hyun; Jeong, Soon Kwan; Alagar, Muthukaruppan

    2011-05-17

    A biocatalyst was synthesized by immobilizing human carbonic anhydrase onto gold nanoparticles assembled over amine/thiol-functionalized mesoporous SBA-15. The physicochemical properties of the functionalized mesoporous SBA-15 were obtained by XRD, BET, FE SEM, HR TEM, EDS, and zeta potential analysis. The biocatalytic performance was studied for para-nitrophenyl acetate (p-NPA) hydrolysis. The kinetic parameters K(m) were found to be 22.35 and 27.75 mM, and K(cat)/K(m) values were 1514.09 and 1612.25 M(-1) s(-1) for HCA immobilized on gold nanoparticles assembled on amine/thiol-functionalized mesoporous SBA-15 (HCA/Au/APTES/SBA-15 and HCA/Au/MPTES/SBA-15), respectively. These HCA/Au/APTES/SBA-15 and HCA/Au/MPTES/SBA-15 were investigated for biocatalytic hydration of CO(2) and its precipitation as CaCO(3). The amount of CaCO(3) precipitated over HCA/Au/MPTES/SBA-15 was nearly the same as that precipitated over free HCA. Storage stability and reusability studies suggested that HCA/Au/MPTES/SBA-15 retained its activity even after 20 days storage at 25 °C and 20 recycling runs. The present results demonstrate that HCA/Au/MPTES/SBA-15 and HCA/Au/APTES/SBA-15 are highly efficient potential nanobiocatalysts for industrial-scale CO(2) sequestration. PMID:21488617

  16. Conjugating folate on superparamagnetic Fe{sub 3}O{sub 4}@Au nanoparticles using click chemistry

    SciTech Connect

    Shen, Xiaofang Ge, Zhaoqiang; Pang, Yuehong

    2015-02-15

    Gold-coated magnetic core@shell nanoparticles, which exhibit magneto-optical properties, not only enhance the chemical stability of core and biocompatibility of surface, but also provide a combination of multimodal imaging and therapeutics. The conjugation of these tiny nanoparticles with specific biomolecules allows researchers to target the desired location. In this paper, superparamagnetic Fe{sub 3}O{sub 4}@Au nanoparticles were synthesized and functionalized with the azide group on the surface by formation of self-assembled monolayers. Folate (FA) molecules, non-immunogenic target ligands for cancer cells, are conjugated with alkyne and then immobilized on the azide-terminated Fe{sub 3}O{sub 4}@Au nanoparticles through copper(I)-catalyzed azide-alkyne cycloaddition (click reaction). Myelogenous leukemia K562 cells were used as a folate receptor (FR) model, which can be targeted and extracted by magnetic field after interaction with the Fe{sub 3}O{sub 4}@Au–FA nanoparticles. - Graphical abstract: Self-assembled azide-terminated group on superparamagnetic Fe{sub 3}O{sub 4}@Au nanoparticles followed by click reaction with alkyne-functionalized folate, allowing the nanoparticles target folate receptor of cancer cells. - Highlights: • Azidoundecanethiol was coated on the superparamagnetic Fe{sub 3}O{sub 4}@Au nanoparticles by forming self-assembled monolayers. • Alkyne-terminated folate was synthesized from a reaction between the amine and the carboxylic acid. • Conjugation of Fe{sub 3}O{sub 4}@Au nanoparticles with folate was made by copper-catalyzed azide-alkyne cycloaddition click chemistry.

  17. Magnetic mesoporous silica nanoparticles: fabrication and their laccase immobilization performance.

    PubMed

    Wang, Feng; Guo, Chen; Yang, Liang-rong; Liu, Chun-Zhao

    2010-12-01

    Newly large-pore magnetic mesoporous silica nanoparticles (MMSNPs) with wormhole framework structures were synthesized for the first time by using tetraethyl orthosilicate as the silica source and amine-terminated Jeffamine surfactants as template. Iminodiacerate was attached on these MMSNPs through a silane-coupling agent and chelated with Cu(2+). The Cu(2+)-chelated MMSNPs (MMSNPs-CPTS-IDA-Cu(2+)) showed higher adsorption capacity of 98.1 mg g(-1)-particles and activity recovery of 92.5% for laccase via metal affinity adsorption in comparison with MMSNPs via physical adsorption. The Michaelis constant (K(m)) and catalytic constant (k(cat)) of laccase immobilized on the MMSNPs-CPTS-IDA-Cu(2+) were 3.28 mM and 155.4 min(-1), respectively. Storage stability and temperature endurance of the immobilized laccase on MMSNPs-CPTS-IDA-Cu(2+) increased significantly, and the immobilized laccase retained 86.6% of its initial activity after 10 successive batch reactions operated with magnetic separation. PMID:20655206

  18. Hierarchical organization of Au nanoparticles in a poly(vinyl carbazole) matrix for hybrid electronic devices

    NASA Astrophysics Data System (ADS)

    Lee, Sangkyu; Yoon, Seon-Mi; Shin, Hyeon-Jin; Joo, Won-Jae; Yi, Dong Kee; Choi, Jae-Young; Amarnath, Chellachamy A.; Paik, Ungyu

    2008-02-01

    We report a novel one-step method for the preparation of hierarchically patterned Au nanoparticles in a conducting polymer matrix by controlling the interface properties between Au nanoparticles and the conducting polymer matrix. The terminal group of capping molecules for the Au nanoparticles was modified to change the interface properties, not to change the size of the Au nanoparticles which affects their intrinsic properties. By modulating the interface properties, it is possible to construct Au nanoparticle-conducting polymer composites with two different structures: one presents a triple layer in which the conducting polymer layer is sandwiched between Au nanoparticle layers at the top and bottom; the other exhibits a form like a raisin cake in which Au nanoparticles are homogeneously organized in the conducting polymer matrix. High-resolution transmission electron microscopy was used to study the morphology and patterning of Au nanoparticles in the conducting polymer matrix.

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

    PubMed

    Seelert, Trevor; Ghosh, Dipankar; Yargeau, Viviane

    2015-05-01

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

  20. Enhanced electrochromic coloration of poly(3-hexylthiophene) films by electrodeposited Au nanoparticles.

    PubMed

    Nah, Yoon-Chae

    2013-05-01

    Au nanoparticles and poly(3-hexylthiophene) (P3HT) composite films were prepared by electrodeposition of Au nanoparticles using pulse-current electrodeposition followed by the spin coating of P3HT and their enhanced electrochromic coloration was investigated. A relatively uniformed Au nanoparticle was obtained by the controlled electrodeposition on indium tin oxide (ITO) substrate and plasmon absorption band of Au nanoparticles were observed. Optical and electrochemical properties of Au/P3HT composite films were compared with the pure P3HT films. The enhanced electrochromic absorption of the composite films was observed due to the surface plasmon resonance of the Au nanoparticles. PMID:23858881

  1. Glucose biosensor based on glucose oxidase immobilized at gold nanoparticles decorated graphene-carbon nanotubes.

    PubMed

    Devasenathipathy, Rajkumar; Mani, Veerappan; Chen, Shen-Ming; Huang, Sheng-Tung; Huang, Tsung-Tao; Lin, Chun-Mao; Hwa, Kuo-Yuan; Chen, Ting-Yo; Chen, Bo-Jun

    2015-10-01

    Biopolymer pectin stabilized gold nanoparticles were prepared at graphene and multiwalled carbon nanotubes (GR-MWNTs/AuNPs) and employed for the determination of glucose. The formation of GR-MWNTs/AuNPs was confirmed by scanning electron microscopy, X-ray diffraction, UV-vis and FTIR spectroscopy methods. Glucose oxidase (GOx) was successfully immobilized on GR-MWNTs/AuNPs film and direct electron transfer of GOx was investigated. GOx exhibits highly enhanced redox peaks with formal potential of -0.40 V (vs. Ag/AgCl). The amount of electroactive GOx and electron transfer rate constant were found to be 10.5 × 10(-10) mol cm(-2) and 3.36 s(-1), respectively, which were significantly larger than the previous reports. The fabricated amperometric glucose biosensor sensitively detects glucose and showed two linear ranges: (1) 10 μM - 2 mM with LOD of 4.1 μM, (2) 2 mM - 5.2 mM with LOD of 0.95 mM. The comparison of the biosensor performance with reported sensors reveals the significant improvement in overall sensor performance. Moreover, the biosensor exhibited appreciable stability, repeatability, reproducibility and practicality. The other advantages of the fabricated biosensor are simple and green fabrication approach, roughed and stable electrode surface, fast in sensing and highly reproducible. PMID:26215343

  2. Heatless synthesis of well dispersible Au nanoparticles using pectin biopolymer.

    PubMed

    Ahmed, Hanan B; Zahran, M K; Emam, Hossam E

    2016-10-01

    Due to its potency to utilize in enormous applications, preparation of nanogold is of interest. Moreover, getting of highly dispersed nanogold with small size is extremely needful in specific fields. Herein, Au nanocolloid was prepared using alkali catalyzed pectin biopolymer. Pectin was concurrently used as reductant for Au ions and stabilizer for the produced Au nanoparticles (AuNPs). Reducing sugars were evaluated in the colloidal solution reflecting the role alkali in catalytic degradation of pectin to produce much powerful reducing moieties. The obtained Au nanocolloid was monitored via changing in color, UV-visible spectral and transmission electron microscopy. Using of NaOH as strong alkali achieving rapid rate of degradation reaction, resulted in 0.45g/L reducing sugars from 0.2g/L pectin which produced AuNPs with mean size of 6.5nm. In case of Na2CO3 which attained slow degradation rate led to, slightly low reducing sugar content (0.41g/L), fabricated comparatively size of AuNPs (7.5nm). In both cases, well distributed AuNPs was obtained with suitable stabilization up to 5 months and Na2CO3 exhibited higher stability. The current successful method used to produce small sized AuNPs with high dispersion is an innovative, one-step, easily, costless, energy saving and eco-friendly method. PMID:27212212

  3. Tuning surface plasmon resonance by the plastic deformation of Au nanoparticles within a diamond anvil cell

    NASA Astrophysics Data System (ADS)

    Bao, Yongjun; Zhao, Bin; Tang, Xinyu; Hou, Dongjie; Cai, Jian; Tang, Shan; Liu, Junsong; Wang, Fei; Cui, Tian

    2015-11-01

    In this work, surface plasmon resonance (SPR) is tuned by controlling the deformation of Au nanoparticles within a diamond anvil cell (DAC). Colloidal Au nanoparticles were loaded into a DAC and pressurized into a mixture of ice and Au nanoparticles. The Au nanoparticles were reshaped by their anisotropic compression of surrounding ice, which leads to the spectral variations of absorption peaks, broadening or red-shifting. These spectral features are well tuned by controlling the deformation process of Au nanoparticle with choosing the initial intended thickness of DAC gasket. The mechanical properties of Au nanoparticles are also revealed by the shape-dependent SPR in nanometer scale. This result provides us a way to fabricate Au nanoparticles into new shapes and tune SPR of metallic nanoparticles with pressure.

  4. Characterization of Au and Bimetallic PtAu Nanoparticles on PDDA-Graphene Sheets as Electrocatalysts for Formic Acid Oxidation

    NASA Astrophysics Data System (ADS)

    Yung, Tung-Yuan; Liu, Ting-Yu; Huang, Li-Ying; Wang, Kuan-Syun; Tzou, Huei-Ming; Chen, Po-Tuan; Chao, Chi-Yang; Liu, Ling-Kang

    2015-09-01

    Nanocomposite materials of the Au nanoparticles (Au/PDDA-G) and the bimetallic PtAu nanoparticles on poly-(diallyldimethylammonium chloride) (PDDA)-modified graphene sheets (PtAu/PDDA-G) were prepared with hydrothermal method at 90 °C for 24 h. The composite materials Au/PDDA-G and PtAu/PDDA-G were evaluated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) for exploring the structural characterization for the electrochemical catalysis. According to TEM results, the diameter of Au and bimetallic PtAu nanoparticles is about 20-50 and 5-10 nm, respectively. X-ray diffraction (XRD) results indicate that both of PtAu and Au nanoparticles exhibit the crystalline plane of (111), (200), (210), and (311). Furthermore, XRD data also show the 2°-3° difference between pristine graphene sheets and the PDDA-modified graphene sheets. For the catalytic activity tests of Au/PDDA-G and PtAu/PDDA-G, the mixture of 0.5 M aqueous H2SO4 and 0.5 M aqueous formic acid was used as model to evaluate the electrochemical characterizations. The catalytic activities of the novel bimetallic PtAu/graphene electrocatalyst would be anticipated to be superior to the previous electrocatalyst of the cubic Pt/graphene.

  5. Cell adhesion and proliferation on polyethylene grafted with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Kasálková, N. Slepičková; Slepička, P.; Kolská, Z.; Sajdl, P.; Bačáková, L.; Rimpelová, S.; Švorčík, V.

    2012-02-01

    Plasma treatment and subsequent Au nano-particles grafting of polyethylene (PE) lead to changes in surface morphology, roughness and wettability, significantly increasing the attractiveness of the material for cells. The PE samples were exposed to argon plasma. Plasma modified PE was chemically grafted by immersion to biphenyldithiol and consequently into solution of Au nano-particles. Changes in chemical structure of the modified PE were studied using X-ray Photoelectron Spectroscopy (XPS) and electrokinetic analysis ( ζ-potential). The surface wettability of the modified PE samples was examined by measurement of the contact angle by standard goniometry. The surface morphology of the plasma modified PE and that grafted with Au nano-particles was studied by Atomic Force Microscopy (AFM). The modified PE samples were seeded with rat vascular smooth muscle cells (VSMCs) and their adhesion and proliferation were studied. Chemically bounded biphenyldithiol increases the number of the incorporated gold nano-particles and changes sample surface properties. The presence of the biphenyldithiol and the gold nano-particles on the PE surface influences dramatically adhesion and proliferation of VSMCs.

  6. Esterases immobilized on aminosilane modified magnetic nanoparticles as a catalyst for biotransformation reactions.

    PubMed

    Alex, Deepthy; Mathew, Abraham; Sukumaran, Rajeev K

    2014-09-01

    Magnetite nanoparticles were prepared by reacting ferrous and ferric salts in presence of aqueous ammonia. The magnetic nanoparticles (MNPs) were amino functionalized by treating with 3-aminopropyl triethoxy silane (APTES) and was coupled with glutaraldehyde. A novel solvent tolerant esterase from Pseudozyma sp. NII 08165 was immobilized on the MNPs through covalent bonding to the glutaraldehyde. The magnetite nanoparticles had a size range of 10-100 nm, confirmed by DLS. Lipases immobilized on MNPs were evaluated for biotransformation reactions including synthesis of ethyl acetate and transesterification of vegetable oil for producing biodiesel. The MNP immobilized esterase had prolonged shelf life and there was no loss in enzyme activity. PMID:24968816

  7. Surface segregation phenomena in extended and nanoparticle surfaces of Cu-Au alloys

    NASA Astrophysics Data System (ADS)

    Li, Jonathan; Wang, Guofeng; Zhou, Guangwen

    2016-07-01

    Using density functional theory (DFT) and Monte Carlo (MC) simulations, we studied the surface segregation phenomena of Au atoms in the extended and nanoparticle surfaces of Cu-Au alloys. Our MC simulations predicted significant Au enrichment in the outermost layer of (111) and (100) extended surfaces, and Au enrichment in the two outermost layers of (110) extended surfaces. The equilibrium Cu-Au nanoparticles were predicted to develop into an Au-enriched shell structure, where Au atoms preferably segregate to the (100) facets while Cu atoms are mainly located on the (111) facet of the nanoparticles. Our simulation predictions agree with experimental measurements.

  8. Titanium dental implants surface-immobilized with gold nanoparticles as osteoinductive agents for rapid osseointegration.

    PubMed

    Heo, Dong Nyoung; Ko, Wan-Kyu; Lee, Hak Rae; Lee, Sang Jin; Lee, Donghyun; Um, Soong Ho; Lee, Jung Haeng; Woo, Yi-Hyung; Zhang, Lijie Grace; Lee, Deok-Won; Kwon, Il Keun

    2016-05-01

    Gold nanoparticles (GNPs) are quite attractive materials for use as osteogenic agents due to their potential effects on the stimulation of osteoblast differentiation. In this study, an osseo-integrated titanium (Ti) implant surface coated with GNPs was used for promotion of bone regeneration. We prepared a silanized Ti surface by chemical treatment of (3-Mercaptopropyl) trimethoxysilane (MPTMS) and immobilized the GNP layer (Ti-GNP) on their surfaces via Au-S bonding. The GNP layer is uniformly immobilized on the surface and the layer covers the titanium oxide surface well, as confirmed by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The Ti-GNP was used to investigate the effectiveness of this system both in vitro and in vivo. The in vitro results showed that the Ti-GNP significantly enhances the osteogenic differentiation with increased mRNA expression of osteogenic differentiation specific genes in human adipose-derived stem cells (ADSCs). Furthermore, the in vivo results showed that Ti-GNP had a significant influence on the osseous interface formation. Through these in vitro and vivo tests, we found that Ti-GNP can be useful as osseo-integration inducing dental implants for formation of an osseous interface and maintenance of nascent bone formation. PMID:26874978

  9. Assembling Bare Au Nanoparticles at Positively Charged Templates.

    PubMed

    Wang, Wenjie; Zhang, Honghu; Kuzmenko, Ivan; Mallapragada, Surya; Vaknin, David

    2016-01-01

    In-situ X-ray reflectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctionalized (bare) gold nanoparticles (AuNP) spontaneously adsorb to a cationic lipid template formed by a Langmuir monolayer of DPTAP (1,2-dihexadecanoyl-3-trimethylammonium-propane) at vapor/aqueous interfaces. Analysis of the XRR yields the electron density profile across the charged-interfaces along the surface normal showing the AuNPs assemble with vertical thickness comparable to the particle size. The GISAXS analysis indicates that the adsorbed mono-particle layer exhibits short-range in-plane correlations. By contrast, single-stranded DNA-functionalized AuNPs, while attracted to the positively charged surface (more efficiently with the addition of salt to the solution), display less in-plane regular packing compared to bare AuNPs. PMID:27225047

  10. Assembling Bare Au Nanoparticles at Positively Charged Templates

    PubMed Central

    Wang, Wenjie; Zhang, Honghu; Kuzmenko, Ivan; Mallapragada, Surya; Vaknin, David

    2016-01-01

    In-situ X-ray reflectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctionalized (bare) gold nanoparticles (AuNP) spontaneously adsorb to a cationic lipid template formed by a Langmuir monolayer of DPTAP (1,2-dihexadecanoyl-3-trimethylammonium-propane) at vapor/aqueous interfaces. Analysis of the XRR yields the electron density profile across the charged-interfaces along the surface normal showing the AuNPs assemble with vertical thickness comparable to the particle size. The GISAXS analysis indicates that the adsorbed mono-particle layer exhibits short-range in-plane correlations. By contrast, single-stranded DNA-functionalized AuNPs, while attracted to the positively charged surface (more efficiently with the addition of salt to the solution), display less in-plane regular packing compared to bare AuNPs. PMID:27225047

  11. Assembling Bare Au Nanoparticles at Positively Charged Templates

    NASA Astrophysics Data System (ADS)

    Wang, Wenjie; Zhang, Honghu; Kuzmenko, Ivan; Mallapragada, Surya; Vaknin, David

    2016-05-01

    In-situ X-ray reflectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctionalized (bare) gold nanoparticles (AuNP) spontaneously adsorb to a cationic lipid template formed by a Langmuir monolayer of DPTAP (1,2-dihexadecanoyl-3-trimethylammonium-propane) at vapor/aqueous interfaces. Analysis of the XRR yields the electron density profile across the charged-interfaces along the surface normal showing the AuNPs assemble with vertical thickness comparable to the particle size. The GISAXS analysis indicates that the adsorbed mono-particle layer exhibits short-range in-plane correlations. By contrast, single-stranded DNA-functionalized AuNPs, while attracted to the positively charged surface (more efficiently with the addition of salt to the solution), display less in-plane regular packing compared to bare AuNPs.

  12. 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

  13. Electrochemical synthesis of reduced graphene sheet-AuPd alloy nanoparticle composites for enzymatic biosensing.

    PubMed

    Yang, Jiang; Deng, Shengyuan; Lei, Jianping; Ju, Huangxian; Gunasekaran, Sundaram

    2011-11-15

    A simple, fast, green and controllable approach was developed for electrochemical synthesis of a novel nanocomposite of electrochemically reduced graphene oxide (ERGO) and gold-palladium (1:1) bimetallic nanoparticles (AuPdNPs), without the aid of any reducing reagent. The electrochemical reduction efficiently removed oxygen-containing groups in ERGO, which was then modified with homogeneously dispersed AuPdNPs in a good size distribution. ERGO-AuPdNPs nanocomposite showed excellent biocompatibility, enhanced electron transfer kinetics and large electroactive surface area, and were highly sensitive and stable towards oxygen reduction. A biosensor was constructed by immobilizing glucose oxidase as a model enzyme on the nanocomposites for glucose detection through oxygen consumption during the enzymatic reaction. The biosensor had a detection limit of 6.9μM, a linear range up to 3.5mM and a sensitivity of 266.6μAmM(-1)cm(-2). It exhibited acceptable reproducibility and good accuracy with negligible interferences from common oxidizable interfering species. These characteristics make ERGO-AuPdNPs nanocomposite highly suitable for oxidase-based biosensing. PMID:21903376

  14. Ultrasensitive electrochemical sensor for Hg(2+) by using hybridization chain reaction coupled with Ag@Au core-shell nanoparticles.

    PubMed

    Li, Zongbing; Miao, Xiangmin; Xing, Ke; Peng, Xue; Zhu, Aihua; Ling, Liansheng

    2016-06-15

    A novel electrochemical biosensor for Hg(2+) detection was reported by using DNA-based hybridization chain reaction (HCR) coupled with positively charged Ag@Au core-shell nanoparticles ((+)Ag@Au CSNPs) amplification. To construct the sensor, capture probe (CP ) was firstly immobilized onto the surface of glass carbon electrode (GCE). In the presence of Hg(2+), the sandwiched complex can be formed between the immobilized CP on the electrode surface and the detection probe (DP) modified on the gold nanoparticles (AuNPs) based on T-Hg(2+)-T coordination chemistry. The carried DP then opened two ferrocene (Fc) modified hairpin DNA (H1 and H2) in sequence and propagated the happen of HCR to form a nicked double-helix. Numerous Fc molecules were formed on the neighboring probe and produced an obvious electrochemical signal. Moreover, (+)Ag@Au CSNPs were assembly onto such dsDNA polymers as electrochemical signal enhancer. Under optimal conditions, such sensor presents good electrochemical responses for Hg(2+) detection with a detection limit of 3.6 pM. Importantly, the methodology has high selectivity for Hg(2+) detection. PMID:26852203

  15. Photochromic reaction of the diarylethene derivative on Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Takahashi, Ryoji; Kaneko, Satoshi; Fujii, Shintaro; Kiguchi, Manabu

    2015-03-01

    We have studied the photochromic reaction of the diarylethene derivative on Au nanoparticles using the incoherent excitation as a function of the wavelength of the irradiation light with the aim to clarify the effect of metal nanoparticles on the reaction yield. The photochemical reaction was suppressed by the Au nanoparticles under the irradiation of light whose wave length was shorter than 700 nm, while photochemical reaction was enhanced by the irradiation of light whose wavelength was longer than 750 nm via two-photon absorption process. The suppression of the photochemical reaction could be explained by the quenching of the excited state via radiative and non-radiative decay through energy or charge transfer to the metal substrate (e.g. electron-hole pair formation, surface plasmon excitation, formation of induced-dipole induced-dipole coupling), and the absorption of light by the Au nanoparticle. Invited talk at the 7th International Workshop on Advanced Materials Science and Nanotechnology IWAMSN2014, 2-6 November, 2014, Ha Long, Vietnam.

  16. Development of a simple bioelectrode for the electrochemical detection of hydrogen peroxide using Pichia pastoris catalase immobilized on gold nanoparticle nanotubes and polythiophene hybrid.

    PubMed

    Nandini, Seetharamaiah; Nalini, Seetharamaiah; Sanetuntikul, Jakkid; Shanmugam, Sangaraju; Niranjana, Pathappa; Melo, Jose Savio; Suresh, Gurukar Shivappa

    2014-11-21

    In this paper, a simple and innovative electrochemical hydrogen peroxide biosensor has been proposed using catalase (CATpp) derived from Pichia pastoris as bioelectrocatalyst. The model biocomponent was immobilized on gold nanoparticle nanotubes (AuNPNTs) and polythiophene composite using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-hydroxysuccinimide (EDC-NHS) coupling reagent. In this present work, we have successfully synthesized gold nanoparticles (AuNPs) by ultrasonic irradiation. The tubular gold nanostructures containing coalesced AuNPs were obtained by sacrificial template synthesis. The assembly of AuNPNTs onto the graphite (Gr) electrode was achieved via S-Au chemisorption. The latter was pre-coated with electropolymerized thiophene (PTh) to enable S groups to bind AuNPNTs. The combination of AuNPNTs-PTh, i.e., an inorganic-organic hybrid, provides a stable enzyme immobilization platform. The physical morphology of the fabricated biosensor Gr/PTh/AuNPNTs/EDC-NHS/CATpp was investigated using scanning electron microscopy and energy-dispersive microscopy. The analytical performance of the bioelectrode was examined using cyclic voltammetry, differential pulse voltammetry and chronoamperometry. Operational parameters such as working potential, pH, and thermal stability of the modified electrode were examined. The beneficial analytical characteristics of the proposed electrode were demonstrated. Our results indicate that the Gr/PTh/AuNPNTs/EDC-NHS/CATpp bioelectrode exhibits a wide linear range from 0.05 mM to 18.5 mM of H2O2, fast response time of 7 s, excellent sensitivity of 26.2 mA mM(-1) cm(-2), good detection limit of 0.12 μM and good Michaelis-Menten constant of 1.4 mM. In addition, the bioelectrode displayed good repeatability, high stability and acceptable reproducibility, which can be attributed to the AuNPNTs-PTh composite that provides a biocompatible micro-environment. PMID:25208248

  17. Immobilization and Characterization of Penicillin G Acylase (PGA) Immobilized on Magnetic Ni₀.₅Zn₀.₅Fe₂O₄ Nanoparticles.

    PubMed

    Liu, Ruijiang; Fan, Jiawen; Zhang, Yewang; Wang, Peng; Shen, Xiangqian

    2016-01-01

    Magnetic Ni₀.₅Zn₀.₅Fe₂O₄ nanoparticles were prepared via the solution combustion process and their microstructure and magnetic properties were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). The as-prepared magnetic Ni₀.₅Zn₀.₅Fe₂O₄ nanoparticles are characterized with average grain size of about 20 nm and magnetization of 90.3 Am²/kg. The surface of magnetic Ni₀.₅Zn₀.₅Fe₂O₄ nanoparticles was modified by use of sodium silicate and N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride, and the penicillin G acylase (PGA) was successfully immobilized on the surface-modified magnetic Ni₀.₅Zn₀.₅Fe₂O₄ nanoparticles. The results show that the activity for the immobilized PGA is affected less by pH and temperature than that for the free PGA, and the immobilized PGA exhibits a high effective activity, good stability of enzyme catalyst. This immobilized PGA on magnetic Ni₀.₅Zn₀.₅Fe₂O₄ nanoparticles can be separated from the solution by the external magnetic field for cyclic utilization, and they could retain about 70% of initial enzyme activity after 11 consecutive operations. The kinetic parameters (Km and Vmax) were determined, and the value of Km for the immobilized PGA (204.53 mmol/L) is higher than that of the free enzyme (3.50 mmol/L), while Vmax (1.93 mmol/min) is also larger than that of the free enzyme (0.838 mmol/min). PMID:27398443

  18. Au/Pd core-shell nanoparticles with varied hollow Au cores for enhanced formic acid oxidation

    PubMed Central

    2013-01-01

    A facile method has been developed to synthesize Au/Pd core-shell nanoparticles via galvanic replacement of Cu by Pd on hollow Au nanospheres. The unique nanoparticles were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, ultraviolet–visible spectroscopy, and electrochemical measurements. When the concentration of the Au solution was decreased, grain size of the polycrystalline hollow Au nanospheres was reduced, and the structures became highly porous. After the Pd shell formed on these Au nanospheres, the morphology and structure of the Au/Pd nanoparticles varied and hence significantly affected the catalytic properties. The Au/Pd nanoparticles synthesized with reduced Au concentrations showed higher formic acid oxidation activity (0.93 mA cm-2 at 0.3 V) than the commercial Pd black (0.85 mA cm-2 at 0.3 V), suggesting a promising candidate as fuel cell catalysts. In addition, the Au/Pd nanoparticles displayed lower CO-stripping potential, improved stability, and higher durability compared to the Pd black due to their unique core-shell structures tuned by Au core morphologies. PMID:23452438

  19. Au/Pd core-shell nanoparticles with varied hollow Au cores for enhanced formic acid oxidation

    NASA Astrophysics Data System (ADS)

    Hsu, Chiajen; Huang, Chienwen; Hao, Yaowu; Liu, Fuqiang

    2013-03-01

    A facile method has been developed to synthesize Au/Pd core-shell nanoparticles via galvanic replacement of Cu by Pd on hollow Au nanospheres. The unique nanoparticles were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, ultraviolet-visible spectroscopy, and electrochemical measurements. When the concentration of the Au solution was decreased, grain size of the polycrystalline hollow Au nanospheres was reduced, and the structures became highly porous. After the Pd shell formed on these Au nanospheres, the morphology and structure of the Au/Pd nanoparticles varied and hence significantly affected the catalytic properties. The Au/Pd nanoparticles synthesized with reduced Au concentrations showed higher formic acid oxidation activity (0.93 mA cm-2 at 0.3 V) than the commercial Pd black (0.85 mA cm-2 at 0.3 V), suggesting a promising candidate as fuel cell catalysts. In addition, the Au/Pd nanoparticles displayed lower CO-stripping potential, improved stability, and higher durability compared to the Pd black due to their unique core-shell structures tuned by Au core morphologies.

  20. Assembly of hybrid oligonucleotide modified gold (Au) and alloy nanoparticles building blocks.

    PubMed

    Kuo, Yu-Ching; Jen, Chun-Ping; Chen, Yu-Hung; Su, Chia-Hao; Tsai, Shu-Hui; Yeh, Chen-Sheng

    2006-01-01

    The alloy-based hybrid materials with macroscopic network arrays were developed by AuAg/Au and AuAgPd/Au nanoparticle composites through oligonucleotides hybridization. AuAg/Au and AuAgPd/Au exhibited distinct organization. The morphology of AuAg/Au conjugation assembled mainly as compact aggregates while AuAgPd/Au hybrid conjugated into the loosen network assemblies. The dehybridization temperatures were studied as a function of molar ratio of alloy/Au. It was found that higher alloy/gold molar ratio led to stronger hybridization for alloy/gold composite, accompanied with increased melting temperature. These results could be interpreted in terms of more alloy nanoparticles bound to a Au particle when the molar ratio of alloy/gold increased. The thermal analysis also showed that AuAg/Au exhibited higher dehybridization temperature. A modified model describing the dehybridization probability of an intact Au/alloy aggregate was performed to support the dehybridization temperature increased with increasing alloy/Au molar ratio. As to more oligonucleotides carried by AuAg (4.9 +/- 1.9 nm) than by AuAgPd (4.4 +/- 1.5 nm) due to larger size in AuAg, the efficient hybridization could result in higher dehybridization temperature in AuAg/Au. PMID:16573077

  1. Synthesis and characterization of cysteine functionalized silver nanoparticles for biomolecule immobilization.

    PubMed

    Upadhyay, Lata Sheo Bachan; Verma, Nishant

    2014-11-01

    A facile method for the aqueous phase synthesis of cysteine-functionalized silver nanoparticles by potato extract has been reported in the present work. These functionalized nanoparticles were then used for the covalent immobilization of a biomolecule, alkaline phosphatase, on its surface through carbodiimide coupling. Different reaction parameters such as cysteine concentration, reducing agent concentration, temperature, pH and reaction time were varied during the nanoparticles' formation, and their effects on plasmon resonance were studied using Ultraviolet-visible spectroscopy. Fourier transform infrared spectroscopy was used to confirm the surface modification of silver nanoparticles by cysteine and the particle size analysis was done using particle size analyzer, which showed the average nanoparticles' size of 61 nm for bare silver nanoparticles and 201 nm for the enzyme-immobilized nanoparticles. The synthesized nanoparticles were found to be highly efficient for the covalent immobilization of alkaline phosphatase on its surface and retained 67% of its initial enzyme activity (9.44 U/mg), with 75% binding efficiency. The shelf life of the enzyme-nanoparticle bioconjugates was found to be 60 days, with a 12% loss in the initial enzyme activity. With a simple synthesis strategy, high immobilization efficiency and enhanced stability, these enzyme-coated nanoparticles have the potential for further integration into the biosensor technology. PMID:24760173

  2. Immobilization of gold nanoparticles on cell culture surfaces for safe and enhanced gold nanoparticle-mediated laser transfection

    NASA Astrophysics Data System (ADS)

    Kalies, Stefan; Heinemann, Dag; Schomaker, Markus; Gentemann, Lara; Meyer, Heiko; Ripken, Tammo

    2014-07-01

    In comparison to standard transfection methods, gold nanoparticle-mediated laser transfection has proven to be a versatile alternative. This is based on its minor influence on cell viability and its high efficiency, especially for the delivery of small molecules like small interfering RNA. However, in order to transfer it to routine usage, a safety aspect is of major concern: The avoidance of nanoparticle uptake by the cells is desired. The immobilization of the gold nanoparticles on cell culture surfaces can address this issue. In this study, we achieved this by silanization of the appropriate surfaces and the binding of gold nanoparticles to them. Comparable perforation efficiencies to the previous approaches of gold nanoparticle-mediated laser transfection with free gold nanoparticles are demonstrated. The uptake of the immobilized particles by the cells is unlikely. Consequently, these investigations offer the possibility of bringing gold nanoparticle-mediated laser transfection closer to routine usage.

  3. Immobilization of dehydrogenase onto epoxy-functionalized nanoparticles for synthesis of (R)-mandelic acid.

    PubMed

    Jiang, Xiao-Ping; Lu, Ting-Ting; Liu, Cai-Hong; Ling, Xiao-Ming; Zhuang, Meng-Yao; Zhang, Jiu-Xun; Zhang, Ye-Wang

    2016-07-01

    Epoxy functionalized magnetic Fe3O4@SiO2 nanoparticles were successfully prepared and characterized by Fourier-transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The prepared nanoparticles were used for immobilization of alcohol dehydrogenase (ADH) from Saccharomyces cerevisiae by covalent attachment. The optimal immobilization conditions were obtained as follows: enzyme/support 4.49mg/g, pH 8.0, buffer concentration 0.05M, time 12h and temperature 30°C. Under these conditions, a high immobilization yield and efficiency of above 92% were obtained after the optimization. Broad pH tolerance and high thermostability were achieved by the immobilization. The immobilized ADH retained about 84% initial activity after five cycles. Kinetic parameters Vmax and Km of free and immobilized ADH were determined as 56.72μM/min, 44.27μM/min and 11.54mM, 31.32mM, respectively. (R)-mandelic acid synthesis with the immobilized ADH was carried out, and the yield of (R)-mandelic acid was as high as 64%. These results indicate that the ADH immobilized onto epoxy-functionalized nanoparticles is an efficient and simple way for preparation of stable ADH, and the immobilized ADH has potential applications in the production of (R)-mandelic acid. PMID:26995611

  4. Controlled deposition of Au on (BiO)2CO3 microspheres: the size and content of Au nanoparticles matter.

    PubMed

    Li, Qiuyan; Hao, Xiaodong; Guo, Xiaolong; Dong, Fan; Zhang, Yuxin

    2015-05-21

    Novel 3D Au/(BiO)2CO3 (Au/BOC) heterostructures with size-controlled Au nanoparticles (NPs) (2-10 nm) were first synthesized and used in photocatalytic removal of ppb-level NO for air cleaning. The photocatalytic performance of Au/BOC heterostructures was enhanced by fine-tuning the content of Au and the size of Au NPs. A new photocatalysis mechanism of surface scattering and reflecting (SSR) coupled with surface plasmon resonance (SPR) was proposed to understand the enhanced photocatalytic activity. PMID:25906416

  5. Preparation and characterization of tannase immobilized onto carboxyl-functionalized superparamagnetic ferroferric oxide nanoparticles.

    PubMed

    Wu, Changzheng; Xu, Caiyun; Ni, Hui; Yang, Qiuming; Cai, Huinong; Xiao, Anfeng

    2016-04-01

    Tannase from Aspergillus tubingensis was immobilized onto carboxyl-functionalized Fe3O4 nanoparticles (CMNPs), and conditions affecting tannase immobilization were investigated. Successful binding between CMNPs and tannase was confirmed by Fourier transform infrared spectroscopy and thermogravimetric analysis. Vibrating sample magnetometry and X-ray diffraction showed that the CMNPs and immobilized tannase exhibit distinct magnetic responses and superparamagnetic properties. Free and immobilized tannase exhibited identical optimal temperatures of 50°C and differing pH optima at 6 and 7, respectively. The thermal, pH, and storage stabilities of the immobilized tannase were superior to those of free tannase. After six cycles of catalytic hydrolysis of propyl gallate, the immobilized tannase maintained over 60% of its initial activity. The Michaelis constant (Km) of the immobilized enzyme indicated its higher affinity for substrate binding than the free enzyme. PMID:26809129

  6. The impact of immobile zones on the transport and retention of nanoparticles in porous media

    NASA Astrophysics Data System (ADS)

    Molnar, Ian L.; Gerhard, Jason I.; Willson, Clinton S.; O'Carroll, Denis M.

    2015-11-01

    Nanoparticle transport and retention within porous media is treated by conceptualizing the porous media as a series of independent collectors (e.g., Colloid Filtration Theory). This conceptualization assumes that flow phenomena near grain-grain contacts, such as immobile zones (areas of low flow), exert a negligible influence on nanoparticle transport and assumes that retention and release of particles depends only on surface chemistry. This study investigated the impact of immobile zones on nanoparticle transport and retention by employing synchrotron X-ray computed microtomography (SXCMT) to examine pore-scale silver nanoparticle distributions during transport through three sand columns: uniform iron oxide, uniform quartz, and well-graded quartz. Extended tailing was observed during the elution phase of all experiments suggesting that hydraulic retention in immobile zones, not detachment from grains, was the source of tailing. A numerical simulation of fluid flow through an SXCMT data set predicted the presence of immobile zones near grain-grain contacts. SXCMT-determined silver nanoparticle concentrations observed that significantly lower nanoparticle concentrations existed near grain-grain contacts throughout the duration of all experiments. In addition, the SXCMT-determined pore-scale concentration gradients were found to be independent of surface chemistry and grain size distribution, suggesting that immobile zones limit the diffusive transport of nanoparticles toward the collectors. These results suggest that the well-known overprediction of nanoparticle retention by traditional CFT may be due to ignoring the influences of grain-grain contacts and immobile zones. As such, accurate prediction of nanoparticle transport requires consideration of immobile zones and their influence on both hydraulic and surface retention.

  7. Urease immobilized fluorescent gold nanoparticles for urea sensing.

    PubMed

    Parashar, Upendra Kumar; Nirala, Narsingh R; Upadhyay, Chandan; Saxena, P S; Srivastava, Anchal

    2015-05-01

    We report a surfactant-free synthesis of monodispersed gold nanoparticles (AuNPs) with average size of 15 nm. An approach for visual and fluorescent sensing of urea in aqueous solution based on shift in surface plasmon band (SPB) maxima as well as quench in fluorescence intensity. To enable the urea detection, we functionalized the thiol-capped gold nanoparticles with urease, the enzyme specific to urea using carbodiimide chemistry. The visible color changed of the gold colloidal solution from red to blue (or purple); this was evident from quenching in absorbance and fluorescence intensity, is the principle applied here for the sensing of urea. The solution turns blue when the urea concentration exceeds 8 mg/dL which reveals visual lower detection limit. The lower detection limits governed by the fluorescence quenching were found 5 mg/dL (R(2) = 0.99) which is highly sensitive and selective compared to shift in SPB maxima. The approach depicted here seems to be important in clinical diagnosis. PMID:25809996

  8. Heterostructured Au/Pd-M (M = Au, Pd, Pt) nanoparticles with compartmentalized composition, morphology, and electrocatalytic activity.

    PubMed

    Lutz, Patrick S; Bae, In-Tae; Maye, Mathew M

    2015-10-14

    The synthesis, processing, and galvanic exchange of three heterostructured nanoparticle systems is described. The surface accessibility and redox potential of a Au/Pd-Ag dumbbell nanoparticle, where a Au/Pd core/shell region, and a silver region make up the domains, was used to prepare the new nanostructures with controlled composition, morphology, and microstructure. Results indicate that the silver domain was particularly susceptible to galvanic displacement, and was exchanged to Au/Pd-M (M = Au, Pd, Pt). Interestingly, the dumbbell morphology remained after exchange, and the silver region was transformed to hollow, parachute, or concentric domains respectively. The morphology and microstructure change was visualized via TEM and HRTEM, and the composition changes were probed via STEM-EDS imaging and XPS. The electrocatalytic activity of the Au/Pd-M towards methanol oxidation was studied, with results indicating that the Au/Pd-Pt nanoparticles had high activity attributed to the porous nature of the platinum domains. PMID:26351824

  9. Controlling Au Photodeposition on Large ZnO Nanoparticles.

    PubMed

    Fernando, Joseph F S; Shortell, Matthew P; Noble, Christopher J; Harmer, Jeffrey R; Jaatinen, Esa A; Waclawik, Eric R

    2016-06-01

    This study investigated how to control the rate of photoreduction of metastable AuCl2(-) at the solid-solution interface of large ZnO nanoparticles (NPs) (50-100 nm size). Band-gap photoexcitation of electronic charge in ZnO by 370 nm UV light yielded Au NP deposition and the formation of ZnO-Au NP hybrids. Au NP growth was observed to be nonepitaxial, and the patterns of Au photodeposition onto ZnO NPs observed by high-resolution transmission electron microscopy were consistent with reduction of AuCl2(-) at ZnO facet edges and corner sites. Au NP photodeposition was effective in the presence of labile oleylamine ligands attached to the ZnO surface; however, when a strong-binding dodecanethiol ligand coated the surface, photodeposition was quenched. Rates of interfacial electron transfer at the ZnO-solution interface were adjusted by changing the solvent, and these rates were observed to strongly depend on the solvent's permittivity (ε) and viscosity. From measurements of electron transfer from ZnO to the organic dye toluidine blue at the ZnO-solution interface, it was confirmed that low ε solvent mixtures (ε ≈ 9.5) possessed markedly higher rates of photocatalytic interfacial electron transfer (∼3.2 × 10(4) electrons·particle(-1)·s(-1)) compared to solvent mixtures with high ε (ε = 29.9, ∼1.9 × 10(4) electrons·particle(-1)·s(-1)). Dissolved oxygen content in the solvent and the exposure time of ZnO to band-gap, near-UV photoexcitation were also identified as factors that strongly affected Au photodeposition behavior. Production of Au clusters was favored under conditions that caused electron accumulation in the ZnO-Au NP hybrid. Under conditions where electron discharge was rapid (such as in low ε solvents), AuCl2(-) precursor ions photoreduced at ZnO surfaces in less than 5 s, leading to deposition of several small, isolated ∼6 nm Au NP on the ZnO host instead. PMID:27196721

  10. Application of Molecular Imprinted Magnetic Fe3O4@SiO2 Nanoparticles for Selective Immobilization of Cellulase.

    PubMed

    Tao, Qing-Lan; Li, Yue; Shi, Ying; Liu, Rui-Jiang; Zhang, Ye-Wang; Guo, Jianyong

    2016-06-01

    Magnetic Fe3O4@SiO2 nanoparticles were prepared with molecular imprinting method using cellulase as the template. And the surface of the nanoparticles was chemically modified with arginine. The prepared nanoparticles were used as support for specific immobilization of cellulase. SDS-PAGE results indicated that the adsorption of cellulase onto the modified imprinted nanoparticles was selective. The immobilization yield and efficiency were obtained more than 70% after the optimization. Characterization of the immobilized cellulase revealed that the immobilization didn't change the optimal pH and temperature. The half-life of the immobilized cellulase was 2-fold higher than that of the free enzyme at 50 degrees C. After 7 cycles reusing, the immobilized enzyme still retained 77% of the original activity. These results suggest that the prepared imprinted nanoparticles have the potential industrial applications for the purification or immobilization of enzymes. PMID:27427671

  11. Photoreduction of Au(III) to form Au(0) nanoparticles using ferritin as a photocatalyst

    NASA Astrophysics Data System (ADS)

    Hilton, Robert J.; Keyes, Jeremiah D.; Watt, Richard K.

    2010-04-01

    Gold metal nanoparticles have applications in bio sensing technology, nano-tube formation, and cancer therapy. We report attempts to synthesize gold nanoparticles within the ferritin cavity (8 nm) or to use ferritin as a scaffold for coating gold on the outside surface (12 nm). The intrinsic iron oxide core of ferritin is a semi-conductor and light can excite electrons to a conduction band producing a powerful reductant when a sacrificial electron donor fills the electron hole. We present a method using ferritin to photo chemically reduce Au(III) to metallic gold nanoparticles. During initial studies we observed that the choice of buffers influenced the products that formed as evidenced by a red product formed in TRIS and a purple produce formed in MOPS. Gold nanoparticles formed in MOPS buffer in the absence of illumination have diameters of 15-30 nm whereas illumination in TRIS buffer produced 5-10 nm gold nanoparticles. Increases in temperature cause the gold nanoparticles to form more rapidly. Chemical reduction and photochemical reduction methods have very different reaction profiles with photochemical reduction possessing a lag phase prior to the formation of gold nanoparticles.

  12. Photoacoustic emission from Au nanoparticles arrayed on thermal insulation layer.

    PubMed

    Namura, Kyoko; Suzuki, Motofumi; Nakajima, Kaoru; Kimura, Kenji

    2013-04-01

    Efficient photoacoustic emission from Au nanoparticles on a porous SiO(2) layer was investigated experimentally and theoretically. The Au nanoparticle arrays/porous SiO(2)/SiO(2)/Ag mirror sandwiches, namely, local plasmon resonators, were prepared by dynamic oblique deposition (DOD). Photoacoustic measurements were performed on the local plasmon resonators, whose optical absorption was varied from 0.03 (3%) to 0.95 by varying the thickness of the dielectric SiO(2) layer. The sample with high absorption (0.95) emitted a sound that was eight times stronger than that emitted by graphite (0.94) and three times stronger than that emitted by the sample without the porous SiO(2) layer (0.93). The contribution of the porous SiO(2) layer to the efficient photoacoustic emission was analyzed by means of a numerical method based on a one-dimensional heat transfer model. The result suggested that the low thermal conductivity of the underlying porous layer reduces the amount of heat escaping from the substrate and contributes to the efficient photoacoustic emission from Au nanoparticle arrays. Because both the thermal conductivity and the spatial distribution of the heat generation can be controlled by DOD, the local plasmon resonators produced by DOD are suitable for the spatio-temporal modulation of the local temperature. PMID:23571958

  13. Stabilization of D-amino acid oxidase from Rhodosporidium toruloides by immobilization onto magnetic nanoparticles.

    PubMed

    Hsieh, Hao-Chieh; Kuan, I-Ching; Lee, Shiow-Ling; Tien, Gee-Yeng; Wang, Yi-Jen; Yu, Chi-Yang

    2009-04-01

    D-amino acid oxidase from Rhodosporidium toruloides was immobilized onto glutaraldehyde-activated magnetic nanoparticles. Approximately four enzyme molecules were attached to one magnetic nanoparticle when the weight ratio of the enzyme to the support was 0.12. After immobilization, the T(m) was increased from 45 degrees C of the free form to 55 degrees C. In the presence of 20 mM H2O2, the immobilized form retained 93% of its activity after 5 h while the free form was completely inactivated after 3.5 h. PMID:19066733

  14. Oxidation of Chlorpromazine by Lipoxygenase Immobilized on Magnetic Fe3O4 Nanoparticles.

    PubMed

    Ding, Wenwu; Hou, Zhaosheng; Che, Zhenming; Li, Mingyuan; Chen, Xianggui; Zhang, Junqing; Zhang, Qikun

    2016-06-01

    In this work, soybean lipoxygenase enzyme was immobilized on the magnetic Fe3O4 nanoparticles to oxidate chlorpromazine (CPZ). The physicochemical properties of the nanoparticles were characterized with transmission electronic microscopy (TEM), fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and thermal gravimetric analysis (TGA), and the magnetic properties were detected by a vibrating sample magnetometer (VSM). The TEM images indicated the surface and the size of the immobilized enzyme were much rougher and thicker than those of the naked particles. The analyses of XRD patterns showed that the structure of the magnetic nanoparticles had no significant change while the nanoparticles also exhibited higher superparamagnetism at room temperature. Compared to free enzyme or the enzyme immobilized with other methods, the optimal pH, temperature and H2O2 concentration for the activity of immobilized enzyme did not have great changes, but the immobilized enzyme was more stable and less sensitive to the change of the influence factors than free counterpart. The immobilized enzyme could be recovered easily by magnetic separation and could be reused for many times in the process of CPZ oxidation. The results obtained by simulating the model of Michaelis-Menten indicated that the reaction of CPZ oxidation followed Michaelis-Menten kinetics and the enzyme still retained its affinity for CPZ while the enzyme was immobilized. PMID:27427602

  15. Efficient synthesis of core@shell Fe3O4@Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Alonso-Cristobal, Paulino; Laurenti, Marco; Lopez-Cabarcos, Enrique; Rubio-Retama, Jorge

    2015-07-01

    The synthesis of Fe3O4@Au nanoparticles has received much attention due to promising applications in the biomedical field. In this work, we produced Fe3O4@Au nanoparticles by using a two-step solvothermal route that employed Fe3O4 nanoparticles as seeds for the Au deposition. Although this protocol leads to highly monodisperse and reproducible Fe3O4@Au nanoparticles it was necessary to perform a systematic study to have a better understanding, improve the yield and allow us to obtain a tunable result. We demonstrated that the Au:Fe3O4 ratio is a key parameter that, contrary to what could be expected, does not influence the Au shell thickness. However, this parameter should be optimized because it strongly influences the yield. When the Au:Fe3O4 ratio was low there were plenty of uncoated Fe3O4 nanoparticles, whereas when the Au:Fe3O4 ratio was high there could be some pure Au nanoparticles together with the desired Fe3O4@Au nanoparticles. Furthermore we demonstrated that the Au shell thickness can be tuned by varying the reaction temperature. This paper describes the influence of both parameters and proposes a mechanism of the synthetic process by studying parametrically the morphological and structural evolution of the nanoparticles by TEM, DLS, SQUID and UV-vis spectroscopy.

  16. Selective oxidation of veratryl alcohol with composites of Au nanoparticles and graphene quantum dots as catalysts.

    PubMed

    Wu, Xiaochen; Guo, Shouwu; Zhang, Jingyan

    2015-04-14

    Veratryl alcohol can be oxidized to veratryl aldehyde or veratric acid with excellent selectivity and efficient conversion under acidic and alkaline conditions using Au nanoparticles and graphene quantum dot composites (Au/GQDs) as catalysts. PMID:25760658

  17. Immobilization of aptamer-modified gold nanoparticles on BiOCl nanosheets: Tunable peroxidase-like activity by protein recognition.

    PubMed

    Hsu, Chia-Lun; Lien, Chia-Wen; Wang, Chia-Wei; Harroun, Scott G; Huang, Chih-Ching; Chang, Huan-Tsung

    2016-01-15

    A self-assembled nanocomposite is prepared from an aqueous mixture of aptamer-modified gold nanoparticles (Apt-Au NPs), bismuth ions and chloride ions. The Apt-Au NPs are immobilized on bismuth oxychloride (BiOCl) nanosheets in situ to form Apt-Au NPs/BiOCl nanocomposites. The as-prepared nanocomposites exhibit high peroxidase-like activity for the catalytic conversion of Amplex Red (AR) to fluorescent resorufin in the presence of H2O2. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is at least 90-fold higher than that of Apt-Au NPs or BiOCl nanosheets, revealing synergistic effects on their activity. The catalytic activity of Apt-Au NPs/BiOCl nanocomposites is suppressed by vascular endothelial growth factor-A165 (VEGF-A165) molecules that specifically interact with the aptamer units (Del-5-1 and v7t-1) on the nanocomposite surface. The AR/H2O2-Apt-Au NPs/BiOCl nanocomposites probe shows high selectivity (>1000-fold over other proteins) and sensitivity (detection limit ~0.5nM) for the detection of VEGF-A165. Furthermore, the probe is employed for the detection of VEGF isoforms and for the study of interactions between VEGF and VEGF receptors. The practicality of this simple, rapid, cost-effective probe is validated by the analysis of VEGF-A165 in cell culture media, showing its great potential for the analysis of VEGF in biological samples. PMID:26318787

  18. Immobilization of Lipase by Adsorption Onto Magnetic Nanoparticles in Organic Solvents.

    PubMed

    Shi, Ying; Liu, Wei; Tao, Qing-Lan; Jiang, Xiao-Ping; Liu, Cai-Hong; Zeng, Sha; Zhang, Ye-Wang

    2016-01-01

    In order to improve the performance of lipase in organic solvents, a simple immobilization method was developed by adsorption of lipase onto Fe₃O₄@ SiO₂magnetic nanoparticles in organic solvent. Among the solvents tested, toluene was found to be the most effective solvent for the immobilization. A maximum immobilization yield of 97% and relative activity of 124% were achieved in toluene at 30 °C. The optimal temperature, enzyme loading and water activity were 30 °C, 1.25 mg/mg support and 0.48 aw, respectively. The residual activity of immobilized lipase was 67% after 10 cycles of use. The advantages of the immobilized lipase including easy recovery, high stability, and enhanced activity of immobilized lipase in organic solvents show potential industrial applications in anhydrous solvents. PMID:27398494

  19. Structure analysis of bimetallic Co-Au nanoparticles formed by sequential ion implantation

    NASA Astrophysics Data System (ADS)

    Chen, Hua-jian; Wang, Yu-hua; Zhang, Xiao-jian; Song, Shu-peng; chen, Hong; Zhang, Ke; Xiong, Zu-zhao; Ji, Ling-ling; Dai, Hou-mei; Wang, Deng-jing; Lu, Jian-duo; Wang, Ru-wu; Zheng, Li-rong

    2016-08-01

    Co-Au alloy Metallic nanoparticles (MNPs) are formed by sequential ion implantation of Co and Au into silica glass at room temperature. The ion ranges of Au ions implantation process have been displayed to show the ion distribution. We have used the atomic force microscopy (AFM) and transmission electron microscopy (TEM) to investigate the formation of bimetallic nanoparticles. The extended X-ray absorption fine structure (EXAFS) has been used to study the local structural information of bimetallic nanoparticles. With the increase of Au ion implantation, the local environments of Co ions are changed enormously. Hence, three oscillations, respectively, Co-O, Co-Co and Co-Au coordination are determined.

  20. Enzymatic biosensor of horseradish peroxidase immobilized on Au-Pt nanotube/Au-graphene for the simultaneous determination of antioxidants.

    PubMed

    Wu, Long; Yin, Wenmin; Tang, Kun; Li, Dian; Shao, Kang; Zuo, Yunpeng; Ma, Jing; Liu, Jiawei; Han, Heyou

    2016-08-24

    A new electrochemical method has been proposed for the simultaneous determination of butylated hydroxyanisole (BHA) and propyl gallate (PG) in food matrices based on enzymatic biosensors. Spiny Au-Pt nanotubes (SAP NTs) was first synthesized and demonstrated to exhibit intrinsic peroxidase and catalase-like activity. The structure of SAP NTs provides large surface area and favorable medium for electron transfer, on which HRP were immobilized and acted as enzymatic biosensor for the simultaneous detection of BHA and PG. The results revealed that BHA and PG both have well-defined oxidation waves with peak potentials of 624 and 655 mV, respectively. Under the optimal conditions, the method behaved satisfactory analytical performance towards BHA and PG with a wide linear range of 0.3-50 mg L(-1) and 0.1-100 mg L(-1), as well as a detection limit of 0.046 mg L(-1) and 0.024 mg L(-1) (3σ/slope), respectively. Besides, the proposed method exhibits good sensitivity, stability and reproducibility, providing an alternative to fabricate electrode and construct sensitive biosensors. PMID:27497001

  1. Highly efficient antibody immobilization with multimeric protein Gs coupled magnetic silica nanoparticles

    NASA Astrophysics Data System (ADS)

    Lee, J. H.; Choi, H. K.; Chang, J. H.

    2011-10-01

    This work reports the immobilization of monomeric, dimeric and trimer protein Gs onto silica magnetic nanoparticles for self-oriented antibody immobilization. To achieve this, we initially prepared the silica-coated magnetic nanoparticle having about 170 nm diameters. The surface of the silica coated magnetic nanoparticles was modified with 3- aminopropyl-trimethoxysilane (APTMS) to chemically link to multimeric protein Gs. The conjugation of amino groups on the SiO2-MNPs to cysteine tagged in multimeric protein Gs was performed using a sulfo-SMCC coupling procedure. The binding efficiencies of monomer, dimer and trimer were 77 %, 67 % and 55 % respectively. However, the efficiencies of antibody immobilization were 70 %, 83 % and 95 % for monomeric, dimeric and trimeric protein G, respectively. To prove the enhancement of accessibility by using multimeric protein G, FITC labeled goat-anti-mouse IgG was treated to mouse IgG immobilized magnetic silica nanoparticles through multimeric protein G. FITC labeled goat anti-mouse IgGs were more easily bound to mouse IgG immobilized by trimeric protein G than others. Finally protein G bound silica magnetic nanoparticles were utilized to develop highly sensitive immunoassay to detect hepatitis B antigen.

  2. Immobilized protease on the magnetic nanoparticles used for the hydrolysis of rapeseed meals

    NASA Astrophysics Data System (ADS)

    Jin, Xin; Li, Ju-Fang; Huang, Ping-Ying; Dong, Xu-Yan; Guo, Lu-Lu; Yang, Liang; Cao, Yuan-Cheng; Wei, Fang; Zhao, Yuan-Di; Chen, Hong

    2010-07-01

    (3-aminopropl) triethoxysilaneand modified magnetic nanoparticles with the average diameter of 25.4 nm were synthesized in water-phase co-precipitation method. And then these nanoparticles were covalently coupled with alkaline protease as enzyme carrier by using 1,4-phenylene diisothlocyanate as coupling agent. Experiments showed that the immobilized protease can keep the catalytic bioactivity, which can reach to 47.8% when casein was served as substrate. Results showed that the catalytic activity of immobilized protease on these magnetic nanoparticles could retain 98.63±2.37% after 60 days. And it is more stable than the free protease during the shelf-life test. The enzyme reaction conditions such as optimum reaction temperature and pH are the same as free protease. Furthermore, mix-and-separate experiments showed that the immobilized protease could be recycled through the magnetic nanoparticles after the biocatalysis process. When the rapeseed meals were used as substrate, the degree of hydrolysis of immobilized alkaline protease achieved 9.86%, while it was 10.41% for the free protease. The macromolecular proteins of rapeseed meals were hydrolyzed by immobilized protease into small molecules such as polypeptides or amino acids. Thus, a novel efficient and economic way for the recycling of enzymes in the application of continuous production of active peptides was provided based on these magnetic nanoparticles.

  3. Facile and high-efficient immobilization of histidine-tagged multimeric protein G on magnetic nanoparticles

    PubMed Central

    2014-01-01

    This work reports the high-efficient and one-step immobilization of multimeric protein G on magnetic nanoparticles. The histidine-tagged (His-tag) recombinant multimeric protein G was overexpressed in Escherichia coli BL21 by the repeated linking of protein G monomers with a flexible linker. High-efficient immobilization on magnetic nanoparticles was demonstrated by two different preparation methods through the amino-silane and chloro-silane functionalization on silica-coated magnetic nanoparticles. Three kinds of multimeric protein G such as His-tag monomer, dimer, and trimer were tested for immobilization efficiency. For these tests, bicinchoninic acid (BCA) assay was employed to determine the amount of immobilized His-tag multimeric protein G. The result showed that the immobilization efficiency of the His-tag multimeric protein G of the monomer, dimer, and trimer was increased with the use of chloro-silane-functionalized magnetic nanoparticles in the range of 98% to 99%, rather than the use of amino-silane-functionalized magnetic nanoparticles in the range of 55% to 77%, respectively. PMID:25593554

  4. Covalent Immobilization of Penicillin G Acylase onto Fe3O4@Chitosan Magnetic Nanoparticles.

    PubMed

    Ling, Xiao-Min; Wang, Xiang-Yu; Ma, Ping; Yang, Yi; Qin, Jie-Mei; Zhang, Xue-Jun; Zhang, Ye-Wang

    2016-05-28

    Penicillin G acylase (PGA) was immobilized on magnetic Fe3O4@chitosan nanoparticles through the Schiff base reaction. The immobilization conditions were optimized as follows: enzyme/support 8.8 mg/g, pH 6.0, time 40 min, and temperature 25°C. Under these conditions, a high immobilization efficiency of 75% and a protein loading of 6.2 mg/g-support were obtained. Broader working pH and higher thermostability were achieved by the immobilization. In addition, the immobilized PGA retained 75% initial activity after ten cycles. Kinetic parameters Vmax and Km of the free and immobilized PGAs were determined as 0.91 mmol/min and 0.53 mmol/min, and 0.68 mM and 1.19 mM, respectively. Synthesis of amoxicillin with the immobilized PGA was carried out in 40% ethylene glycol at 25°C and a conversion of 72% was obtained. These results showed that the immobilization of PGA onto magnetic chitosan nanoparticles is an efficient and simple way for preparation of stable PGA. PMID:26869599

  5. Reduced graphene oxide supported Au nanoparticles as an efficient catalyst for aerobic oxidation of benzyl alcohol

    NASA Astrophysics Data System (ADS)

    Yu, Xianqin; Huo, Yujia; Yang, Jing; Chang, Sujie; Ma, Yunsheng; Huang, Weixin

    2013-09-01

    Various Au/C catalysts were prepared by Au nanoparticels supported on different carbonaceous supports including reduced graphene oxide (RGO), activated carbon (AC) and graphite (GC) using sol-immobilization method. Au/RGO shows a much higher activity than Au/AC and Au/GC in the liquid phase aerobic oxidation of benzyl alcohol. The superior catalytic performance of Au/RGO may be related to the presence of surface O-containing functional groups and moderate graphite character of RGO supports.

  6. Rhodamine B immobilized on hollow Au-HMS material for naked-eye detection of Hg2+ in aqueous media.

    PubMed

    Zhang, Na; Li, Gang; Cheng, Zhuhong; Zuo, Xiujin

    2012-08-30

    A simple, effective method has been demonstrated to immobilize Rhodamine B (RhB) probes on mesoporous silica (Au-HMS). The prepared chemosensor (Au-HMS-Probe) was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), UV-vis spectrum and Fourier transform infrared spectroscopy (FT-IR). Further application of Au-HMS-Probe in sensing Hg(2+) was confirmed by fluorescence titration experiment. Au-HMS-Probe afforded "turn-on" fluorescence enhancement and displayed high brightness in water, and it also showed excellent selectivity for Hg(2+) over alkali (Na(+), K(+)), alkaline earth (Mg(2+), Ca(2+)) and other heavy metal ions (Ag(+), Cd(2+), Co(2+), Pb(2+), Ni(2+), Cu(2+), Fe(2+)). Importantly, Au-HMS-Probe could be regenerated by treatment with tetrapropylammonium hydroxide solution. PMID:22771346

  7. Optical properties of Ag nanoparticle-polymer composite film based on two-dimensional Au nanoparticle array film

    NASA Astrophysics Data System (ADS)

    Wang, Long-De; Zhang, Tong; Zhang, Xiao-Yang; Song, Yuan-Jun; Li, Ruo-Zhou; Zhu, Sheng-Qing

    2014-03-01

    The nanocomposite polyvinyl pyrrolidone (PVP) films containing Ag nanoparticles and Rhodamine 6G are prepared on the two-dimensional distinctive continuous ultrathin gold nanofilms. We investigate the optical properties and the fluorescence properties of silver nanoparticles-PVP polymer composite films influenced by Ag nanoparticles and Au nanoparticles. Absorption spectral analysis suggests that the prominently light absorption in Ag nanowire/PVP and Ag nanowire/PVP/Au film arises from the localized surface plasmon resonance of Ag nanowire and Au nanofilm. The enhanced fluorescence is observed in the presence of Ag nanowire and Au nanofilm, which is attributed to the excitation of surface plasmon polariton resonance of Ag nanowire and Au nanofilm. The gold nanofilm is proven to be very effective fluorescence resonance energy transfer donors. The fabricated novel structure, gold ultrathin continuous nanofilm, possesses high surface plasmon resonance properties and prominent fluorescence enhancement effect. Therefore, the ultrathin continuous gold nanofilm is an active substrate on nanoparticle-enhanced fluorescence.

  8. Synthesis of triangular Au core-Ag shell nanoparticles

    SciTech Connect

    Rai, Akhilesh; Chaudhary, Minakshi; Ahmad, Absar; Bhargava, Suresh; Sastry, Murali . E-mail: msastry@tatachemicals.com

    2007-07-03

    In this paper, we demonstrate a simple and reproducible method for the synthesis of triangular Au core-Ag shell nanoparticles. The triangular gold core is obtained by the reduction of gold ions by lemongrass extract. Utilizing the negative charge on the gold nanotriangles, silver ions are bound to their surface and thereafter reduced by ascorbic acid under alkaline conditions. The thickness of the silver shell may be modulated by varying the pH of the reaction medium. The formation of the Au core-Ag shell triangular nanostructures has been followed by UV-vis-NIR Spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy (TEM) and atomic force microscopy (AFM) measurements. The sharp vertices of the triangles coupled with the core-shell structure is expected to have potential for application in surface enhanced Raman spectroscopy and in the sensitive detection of biomolecules.

  9. Facile Synthesis of Au Nanoparticles Embedded in an Ultrathin Hollow Graphene Nanoshell with Robust Catalytic Performance.

    PubMed

    Liu, Hongyang; Wang, Jia; Feng, Zhenbao; Lin, Yangming; Zhang, Liyun; Su, Dangsheng

    2015-10-01

    Au nanoparticles (NPs) uniformly embedded into an ultrathin hollow graphene nanoshell (Au@HGN) are synthesized using a facile template-based procedure. The obtained Au@HGN catalyst exhibits robust and stable catalytic performance in the reduction of 4-nitrophenol to 4-aminophenol, compared with that of traditional Au/TiO2 and previously reported Au- and Ag-based catalysts. PMID:26280245

  10. Activity of Candida rugosa lipase immobilized on gamma-Fe2O3 magnetic nanoparticles.

    PubMed

    Dyal, Ansil; Loos, Katja; Noto, Mayumi; Chang, Seung W; Spagnoli, Chiara; Shafi, Kurikka V P M; Ulman, Abraham; Cowman, Mary; Gross, Richard A

    2003-02-19

    We report the stability and enzymatic activity of Candida rugosa Lipase (E.C.3.1.1.3) immobilized on gamma-Fe2O3 magnetic nanoparticles. The immobilization strategies were either reacting the enzyme amine group with a nanoparticle surface acetyl, or amine groups. In the former, the enzyme was attached through a C=N bond, while in the latter it was connected using glutaraldehyde. AFM images show an average particle size of 20 +/- 10 nm after deconvolution. The enzymatic activity of the immobilized lipase was determined by following the ester cleavage of p-nitrophenol butyrate. The covalently immobilized enzyme was stabile and reactive over 30 days. PMID:12580578

  11. Phenolics Impart Au3+-Stress Tolerance to Cowpea by Generating Nanoparticles

    PubMed Central

    Shabnam, Nisha; Pardha-Saradhi, P.; Sharmila, P.

    2014-01-01

    While evaluating impact of Au nanoparticles on seed germination and early seedling growth of cowpea, HAuCl4 was used as control. Seedlings of cowpea raised in HAuCl4, even at concentration as high as 1 mM, did not show any suppression in growth. Accordingly, Au3+, despite being a heavy metal, did not alter levels of stress markers (viz. proline and malondialdehyde) in cowpea. Interestingly, cowpea turned clear pale yellow HAuCl4 solutions colloidal purple during the course of seed germination and seedling growth. These purple colloidal suspensions showed Au-nanoparticle specific surface plasmon resonance band in absorption spectra. Transmission electron microscopic and powder X-ray diffraction investigations confirmed presence of crystalline Au-nanoparticles in these purple suspensions. Each germinating seed of cowpea released ∼35 nmoles of GAE of phenolics and since phenolics promote generation of Au-nanoparticles, which are less/non toxic compared to Au3+, it was contemplated that potential of cowpea to withstand Au3+ is linked to phenolics. Of the different components of germinating seed of cowpea tested, seed coat possessed immense power to generate Au-nanoparticles, as it was the key source of phenolics. To establish role of phenolics in generation of Au-nanoparticles (i) seed coat and (ii) the incubation medium in which phenolics were released by germinating seeds, were tested for their efficacy to generate Au-nanoparticles. Interestingly, incubation of either of these components with Au3+ triggered increase in generation of Au-nanoparticles with concomitant decrease in phenolics. Accordingly, with increase in concentration of Au3+, a proportionate increase in generation of Au-nanoparticles and decrease in phenolics was recorded. In summary, our findings clearly established that cowpea possessed potential to withstand Au3+-stress as the phenolics released by seed coat of germinating seeds possess potential to reduce toxic Au3+ to form non/less toxic Au-nanoparticles

  12. Photocatalytic degradation of agricultural N-heterocyclic organic pollutants using immobilized nanoparticles of titania.

    PubMed

    Mahmoodi, Niyaz Mohammad; Arami, Mokhtar; Limaee, Nargess Yousefi; Gharanjig, Kamaladin

    2007-06-25

    Degradation and mineralization of two agricultural organic pollutants (Diazinon and Imidacloprid as N-heterocyclic aromatics) in aqueous solution by nanophotocatalysis using immobilized titania nanoparticles were investigated. Insecticides, Diazinon and Imidacloprid, are persistent pollutants in agricultural soil and watercourses. A simple and effective method was developed to immobilization of titania nanoparticles. UV-vis, ion chromatography (IC) and chemical oxygen demand (COD) analyses were employed. The effects of operational parameters such as H(2)O(2) and inorganic anions (NO(3)(-), Cl(-) and SO(4)(2-)) were investigated. The mineralization of Diazinon and Imidacloprid was evaluated by monitoring of the formed inorganic anions. The selected pollutants are effectively degraded following first order kinetics model. Results show that the nanophotocatalysis using immobilized titania nanoparticle is an effective method for treatment Diazinon and Imidacloprid from contaminated water. PMID:17145132

  13. Solvent-induced desorption of alkanethiol ligands from Au nanoparticles.

    PubMed

    Huang, Yuanyuan; Liu, Wei; Cheng, Hao; Yao, Tao; Yang, Lina; Bao, Jie; Huang, Ting; Sun, Zhihu; Jiang, Yong; Wei, Shiqiang

    2016-06-21

    Removing surfactants from a colloidal metal nanoparticle surface is necessary for their realistic applications, and how they could be stripped is a subject of active investigation. Here, we report a solvent-induced desorption of dodecanethiol ligands from the gold nanoparticle surface, and traced this desorption process using a combination of in situ X-ray absorption fine structure (XAFS) and Raman spectroscopic techniques. In situ analysis results reveal that the solvent exchange of ethanol with tetrahydrofuran (THF) can effectively remove dodecanethiol ligands while keeping the particle morphology unchanged. Upon increasing the THF/ethanol ratio from 0 : 1 to 5 : 1, the surface coverage of thiol on the Au surface is reduced from 0.47 to 0.07, suggesting the depletion of ligands first from the nanoparticle facet sites, then from the edge sites, while the ligands at the corner sites are intact. This work enriches our knowledge on surfactant removal and may pave the way towards preparing surface-clean nanoparticles for practical applications. PMID:27241025

  14. Gold surfaces and nanoparticles are protected by Au(0)-thiyl species and are destroyed when Au(I)-thiolates form.

    PubMed

    Reimers, Jeffrey R; Ford, Michael J; Halder, Arnab; Ulstrup, Jens; Hush, Noel S

    2016-03-15

    The synthetic chemistry and spectroscopy of sulfur-protected gold surfaces and nanoparticles is analyzed, indicating that the electronic structure of the interface is Au(0)-thiyl, with Au(I)-thiolates identified as high-energy excited surface states. Density-functional theory indicates that it is the noble character of gold and nanoparticle surfaces that destabilizes Au(I)-thiolates. Bonding results from large van der Waals forces, influenced by covalent bonding induced through s-d hybridization and charge polarization effects that perturbatively mix in some Au(I)-thiolate character. A simple method for quantifying these contributions is presented, revealing that a driving force for nanoparticle growth is nobleization, minimizing Au(I)-thiolate involvement. Predictions that Brust-Schiffrin reactions involve thiolate anion intermediates are verified spectroscopically, establishing a key feature needed to understand nanoparticle growth. Mixing of preprepared Au(I) and thiolate reactants always produces Au(I)-thiolate thin films or compounds rather than monolayers. Smooth links to O, Se, Te, C, and N linker chemistry are established. PMID:26929334

  15. Multifunctional hybrid Fe2O3-Au nanoparticles for efficient plasmonic heating

    DOE PAGESBeta

    Murph, Simona E. Hunyadi; Larsen, George K.; Lascola, Robert J.

    2016-02-20

    We describe the synthesis and properties of multifunctional Fe2O3-Au nanoparticles produced by a wet chemical approach and investigate their photothermal properties using laser irradiation. Here, the composite Fe2O3-Au nanoparticles retain the properties of both materials, creating a multifunctional structure with excellent magnetic and plasmonic properties.

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

    PubMed

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

    2016-01-01

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

  17. Visible light photoactivity of TiO2 loaded with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles

    NASA Astrophysics Data System (ADS)

    Gołąbiewska, Anna; Lisowski, Wojciech; Jarek, Marcin; Nowaczyk, Grzegorz; Zielińska-Jurek, Anna; Zaleska, Adriana

    2014-10-01

    TiO2 modified with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles have been prepared using a water-in-oil microemulsion system (water/AOT/cyclohexane) followed by calcination step. The effect of metal ratio, reducing agent type (NaBH4 or N2H4), TiO2 matrix type (P-25, ST-01, TiO-5, TiO2 nanotubes or TiO2 obtained by TIP hydrolysis) as well as calcination temperature (from 350 to 650 °C) were systematically investigated. Obtained photocatalysts were characterized by UV-vis diffuse-reflectance spectroscopy (DRS), BET surface area measurements, scanning transmission microscopy (STEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). Photocatalytic activity under visible light (λ > 420 nm) has been estimated in phenol degradation reaction in aqueous phase. The results showed that phenol degradation rate under visible light in the presence of TiO2 loaded with Au/Pt nanoparticles differed from 0.7 to 2.2 μmol dm-3 min-1 for samples prepared using different reducing agent. Sodium borohydride (NaBH4) favors formation of smaller Au/Pt nanoparticles and higher amount gold in Au/Pt is in the form of electronegative species (Auδ-) resulted in higher photoactivity. TiO2 obtained by TIP hydrolysis in microemulsion system seems to be the best support for Au/Pt nanoparticles from all among investigated matrix. It was also observed that enhancement of calcination temperature from 450 to 650 °C resulted in rapid drop of Au/Pt-TiO2 photoactivity under visible light due to surface area shrinkage, crystal structure change and probably change in Au/Pt nanoparticles morphology.

  18. XAFS study on structural order in highly monodispersed thiol-stabilized Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Huang, Y.; Liu, W.; Yang, L.; Huang, T.; Jiang, Y.; Yao, T.; Wei, S.

    2016-05-01

    Understanding the influence of thiol on nanoparticle size and structure is essential for the fundamental and applied researches. Here, using x-ray absorption fine structure (XAFS) spectroscopy, we investigate the structural order of Au nanoparticles (NPs) in the protection of thiol ligands with different contents. We found that besides protecting Au NPs against aggregation and growth, thiolates can effectively eliminate the dangling bonds of unsaturated Au atoms, and thus increase the structural order. This work enriches our knowledge of Au-S interface interaction and guides the way towards preparing size-controllable nanoparticles with specific physical/chemical properties.

  19. Core-size-dependent catalytic properties of bimetallic Au/Ag core-shell nanoparticles.

    PubMed

    Haldar, Krishna Kanta; Kundu, Simanta; Patra, Amitava

    2014-12-24

    Bimetallic core-shell nanoparticles have recently emerged as a new class of functional materials because of their potential applications in catalysis, surface enhanced Raman scattering (SERS) substrate and photonics etc. Here, we have synthesized Au/Ag bimetallic core-shell nanoparticles with varying the core diameter. The red-shifting of the both plasmonic peaks of Ag and Au confirms the core-shell structure of the nanoparticles. Transmission electron microscopy (TEM) analysis, line scan EDS measurement and UV-vis study confirm the formation of core-shell nanoparticles. We have examined the catalytic activity of these core-shell nanostructures in the reaction between 4-nitrophenol (4-NP) and NaBH4 to form 4-aminophenol (4-AP) and the efficiency of the catalytic reaction is found to be increased with increasing the core size of Au/Ag core-shell nanocrystals. The catalytic efficiency varies from 41.8 to 96.5% with varying core size from 10 to 100 nm of Au/Ag core-shell nanoparticles, and the Au100/Ag bimetallic core-shell nanoparticle is found to be 12-fold more active than that of the pure Au nanoparticles with 100 nm diameter. Thus, the catalytic properties of the metal nanoparticles are significantly enhanced because of the Au/Ag core-shell structure, and the rate is dependent on the size of the core of the nanoparticles. PMID:25456348

  20. Enhanced electron field emission from CuO nanoplate arrays decorated with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Li, Fei; Wu, Shumao; Zhang, Liangji; Li, Zhen

    2015-09-01

    A simple and controllable method was reported for the decoration of CuO nanoplate arrays with Au nanoparticles. It had been achieved through the reaction between Sn2+ and AuCl4 - in the presence of CuO nanoplate arrays. The structure and electron field emission properties of CuO nanoplate arrays decorated with different amounts of Au nanoparticles were investigated. The results demonstrated a remarkable enhancement of field emission performance of CuO nanoplate arrays decorated with Au nanoparticles. The effect of Au amount on the field emission performance was studied in detail, and excellent field emission properties such as a low turn-on electric field of 6.7 V/μm and a high field enhancement factor of 516 could be realized from the optimized sample. On the basis of experimental results, a possible mechanism for the formation of the CuO nanoplate arrays decorated with Au nanoparticles was speculated.

  1. One pot green synthesis of Ag, Au and Au-Ag alloy nanoparticles using isonicotinic acid hydrazide and starch.

    PubMed

    Malathi, Sampath; Ezhilarasu, Tamilarasu; Abiraman, Tamilselvan; Balasubramanian, Sengottuvelan

    2014-10-13

    Gold-silver alloy nanoparticles were synthesized via chemical reduction of varying mole fractions of chloroauric acid (HAuCl4) and silver nitrate (AgNO3) by environmentally benign isonicotinic acid hydrazide (INH) in the presence of starch as a capping agent in aqueous medium. The absorption spectra of Au-Ag nanoparticles show blue shift with increasing silver content indicating the formation of alloy nanoparticles. When the Ag content in the alloy decreases the size of the nanoparticles increases and as a result of which the oxidation potential also increases. The emission maximum undergoes a red shift from 443 to 614 nm. The nanoparticles are monodisperse and spherical with an average particle size of 3-18 nm. The catalytic behavior of alloy nanoparticles indicate that the rate constant for the reduction of 4-nitro phenol to 4-amino phenol increases exponentially from metallic Ag to metallic Au as Au content increases in the Au-Ag alloy nanoparticles. PMID:25037410

  2. Immobilization of uranium by biomaterial stabilized FeS nanoparticles: Effects of stabilizer and enrichment mechanism.

    PubMed

    Shao, Dadong; Ren, Xuemei; Wen, Jun; Hu, Sheng; Xiong, Jie; Jiang, Tao; Wang, Xiaolin; Wang, Xiangke

    2016-01-25

    Iron sulfide (FeS) nanoparticles have been recognized as effective scavengers for multi-valent metal ions. However, the aggregation of FeS nanoparticles in aqueous solution greatly restricts their application in real work. Herein, different biomaterial-FeS nanoparticles were developed for the in-situ immobilization of uranium(VI) in radioactive waste management. TEM images suggested that sodium carboxymethyl cellulose (CMC) and gelatin can effectively suppress the aggregation of FeS nanoparticles in aqueous solutions. The resulting CMC-FeS and gelatin-FeS were stable in aqueous solutions and showed high adsorption capacity for U(VI). Specially, gelatin-FeS showed the best performance in U(VI) adsorption-reduction immobilization under experimental conditions. The maximum enrichment capacity of U(VI) on CMC-FeS and gelatin-FeS at pH 5.0 and 20 °C achieved to ∼430 and ∼556 mg/g, respectively. Additionally, gelatin-FeS and CMC-FeS nanoparticles presented excellent tolerance to environmental salinity. The immobilized U(VI) on the surfaces of CMC-FeS and gelatin-FeS remained stable more than one year. These findings highlight the possibility of using ggelatin-FeS for efficient immobilization of U(VI) from radioactive wastewater. PMID:26448488

  3. Growth of textured thin Au coatings on iron oxide nanoparticles with near infrared absorbance

    PubMed Central

    Ma, L L; Borwankar, A U; Willsey, B W; Yoon, K Y; Tam, J O; Sokolov, K V; Feldman, M D; Milner, T E; Johnston, K P

    2013-01-01

    A homologous series of Au-coated iron oxide nanoparticles, with hydrodynamic diameters smaller than 60 nm was synthesized with very low Auto-iron mass ratios as low as 0.15. The hydrodynamic diameter was determined by dynamic light scattering and the composition by atomic absorption spectroscopy and energy dispersive x-ray spectroscopy (EDS). Unusually low Au precursor supersaturation levels were utilized to nucleate and grow Au coatings on iron oxide relative to formation of pure Au nanoparticles. This approach produced unusually thin coatings, by lowering autocatalytic growth of Au on Au, as shown by transmission electron microscopy (TEM). Nearly all of the nanoparticles were attracted by a magnet indicating a minimal amount of pure Au particles The coatings were sufficiently thin to shift the surface plasmon resonance (SPR) to the near infrared (NIR), with large extinction coefficients., despite the small particle hydrodynamic diameters, observed from dynamic light scattering to be less than 60 nm. PMID:23238021

  4. Optical properties of ion-beam-synthesized Au nanoparticles in SiO2 matrix

    NASA Astrophysics Data System (ADS)

    Hsieh, Chang-Lin; Oyoshi, Keiji; Chao, Der-Sheng; Tsai, Hsu-Sheng; Hong, Wei-Lun; Takeda, Yoshihiko; Liang, Jenq-Horng

    2016-05-01

    In recent years, gold (Au) nanoparticles have been synthesized via various methods and used in optical and biomedical detection. Au nanoparticles contain some remarkable dimension-dependent optical properties due to surface plasmon resonance (SPR) in Au nanoparticles which causes high absorption in visible light regions. Since SPR in well-crystallized Au nanoparticles can enhance the local electromagnetic field, it is thus expected that greater efficiency in the photoluminescence (PL) originating from oxygen deficiency centers (ODC) can be achieved in Au-implanted SiO2 matrix. In order to demonstrate the enhancement of PL, Au nanoparticles were formed in SiO2 film using ion beam synthesis and their optical and microstructural properties were also investigated in this study. The results revealed that a clear absorption peak at approximately 530 nm was identified in the UV-Vis spectra and was attributed to SPR induced by Au nanoparticles in SiO2. The SPR of Au nanoparticles is also dependent on thermal treatment conditions, such as post-annealing temperature and ambient. The Au nanoparticle-containing SiO2 film also displayed several distinctive peaks at approximately 320, 360, 460, and 600 nm in the PL spectra and were found to be associated with ODC-related defects and non-bridging oxygen hole centers (NBOHC) in SiO2. In addition, the PL peak intensities increased as post-annealing temperature increased, a finding contradictory to the defect recovery but highly consistent with the SPR tendency. A maximum PL emission was achieved when the Au-implanted SiO2 film was annealed at 1100 °C for 1 h under N2. Therefore, the existence of Au nanoparticles in SiO2 film can induce SPR effects as well as enhance PL emission resulting from defect-related luminescence centers.

  5. Facile synthesis of ultrathin Au nanorods by aging the AuCl(oleylamine) complex with amorphous Fe nanoparticles in chloroform.

    PubMed

    Li, Zhengquan; Tao, Jing; Lu, Xianmao; Zhu, Yimei; Xia, Younan

    2008-09-01

    Despite plenty of reports on the preparation of Au nanorods, it remains challenging to grow uniform Au nanorods with diameters below 5 nm. In this communication, we demonstrate the facile synthesis of ultrathin Au nanorods with a uniform diameter of 2 nm and an average aspect ratio of 30. The synthesis involves the room-temperature aging of a mixture of the [AuCl(oleylamine)] complex with amorphous Fe nanoparticles in chloroform. Analysis of the growth mechanism indicates that Au nanoparticles with a high density of defects were formed at early stages, followed by etching and redeposition process that gradually led to the growth of ultrathin Au nanorods along the 111 direction. This growth mechanism is different from the mechanism recently reported for ultrathin Au nanowires (ref ), where the [AuCl(oleylamine)] complex is assembled into polymer chains followed by reduction to form wires, although the template effect of oleylamine for the formation of ultrathin Au nanorods cannot be completely ruled out. PMID:18681484

  6. Sonochemical synthesis of (3-aminopropyl)triethoxysilane-modified monodispersed silica nanoparticles for protein immobilization

    SciTech Connect

    Shen, Shou-Cang; Ng, Wai Kiong; Chia, Leonard; Dong, Yuan-Cai; Tan, Reginald B.H.

    2011-10-15

    Graphical abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by rapid sonochemical co-condensation to achieve high capability for protein immobilization. Highlights: {yields} Amino-modified monodispersed silica nanoparticles were synthesized by rapid co-condensation. {yields} Strong positive charge was created by aminopropyl-modification. {yields} Capability for immobilization of negatively charged protein was enhanced. {yields} Electrostatic interaction between proteins and surface contributed to the enhanced adsorption. -- Abstract: 3-Aminopropyltriethoxysilane modified monodispersed silica nanoparticles were synthesized by a rapid sonochemical co-condensation synthesis procedure. The chemical nature of surface organic modifier on the obtained modified silica nanoparticle was characterized by {sup 13}C and {sup 29}Si MAS Nuclear Magnetic Resonance (NMR) spectroscopies, Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA)- differential scanning calorimetry (DSC). Due to the strengthened positive surface charge of the silica nanoparticles by the modification with aminopropyl groups, the capability for bovine serum albumin (BSA) adsorption was significantly increased as compared with bare silica nanoparticles. 80 mg/g BSA was adsorbed on modified silica nanoparticles, whereas only 20 mg/g BSA could be loaded on pure silica nanoparticles. The enhanced positive surface charge repelled proteins with net positive charge and the modified silica nanoparticles exhibited negligible adsorption of lysozyme, thus a selective adsorption of proteins could be achieved.

  7. Metanephrine neuroendocrine tumor marker detection by SERS using Au nanoparticle/Au film sandwich architecture.

    PubMed

    Boca, Sanda; Farcau, Cosmin; Baia, Monica; Astilean, Simion

    2016-02-01

    Neuroendocrine tumors, such as pheochromocytoma or paraganglioma, are dangerous tumors that constitute a potential threat for a large number of patients. Currently, the biochemical diagnosis of neuroendocrine tumors is based on measurement of the direct secretory products of the adrenomedullary-sympathetic system or of their metabolites, such as catecholamines or their metanephrine derivatives, from plasma or urine. The techniques used for analysis of plasma free metanephrines, i.e. high-performance liquid chromatography or high-performance liquid chromatography coupled with mass-spectrometry are technically-demanding and time consuming, which limit their availability. Here we demonstrate a simple, fast and low-cost method for detecting metanephrine by Surface Enhanced Raman Scattering (SERS). The protocol consists in using evaporation-induced self-assembly of gold (Au) nanoparticles incubated with the analyte, on planar gold films. The assembly process produces regions with a dense distribution of both inter-particle gaps and particle-film gaps. Finite-difference time-domain simulations confirm that both kinds of gaps are locations of enhanced electromagnetic fields resulting from inter-particle and particle-film plasmonic coupling, useful for SERS amplification. Metanephrine vibrational bands assignment was performed according to density functional theory calculations. Metanephrine metabolite was detected in liquid at concentration levels lower than previously reported for other similar metabolites. The obtained results demonstrate that the Au nanoparticle/Au film exhibits noticeable SERS amplification of the adsorbed metabolite and can be used in the design of efficient, stable SERS-active substrates for the detection and identification of specific tumor markers. PMID:26820563

  8. Heterostructured Au/Pd-M (M = Au, Pd, Pt) nanoparticles with compartmentalized composition, morphology, and electrocatalytic activity

    NASA Astrophysics Data System (ADS)

    Lutz, Patrick S.; Bae, In-Tae; Maye, Mathew M.

    2015-09-01

    The synthesis, processing, and galvanic exchange of three heterostructured nanoparticle systems is described. The surface accessibility and redox potential of a Au/Pd-Ag dumbbell nanoparticle, where a Au/Pd core/shell region, and a silver region make up the domains, was used to prepare the new nanostructures with controlled composition, morphology, and microstructure. Results indicate that the silver domain was particularly susceptible to galvanic displacement, and was exchanged to Au/Pd-M (M = Au, Pd, Pt). Interestingly, the dumbbell morphology remained after exchange, and the silver region was transformed to hollow, parachute, or concentric domains respectively. The morphology and microstructure change was visualized via TEM and HRTEM, and the composition changes were probed via STEM-EDS imaging and XPS. The electrocatalytic activity of the Au/Pd-M towards methanol oxidation was studied, with results indicating that the Au/Pd-Pt nanoparticles had high activity attributed to the porous nature of the platinum domains.The synthesis, processing, and galvanic exchange of three heterostructured nanoparticle systems is described. The surface accessibility and redox potential of a Au/Pd-Ag dumbbell nanoparticle, where a Au/Pd core/shell region, and a silver region make up the domains, was used to prepare the new nanostructures with controlled composition, morphology, and microstructure. Results indicate that the silver domain was particularly susceptible to galvanic displacement, and was exchanged to Au/Pd-M (M = Au, Pd, Pt). Interestingly, the dumbbell morphology remained after exchange, and the silver region was transformed to hollow, parachute, or concentric domains respectively. The morphology and microstructure change was visualized via TEM and HRTEM, and the composition changes were probed via STEM-EDS imaging and XPS. The electrocatalytic activity of the Au/Pd-M towards methanol oxidation was studied, with results indicating that the Au/Pd-Pt nanoparticles had

  9. pH-dependent immobilization of urease on glutathione-capped gold nanoparticles.

    PubMed

    Garg, Seema; De, Arnab; Mozumdar, Subho

    2015-05-01

    Urease is a nickel-dependent metalloenzyme that catalyzes the hydrolysis of urea to form ammonia and carbon dioxide. Although the enzyme serves a significant role in several detoxification and analytical processes, its usability is restricted due to high cost, availability in small amounts, instability, and a limited possibility of economic recovery from a reaction mixture. Hence, there is a need to develop an efficient, simple, and reliable immobilization strategy for the enzyme. In this study, the carboxyl terminated surface of glutathione-capped gold nanoparticles have been utilized as a solid support for the covalent attachment of urease. The immobilization has been carried out at different pH conditions so as to elucidate its effect on the immobilization efficiency and enzyme bioactivity. The binding of the enzyme has been quantitatively and qualitatively analyzed through techniques like ultraviolet-visible spectroscopy, intrinsic steady state fluorescence, and circular dichorism. The bioactivity of the immobilized enzyme was investigated with respect to the native enzyme under different thermal conditions. Recyclability and shelf life studies of the immobilized enzyme have also been carried out. Results reveal that the immobilization is most effective at pH of 7.4 followed by that in an acidic medium and is least in alkaline environment. The immobilized enzyme also exhibits enhance activity in comparison to the native form at physiological temperature. The immobilized urease (on gold glutathione nanoconjugates surface) can be effectively employed for biosensor fabrication, immunoassays and as an in vivo diagnostic tool in the future. PMID:25227875

  10. Control of the spatial distribution and crystal orientation of self-organized Au nanoparticles.

    PubMed

    Yasukawa, Yukiko; Liu, Xiaoxi; Shirsath, Sagar E; Suematsu, Hisayuki; Kotaki, Yukio; Nemoto, Yoshihiro; Takeguchi, Masaki; Morisako, Akimitsu

    2016-09-23

    Ordered, two-dimensional, self-organized Au nanoparticles were fabricated using radiofrequency (RF) magnetron sputtering. The particles were uniformly spherical in shape and ultrafine in size (3-7 nm) and showed an ultrahigh density in the order of ∼10(12) inch(-2). A custom-developed sputtering apparatus that employs low sputtering power density and a minimized sputtering time (1 min) was used to markedly simplify the preparation conditions for Au nanoparticle fabrication. The spatial distribution of Au nanoparticles was rigorously controlled by placing a Ta interfacial layer between the Au nanoparticles and substrate as well as by post-annealing samples in an Ar atmosphere after the formation of Au nanoparticles. The interfacial layer and the post-annealing step caused approximately 40% of the Au nanoparticles on the substrate surface to orient in the (111) direction. This method was shown to produce ultrafine Au nanoparticles showing an ultrahigh surface density. The crystal orientation of the nanoparticles can be precisely controlled with respect to the substrate surface. Therefore, this technique promises to deliver tunable nanostructures for applications in the field of high-performance electronic devices. PMID:27528598

  11. Phytosynthesis of Au, Ag and Au-Ag bimetallic nanoparticles using aqueous extract and dried leaf of Anacardium occidentale

    NASA Astrophysics Data System (ADS)

    Sheny, D. S.; Mathew, Joseph; Philip, Daizy

    2011-06-01

    Present study reports a green chemistry approach for the biosynthesis of Au, Ag, Au-Ag alloy and Au core-Ag shell nanoparticles using the aqueous extract and dried powder of Anacardium occidentale leaf. The effects of quantity of extract/powder, temperature and pH on the formation of nanoparticles are studied. The nanoparticles are characterized using UV-vis and FTIR spectroscopies, XRD, HRTEM and SAED analyses. XRD studies show that the particles are crystalline in the cubic phase. The formation of Au core-Ag shell nanoparticles is evidenced by the dark core and light shell images in TEM and is supported by the appearance of two SPR bands in the UV-vis spectrum. FTIR spectra of the leaf powder before and after the bioreduction of nanoparticles are used to identify possible functional groups responsible for the reduction and capping of nanoparticles. Water soluble biomolecules like polyols and proteins are expected to bring about the bio-reduction.

  12. Biogenic synthesis of Ag, Au and bimetallic Au/Ag alloy nanoparticles using aqueous extract of mahogany (Swietenia mahogani JACQ.) leaves.

    PubMed

    Mondal, Samiran; Roy, Nayan; Laskar, Rajibul A; Sk, Ismail; Basu, Saswati; Mandal, Debabrata; Begum, Naznin Ara

    2011-02-01

    In this paper, we have demonstrated for the first time, the superb efficiency of aqueous extract of dried leaves of mahogany (Swietenia mahogani JACQ.) in the rapid synthesis of stable monometallic Au and Ag nanoparticles and also Au/Ag bimetallic alloy nanoparticles having spectacular morphologies. Our method was clean, nontoxic and environment friendly. When exposed to aqueous mahogany leaf extract, competitive reduction of Au(III) and Ag(I) ions present simultaneously in same solution leads to the production of bimetallic Au/Ag alloy nanoparticles. UV-visible spectroscopy was used to monitor the kinetics of nanoparticles formation. UV-visible spectroscopic data and TEM images revealed the formation of bimetallic Au/Ag alloy nanoparticles. Mahogany leaf extract contains various polyhydroxy limonoids which are responsible for the reduction of Au(III) and Ag(I) ions leading to the formation and stabilization of Au and Ag nanopaticles. PMID:21030220

  13. Facile, high efficiency immobilization of lipase enzyme on magnetic iron oxide nanoparticles via a biomimetic coating

    PubMed Central

    2011-01-01

    Background Immobilization of lipase on appropriate solid supports is one way to improve their stability and activity, and can be reused for large scale applications. A sample, cost- effective and high loading capacity method is still challenging. Results A facile method of lipase immobilization was developed in this study, by the use of polydopamine coated magnetic nanoparticles (PD-MNPs). Under optimal conditions, 73.9% of the available lipase was immobilized on PD-MNPs, yielding a lipase loading capacity as high as 429 mg/g. Enzyme assays revealed that lipase immobilized on PD-MNPs displayed enhanced pH and thermal stability compared to free lipase. Furthermore, lipase immobilized on PD-MNPs was easily isolated from the reaction medium by magnetic separation and retained more than 70% of initial activity after 21 repeated cycles of enzyme reaction followed by magnetic separation. Conclusions Immobilization of enzyme onto magnetic iron oxide nanoparticles via poly-dopamine film is economical, facile and efficient. PMID:21649934

  14. A novel electrochemical sensor based on magneto Au nanoparticles/carbon paste electrode for voltammetric determination of acetaminophen in real samples.

    PubMed

    Haghshenas, Esmaeel; Madrakian, Tayyebeh; Afkhami, Abbas

    2015-12-01

    An electrochemical magneto Au nanoparticles/carbon paste electrodes (MAuNP/CPE) which is used for the determination of acetaminophen (AC) in real samples was developed. Initially, Au nanoparticles were immobilized at the surface of Fe3O4 (AuNPs@Fe3O4), which was used as a sorbent for capturing AC molecules. After adding AuNPs@Fe3O4 to the AC solution and stirring for 20 min, the AuNPs@Fe3O4 was gathered on the magneto electrode based on its magnetic field. The AC molecules which became adsorbed at AuNPs@Fe3O4 were analyzed by differential pulse voltammetry (DPV). For characterization and investigation of the performance of AuNPs@Fe3O4 and MAuNPs/CPE, various methods, including scanning electron microscopy, X-ray diffraction, UV-Vis spectroscopy, electrochemical impedance spectroscopy, cyclic voltammetry and DPV were used. Under the optimized conditions, the anodic peak current was linear to the concentration of AC in the range of 0.1 to 70.0μmol L(-1) with the detection limit of 4.5×10(-2)μmol L(-1). This method was also successfully used to detect the concentration of AC in pharmaceutical formulations and human serum samples. In addition, the proposed magneto sensor exhibited good reproducibility, long-term stability and fast current response. PMID:26354256

  15. Thermal stability of bimetallic Au/Fe nanoparticles in silica matrix

    SciTech Connect

    Pannu, Compesh Singh, Udai B. Hooda, Sonu Kabiraj, D. Avasthi, D. K.

    2014-04-24

    Thin silica film containing Au and Fe bimetallic nanoparticles were prepared by atom beam cosputtering. The samples were annealed at different temperatures from 400 to 800° C to study the thermal stability of bimetallic nanoparticles using X ray diffraction. It is observed that at 800° C strong structural rearrangement took place leading to thermal decomposition of bimetallic nanoparticles.

  16. Immobilization of lipases on hydrophobilized zirconia nanoparticles: highly enantioselective and reusable biocatalysts.

    PubMed

    Chen, Yi Zhao; Yang, Cai Ting; Ching, Chi Bun; Xu, Rong

    2008-08-19

    Our study has demonstrated for the first time that zirconia nanoparticles modified by a simple carboxylic surfactant of a very long alkyl chain can significantly enhance the activity of the immobilized lipases for asymmetric synthesis in organic media. Zirconia nanoparticles of ca. 20 nm diameter were grafted with carboxylic surfactant modifiers from Tween 85 and erucic acid. The surface of nanoparticles was successfully changed from hydrophilic to hydrophobic. Lipases from Candida rugosa and Pseudomonas cepacia were immobilized on the modified zirconia nanoparticles by adsorption in aqueous solution. The immobilized lipases were used for the resolution of ( R, S)-ibuprofen and ( R, S)-1-phenylethanol through esterification and acylation, respectively, in isooctane organic solvent. When immobilized on erucic acid-modified zirconia, both lipases gave significantly higher activity and enantioselectivity compared with those from their corresponding crude lipase powders. The nanohybrid biocatalysts are stable and can be reused for eight cycles without loss in activity and selectivity. The interaction between the hydrophobic surface of zirconia support and lipases probably induces the conformational rearrangement of lipases into an active, stable form. PMID:18656972

  17. Xylanase Immobilized on Novel Multifunctional Hyperbranched Polyglycerol-Grafted Magnetic Nanoparticles: An Efficient and Robust Biocatalyst.

    PubMed

    Landarani-Isfahani, Amir; Taheri-Kafrani, Asghar; Amini, Mina; Mirkhani, Valiollah; Moghadam, Majid; Soozanipour, Asieh; Razmjou, Amir

    2015-08-25

    Although several strategies are now available for immobilization of enzymes to magnetic nanoparticles for bioapplications, little progresses have been reported on the use of dendritic or hyperbranched polymers for the same purpose. Herein, we demonstrated synthesis of magnetic nanoparticles supported hyperbranched polyglycerol (MNP/HPG) and a derivative conjugated with citric acid (MNP/HPG-CA) as unique and convenient nanoplatforms for immobilization of enzymes. Then, an important industrial enzyme, xylanase, was immobilized on the nanocarriers to produce robust biocatalysts. A variety of analytical tools were used to study the morphological, structural, and chemical properties of the biocatalysts. Additionally, the results of biocatalyst systems exhibited the substantial improvement of reactivity, reusability, and stability of xylanase due to this strategy, which might confer them a wider range of applications. PMID:26258956

  18. Hybrid nanoparticle architecture for cellular uptake and bioimaging: direct crystallization of a polymer immobilized with magnetic nanoparticles on carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Depan, D.; Misra, R. D. K.

    2012-09-01

    We describe here the success of an innovative approach of direct immobilization of magnetic nanoparticles (MNPs) onto carbon nanotubes (CNTs). The approach involved functionalization of magnetic nanoparticles and consequent covalent linkage to a copolymer (PE-b-PEG). Next, the immobilized magnetic nanoparticles on the copolymer were directly crystallized on the long axis of CNTs, where the interfacial adhesion comes from electrostatic and van der Waals interaction. The intracellular trafficking of a hybrid nanoparticle system [(PE-b-PEG)-MNP-CNT-FITC] in HeLa cells was monitored using a fluorescent marker, FITC, conjugated to the nanoparticle system. The distribution of the nanoparticle system inside cells was studied by fluorescence microscopy in a time and dose dependent manner, and it was observed that the nanoparticles are located in the cytoplasm and no apparent cell death was observed at the concentration studied. Also, the effect of an externally applied magnetic field on actin cytoskeleton, cell morphology and intracellular uptake of iron was studied. The approach described here is promising for simultaneous imaging and monitoring intracellular uptake.

  19. Electrophoretic deposition on graphene of Au nanoparticles generated by laser ablation of a bulk Au target in water

    NASA Astrophysics Data System (ADS)

    Semaltianos, N. G.; Hendry, E.; Chang, H.; Wears, M. L.

    2015-04-01

    The characteristic property of nanoparticles generated by laser ablation of metallic targets in liquids to be surface electrically charged can be exploited for the deposition of the nanoparticles onto electrically conducting substrates directly from the synthesized colloidal solution by using the method of electrophoretic deposition (EPD). The method benefits from the high quality of the interface between the deposited nanoparticles and the substrate due to the ligand-free nanoparticle surfaces and thus providing hybrid materials with advanced and novel properties. In this letter, an Au bulk target was laser ablated in deionized (DI) water for the generation of an Au nanoparticle colloidal solution. Under the present conditions of ablation, nanoparticles with diameters from 4 and up to 67 nm are formed in the solution with 80% of the nanoparticles having diameters below ~20 nm. Their size distribution follows a log-normal function with a median diameter of 8.6 nm. The nanoparticles were deposited onto graphene on a quartz surface by anodic EPD performed at 30 V for 20 min and a longer time of 1 h. A quite uniform surface distribution of the nanoparticles was achieved with surface densities ranging from ~15 to ~40 nanoparticles per μm2. The hybrid materials exhibit clearly the plasmon resonance absorption of the Au nanoparticles. Deposition for short times preserves the integrity of graphene while longer time deposition leads to the conversion of graphene to graphene oxide, which is attributed to the electrochemical oxidation of graphene.

  20. Nanoscale mapping of plasmon and exciton in ZnO tetrapods coupled with Au nanoparticles

    PubMed Central

    Bertoni, Giovanni; Fabbri, Filippo; Villani, Marco; Lazzarini, Laura; Turner, Stuart; Van Tendeloo, Gustaaf; Calestani, Davide; Gradečak, Silvija; Zappettini, Andrea; Salviati, Giancarlo

    2016-01-01

    Metallic nanoparticles can be used to enhance optical absorption or emission in semiconductors, thanks to a strong interaction of collective excitations of free charges (plasmons) with electromagnetic fields. Herein we present direct imaging at the nanoscale of plasmon-exciton coupling in Au/ZnO nanostructures by combining scanning transmission electron energy loss and cathodoluminescence spectroscopy and mapping. The Au nanoparticles (~30 nm in diameter) are grown in-situ on ZnO nanotetrapods by means of a photochemical process without the need of binding agents or capping molecules, resulting in clean interfaces. Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than presenting an isotropic distribution around the nanoparticle. On the contrary, a localization of the ZnO signal has been observed inside the Au nanoparticle, as also confirmed by numerical simulations. PMID:26754789

  1. Nanoscale mapping of plasmon and exciton in ZnO tetrapods coupled with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Bertoni, Giovanni; Fabbri, Filippo; Villani, Marco; Lazzarini, Laura; Turner, Stuart; van Tendeloo, Gustaaf; Calestani, Davide; Gradečak, Silvija; Zappettini, Andrea; Salviati, Giancarlo

    2016-01-01

    Metallic nanoparticles can be used to enhance optical absorption or emission in semiconductors, thanks to a strong interaction of collective excitations of free charges (plasmons) with electromagnetic fields. Herein we present direct imaging at the nanoscale of plasmon-exciton coupling in Au/ZnO nanostructures by combining scanning transmission electron energy loss and cathodoluminescence spectroscopy and mapping. The Au nanoparticles (~30 nm in diameter) are grown in-situ on ZnO nanotetrapods by means of a photochemical process without the need of binding agents or capping molecules, resulting in clean interfaces. Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than presenting an isotropic distribution around the nanoparticle. On the contrary, a localization of the ZnO signal has been observed inside the Au nanoparticle, as also confirmed by numerical simulations.

  2. Nanoscale mapping of plasmon and exciton in ZnO tetrapods coupled with Au nanoparticles.

    PubMed

    Bertoni, Giovanni; Fabbri, Filippo; Villani, Marco; Lazzarini, Laura; Turner, Stuart; Van Tendeloo, Gustaaf; Calestani, Davide; Gradečak, Silvija; Zappettini, Andrea; Salviati, Giancarlo

    2016-01-01

    Metallic nanoparticles can be used to enhance optical absorption or emission in semiconductors, thanks to a strong interaction of collective excitations of free charges (plasmons) with electromagnetic fields. Herein we present direct imaging at the nanoscale of plasmon-exciton coupling in Au/ZnO nanostructures by combining scanning transmission electron energy loss and cathodoluminescence spectroscopy and mapping. The Au nanoparticles (~30 nm in diameter) are grown in-situ on ZnO nanotetrapods by means of a photochemical process without the need of binding agents or capping molecules, resulting in clean interfaces. Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than presenting an isotropic distribution around the nanoparticle. On the contrary, a localization of the ZnO signal has been observed inside the Au nanoparticle, as also confirmed by numerical simulations. PMID:26754789

  3. Nanoscale mapping of plasmon and exciton in ZnO tetrapods coupled with Au nanoparticles

    DOE PAGESBeta

    Bertoni, Giovanni; Fabbri, Filippo; Villani, Marco; Lazzarini, Laura; Turner, Stuart; Van Tendeloo, Gustaaf; Calestani, Davide; Gradečak, Silvija; Zappettini, Andrea; Salviati, Giancarlo

    2016-01-12

    Metallic nanoparticles can be used to enhance optical absorption or emission in semiconductors, thanks to a strong interaction of collective excitations of free charges (plasmons) with electromagnetic fields. Herein we present direct imaging at the nanoscale of plasmon-exciton coupling in Au/ZnO nanostructures by combining scanning transmission electron energy loss and cathodoluminescence spectroscopy and mapping. The Au nanoparticles (~30 nm in diameter) are grown in-situ on ZnO nanotetrapods by means of a photochemical process without the need of binding agents or capping molecules, resulting in clean interfaces. Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than presentingmore » an isotropic distribution around the nanoparticle. Moreover, on the contrary, a localization of the ZnO signal has been observed inside the Au nanoparticle, as also confirmed by numerical simulations.« less

  4. Surface immobilization of kanamycin-chitosan nanoparticles on polyurethane ureteral stents to prevent bacterial adhesion.

    PubMed

    Venkat Kumar, Govindarajan; Su, Chia-Hung; Velusamy, Palaniyandi

    2016-09-13

    Bacterial adhesion is a major problem that can lead to the infection of implanted urological stents. In this study, kanamycin-chitosan nanoparticles (KMCSNPs) were immobilized on the surface of a polyurethane ureteral stent (PUS) to prevent urinary bacterial infection. KMCSNPs were synthesized using the ionic gelation method. The synthesized KMCSNPs appeared spherical with a ζ-average particle size of 225 nm. KMCSNPs were immobilized on the PUS surface by covalent immobilization techniques. The surface-modified PUS was characterized using attenuated total reflectance Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and energy dispersive X-ray spectroscopy. The surface-modified PUS showed significantly increased antibacterial activity against Escherichia coli MTCC 729 and Proteus mirabilis MTCC 425 relative to the surface of an unmodified PUS. These findings suggest that the KMCSNP-immobilized PUS has the potential to prevent bacterial infection in the human urinary tract. PMID:27436679

  5. Immobilization of Lipases on Alkyl Silane Modified Magnetic Nanoparticles: Effect of Alkyl Chain Length on Enzyme Activity

    PubMed Central

    Wang, Jiqian; Meng, Gang; Tao, Kai; Feng, Min; Zhao, Xiubo; Li, Zhen; Xu, Hai; Xia, Daohong; Lu, Jian R.

    2012-01-01

    Background Biocatalytic processes often require a full recycling of biocatalysts to optimize economic benefits and minimize waste disposal. Immobilization of biocatalysts onto particulate carriers has been widely explored as an option to meet these requirements. However, surface properties often affect the amount of biocatalysts immobilized, their bioactivity and stability, hampering their wide applications. The aim of this work is to explore how immobilization of lipases onto magnetite nanoparticles affects their biocatalytic performance under carefully controlled surface modification. Methodology/Principal Findings Magnetite nanoparticles, prepared through a co-precipitation method, were coated with alkyl silanes of different alkyl chain lengths to modulate their surface hydrophobicity. Candida rugosa lipase was then directly immobilized onto the modified nanoparticles through hydrophobic interaction. Enzyme activity was assessed by catalytic hydrolysis of p-nitrophenyl acetate. The activity of immobilized lipases was found to increase with increasing chain length of the alkyl silane. Furthermore, the catalytic activities of lipases immobilized on trimethoxyl octadecyl silane (C18) modified Fe3O4 were a factor of 2 or more than the values reported from other surface immobilized systems. After 7 recycles, the activities of the lipases immobilized on C18 modified nanoparticles retained 65%, indicating significant enhancement of stability as well through hydrophobic interaction. Lipase immobilized magnetic nanoparticles facilitated easy separation and recycling with high activity retaining. Conclusions/Significance The activity of immobilized lipases increased with increasing alkyl chain length of the alkyl trimethoxy silanes used in the surface modification of magnetite nanoparticles. Lipase stability was also improved through hydrophobic interaction. Alkyl silane modified magnetite nanoparticles are thus highly attractive carriers for enzyme immobilization

  6. Site-specific immobilization of enzymes on magnetic nanoparticles and their use in organic synthesis.

    PubMed

    Yu, Ching-Ching; Kuo, Yu-Ying; Liang, Chien-Fu; Chien, Wei-Ting; Wu, Huan-Ting; Chang, Tsung-Che; Jan, Fan-Dan; Lin, Chun-Cheng

    2012-04-18

    Magnetic nanoparticles (MNPs) are attractive materials that serve as a support for enzyme immobilization and facilitate separations by applying an external magnetic field; this could facilitate the recycling of enzymes and broaden their applications in organic synthesis. Herein, we report the methods for the immobilization of water-soluble and membrane-bound enzymes, and the activity difference between free and immobilized enzymes is discussed. Sialyltransferase (PmST1, from Pasteurella multocida ) and cytidine monophosphate (CMP)-sialic acid synthetase (CSS, from Neisseria meningitides ) were chosen as water-soluble enzymes and expressed using an intein expression system. The enzymes were site-specifically and covalently immobilized on PEGylated-N-terminal cysteine MNPs through native chemical ligation (NCL). Increasing the length of the PEG linker between the enzyme and the MNP surface increased the activity of the immobilized enzymes relative to the free parent enzymes. In addition, the use of a fluorescent acceptor tag for PmST1 affected enzyme kinetics. In contrast, sialyltransferase from Neisseria gonorrheae (NgST, a membrane-bound enzyme) was modified with a biotin-labeled cysteine at the C-terminus using NCL, and the enzyme was then assembled on streptavidin-functionalized MNPs. Using a streptavidin-biotin interaction, it was possible to immobilize NgST on a solid support under mild ligation conditions, which prevented the enzyme from high-temperature decomposition and provided an approximately 2-fold increase in activity compared to other immobilization methods on MNPs. Finally, the ganglioside GM3-derivative (sialyl-lactose derivative) was synthesized in a one-pot system by combining the use of immobilized PmST1 and CSS. The enzymes retained 50% activity after being reused ten times. Furthermore, the results obtained using the one-pot two-immobilized-enzyme system demonstrated that it can be applied to large-scale reactions with acceptable yields and

  7. Modification of TiO2 by Bimetallic Au-Cu Nanoparticles for Wastewater Treatment

    PubMed Central

    Hai, Zibin; Kolli, Nadia EL; Uribe, Daniel Bahena; Beaunier, Patricia; José-Yacaman, Miguel; Vigneron, Jackie; Etcheberry, Arnaud; Sorgues, Sébastien; Colbeau-Justin, Christophe; Chen, Jiafu; Remita, Hynd

    2016-01-01

    Au, Cu and bimetallic Au-Cu nanoparticles were synthesized on the surface of commercial TiO2 compounds (P25) by reduction of the metal precursors with tetrakis (hydroxymethyl) phosphonium chloride (THPC) (0.5 % in weight). The alloyed structure of Au-Cu NPs was confirmed by HAADF-STEM, EDS, HRTEM and XPS techniques. The photocatalytic properties of the modified TiO2 have been studied for phenol photodegradation in aqueous suspensions under UV-visible irradiation. The modification by the metal nanoparticles induces an increase in the photocatalytic activity. The highest photocatalytic activity is obtained with Au-Cu/TiO2 (Au/Cu 1:3). Their electronic properties have been studied by time resolved microwave conductivity (TRMC) to follow the charge-carrier dynamics. TRMC measurements show that the TiO2 modification with Au, Cu and Au-Cu nanoparticles plays a role in charge-carrier separations increasing the activity under UV-light. Indeed, the metal nanoparticles act as a sink for electron, decreasing the charge carrier recombination. The TRMC measurements show also that the bimetallic Au-Cu nanoparticles are more efficient in electron scavenging than the monometallic Au and Cu ones. PMID:27274844

  8. An amperometric β-glucan biosensor based on the immobilization of bi-enzyme on Prussian blue-chitosan and gold nanoparticles-chitosan nanocomposite films.

    PubMed

    Wang, Beibei; Ji, Xueping; Zhao, Haiyan; Wang, Na; Li, Xianrui; Ni, Ruixing; Liu, Yuheng

    2014-05-15

    A novel β-glucan biosensor was fabricated by immobilizing β-glucanase (β-G) with glucose oxidase (GOD) on nano-Prussian blue-chitosan (PB-CS) and gold nanoparticles-chitosan (AuNPs-CS) composites. Both the PB-CS and AuNPs_CS film were directly electrodeposited on the surface of gold electrode. The morphology of the AuNPs-CS/PB-CS nanocomposites was characterized by scanning electron microscope (SEM). The electrochemical behavior of the resulting sensor was investigated using cyclic voltammetry (CV) and amperometry. It was found that PB-CS nanocomposite exhibited an excellent electrocatalytic reduction towards hydrogen peroxide at a low applied potential window. The synergistic effect of AuNPs-CS/PB-CS nanocomposites could remarkably improve the performances of the biosensor. Under optimal conditions, the biosensor showed a wide linear range of 6.25-93.75 μM, with a correlation coefficient of 0.9991. The sensitivity at an applied potential of 0.0 V was 100 nA μM(-1) cm(-2), with a detection limit of 1.56 μM. The apparent Michaelis-Menten constant (Km) was found to be 1.0mM, showed a high affinity of the immobilizing β-G for β-glucan. The biosensor displayed a rapid response (within 10s) toward β-glucan, with a good selectivity and stability. PMID:24368228

  9. Plasmonic interactions and optical forces between Au bypyramidal nanoparticle dimers.

    SciTech Connect

    Nome, R. A.; Guffey, M. J.; Scherer, N. F.; Gray, S. K.; Univ. of Chicago

    2009-04-23

    Interparticle forces that can be driven by applied (optical) fields could lead to the formation of new particle arrangements when assembled in arrays. Furthermore, the potentially large interactions and large local fields associated with plasmon excitations in anisotropic nanoparticles can lead to enhanced nonlinear responses and applications for sensing. These and other applications would benefit from simulations of spectra and forces arising from plasmonic interactions. We present the results of rigorous three-dimensional, finite-difference, time-domain calculations of near- and far-field properties of pairs of Au bipyramidal nanoparticles in three different configurations: side-by-side, head-to-tail, and face-on. The absorption and scattering spectra depend strongly on the geometry as well as on the interparticle separation, as intuitively expected from a dipole coupling picture. Bipyramidal dimers in head-to-tail and face-on geometries exhibit an increasingly red-shifted (longitudinal) plasmon resonance with decreasing separation, whereas side-by-side dimers exhibit a blue shift. Large resonant field enhancements at the gap between particles in a head-to-tail configuration indicate the strong coupling of plasmonic modes. The Maxwell stress tensor formalism is employed to calculate the optical force one particle exerts on the other. Both significant attraction and weak repulsion can be obtained, depending on the relative arrangement of the particles. The force between bipyramids in the head-to-tail configuration can be greater than 10 times the force between pairs of Au nanospheres with the same volume. Experimental linear scattering spectra of particles trapped using the plasmon-resonance-based optical trapping method are found to be consistent with two particles trapped in the side-by-side configuration.

  10. Synthesis and optical properties of Au decorated colloidal tungsten oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Tahmasebi, Nemat; Mahdavi, Seyed Mohammad

    2015-11-01

    In this study, colloidal tungsten oxide nanoparticles were fabricated by pulsed laser ablation of tungsten target using the first harmonic of a Nd:YAG laser (1064 nm) in deionized water. After ablation, a 0.33 g/lit HAuCl4 aqueous solution was added into as-prepared colloidal nanoparticles. In this process, Au3+ ions were reduced to decorate gold metallic state (Au0) onto colloidal tungsten oxide nanoparticles surface. The morphology and chemical composition of the synthesized nanoparticles were studied by AFM, XRD, TEM and XPS techniques. UV-Vis analysis reveals a distinct absorption peak at ∼530 nm. This peak can be attributed to the surface plasmon resonance (SPR) of Au and confirms formation of gold state. Moreover, X-ray photoelectron spectroscopy reveals that Au ions' reduction happens after adding HAuCl4 solution into as-prepared colloidal tungsten oxide nanoparticles. Transmission electron microscope shows that an Au shell has been decorated onto colloidal WO3 nanoparticles. Noble metal decorated tungsten oxide nanostructure could be an excellent candidate for photocatalysis, gas sensing and gasochromic applications. Finally, the gasochromic behavior of the synthesized samples was investigated by H2 and O2 gases bubbling into the produced colloidal Au/WO3 nanoparticles. Synthesized colloidal nanoparticles show excellent coloration contrast (∼80%) through NIR spectra.

  11. Shape-dependent adhesion and friction of Au nanoparticles probed with atomic force microscopy

    NASA Astrophysics Data System (ADS)

    Yuk, Youngji; Hong, Jong Wook; Lee, Hyunsoo; Han, Sang Woo; Park, Jeong Young

    2015-03-01

    The relation between surface structure and friction and adhesion is a long-standing question in tribology. Tuning the surface structure of the exposed facets of metal nanoparticles is enabled by shape control. We investigated the effect of the shape of Au nanoparticles on friction and adhesion. Two nanoparticle systems, cubic nanoparticles with a low-index (100) surface and hexoctahedral nanoparticles with a high-index (321) surface, were used as model nanoparticle surfaces. Atomic force microscopy was used to probe the nanoscale friction and adhesion on the nanoparticle surface. Before removing the capping layers, the friction results include contributions from both the geometric factor and the presence of capping layers. After removing the capping layers, we can see the exclusive effect of the surface atomic structure while the geometric effect is maintained. We found that after removing the capping layer, the cubic Au nanoparticles exhibited higher adhesion and friction, compared with cubes capped with layers covering 25% and 70%, respectively. On the other hand, the adhesion and friction of hexoctahedral Au nanoparticles decreased after removing the capping layers, compared with nanoparticles with capping layers. The difference in adhesion and friction forces between the bare Au surfaces and Au nanoparticles with capping layers cannot be explained by geometric factors, such as the slope of the nanoparticle surfaces. The higher adhesion and friction forces on cubic nanoparticles after removing the capping layers is associated with the atomic structure of (100) and (321) (i.e., the flat (100) surfaces of the cubic nanoparticles have a larger contact area, compared with the rough (321) surfaces of the hexoctahedral nanoparticles). This study implies an intrinsic relation between atomic structure and nanomechanical properties, with potential applications for controlling nanoscale friction and adhesion via colloid chemistry.

  12. Shape-dependent adhesion and friction of Au nanoparticles probed with atomic force microscopy.

    PubMed

    Yuk, Youngji; Hong, Jong Wook; Lee, Hyunsoo; Han, Sang Woo; Young Park, Jeong

    2015-03-27

    The relation between surface structure and friction and adhesion is a long-standing question in tribology. Tuning the surface structure of the exposed facets of metal nanoparticles is enabled by shape control. We investigated the effect of the shape of Au nanoparticles on friction and adhesion. Two nanoparticle systems, cubic nanoparticles with a low-index (100) surface and hexoctahedral nanoparticles with a high-index (321) surface, were used as model nanoparticle surfaces. Atomic force microscopy was used to probe the nanoscale friction and adhesion on the nanoparticle surface. Before removing the capping layers, the friction results include contributions from both the geometric factor and the presence of capping layers. After removing the capping layers, we can see the exclusive effect of the surface atomic structure while the geometric effect is maintained. We found that after removing the capping layer, the cubic Au nanoparticles exhibited higher adhesion and friction, compared with cubes capped with layers covering 25% and 70%, respectively. On the other hand, the adhesion and friction of hexoctahedral Au nanoparticles decreased after removing the capping layers, compared with nanoparticles with capping layers. The difference in adhesion and friction forces between the bare Au surfaces and Au nanoparticles with capping layers cannot be explained by geometric factors, such as the slope of the nanoparticle surfaces. The higher adhesion and friction forces on cubic nanoparticles after removing the capping layers is associated with the atomic structure of (100) and (321) (i.e., the flat (100) surfaces of the cubic nanoparticles have a larger contact area, compared with the rough (321) surfaces of the hexoctahedral nanoparticles). This study implies an intrinsic relation between atomic structure and nanomechanical properties, with potential applications for controlling nanoscale friction and adhesion via colloid chemistry. PMID:25765817

  13. Dual immobilization and magnetic manipulation of magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Yang, S. Y.; Jian, Z. F.; Horng, H. E.; Hong, Chin-Yih; Yang, H. C.; Wu, C. C.; Lee, Y. H.

    By suitably bio-functionalizing the surfaces, magnetic nanoparticles are able to bind specific biomolecules, and may serve as vectors for delivering bio-entities to target tissues. In this work, the synthesis of bio-functionalized magnetic nanoparticles with two kinds of bio-probes is developed. Here, the stem cell is selected as a to-be-delivered bio-entity and infarcted myocardium is the target issue. Thus, cluster designation-34 (CD-34) on stem cell and creatine kinase-MB (CK-MB) (or troponin I) on infarcted myocardium are the specific biomolecules to be bound with bio-functionalized magnetic nanoparticles. In addition to demonstrating the co-coating of two kinds of bio-probes on a magnetic nanoparticle, the feasibility of manipulation on bio-functionalized magnetic nanoparticles by external magnetic fields is investigated.

  14. Rationalization of Au concentration and distribution in AuNi@Pt core-shell nanoparticles for oxygen reduction reaction

    SciTech Connect

    An, Wei; Liu, Ping

    2015-09-18

    Improving the activity and stability of Pt-based core–shell nanocatalysts for proton exchange membrane fuel cells while lowering Pt loading has been one of the big challenges in electrocatalysis. Here, using density functional theory, we report the effect of adding Au as the third element to enhance the durability and activity of Ni@Pt core–shell nanoparticles (NPs) during the oxygen reduction reaction (ORR). Our results show that the durability and activity of a Ni@Pt NP can be finely tuned by controlling Au concentration and distribution. For a NiAu@Pt NP, the durability can be greatly promoted by thermodynamically favorable segregation of Au to replace the Pt atoms at vertex, edge, and (100) facets on the shell, while still keeping the ORR activity on the active Pt(111) shell as high as that of Ni@Pt nanoparticles. Such behavior strongly depends on a direct interaction with the Ni interlayer. The results not only highlight the importance of interplay between surface strain on the shell and the interlayer–shell interaction in determining the durability and activity but also provide guidance on how to maximize the usage of Au to optimize the performance of core–shell (Pt) nanoparticles. As a result, such understanding has allowed us to discover a novel NiAu@Pt nanocatalyst for the ORR.

  15. Rationalization of Au concentration and distribution in AuNi@Pt core-shell nanoparticles for oxygen reduction reaction

    DOE PAGESBeta

    An, Wei; Liu, Ping

    2015-09-18

    Improving the activity and stability of Pt-based core–shell nanocatalysts for proton exchange membrane fuel cells while lowering Pt loading has been one of the big challenges in electrocatalysis. Here, using density functional theory, we report the effect of adding Au as the third element to enhance the durability and activity of Ni@Pt core–shell nanoparticles (NPs) during the oxygen reduction reaction (ORR). Our results show that the durability and activity of a Ni@Pt NP can be finely tuned by controlling Au concentration and distribution. For a NiAu@Pt NP, the durability can be greatly promoted by thermodynamically favorable segregation of Au tomore » replace the Pt atoms at vertex, edge, and (100) facets on the shell, while still keeping the ORR activity on the active Pt(111) shell as high as that of Ni@Pt nanoparticles. Such behavior strongly depends on a direct interaction with the Ni interlayer. The results not only highlight the importance of interplay between surface strain on the shell and the interlayer–shell interaction in determining the durability and activity but also provide guidance on how to maximize the usage of Au to optimize the performance of core–shell (Pt) nanoparticles. As a result, such understanding has allowed us to discover a novel NiAu@Pt nanocatalyst for the ORR.« less

  16. Immobilization of horseradish peroxidase on β-cyclodextrin-capped silver nanoparticles: Its future aspects in biosensor application.

    PubMed

    Karim, Zoheb; Khan, Mohd Jahir; Maskat, Mohamad Yusof; Adnan, Rohana

    2016-05-18

    This study aimed to work out a simple and high-yield procedure for the immobilization of horseradish peroxidase on silver nanoparticle. Ultraviolet-visible (UV-vis) and Fourier-transform infrared spectroscopy and transmission electron microscopy were used to characterize silver nanoparticles. Horseradish peroxidase was immobilized on β-cyclodextrin-capped silver nanoparticles via glutaraldehyde cross-linking. Single-cell gel electrophoresis (Comet assay) was also performed to confirm the genotoxicity of silver nanoparticles. To decrease toxicity, silver nanoparticles were capped with β-cyclodextrin. A comparative stability study of soluble and immobilized enzyme preparations was investigated against pH, temperature, and chaotropic agent, urea. The results showed that the cross-linked peroxidase was significantly more stable as compared to the soluble counterpart. The immobilized enzyme exhibited stable enzyme activities after repeated uses. PMID:25830286

  17. UV Spectra of Amino Acid Immobilized at Nanoparticles Formation through Nanosphere Lithography (NSL) by Plasma Treatment

    SciTech Connect

    Mohamad, Farizan; Agam, Mohd Arif; Nur, Hadi

    2011-05-25

    The modifying of nanospheres structures by plasma treatments to the fabricated nanoparticles arrays by Nanosphere Lithography (NSL) techniques to create Periodic Particles Arrays (PPAs) with different size, shape and orientation. Spectra of amino acid that immobilized to the nanoparticles arrays under Ultra Violet (UV) spectrums were studied. The PPAs with different sizes, shapes and orientation were fabricated by plasma treatment of 5 sec, 7 sec and 10 sec to the Polystyrene Nanosphere (PSN). Plasma treatment will effect to the PSN including etching part of the PSN to produce a much bigger channel to the single layer template of the PSN. Metal was deposited at interstitial sites between of the polymer balls and later removed by dissolving them in organic solvent, leaving a hexagonal pattern of metal structures at the interstitial sites. The nanoparticles immobilized with the standard amino acid, which later investigated under UV spectrums. The spectrums shows the possibilities use as biosensor devices.

  18. Synthesis of tripodal catecholates and their immobilization on zinc oxide nanoparticles

    PubMed Central

    Klitsche, Franziska; Ramcke, Julian; Migenda, Julia; Hensel, Andreas; Vossmeyer, Tobias; Weller, Horst

    2015-01-01

    Summary A common approach to generate tailored materials and nanoparticles (NPs) is the formation of molecular monolayers by chemisorption of bifunctional anchor molecules. This approach depends critically on the choice of a suitable anchor group. Recently, bifunctional catecholates, inspired by mussel-adhesive proteins (MAPs) and bacterial siderophores, have received considerable interest as anchor groups for biomedically relevant metal surfaces and nanoparticles. We report here the synthesis of new tripodal catecholates as multivalent anchor molecules for immobilization on metal surfaces and nanoparticles. The tripodal catecholates have been conjugated to various effector molecules such as PEG, a sulfobetaine and an adamantyl group. The potential of these conjugates has been demonstrated with the immobilization of tripodal catecholates on ZnO NPs. The results confirmed a high loading of tripodal PEG-catecholates on the particles and the formation of stable PEG layers in aqueous solution. PMID:26124871

  19. Electrochemical Insight into the Brust-Schiffrin Synthesis of Au Nanoparticles.

    PubMed

    Uehara, Akihiro; Booth, Samuel G; Chang, Sin Yuen; Schroeder, Sven L M; Imai, Takahito; Hashimoto, Teruo; Mosselmans, J Frederick W; Dryfe, Robert A W

    2015-12-01

    The mechanism of the Brust-Schiffrin gold nanoparticle synthesis has been investigated through the use of ion transfer voltammetry at the water/1,2-dichloroethane (DCE) solution interface, combined with X-ray absorption fine structure (XAFS) of the reaction between [AuCl4](-) and thiol (RSH) in homogeneous toluene (TL) solution. Ion transfer calculations indicate the formation of [AuCl2](-) at RSH/Au ratios from 0.2-2 with a time-dependent variation observed over several days. At RSH/Au ratios above 2 and after time periods greater than 24 h, the formation of Au(I)SR is also observed. The relative concentrations of reaction products observed at the liquid/liquid interface are in excellent agreement with those observed by XAFS for the corresponding reaction in a single homogeneous phase. BH4(-) ion transfer reactions between water and DCE indicate that the reduction of [AuCl4](-) or [AuCl2](-) to Au nanoparticles by BH4(-) proceeds in the bulk organic phase. On the other hand, BH4(-) was unable to reduce the insoluble [Au(I)SR]n species to Au nanoparticles. The number and size of the nanoparticles formed was dependent on the concentration ratio of RSH/Au, as well as the experimental duration because of the competing formation of the [Au(I)SR]n precipitate. Higher concentrations of nanoparticles, with diameters of 1.0-1.5 nm, were formed at RSH/Au ratios from 1 to 2. PMID:26559785

  20. Immobilization of selenite in soil and groundwater using stabilized Fe-Mn binary oxide nanoparticles.

    PubMed

    Xie, Wenbo; Liang, Qiqi; Qian, Tianwei; Zhao, Dongye

    2015-03-01

    Stabilized Fe-Mn binary oxide nanoparticles were synthesized and tested for removal and in-situ immobilization of Se(IV) in groundwater and soil. A water-soluble starch or food-grade carboxymethyl cellulose (CMC) was used as a stabilizer to facilitate in-situ delivery of the particles into contaminated soil. While bare and stabilized nanoparticles showed rapid sorption kinetics, starch-stabilized Fe-Mn offered the greatest capacity for Se(IV). The Langmuir maximum capacity was determined to be 109 and 95 mg-Se/g-Fe for starch- and CMC-stabilized nanoparticles, respectively, and the high Se(IV) uptake was observed over the typical groundwater pH range of 5-8. Column breakthrough tests indicated that the stabilized nanoparticles were deliverable in a model sandy soil while non-stabilized particles were not. When a Se(IV)-spiked soil was treated in situ with the nanoparticles, >90% water leachable Se(IV) was transferred to the nanoparticle phase, and thereby immobilized as the particles were retained in the downstream soil matrix. The nanoparticle amendment reduced the TCLP (toxicity characteristic leaching procedure) leachability and the California WET (waste extraction test) leachability of Se(IV) by 76% and 71%, respectively. The technology holds the potential to fill a major technology gap in remediation of metals-contaminated soil and groundwater. PMID:25577492

  1. Au nanoparticles on graphitic petal arrays for surface-enhanced Raman spectroscopy

    SciTech Connect

    Rout, Chandra Sekhar; Kumar, Anurag; Xiong Guoping; Fisher, Timothy S.; Irudayaraj, Joseph

    2010-09-27

    We report a unique substrate for surface-enhanced Raman scattering (SERS) based on Au nanoparticle-decorated, thin graphitic petals. The petals were grown on Si substrates by microwave plasma chemical vapor deposition without catalyst, followed by Au nanoparticle decoration on the oxygen plasma-treated petals by electrodeposition. The substrates possess high surface area and sharp nanoscale features that enable high SERS sensitivity to detect 1x10{sup -7} M rhodamine 6G in methanol solution. The obtained SERS enhancement is comparable to the best values reported in the literature and is determined to result from high surface area and increased density of Au nanoparticles on the petal surfaces.

  2. Facile synthesis of PtAu alloy nanoparticles with high activity for formic acid oxidation

    SciTech Connect

    Zhang, Sheng; Shao, Yuyan; Yin, Geping; Lin, Yuehe

    2010-02-15

    We report the facile synthesis of carbon supported PtAu alloy nanoparticles with high electrocatalytic activity as the anode catalyst for direct formic acid fuel cells (DFAFCs). PtAu alloy nanopaticles are synthesized by co-reducing HAuCl4 and H2PtCl6 with NaBH4 in the presence of sodium citrate and then the nanoparticles are deposited on Vulcan XC-72R carbon support (PtAu/C). The obtained catalysts are characterized with X-ray diffraction (XRD) and transmission electron microscope (TEM), which reveal PtAu alloy formation with an average diameter of 4.6 nm. PtAu/C exhibits 8 times higher catalytic activity toward formic acid oxidation than Pt/C. The enhanced activity of PtAu/C catalyst is attributed to noncontinuous Pt sites formed in the presence of the neighbored Au sites, which promotes direct oxidation of formic acid by avoiding poison CO.

  3. Immobilization of cholesterol oxidase on magnetic fluorescent core-shell-structured nanoparticles.

    PubMed

    Huang, Jun; Liu, Huichao; Zhang, Peipei; Zhang, Pengfei; Li, Mengshi; Ding, Liyun

    2015-12-01

    The magnetic fluorescent core-shell structured nanoparticles, Fe3O4@SiO2(F)@meso-SiO2 nanoparticles, were prepared. Cholesterol oxidase (COD) was immobilized on their surface to form Fe3O4@SiO2(F)@meso-SiO2@COD nanoparticles. Optimal immobilization was achieved with 2.5% (v/v) APTES, 2.0% (v/v) GA, 10mg COD (in 15 mg carrier) and solution pH of 7.0. Fe3O4@SiO2(F)@meso-SiO2@COD nanoparticles showed maximal catalytic activity at pH7.0 and 50°C. The thermal, storage and operational stabilities of COD were improved greatly after its immobilization. After the incubation at 50°C for 5h, the nanoparticles and free COD retained 80% and 46% of its initial activity, respectively. After kept at 4°C for 30 days, the nanoparticles and free COD maintained 86% and 65% of initial activity, respectively. The nanoparticles retained 71% of its initial activity after 7 consecutive operations. Since Fe3O4@SiO2(F)@meso-SiO2@COD nanoparticles contained tris(2,2-bipyridyl)dichloro-ruthenium(II) hexahydrate (Ru(bpy)3Cl2) and were optical sensitive to oxygen in solution, it might be used as the sensing material and has the application potential in multi parameter fiber optic biosensor based on enzyme catalysis and oxygen consumption. PMID:26354237

  4. Direct imaging Au nanoparticle migration inside mesoporous silica channels.

    PubMed

    Liu, Zhengwang; Che, Renchao; Elzatahry, Ahmed A; Zhao, Dongyuan

    2014-10-28

    Supported metal nanoparticle (NP) catalysts have been widely used in many industry processes and catalytic reactions. Catalyst deactivation is mainly caused by the sintering of supported metal NPs. Hence, understanding the metal NPs' sintering behaviors has great significance in preventing catalyst deactivation. Here we report the metal particle migration inside/between mesochannels by scanning transmission electron microscopy and electron energy loss spectroscopy via an in situ TEM heating technique. A sintering process is proposed that particle migration predominates, driven by the difference of gravitational potential from the height of the uneven internal surface of the mesopores; when the distance of the gold nanoparticles with a size of about 3 and 5 nm becomes short after migration, the coalescence process is completed, which is driven by an "octopus-claw-like" expansion of a conduction electron cloud outside the Au NPs. The supports containing an abundance of micropores help to suppress particle migration and coalescence. Our findings provide the understanding toward the rational design of supported industrial catalysts and other nanocomposites with enhanced activity and stability for applications such as batteries, catalysis, drug delivery, gas sensors, and solar cells. PMID:25264601

  5. An electrochemical DNA biosensor based on nitrogen-doped graphene/Au nanoparticles for human multidrug resistance gene detection.

    PubMed

    Chen, Mei; Hou, Changjun; Huo, Danqun; Bao, Jing; Fa, Huanbao; Shen, Caihong

    2016-11-15

    Multidrug resistance (MDR) has become a major obstacle to the adequate treatment of cancer patients; thus, there is an urgent need for exploring new strategies for early diagnosis of MDR in clinic. Here, we report a novel electrochemical biosensor based on nitrogen-doped graphene nanosheets functionalized with Au nanoparticles (N-G/Au) for sensitive and selective DNA detection. The highly conductive nanocomposite layer was characterized by using scanning and transmission electron microscopy, X-ray photoelectron spectroscopy, and cyclic voltammetry. DNA with thiol groups at the 5' end was immobilized on the N-G/Au surface via the strong Au-S bond. Differential pulse voltammetry was applied to monitor the target DNA hybridization event using methylene blue as an electrochemical indicator. Under optimal conditions, the biosensor could detect target DNA down to 3.12×10(-15)M with a linear range from 1.0×10(-14) to 1.0×10(-7)M, showing high sensitivity. Further, the sensing strategy was successfully used for detecting MDR1 DNA in real clinical samples. These results will aid in developing a new portable detection system for MDR that will allow effective diagnosis in the early stages of related cancer. PMID:27258172

  6. A fluorescence-based method to directly quantify antibodies immobilized on gold nanoparticles.

    PubMed

    Filbrun, Seth L; Driskell, Jeremy D

    2016-06-21

    The ability to evaluate antibody immobilization onto gold nanoparticles is critical for assessing coupling chemistry and optimizing the sensitivity of nanoparticle-enabled biosensors. Herein, we developed a fluorescence-based method for directly quantifying antibodies bound onto gold nanoparticles. Antibody-modified gold nanoparticles were treated with KI/I2 etchant to dissolve the gold nanoparticles. A desalting spin column was used to recover the antibody released from the nanoparticles, and NanoOrange, a fluorescent dye, was used to quantify the antibody. We determined 309 ± 93 antibodies adsorb onto a 60 nm gold nanoparticles (2.6 × 10(10) NP mL(-1)), which is consistent with a fully adsorbed monolayer based on the footprint of an IgG molecule. Moreover, the increase in hydrodynamic diameter of the conjugated nanoparticle (76 nm) compared to that of the unconjugated nanoparticle (62 nm) confirmed that multilayers did not form. A more conventional method of indirectly quantifying the adsorbed antibody by analysis of the supernatant overestimated the antibody surface coverage (660 ± 87 antibodies per nanoparticle); thus we propose the method described herein as a more accurate alternative to the conventional approach. PMID:27113720

  7. Synthesis and immobilization of silver nanoparticles on aluminosilicate nanotubes and their antibacterial properties

    NASA Astrophysics Data System (ADS)

    Ipek Yucelen, G.; Connell, Rachel E.; Terbush, Jessica R.; Westenberg, David J.; Dogan, Fatih

    2016-04-01

    A novel colloidal method is presented to synthesize silver nanoparticles on aluminosilicate nanotubes. The technique involves decomposition of AgNO3 solution to Ag nanoparticles in the presence of aluminosilicate nanotubes at room temperature without utilizing of reducing agents or any organic additives. Aluminosilicate nanotubes are shown to be capable of providing a unique chemical environment, not only for in situ conversion of Ag+ into Ag0, but also for stabilization and immobilization of Ag nanoparticles. The synthesis strategy described here could be implemented to obtain self-assembled nanoparticles on other single-walled metal oxide nanotubes for unique applications. Finally, we demonstrated that nanotube/nanoparticle hybrid show strong antibacterial activity toward Gram-positive Staphylococcus epidermidis and Gram-negative Escherichia coli.

  8. Selective Hydrogenation of Acetylene over Pd, Au, and PdAu Supported Nanoparticles

    NASA Astrophysics Data System (ADS)

    Walker, Michael P.

    The removal of trace amounts of acetylene in ethylene streams is a high-volume industrial process that must possess high selectivity of alkyne hydrogenation over hydrogenation of alkenes. Current technology uses metallic nanoparticles, typically palladium or platinum, for acetylene removal. However, problems arise due to the deactivation of the catalysts at high temperatures as well as low selectivities at high conversions. Pore expanded MCM-41 is synthesized via a two-step strategy in which MCM-41 was prepared via cetyltrimethylammonium bromide (CTMABr) followed by the hydrothermal treatment with N,N-dimethyldecylamine (DMDA). This material was washed with ethanol to remove DMDA, or calcined to remove both surfactants. PE-MCM-41 based materials were impregnated with palladium, gold, and palladium-gold nanoparticles. The removal of DMDA had an effect on both the conversion and selectivity, in which they were found to drop significantly. However, by using the bimetallic PdAu catalysts, higher selectivity could be achieved due to increased electron density.

  9. Evaluation of nanoparticle-immobilized cellulase for improved ethanol yield in simultaneous saccharification and fermentation reactions

    SciTech Connect

    Lupoi, Jason; Smith, Emily

    2011-12-01

    Ethanol yields were 2.1 (P = 0.06) to 2.3 (P = 0.01) times higher in simultaneous saccharification and fermentation (SSF) reactions of microcrystalline cellulose when cellulase was physisorbed on silica nanoparticles compared to enzyme in solution. In SSF reactions, cellulose is hydrolyzed to glucose by cellulase while yeast simultaneously ferments glucose to ethanol. The 35 C temperature and the presence of ethanol in SSF reactions are not optimal conditions for cellulase. Immobilization onto solid supports can stabilize the enzyme and promote activity at non-optimum reaction conditions. Mock SSF reactions that did not contain yeast were used to measure saccharification products and identify the mechanism for the improved ethanol yield using immobilized cellulase. Cellulase adsorbed to 40 nm silica nanoparticles produced 1.6 times (P = 0.01) more glucose than cellulase in solution in 96 h at pH 4.8 and 35 C. There was no significant accumulation (<250 {mu}g) of soluble cellooligomers in either the solution or immobilized enzyme reactions. This suggests that the mechanism for the immobilized enzyme's improved glucose yield compared to solution enzyme is the increased conversion of insoluble cellulose hydrolysis products to soluble cellooligomers at 35 C and in the presence of ethanol. The results show that silica-immobilized cellulase can be used to produce increased ethanol yields in the conversion of lignocellulosic materials by SSF.

  10. Effects of Au/Fe and Fe nanoparticles on Serratia bacterial growth and production of biosurfactant.

    PubMed

    Liu, Jia; Vipulanandan, Cumaraswamy

    2013-10-01

    The overall objective of this study was to compare the effects of Au/Fe and Fe nanoparticles on the growth and performance of Serratia Jl0300. The nanoparticle effect was quantified not only by the bacterial growth on agar plate after 1 hour interaction with the nanoparticles, but also by its production of a biosurfactant from used vegetable oil. The nanoparticles were prepared using the foam method. The concentrations of the nanoparticles used for the bacterial interaction study were varied from 1 mg/L to 1 g/L. The test results showed that the effect of nanoparticles on the bacterial growth and biosurfactant production varied with nanoparticle type, concentrations, and interaction time with the bacteria. Au/Fe nanoparticles didn't show toxicity to Serratia after short time (1 h) exposure, while during 8 days fermentation Au/Fe nanoparticles inhibited the growth of Serratia as well as the biosurfactant production when the concentration of the nanoparticles was higher than 10mg/L. Fe nanoparticles showed inhibition effects to bacterial growth both after short time and long time interaction with Serratia, as well as to biosurfactant production when its concentration was higher than 100 mg/L. Based on the trends observed in this study, analytical models have been developed to predict the bacterial growth and biosurfactant production with varying concentrations of nanoparticles. PMID:23910295

  11. Immobilizing water-soluble graphene quantum dots with gold nanoparticles for a low potential electrochemiluminescence immunosensor

    NASA Astrophysics Data System (ADS)

    Dong, Yongqiang; Wu, Huan; Shang, Pengxiang; Zeng, Xiaoting; Chi, Yuwu

    2015-10-01

    Hydrazide-modified graphene quantum dots (HM-GQDs) obtained by refluxing GQDs with hydrazine hydrate were hybridized with gold nanoparticles (AuNPs) through a redox reaction between HM-GQDs and AuCl4-. The obtained nano-hybrids (HM-GQD-AuNPs) possess the unique electrochemiluminescence (ECL) properties of HM-GQDs and the easy self-assembly with some bio-molecules of AuNPs, which have great potential applications in bio-sensors. HM-GQD-AuNPs were modified on a glassy carbon electrode to develop a novel ECL immunosensor of carcinoembryonic antigen (CEA) as a model target analyte. Due to the increment of electron-transfer resistance after immunoreaction, the ECL intensity decreased as the concentration of CEA was increased. The linear response range was between 0.02 and 80 ng mL-1, and the detection limit was 0.01 ng mL-1.Hydrazide-modified graphene quantum dots (HM-GQDs) obtained by refluxing GQDs with hydrazine hydrate were hybridized with gold nanoparticles (AuNPs) through a redox reaction between HM-GQDs and AuCl4-. The obtained nano-hybrids (HM-GQD-AuNPs) possess the unique electrochemiluminescence (ECL) properties of HM-GQDs and the easy self-assembly with some bio-molecules of AuNPs, which have great potential applications in bio-sensors. HM-GQD-AuNPs were modified on a glassy carbon electrode to develop a novel ECL immunosensor of carcinoembryonic antigen (CEA) as a model target analyte. Due to the increment of electron-transfer resistance after immunoreaction, the ECL intensity decreased as the concentration of CEA was increased. The linear response range was between 0.02 and 80 ng mL-1, and the detection limit was 0.01 ng mL-1. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr04328j

  12. Enzyme-free surface plasmon resonance aptasensor for amplified detection of adenosine via target-triggering strand displacement cycle and Au nanoparticles.

    PubMed

    Yao, Gui-Hong; Liang, Ru-Ping; Huang, Chun-Fang; Zhang, Li; Qiu, Jian-Ding

    2015-04-29

    Herein, we combine the advantage of aptamer technique with the amplifying effect of an enzyme-free signal-amplification and Au nanoparticles (NPs) to design a sensitive surface plasmon resonance (SPR) aptasensor for detecting small molecules. This detection system consists of aptamer, detection probe (c-DNA1) partially hybridizing to the aptamer strand, Au NPs-linked hairpin DNA (Au-H-DNA1), and thiolated hairpin DNA (H-DNA2) previously immobilized on SPR gold chip. In the absence of target, the H-DNA1 possessing hairpin structure cannot hybridize with H-DNA2 and thereby Au NPs will not be captured on the SPR gold chip surface. Upon addition of target, the detection probe c-DNA1 is forced to dissociate from the c-DNA1/aptamer duplex by the specific recognition of the target to its aptamer. The released c-DNA1 hybridizes with Au-H-DNA1 and opens the hairpin structure, which accelerate the hybridization between Au-H-DNA1 and H-DNA2, leading to the displacement of the c-DNA1 through a branch migration process. The released c-DNA1 then hybridizes with another Au-H-DNA1 probe, and the cycle starts anew, resulting in the continuous immobilization of Au-H-DNA1 probes on the SPR chip, generating a significant change of SPR signal due to the electronic coupling interaction between the localized surface plasma of the Au NPs and the surface plasma wave. With the use of adenosine as a proof-of-principle analyte, this sensing platform can detect adenosine specifically with a detection limit as low as 0.21 pM, providing a simple, sensitive and selective protocol for small target molecules detection. PMID:25847158

  13. Size-Induced Chemical and Magnetic Ordering in Individual Fe-Au Nanoparticles

    SciTech Connect

    Mukherjee, Pinaki; Manchanda, Priyanka; Kumar, Pankaj; Zhou, Lin; Kramer, Matthew J; Kashyap, Arti; Skomski, Ralph; Sellmyer, David; Shield, Jeffrey E

    2014-08-26

    Formation of chemically ordered compounds of Fe and Au is inhibited in bulk materials due to their limited mutual solubility. However, here we report the formation of chemically ordered L12-type Fe3Au and FeAu3 compounds in Fe–Au sub-10 nm nanoparticles, suggesting that they are equilibrium structures in size-constrained systems. The stability of these L12-ordered Fe3Au and FeAu3 compounds along with a previously discovered L10-ordered FeAu has been explained by a size-dependent equilibrium thermodynamic model. Furthermore, the spin ordering of these three compounds has been computed using ab initio first-principle calculations. All ordered compounds exhibit a substantial magnetization at room temperature. The Fe3Au had a high saturation magnetization of about 143.6 emu/g with a ferromagnetic spin structure. The FeAu3 nanoparticles displayed a low saturation magnetization of about 11 emu/g. This suggests a antiferromagnetic spin structure, with the net magnetization arising from uncompensated surface spins. First-principle calculations using the Vienna ab initio simulation package (VASP) indicate that ferromagnetic ordering is energetically most stable in Fe3Au, while antiferromagnetic order is predicted in FeAu and FeAu3, consistent with the experimental results.

  14. Growth of Au@Pt coreshell nanoparticles: Probed by in-situ XANES and UV-visible spectroscopy

    NASA Astrophysics Data System (ADS)

    Nayak, C.; Bhattacharyya, K.; Tripathi, A. K.; Jha, S. N.; Bhattacharyya, D.; Sahoo, N. K.

    2016-05-01

    Au@Pt core shell nanoparticles have been synthesized by reducing Au and Pt chloride precursors with Block Co-polymer and Ascorbic acid. The growth and nucleation of Au@Pt nanoparticles have been investigated by in-situ time resolved XANES measurement which gives the evolution of the reduction process of the precursors. Linear combination fitting of the XANES spectra has been carried out to find the fraction of Au and Pt cations reduced at a particular reaction time. UV-Visible spectroscopy is used as a complementary technique which gives the changes in the Au SPR peak as Au@Pt core shell nanoparticles are formed.

  15. Spectroscopic characterization of magnetic Fe3O4@Au core shell nanoparticles.

    PubMed

    Fouad, Dina M; El-Said, Waleed A; Mohamed, Mona B

    2015-04-01

    The magnetic nanoparticles iron oxide (Fe3O4) nanoparticles and iron oxide/gold core-shell (Fe3O4/Au) nanoparticles were synthesized and their catalytic photo-degradation activity towards malathion as example of organophosphorus pesticides were reported. Iron oxide (Fe3O4) magnetic nanoparticle was successfully prepared through co-precipitation method by the reduction of ferric chloride (FeCl3) using ascorbic acid. The morphology of the prepared nanoparticles was characterized by the TEM and XRD (X-ray diffraction) techniques. Degradation of 10 ppm of malathion in the presence of these nanoparticles under UV radiation was monitored using (HPLC) and UV-visible spectra. Fe3O4/Au nanoparticles showed higher efficiency in photo-degradation of malathion than Fe3O4 ones. PMID:25617979

  16. Au 4f spin-orbit coupling effects in supported gold nanoparticles.

    PubMed

    Chenakin, Sergey P; Kruse, Norbert

    2016-08-17

    Using X-ray photoelectron spectroscopy we examine the Au 4f spin-orbit components in Au 4f spectra of nanosized Au particles on a TiO2 support. In general, the peak ratios of the Au 4f7/2 and 4f5/2 excitations are found to deviate from the statistical ratio of 4 : 3 and their linewidths (FWHM) are not equal. We reveal that both the FWHM and the Au 4f7/2-to-4f5/2 peak ratios increase appreciably as the Au atomic concentration on the surface of the TiO2 support and the size of Au nanoparticles decrease. On the contrary, the Au 4f spin-orbit splitting remains essentially unchanged. Our findings are discussed in terms of alterations in the electronic band structure. PMID:27480507

  17. Effect of experimental conditions on size control of Au nanoparticles synthesized by atmospheric microplasma electrochemistry.

    PubMed

    Huang, Xunzhi; Li, Yongsheng; Zhong, Xiaoxia

    2014-01-01

    Atmospheric microplasma electrochemistry was utilized to synthesize Au nanoparticles (NPs). The synthesized Au NPs were investigated as a function of reduction current, solution temperature, and stirring (or not) by using ultraviolet-visible (UV-Vis) absorbance and transmission electron microscopy (TEM). It was illustrated that high current promoted the growth of Au NPs with small size, and more Au NPs with large size were synthesized as a rise of temperature. The Au NPs often with small size were synthesized as a result of stirring. The production rate, the electrostatic repulsion, and the residence time of the Au NPs at the interfacial region play an important role in the growth of Au NPs. The results shed light upon the roadmap to control the size and particle size distribution (PSD) of Au NPs synthesized by atmospheric microplasma electrochemistry. PMID:25364315

  18. Electrochemical Deposition and Re-oxidation of Au at Highly Oriented Pyrolytic Graphite. Stabilization of Au Nanoparticles on the Upper Plane of Step Edges

    SciTech Connect

    Pinhero, Patrick Joseph; Lister, Tedd Edward; Boxley, Chett J.; White, Henry S.

    2003-10-01

    The electrochemical deposition and reoxidation of Au on the basal plane of highly oriented pyrolytic graphite (HOPG) immersed in a 5 mM AuCl4-/6 M LiCl solution is reported. Scanning electron microscopy (SEM) and ex-situ atomic force microscopy (AFM) demonstrate that Au nanoparticles, ~3.3 nm in height and ~10 nm in diameter, are deposited at times less than ~1 s. The density of nanoparticles, 6 × 109 cm-2, is of the same order of magnitude as the surface point defect density, suggesting that point defects act as nucleation sites for Au electrodeposition. A small subset of the Au nanoparticles (~7%) continues to grow between 1 and 50 s, reaching a height of ~150 nm and a diameter of ~300 nm. At times greater than 50 s, the larger particles coalesce to yield a surface comprised of a low density (~2 × 106 cm-2) of micrometer-size Au crystallites surrounded by Au nanoparticles. Double potential step chronocoulometric experiments demonstrate that the electrodeposition of Au is chemically irreversible, a finding supported by SEM and AFM observations of Au nanoparticles and larger crystallites on the surface after long periods of reoxidation (>3600 s). Au nanoparticles are observed to be preferentially deposited on the upper plane of step edges, a consequence of the nonuniform surface electron density that results from relaxation of the graphite lattice near steps.

  19. Core-shell Au@Pd nanoparticles with enhanced catalytic activity for oxygen reduction reaction via core-shell Au@Ag/Pd constructions

    PubMed Central

    Chen, Dong; Li, Chengyin; Liu, Hui; Ye, Feng; Yang, Jun

    2015-01-01

    Core-shell nanoparticles often exhibit improved catalytic properties due to the lattice strain created in these core-shell particles. Herein, we demonstrate the synthesis of core-shell Au@Pd nanoparticles from their core-shell Au@Ag/Pd parents. This strategy begins with the preparation of core-shell Au@Ag nanoparticles in an organic solvent. Then, the pure Ag shells are converted into the shells made of Ag/Pd alloy by galvanic replacement reaction between the Ag shells and Pd2+ precursors. Subsequently, the Ag component is removed from the alloy shell using saturated NaCl solution to form core-shell Au@Pd nanoparticles with an Au core and a Pd shell. In comparison with the core-shell Au@Pd nanoparticles upon directly depositing Pd shell on the Au seeds and commercial Pd/C catalysts, the core-shell Au@Pd nanoparticles via their core-shell Au@Ag/Pd templates display superior activity and durability in catalyzing oxygen reduction reaction, mainly due to the larger lattice tensile effect in Pd shell induced by the Au core and Ag removal. PMID:26144550

  20. Carbon nanofiber supported bimetallic PdAu nanoparticles for formic acid electrooxidation

    NASA Astrophysics Data System (ADS)

    Qin, Yuan-Hang; Jiang, Yue; Niu, Dong-Fang; Zhang, Xin-Sheng; Zhou, Xing-Gui; Niu, Li; Yuan, Wei-Kang

    2012-10-01

    Carbon nanofiber (CNF) supported PdAu nanoparticles are synthesized with sodium citrate as the stabilizing agent and sodium borohydride as the reducing agent. High resolution transmission electron microscopy (HRTEM) characterization indicates that the synthesized PdAu particles are well dispersed on the CNF surface and X-ray diffraction (XRD) characterization indicates that the alloying degree of the synthesized PdAu nanoparticles can be improved by adding tetrahydrofuran to the synthesis solution. The results of electrochemical characterization indicate that the addition of Au can promote the electrocatalytic activity of Pd/C catalyst for formic acid oxidation and the CNF supported high-alloying PdAu catalyst possesses better electrocatalytic activity and stability for formic acid oxidation than either the CNF supported low-alloying PdAu catalyst or the CNF supported Pd catalyst.

  1. pH dependent immobilization of Urease on glutathione capped gold nanoparticles.

    PubMed

    Garg, Seema; De, Arnab; Mozumdar, Subho

    2014-09-01

    Urease is a nickel-dependent metallonzyme that catalyzes the hydrolysis of urea to form ammonia and carbon dioxide. Although the enzyme serves a significant role in several detoxification and analytical processes, its usability is restricted due to high cost, availability in small amounts, instability and a limited possibility of economic recovery from a reaction mixture. Hence, there is a need to develop an efficient, simple and reliable immobilization strategy for the enzyme. In this work, the carboxyl terminated surface of glutathione capped gold nanoparticles have been utilized as a solid support for the covalent attachment of Urease. The immobilization has been carried out at different pH conditions so as to elucidate its effect on the immobilization efficiency and enzyme bio-activity. The binding of the enzyme has been quantitatively and qualitatively analyzed through techniques like UV-Vis spectroscopy, intrinsic steady state fluorescence and Circular Dichorism. The bio-activity of the immobilized enzyme was investigated with respect to the native enzyme under different thermal conditions. Recyclability and shelf life studies of the immobilized enzyme have also been carried out. Results reveal that the immobilization is most effective at pH of 7.4 followed by that in an acidic medium and is least in alkaline environment. The immobilized enzyme also exhibits enhance activity in comparison to the native form at physiological temperature. The immobilized urease (on gold glutathione nano-conjugates surface) can be effectively employed for biosensor fabrication, immunoassays and as an in vivo diagnostic tool in the future. PMID:25196908

  2. Superparamagnetic Au-Fe3O4 nanoparticles: one-pot synthesis, biofunctionalization and toxicity evaluation

    NASA Astrophysics Data System (ADS)

    Pariti, A.; Desai, P.; Maddirala, S. K. Y.; Ercal, N.; Katti, K. V.; Liang, X.; Nath, M.

    2014-09-01

    Superparamagnetic Au-Fe3O4 bifunctional nanoparticles have been synthesized using a single step hot-injection precipitation method. The synthesis involved using Fe(CO)5 as iron precursor and HAuCl4 as gold precursor in the presence of oleylamine and oleic acid. Oleylamine helps in reducing Au3+ to Au0 seeds which simultaneously oxidizes Fe(0) to form Au-Fe3O4 bifunctional nanoparticles. Triton® X-100 was employed as a highly viscous solvent to prevent agglomeration of Fe3O4 nanoparticles. Detailed characterization of these nanoparticles was performed by using x-ray powder diffraction, transmission electron microscopy, scanning tunneling electron microscopy, UV-visible spectroscopy, Mössbauer and magnetometry studies. To evaluate these nanoparticles’ applicability in biomedical applications, L-cysteine was attached to the Au-Fe3O4 nanoparticles and cytotoxicity of Au-Fe3O4 nanoparticles was tested using CHO cells by employing MTS assay. L-cysteine modified Au-Fe3O4 nanoparticles were qualitatively characterized using Fourier transform infrared spectroscopy and Raman spectroscopy; and quantitatively using acid ninhydrin assay. Investigations reveal that that this approach yields Au-Fe3O4 bifunctional nanoparticles with an average particle size of 80 nm. Mössbauer studies indicated the presence of Fe in Fe3+ in A and B sites (tetrahedral and octahedral, respectively) and Fe2+ in B sites (octahedral). Magnetic measurements also indicated that these nanoparticles were superparamagnetic in nature due to Fe3O4 region. The saturation magnetization for the bifunctional nanoparticles was observed to be ˜74 emu g-1, which is significantly higher than the previously reported Fe3O4 nanoparticles. Mössbauer studies indicated that there was no significant Fe(0) impurity that could be responsible for the superparamagnetic nature of these nanoparticles. None of the investigations showed any presence of other impurities such as Fe2O3 and FeOOH. These Au-Fe3O4 bifunctional

  3. Multifunctional Hybrid Fe2O3-Au Nanoparticles for Efficient Plasmonic Heating.

    PubMed

    Murph, Simona E Hunyadi; Larsen, George K; Lascola, Robert J

    2016-01-01

    One of the most widely used methods for manufacturing colloidal gold nanospherical particles involves the reduction of chloroauric acid (HAuCl4) to neutral gold Au(0) by reducing agents, such as sodium citrate or sodium borohydride. The extension of this method to decorate iron oxide or similar nanoparticles with gold nanoparticles to create multifunctional hybrid Fe2O3-Au nanoparticles is straightforward. This approach yields fairly good control over Au nanoparticle dimensions and loading onto Fe2O3. Additionally, the Au metal size, shape, and loading can easily be tuned by changing experimental parameters (e.g., reactant concentrations, reducing agents, surfactants, etc.). An advantage of this procedure is that the reaction can be done in air or water, and, in principle, is amenable to scaling up. The use of such optically tunable Fe2O3-Au nanoparticles for hyperthermia studies is an attractive option as it capitalizes on plasmonic heating of gold nanoparticles tuned to absorb light strongly in the VIS-NIR region. In addition to its plasmonic effects, nanoscale Au provides a unique surface for interesting chemistries and catalysis. The Fe2O3 material provides additional functionality due to its magnetic property. For example, an external magnetic field could be used to collect and recycle the hybrid Fe2O3-Au nanoparticles after a catalytic experiment, or alternatively, the magnetic Fe2O3 can be used for hyperthermia studies through magnetic heat induction. The photothermal experiment described in this report measures bulk temperature change and nanoparticle solution mass loss as functions of time using infrared thermocouples and a balance, respectively. The ease of sample preparation and the use of readily available equipment are distinct advantages of this technique. A caveat is that these photothermal measurements assess the bulk solution temperature and not the surface of the nanoparticle where the heat is transduced and the temperature is likely to be higher

  4. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles

    NASA Astrophysics Data System (ADS)

    Chaffin, Elise; O'Connor, Ryan T.; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ˜410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods.

  5. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles.

    PubMed

    Chaffin, Elise; O'Connor, Ryan T; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ∼410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods. PMID:27497571

  6. Temperature-independent formation of Au nanoparticles in ionic liquids by arc plasma deposition

    NASA Astrophysics Data System (ADS)

    Hatakeyama, Yoshikiyo; Kimura, Satoshi; Kameyama, Tatsuya; Agawa, Yoshiaki; Tanaka, Hiroyuki; Judai, Ken; Torimoto, Tsukasa; Nishikawa, Keiko

    2016-08-01

    An effective preparation method of Au nanoparticles (NPs) is presented, wherein an arc plasma deposition technique is combined with ionic liquids (ILs) used as capture media. This method requires no chemical reaction. By selecting ILs, size-controlled Au NPs are produced easily and on a massive scale.

  7. In situ immobilization of tin dioxide nanoparticles by nanoporous polymers scaffold toward monolithic humidity sensing devices.

    PubMed

    Wei, Shu; Han, Dong-Dong; Guo, Li; He, Yinyan; Ding, Hong; Zhang, Yong-Lai; Xiao, Feng-Shou

    2014-10-01

    Reported here is in situ immobilization of tin dioxide (SnO2) nanoparticles (NPs) within nanoporous polymer scaffolds for the development of monolithic humidity sensing devices. Through solvothermal polymerization of divinylbenzene (DVB) monomers in the interspaces of SnO2 fine powders, SnO2 NPs could be homogeneously immobilized in polymer matrices, forming a novel composite material. Immobilization of SnO2 NPs in nanoporous polymer matrices not only simplifies the fabrication process of NPs-based sensing devices, but also improves their adsorptive properties. The resultant nanoporous polymer/SnO2 NPs composites with adjustable SnO2 contents possess high BET surface areas, large pore sizes and pore volumes, thus they exhibit high adsorptive capacities for H2O vapor. As a general approach to NPs/nanoporous polymer composites, this work may open up a new way to nanomaterial-based sensing devices that features enhanced adsorptive property. PMID:24980621

  8. Amperometric immunosensor for α-fetoprotein antigen in human serum based on co-immobilizing dinuclear copper complex and gold nanoparticle doped chitosan film

    NASA Astrophysics Data System (ADS)

    Gan, Ning; Meng, Ling Hua; Wang, Feng

    2009-09-01

    A sensitive amperometric immunosensor for α-fetoprotein (AFP), a tumor marker for the diagnosis of hepatocellular carcinoma (HCC), was constructed, The immunosensor is prepared by co-immobilizing [Cu2(phen)2Cl2] (μ-Cl)2 (CuL), nano-Au/Chitosan(Chit) composite, horseradish peroxidase (HRP) and AFP antibody(anti-AFP) on a glassy carbon electrode (GCE). Firstly, CuL was irreversibly absorb on GCE electrode through π-π stacking interaction; then nano-Au/Chit composite was immobilized onto the electrode because of its excellent membrane-forming ability, finally HRP and anti-AFP was adsorbed onto the surface of the gold nanoparticles to construct GCE | CuL/nanoAu-chit/HRP/anti-AFP immunosensor. The preparation procedure of the electrode was characterized by electrochemical and spectroscopy method. The results showed that this immunosensor exhibited an excellent electrocatalytic response to the reduction of hydrogen peroxide (H2O2) without the aid of an electron mediator, offers a high-sensitivity (1710 nA · ng-1 · ml-1) for the detection of AFP and has good correlation for detection of AFP in the range of 0.2 to 120.0 ng/ml with a detection limit of 0.05 ng/ml. The biosensor showed high selectivity as well as good stability and reproductivity.

  9. Noble metals (Ag, Au) nanoparticles addition effects on superconducting properties of CuTl-1223 phase

    NASA Astrophysics Data System (ADS)

    Jabbar, Abdul; Mumtaz, Muhammad; Nadeem, Kashif

    2015-03-01

    Low anisotropic (Cu0.5Tl0.5) Ba2Ca2Cu3O10 - δ (CuTl-1223) high temperature superconducting phase was synthesized by solid-state reaction, silver (Ag) nanoparticles were prepared by sol-gel method and gold (Au) nanoparticles were extracted from colloidal solution. We added Ag and Au nanoparticles in CuTl-1223 matrix separately with same concentration during the final sintering process to get (M)x/CuTl-1223; M = Ag nanoparticles or Au nanoparticles (x = 0 and 1.0 wt.%) nano-superconductor composites. We investigated and compared the effects of these noble metals nanoparticles addition on structural, morphological and superconducting transport properties of CuTl-1223 phase. The crystal structure of the host CuTl-1223 superconducting phase was not affected significantly after the addition of these nanoparticles. The enhancement of superconducting properties was observed after the addition of both Ag and Au nanoparticles, which is most probably due to improved inter-grains weak-links and reduction of defects such as oxygen deficiencies, etc. The reduction of normal state room temperature resistivity is the finger prints of the reduction of barriers and facilitation to the carriers transport across the inter-crystallite sites due to improved inter-grains weak-links. The greater improvement of superconducting properties in Ag nanoparticles added samples is attributed to the higher conductivity of silver as compared to gold, which also suits for practical applications due to lower cost and easy synthesis of Ag nanoparticles as compared to Au nanoparticles.

  10. Electrochemiluminescence immunosensor using poly(l-histidine)-protected glucose dehydrogenase on Pt/Au bimetallic nanoparticles to generate an in situ co-reactant.

    PubMed

    Xiao, Lijuan; Chai, Yaqin; Wang, Haijun; Yuan, Ruo

    2014-08-21

    In this work, Pt/Au bimetallic nanoparticles (Pt/Au NPs) were used as nanocarriers to develop an electrochemiluminescence (ECL) immunosensor for sensitive cardiac troponin I (cTnI) detection, coupling with enzyme-based signal amplification. First, gold nanoparticles modified Ru(phen)3(2+)-doped silica nanoparticles (Au@RuSiO2 NPs) with numerous luminophores were used as a platform, potentially increasing the signal intensity. Second, Pt/Au NPs with large surface area and rich surface atoms were a superior matrix for the immobilization of numerous antibodies (Ab2), poly(l-histidine) (PLH) and glucose dehydrogenase (GDH). More importantly, the PLH-protected GDH exhibited excellent enzymatic activity for the oxidation of glucose accompanied by the reduction of NAD(+) to NADH. The in situ generated NADH acted as a co-reactant of Ru(phen)3(2+), significantly enhancing the ECL signal. In this manner, the designed immunosensor displayed high sensitivity for the detection of cTnI in the range of 0.010 ng mL(-1) to 10 ng mL(-1) with a detection limit of 3.3 pg mL(-1) (S/N = 3). The proposed strategy holds a new promise for highly sensitive bioassays for application in clinical analyses. PMID:24940578

  11. A sensitive electrochemiluminescence immunosensor based on luminophore capped Pd@Au core-shell nanoparticles as signal tracers and ferrocenyl compounds as signal enhancers.

    PubMed

    Liu, Yuting; Wang, Haijun; Xiong, Chengyi; Yuan, Yali; Chai, Yaqin; Yuan, Ruo

    2016-07-15

    In this work, N-(aminobutyl)-N-(ethylisoluminol) (ABEI), an analogue of luminol, is served as both the reductant and luminescence reagent to synthesize ABEI capped Pd@Au core-shell nanoparticles (ABEI-Pd@AuNPs). The nanoparticles not only exhibit inherent electrochemiluminescence (ECL) property, but also possess advantages of noble-metal nanomaterials such as outstanding electronic property, high specific surface area and good biocompatibility. In order to enhance the luminescence efficiency, ferrocene monocarboxylic acid (Fc) as catalyzer is grafted on the surface of ABEI-Pd@AuNPs with the aid of l-cysteine (l-Cys). When the Fc is electrochemically oxidized to ferricinium cation species (Fc(+)), the decomposition of H2O2 which existed in detection solution can be catalyzed by Fc(+) to generate oxygen-related free radicals, resulting effective signal amplification for ABEI-H2O2 system. For potential applications, the Pd@Au core-shell nanoparticles bifunctionalized by ABEI and catalyzer are employed as nano-carriers to immobilize detection antibody (Ab2). Based on sandwiched immunoreactions, a "signal-on" ECL immunosensor is developed for detection of human collagen type IV (Col IV), a potential biomarker associated with diabetic nephropathy. Consequently, the proposed immunosensor provides a wide linear detection ranging from 1pgmL(-1) to 10ngmL(-1) with a relatively low detection limit of 0.3pgmL(-1) (S/N=3). PMID:26985586

  12. Cation exchange resin immobilized bimetallic nickel-iron nanoparticles to facilitate their application in pollutants degradation.

    PubMed

    Ni, Shou-Qing; Yang, Ning

    2014-04-15

    Nanoscale zerovalent iron (nZVI) usually suffers from reduction of reactivity by aggregation, difficulty of assembling, environmental release and health concerns. Furthermore, data are lacking on the effect of cheap nickel on debromination of decabromodiphenyl ether (DBDE) by immobilized nZVI in aqueous system. In this study, strong acid polystyrene cation-exchange resins with particle diameter from 0.4 to 0.6 mm were utilized as matrices to immobilize bimetallic nickel-iron nanoparticles in order to minimize aggregation and environmental leakage risks of nZVI and to enhance their reactivity. Elemental distribution mapping showed that iron particles distributed uniformly on the surface of the resin and nickel particles were dispersed homogeneously into Fe phase. The reaction rate of resin-bound nZVI is about 55% higher than that of dispersed nZVI. The immobilized bimetallic nanoparticles with 9.69% Ni had the highest debromination percent (96%) and reaction rate (0.493 1/h). The existence of Ni significantly improved the debromination rate, due to the surface coverage of catalytic metal on the reductive metal and the formation of a galvanic cell. The environmental dominant congeners, such as BDE 154, 153, 100, 99 and 47, were produced during the process. Outstanding reactive performance, along with magnetic separation assured that resin-bound bimetallic nickel-iron nanoparticles are promising material that can be utilized to remediate a wide variety of pollutants contaminated sites including polybrominated diphenyl ethers. PMID:24559714

  13. Improvement of the stability and activity of immobilized glucose oxidase on modified iron oxide magnetic nanoparticles

    NASA Astrophysics Data System (ADS)

    Abbasi, Mahboube; Amiri, Razieh; Bordbar, Abdol-Kalegh; Ranjbakhsh, Elnaz; Khosropour, Ahmad-Reza

    2016-02-01

    Immobilized proteins and enzymes are widely investigated in the medical field as well as the food and environmental fields. In this study, glucose oxidase (GOX) was covalently immobilized on the surface of modified iron oxide magnetic nanoparticles (MIMNs) to produce a bioconjugate complex. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) were used to the size, shape and structure characterization of the MIMNs. Binding of GOX to these MIMNs was confirmed by using FT-IR spectroscopy. The stability of the immobilized and free enzyme at different temperature and pH values was investigated by measuring the enzymatic activity. These studies reveal that the enzyme's stability is enhanced by immobilization. Further experiments showed that the storage stability of the enzyme is improved upon binding to the MIMNs. The results of kinetic measurements suggest that the effect of the immobilization process on substrate and product diffusion is small. Such bioconjugates can be considered as a catalytic nanodevice for accelerating the glucose oxidation reaction for biotechnological purposes.

  14. Immobilized Silver Nanoparticles on Chitosan with Special Surface State-Enhanced Antimicrobial Efficacy and Reduced Cytotoxicity.

    PubMed

    He, Miao; Lu, Liying; Zhang, Jinchi; Li, Danzhen

    2015-09-01

    Immobilized chitosan-Ag nanoparticles (CTS-Ag NPs) with special surface state have been synthesized successfully through immobilizing Ag NPs on the amino-enriched surface of CTS by reducing Ag (I) in situ. The antimicrobial efficiency and potency of CTS-Ag NPs against Escherichia coli and Staphylococcus aureus were studied. Our results reveal that surface-immobilized CTS-Ag NPs show better antimicrobial efficacy than several other reported monodisperse colloidal Ag NPs, because the unique surface state of our CTS-Ag NPs leads to both "contact killing" and "ion mediated killing" functions. Due to the synergetic effect of CTS and Ag NPs, the immobilized CTS-Ag NPs present a broader antimicrobial spectrum and a more effective antifungal activity against Monilia albican. In addition, CTS as an environment friendly dispersant can help to reduce the cytotoxicity of Ag NPs on higher organisms. The immobilized CTS-Ag NPs are stable and can maintain good disinfection potential after 6 months' shelf-time. PMID:26716197

  15. Characterization and immobilization of trypsin on tannic acid modified Fe3O4 nanoparticles.

    PubMed

    Atacan, Keziban; Özacar, Mahmut

    2015-04-01

    Fe3O4 nanoparticles (NPs) were synthesized by co-precipitating Fe2+ and Fe3+ in an ammonia solution. Fe3O4 NPs functionalized with tannic acid were prepared. After functionalization process, trypsin enzyme was immobilized on these Fe3O4 NPs. The influence of pH, temperature, thermal stability, storage time stability and reusability on non-covalent immobilization was studied. The properties of Fe3O4 and its modified forms were examined by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), UV-vis spectrometer (UV) and X-ray diffraction (XRD), magnetization and zeta potential measurements. The immobilized enzyme was slightly more stable than the free enzyme at 45°C. According to the results, the activity of immobilized trypsin was preserved 55% at 45°C after 2 h and 90% after 120 days storage. In addition, the activity of the immobilized trypsin was preserved 40% of its initial activity after eight times of successive reuse. PMID:25686792

  16. Optical properties of Ag nanoparticle-polymer composite film based on two-dimensional Au nanoparticle array film

    PubMed Central

    2014-01-01

    The nanocomposite polyvinyl pyrrolidone (PVP) films containing Ag nanoparticles and Rhodamine 6G are prepared on the two-dimensional distinctive continuous ultrathin gold nanofilms. We investigate the optical properties and the fluorescence properties of silver nanoparticles-PVP polymer composite films influenced by Ag nanoparticles and Au nanoparticles. Absorption spectral analysis suggests that the prominently light absorption in Ag nanowire/PVP and Ag nanowire/PVP/Au film arises from the localized surface plasmon resonance of Ag nanowire and Au nanofilm. The enhanced fluorescence is observed in the presence of Ag nanowire and Au nanofilm, which is attributed to the excitation of surface plasmon polariton resonance of Ag nanowire and Au nanofilm. The gold nanofilm is proven to be very effective fluorescence resonance energy transfer donors. The fabricated novel structure, gold ultrathin continuous nanofilm, possesses high surface plasmon resonance properties and prominent fluorescence enhancement effect. Therefore, the ultrathin continuous gold nanofilm is an active substrate on nanoparticle-enhanced fluorescence. PMID:24685186

  17. Optical properties of Ag nanoparticle-polymer composite film based on two-dimensional Au nanoparticle array film.

    PubMed

    Wang, Long-De; Zhang, Tong; Zhang, Xiao-Yang; Song, Yuan-Jun; Li, Ruo-Zhou; Zhu, Sheng-Qing

    2014-01-01

    The nanocomposite polyvinyl pyrrolidone (PVP) films containing Ag nanoparticles and Rhodamine 6G are prepared on the two-dimensional distinctive continuous ultrathin gold nanofilms. We investigate the optical properties and the fluorescence properties of silver nanoparticles-PVP polymer composite films influenced by Ag nanoparticles and Au nanoparticles. Absorption spectral analysis suggests that the prominently light absorption in Ag nanowire/PVP and Ag nanowire/PVP/Au film arises from the localized surface plasmon resonance of Ag nanowire and Au nanofilm. The enhanced fluorescence is observed in the presence of Ag nanowire and Au nanofilm, which is attributed to the excitation of surface plasmon polariton resonance of Ag nanowire and Au nanofilm. The gold nanofilm is proven to be very effective fluorescence resonance energy transfer donors. The fabricated novel structure, gold ultrathin continuous nanofilm, possesses high surface plasmon resonance properties and prominent fluorescence enhancement effect. Therefore, the ultrathin continuous gold nanofilm is an active substrate on nanoparticle-enhanced fluorescence. PMID:24685186

  18. Effect of Au nano-particle aggregation on the deactivation of the AuCl3/AC catalyst for acetylene hydrochlorination.

    PubMed

    Dai, Bin; Wang, Qinqin; Yu, Feng; Zhu, Mingyuan

    2015-01-01

    A detailed study of the valence state and distribution of the AuCl3/AC catalyst during the acetylene hydrochlorination deactivation process is described and discussed. Temperature-programmed reduction and X-ray photoelectron spectral analysis indicate that the active Au(3+) reduction to metallic Au(0) is one reason for the deactivation of AuCl3/AC catalyst. Transmission electron microscopy characterization demonstrated that the particle size of Au nano-particles increases with increasing reaction time. The results indicated that metallic Au(0) exhibits considerable catalytic activity and that Au nano-particle aggregation may be another reason for the AuCl3/AC catalytic activity in acetylene hydrochlorination. PMID:25994222

  19. Effect of Au nano-particle aggregation on the deactivation of the AuCl3/AC catalyst for acetylene hydrochlorination

    PubMed Central

    Dai, Bin; Wang, Qinqin; Yu, Feng; Zhu, Mingyuan

    2015-01-01

    A detailed study of the valence state and distribution of the AuCl3/AC catalyst during the acetylene hydrochlorination deactivation process is described and discussed. Temperature-programmed reduction and X-ray photoelectron spectral analysis indicate that the active Au3+ reduction to metallic Au0 is one reason for the deactivation of AuCl3/AC catalyst. Transmission electron microscopy characterization demonstrated that the particle size of Au nano-particles increases with increasing reaction time. The results indicated that metallic Au0 exhibits considerable catalytic activity and that Au nano-particle aggregation may be another reason for the AuCl3/AC catalytic activity in acetylene hydrochlorination. PMID:25994222

  20. Modification of light absorption in thin CuInS2 films by sprayed Au nanoparticles.

    PubMed

    Katerski, Atanas; Kärber, Erki; Acik, Ilona Oja; Dolgov, Leonid; Mere, Arvo; Sildos, Ilmo; Mikli, Valdek; Krunks, Malle

    2014-12-01

    The chemical spray pyrolysis method was used to deposit CuInS2 (CIS) thin films and Au nanoparticles (NPs) in two configurations: glass/Au-NP layer covered with CuInS2 film (Au-NP/CIS) and glass/CuInS2 films covered with Au-NP layer (CIS/Au-NP). According to X-ray diffraction (XRD), the spray of 2 mM HAuCl4 aqueous solution with a volume of 2.5 to 15 ml onto a glass substrate at 340°C results in metallic Au nanoparticles with a similar mean crystallite size in the range of 30 - 38 nm. The mean crystallite sizes remain in the range of 15 - 20 nm when grown onto a CIS film. The prepared films show plasmonic light absorption with increasing intensity in the spectral range of 500- 800 nm when increasing the volume of HAuCl4 solution sprayed. When compared to bare CIS on glass, the absorptance was increased ca. 4.5 times in the case of glass/Au-NP/CIS and ca. 3 times in the case of glass/CIS/Au-NP configuration. The glass/Au-NP/CIS configuration had an advantage since Au-NP could be embedded without chemically damaging the CIS. PMID:26088996

  1. On-chip enzymatic microreactor using trypsin-immobilized superparamagnetic nanoparticles for highly efficient proteolysis.

    PubMed

    Liu, Junyan; Lin, Shuang; Qi, Dawei; Deng, Chunhui; Yang, Pengyuan; Zhang, Xiangmin

    2007-12-28

    An easily replaceable microchip enzymatic microreactor has been fabricated based on the glass microchip with trypsin-immobilized superparamagnetic nanoparticles. Magnetic nanoparticles with small size (50 nm in diameter) and strong magnetism were synthesized. At first, amine-functionalized magnetic nanoparticles with high magnetic responsivity and excellent dispersibility were prepared through a facile one-pot strategy. Then, magnetic nanoparticles were functionalized with numerous aldehyde (-CHO) groups by treating the as-synthesized, amine-functionalized magnetic nanoparticles with glutaraldehyde. Finally, immobilization of trypsin onto the aldehyde-functionalized magnetic nanoparticles was achieved through reaction of the aldehyde groups with amine groups of trypsin. The prepared magnetic nanoparticles were then locally packed onto the glass microchip by the application of a strong magnetic field using a magnet to form an on-chip magnetic nanoparticles packing bed. Capability of the proteolytic microreactor was demonstrated by cytochrome c, bovine serum albumin and myoglobin as model proteins. The digestion products were characterized using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry with sequence coverage of 83%, 43% and 79% observed, respectively. Complete protein digestion was achieved in a short time (10 s) under the flow rate of 5 microL/min. These results are expected to open up a new possibility for the proteolysis analysis as well as a new application of magnetic nanoparticles. It is easy to replace the nanoparticles and make the new microreactor. It takes less than 1 min under the condition of extra magnetic to form a new packing bed. The packing bed can be used for at least five times without any treatments. Additionally, since the preparation and surface functionality of magnetic nanoparticles is low-cost and reproducible, the preparation method and application approach of the magnetic nanoparticles may find much

  2. Photocatalytic oxidation of chloroform using immobilized-biogenic TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Kim, Y.; Cho, Y.; Yoo, H.

    2011-12-01

    Although commercial titanium dioxide (TiO2) nanoparticles as a suspension in water are one of the most popular photocatalysts for treatment of chlorinated organic compounds, the reuse and recovery of the nanoscale phtocatalyst is a practical challenge for application in water and groundwater treatment system. As part of efforts to overcome this practical limitation, development of immobilized TiO2 is needed. Diatom Pinnularia sp. were found to be capable of producing nanoscale TiO2 in their microscale silica shells. In order to obtain biogenic TiO2 nanoparticles from Pinnularia sp., soluble Ti was fed to the silicon-starved cells, resulting in deposition of titanium on the microscale features of the silica shells. After thermal treatment at 720 oC for 2 hr, the titanium was eventually converted to nanoscale TiO2. In order to determine the physical and chemical properties of the immobilized TiO2, material characterization such as TEM, STEM-EDS, BET and XRD analysis was carried out. In this study, a novel type of immobilized photocatalytic nanoparticles, biogenic TiO2 on silica shells was used for the mineralization of chloroform in water. Batch tests were conducted to evaluate the chloroform removal efficiency of biogenic and commercial TiO2 nanoparticles. Also, the amount of Cl- ions in water during the mineralization was measured to check mineralization of chloroform by biogenic TiO2 nanoparticles. Kinetic models were used to determine the rate of chloroform mineralization. In addition, the effect of UVA (ultraviolet-A) intensity on chloroform mineralization was investigated. The results obtained from this study could provide useful information for practical application of biogenic TiO2 in the groundwater treatment contaminated with some chlorinated organic compounds.

  3. Facile synthesis of superparamagnetic Fe3O4@Au nanoparticles for photothermal destruction of cancer cells.

    PubMed

    Ren, Jinfeng; Shen, Shun; Pang, Zhiqing; Lu, Xiaohui; Deng, Chunhui; Jiang, Xinguo

    2011-11-14

    Superparamagnetic Fe(3)O(4) nanoparticles with positive surface ξ-potential were synthesized via a solvothermal route. After Fe(3)O(4) was mixed with HAuCl(4) and NaBH(4), the reduced Au nanoparticles could be directly adsorbed onto the surface of Fe(3)O(4) nanoparticles. The as-synthesized nanocomposites were successfully applied to photothermal destruction of cancer cells. PMID:21952492

  4. Highly sensitive electrochemiluminescenc assay of acetylcholinesterase activity based on dual biomarkers using Pd-Au nanowires as immobilization platform.

    PubMed

    Ye, Cui; Wang, Min-Qiang; Zhong, Xia; Chen, Shihong; Chai, Yaqin; Yuan, Ruo

    2016-05-15

    One-dimensional Pd-Au nanowires (Pd-Au NWs) were prepared and applied to fabricate an electrochemiluminescence (ECL) biosensor for the detection of acetylcholinesterase (AChE) activity. Compared with single-component of Pd or Au, the bimetallic nanocomposite of Pd-Au NWs offers a larger surface area for the immobilization of enzyme, and displays superior electrocatalytic activity and efficient electron transport capacity. In the presence of AChE and choline oxidase (ChOx), acetylcholine (ATCl) is hydrolyzed by AChE to generate thiocholine, then thiocholine is catalyzed by ChOx to produce H2O2 in situ, which serves as the coreactant to effectively enhance the ECL intensity in luminol-ECL system. The detection principle is based on the inhibited AChE and reactivated AChE as dual biomarkers, in which AChE was inhibited by organophosphorus (OP) agents, and then reactivated by obidoxime. Such dual biomarkers method can achieve credible evaluation for AChE activity via providing AChE activity before and after reactivation. The liner range for AChE activity detection was from 0.025 U L(-1) to 25 KU L(-1) with a low detection limit down to 0.0083 U L(-1). PMID:26686921

  5. Protein Viability on Au Nanoparticles during an Electrospray and Electrostatic-Force-Directed Assembly Process

    DOE PAGESBeta

    Mao, Shun; Lu, Ganhua; Yu, Kehan; Chen, Junhong

    2010-01-01

    We study the protein viability on Au nanoparticles during an electrospray and electrostatic-force-directed assembly process, through which Au nanoparticle-antibody conjugates are assembled onto the surface of carbon nanotubes (CNTs) to fabricate carbon nanotube field-effect transistor (CNTFET) biosensors. Enzyme-linked immunosorbent assay (ELISA) and field-effect transistor (FET) measurements have been used to investigate the antibody activity after the nanoparticle assembly. Upon the introduction of matching antigens, the colored reaction from the ELISA and the change in the electrical characteristic of the CNTFET device confirm that the antibody activity is preserved during the assembly process.

  6. A facile surface-enhanced Raman scattering (SERS) detection of rhodamine 6G and crystal violet using Au nanoparticle substrates

    NASA Astrophysics Data System (ADS)

    Zhang, Kuibao; Zeng, Tixian; Tan, Xiulan; Wu, Weidong; Tang, Yongjian; Zhang, Haibin

    2015-08-01

    In this study, Au nanoparticle (5 nm) colloid was employed for a facile preparation of SERS substrates from three approaches: (1) original Au nanoparticles, (b) Au colloid coated 200 nm polystyrene (PS) beads, and (3) Au colloid annealed at 200-500 °C. Rhodamine 6G (R6G) and crystal violet were employed as the Raman active probes. The Au colloid deposited PS beads (PS@Au) exhibit intensive SERS signal for R6G detection, which is promising for crystal violet detection after being annealed at 400 °C. The 200 °C annealed Au nanoparticles demonstrate excellent combined SERS sensitivity for both R6G and crystal violet. For the original Au colloid, elevated annealing temperature from 200 °C to 500 °C decreases the SERS intensity as Au particles were coarsened gradually.

  7. Molecular imprinting and immobilization of cellulase onto magnetic Fe3O4@SiO2 nanoparticles.

    PubMed

    Li, Yue; Wang, Xiang-Yu; Zhang, Rui-Zhuo; Zhang, Xiao-Yun; Liu, Wei; Xu, Xi-Ming; Zhang, Ye-Wang

    2014-04-01

    Supermagnetic Fe3O4@SiO2 nanoparticles were molecular-imprinted prepared with cellulase as the template. The molecular imprinted nanoparticles were used as support to immobilization of cellulase. 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 cellulase was immobilized on the nanoparticles successfully from the Fourier transform infrared spectra. The adsorption of cellulase on the nanoparticles was specific and rapid. A high immobilization efficiency of 95% was achieved after the optimization. At 70 degrees C, the half-life of the immobilized cellulase was 3.3-fold of the free enzyme. Compared with the free enzyme, the immobilized cellulase has the same optimal pH, higher optimal temperature, better thermal stability and higher catalytic efficiency. The results strongly suggest that the immobilized cellulase on molecular imprinted Fe3O4@SiO2 has the potential applications in the production of bioethanol, paper and pulp industry, and pharmaceutical industry. PMID:24734713

  8. Au nanoparticle sensitized ZnO nanopencil arrays for photoelectrochemical water splitting

    NASA Astrophysics Data System (ADS)

    Wang, Tuo; Lv, Rui; Zhang, Peng; Li, Changjiang; Gong, Jinlong

    2014-11-01

    This paper describes the synthesis of Au nanoparticle sensitized ZnO nanopencil arrays on F-doped SnO2 substrates by an aqueous chemical growth and subsequent photoreduction method. The Au-ZnO nanopencil arrays yield a photocurrent of ~1.5 mA cm-2 at 1 V versus Ag/AgCl. The enhanced photocurrent is attributed to the surface plasmon resonance effect of Au nanoparticles and the prolonged lifetime of the photo-generated electron-hole pairs. The improved stability of ZnO is due to the plasmon resonance energy transfer process enabled by the Au nanoparticles, which enhances the electric field intensity in a small, well-defined location of the ZnO semiconductor.This paper describes the synthesis of Au nanoparticle sensitized ZnO nanopencil arrays on F-doped SnO2 substrates by an aqueous chemical growth and subsequent photoreduction method. The Au-ZnO nanopencil arrays yield a photocurrent of ~1.5 mA cm-2 at 1 V versus Ag/AgCl. The enhanced photocurrent is attributed to the surface plasmon resonance effect of Au nanoparticles and the prolonged lifetime of the photo-generated electron-hole pairs. The improved stability of ZnO is due to the plasmon resonance energy transfer process enabled by the Au nanoparticles, which enhances the electric field intensity in a small, well-defined location of the ZnO semiconductor. Electronic supplementary information (ESI) available: Illustrative schematic of PEC measurements, XPS of ZnO nanorods and nanopencils. See DOI: 10.1039/c4nr03735a

  9. Enhancement of the thermal transport in a culture medium with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Jiménez-Pérez, J. L.; Fuentes, R. Gutierrez; Alvarado, E. Maldonado; Ramón-Gallegos, E.; Cruz-Orea, A.; Tánori-Cordova, J.; Mendoza-Alvarez, J. G.

    2008-11-01

    In this work, it is reported the gold nanoparticles synthesis, their characterization, and their application to the enhancement of the thermal transport in a cellular culture medium. The Au nanoparticles (NPs), with average size of 10 nm, contained into a culture medium (DMEM (1)/F12(1)) (CM) increased considerably the heat transfer in the medium. Thermal lens spectrometry (TLS) was used to measure the thermal diffusivity of the nanofluids. The characteristic time constant of the transient thermal lens was obtained by fitting the theoretical expression, for transient thermal lens, to the experimental data. Our results show that the thermal diffusivity of the culture medium is highly sensitive to the Au nanoparticle concentration and size. The ability to modify the thermal properties to nanometer scale becomes very important in medical applications as in the case of cancer treatment by using photodynamic therapy (PDT). A complementary study with UV-vis and TEM techniques was performed to characterize the Au nanoparticles.

  10. Enantiomeric separations of chiral pharmaceuticals using chirally modified tetrahexahedral Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Shukla, N.; Yang, D.; Gellman, A. J.

    2016-06-01

    Tetrahexahedral (THH, 24-sided) Au nanoparticles modified with D- or L-cysteine (Cys) have been used as enantioselective separators of the chiral pharmaceutical propranolol (PLL) in solution phase. Polarimetry has been used to measure the rotation of linearly polarized light by solutions containing mixtures of PLL and Cys/THH-Au NPs with varying enantiomeric excesses of each. Polarimetry yields clear evidence of enantiospecific adsorption of PLL onto the Cys/THH-Au NPs. This extends prior work using propylene oxide as a test chiral probe, by using the crystalline THH Au NPs with well-defined facets to separate a real pharmaceutical. This work suggests that chiral nanoparticles, coupled with a density separation method such as centrifugation, could be used for enantiomeric purification of real pharmaceuticals. A simple robust model developed earlier has also been used to extract the enantiospecific equilibrium constants for R- and S-PLL adsorption onto the D- and L-Cys/THH-Au NPs.

  11. Immobilization of Iron Nanoparticles on Multi Substrates and Its Reduction Removal of Chromium (VI) from Waste Streams

    EPA Science Inventory

    This article describes the in-situ synthesis and immobilization of iron nanoparticles on several substrates at room temperature using NaBH4 as a reducing agent and ascorbic acid as capping agent. The method is very effective in protecting iron nanoparticles from air oxidation for...

  12. A facile and effective immobilization of glucose oxidase on tannic acid modified CoFe2O4 magnetic nanoparticles.

    PubMed

    Altun, Seher; Çakıroğlu, Bekir; Özacar, Münteha; Özacar, Mahmut

    2015-12-01

    This article presents a study of glucose oxidase (GOx) immobilization by employing tannic acid (TA) modified-CoFe2O4 (CFO) magnetic nanoparticles which demonstrates novel aspect for enzyme immobilization. By using the strong protein and tannic acid binding, GOx immobilization was carried out via physical adsorption in a simpler way compared with the other immobilization methods which require various chemicals and complicated procedures which is difficult, expensive, time-consuming, and destructive to the enzyme structure. CFO was synthesized by hydrothermal synthesis and modified with TA to immobilize GOx. The immobilized GOx demonstrated maximum catalytic activity at pH 6.5 and 45 °C. The samples were characterized by vibrating sample magnetometer (VSM), thermogravimetric analysis (TGA), zeta potential, and fourier transform infrared spectroscopy (FTIR), all of which confirm the surface modification of CFO and GOx immobilization. Also, field emission scanning electron microscope (FESEM) and X-ray diffraction (XRD) were performed to demonstrate the surface morphology and chemical structure of samples. According to the Lineweaver-Burk plot, GOx possessed lower affinity to glucose after immobilization, and the Michelis-Menten constant (KM) of immobilized and free GOx were found to be 50.05 mM and 28.00 mM, respectively. The immobilized GOx showed excellent reusability, and even after 8 consecutive activity assay runs, the immobilized GOx maintained ca. 60% of its initial activity. PMID:26562188

  13. Real-Time Imaging of the Formation of Au-Ag Core-Shell Nanoparticles.

    PubMed

    Tan, Shu Fen; Chee, See Wee; Lin, Guanhua; Bosman, Michel; Lin, Ming; Mirsaidov, Utkur; Nijhuis, Christian A

    2016-04-27

    We study the overgrowth process of silver-on-gold nanocubes in dilute, aqueous silver nitrate solution in the presence of a reducing agent, ascorbic acid, using in situ liquid-cell electron microscopy. Au-Ag core-shell nanostructures were formed via two mechanistic pathways: (1) nuclei coalescence, where the Ag nanoparticles absorbed onto the Au nanocubes, and (2) monomer attachment, where the Ag atoms epitaxially deposited onto the Au nanocubes. Both pathways lead to the same Au-Ag core-shell nanostructures. Analysis of the Ag deposition rate reveals the growth modes of this process and shows that this reaction is chemically mediated by the reducing agent. PMID:27043921

  14. Phase decomposition of AuFe alloy nanoparticles embedded in silica matrix under swift heavy ion irradiation

    NASA Astrophysics Data System (ADS)

    Pannu, Compesh; Bala, Manju; Singh, U. B.; Srivastava, S. K.; Kabiraj, D.; Avasthi, D. K.

    2016-07-01

    AuFe alloy nanoparticles embedded in silica matrix are synthesized using atom beam sputtering technique and subsequently irradiated with 100 MeV Au ions at various fluences ranging from 1 × 1013 to 6 × 1013 ions/cm2. The X-ray diffraction, absorption spectroscopy, X-ray photo electron spectroscopy and transmission electron microscopy results show that swift heavy ion irradiation leads to decomposition of AuFe alloy nanoparticles from surface region and subsequent reprecipitation of Au and Fe nanoparticles occur. The process of phase decomposition and reprecipitation of individual element nanoparticles is explained on the basis of inelastic thermal spike model.

  15. Enhancing the stability and antibiofilm activity of DspB by immobilization on carboxymethyl chitosan nanoparticles.

    PubMed

    Tan, Yulong; Ma, Su; Liu, Chenguang; Yu, Wengong; Han, Feng

    2015-09-01

    A β-N-acetyl-glucosaminidase (DspB) from Aggregatibacter actinomycetemcomitans CU1000 has been proved to inhibit and detach the biofilms formed by Staphylococcus epidermidis, Staphylococcus aureus and A. actinomycetemcomitans. However, the application of this enzyme is limited by its poor stability. In the present study, a β-N-acetyl-glucosaminidase encoding gene, dspB, was cloned from A. actinomycetemcomitans HK1651 and expressed in Escherichia coli. The recombinant DspB was loaded on hydrogel nanoparticles, which was prepared by using linoleic acid (LA) modified carboxymethyl chitosan (CMCS) after sonication. The nanoparticles were almost saturated by DspB at 0.3 mg/ml, which gave a loading capacity of 76.7%. The immobilization enhanced thermal stability, storage stability and reusability of DspB significantly. Moreover, it also increased antibiofilm activity due to the dual mechanism, including the improvement of the enzyme stability and the antibiofilm activity of CMCS nanoparticles. PMID:26302845

  16. Immobilization of mercury in field soil and sediment using carboxymethyl cellulose stabilized iron sulfide nanoparticles

    NASA Astrophysics Data System (ADS)

    Gong, Yanyan; Liu, Yuanyuan; Xiong, Zhong; Kaback, Dawn; Zhao, Dongye

    2012-07-01

    Mercury (Hg) is one of the most pervasive and bio-accumulative metals in the environment. Yet, effective in situ remediation technologies have been lacking. This study investigated the effectiveness of a class of soil-deliverable FeS nanoparticles for in situ immobilization of Hg in two field-contaminated soils from a New Jersey site and one sediment from an Alabama site. The nanoparticles were prepared using sodium carboxymethyl cellulose (CMC) as a stabilizer. Transmission electron microscopy measurements revealed a particle size of 34.3 ± 8.3 nm (standard deviation), whereas dynamic light scattering gave a hydrodynamic diameter of 222.5 ± 3.2 nm. Batch tests showed that at an FeS-to-Hg molar ratio of 28:1-118:1, the nanoparticles reduced water-leachable Hg by 79%-96% and the TCLP (toxicity characteristic leaching procedure) based leachability by 26%-96%. Column breakthrough tests indicated that the nanoparticles were deliverable in the sediment/soil columns under moderate injection pressure. However, once the external pressure was removed, the delivered nanoparticles remained virtually mobile under typical groundwater flow conditions. When the Hg-contaminated soil and sediment were treated with 52-95 pore volumes of a 500 mg l-1 FeS nanoparticle suspension, water-leachable Hg was reduced by 90%-93% and TCLP-leachable Hg was reduced by 65%-91%. The results warrant further field demonstration of this promising in situ remediation technology.

  17. Gold Nanoparticles Doped with (199) Au Atoms and Their Use for Targeted Cancer Imaging by SPECT.

    PubMed

    Zhao, Yongfeng; Pang, Bo; Luehmann, Hannah; Detering, Lisa; Yang, Xuan; Sultan, Deborah; Harpstrite, Scott; Sharma, Vijay; Cutler, Cathy S; Xia, Younan; Liu, Yongjian

    2016-04-01

    Gold nanoparticles have been labeled with various radionuclides and extensively explored for single photon emission computed tomography (SPECT) in the context of cancer diagnosis. The stability of most radiolabels, however, still needs to be improved for accurate detection of cancer biomarkers and thereby monitoring of tumor progression and metastasis. Here, the first synthesis of Au nanoparticles doped with (199) Au atoms for targeted SPECT tumor imaging in a mouse triple negative breast cancer (TNBC) model is reported. By directly incorporating (199) Au atoms into the crystal lattice of each Au nanoparticle, the stability of the radiolabel can be ensured. The synthetic procedure also allows for a precise control over both the radiochemistry and particle size. When conjugated with D-Ala1-peptide T-amide, the Au nanoparticles doped with (199) Au atoms can serve as a C-C chemokine receptor 5 (CCR5)-targeted nanoprobe for the sensitive and specific detection of both TNBC and its metastasis in a mouse tumor model. PMID:26865221

  18. Structural studies of Au-Pd bimetallic nanoparticles by a genetic algorithm method

    NASA Astrophysics Data System (ADS)

    Shao, Gui-Fang; Tu, Na-Na; Liu, Tun-Dong; Xu, Liang-You; Wen, Yu-Hua

    2015-06-01

    Metallic nanoparticles have attracted particular interests due to their excellent electronic, catalytic and optical properties over the past decades. Atomic-level understanding of structural characteristics of metallic nanoparticles is of great importance for their syntheses and applications because the structural characteristics strongly determine their chemical and physical properties. In this article, we systematically investigated the structural stability and structural features of Au-Pd nanoparticles by using the genetic algorithm with the quantum correction Sutton-Chen potentials. Layered coordinate ranking method and an effective fitness function have been introduced into the genetic algorithm to enhance its searching ability of low-energy configurations. Here were addressed eight representative nanoshapes including single-crystalline and multiple-twinned structures. The results reveal that the developed genetic algorithm exhibits superior searching ability. In all polyhedra, the truncated octahedron possessed the best stability, while the icosahedron did the worst. Moreover, segregation of Au to the surface and that of Pd to the core were disclosed in these polyhedral Au-Pd nanoparticles. Particularly, for Au composition of 50%, the optimized structures of Au-Pd nanoparticles were predicted to exhibit core-shell structures.

  19. Thermal diffusivity of nanofluids containing Au/Pd bimetallic nanoparticles of different compositions.

    PubMed

    Sánchez-Ramírez, J F; Jiménez Pérez, J L; Cruz Orea, A; Gutierrez Fuentes, R; Bautista-Hernández, A; Pal, U

    2006-03-01

    Colloidal suspensions of bimetallic Au/Pd nanoparticles were prepared by simultaneous reduction of the metal ions from their corresponding chloride salts with polymer (PVP) stabilizer. Thermal properties of water containing bimetallic nanoparticles with different nominal compositions (Au/Pd = 12/1, 5/1, 1/1, 1/5) were measured using the mode mismatched dual-beam thermal lens technique to determine the effect of particle composition on the thermal diffusivity of the nanofluids. The characteristic time constant of the transient thermal lens was estimated by fitting the experimental data to the theoretical expression for transient thermal lens. The thermal diffusivity of the nanofluids (water, containing Au/Pd bimetallic nanoparticles) is seen to be strongly dependent on the composition of the particles. The maximum diffusivity was achieved for the nanoparticles with highest Au/Pd molar ratio. A possible mechanism for such high thermal diffusivity of the nanofluids with bimetallic particles is given. UV-Vis spectroscopy, TEM and high-resolution electron microscopy (HREM) techniques were used to characterize the Au/Pd bimetallic nanoparticles. PMID:16573121

  20. Improved Performance of Lipase Immobilized on Tannic Acid-Templated Mesoporous Silica Nanoparticles.

    PubMed

    Jiang, Yanjun; Sun, Wenya; Zhou, Liya; Ma, Li; He, Ying; Gao, Jing

    2016-08-01

    Mesoporous silica nanoparticles were synthesized by using tannic acid as a pore-forming agent, which is an environmentally friendly, cheap, and non-surfactant template. SEM and TEM images indicated that the tannic acid-templated mesoporous silica nanoparticles (TA-MSNs) are monodisperse spherical-like particles with an average diameter of 195 ± 16 nm. The Brunauer-Emmett-Teller (BET) results showed that the TA-MSNs had a relatively high surface area (447 m(2)/g) and large pore volume (0.91 cm(3)/g), and the mean pore size was ca. 10.1 nm. Burkholderia cepacia lipase was immobilized on the TA-MSNs by physical adsorption for the first time, and the properties of immobilized lipase (BCL@TA-MSNs) were investigated. The BCL@TA-MSNs exhibited satisfactory thermal stability; strong tolerance to organic solvents such as methanol, ethanol, isooctane, n-hexane, and tetrahydrofuran; and high operational reusability when BCL@TA-MSNs were applied in esterification and transesterification reactions. After recycling 15 times in the transesterification reaction for biodiesel production, over 85 % of biodiesel yield can be maintained. With these desired characteristics, the TA-MSNs may provide excellent candidates for enzyme immobilization. PMID:27011329

  1. Immobilization of Lipase on Silver Nanoparticles via Adhesive Polydopamine for Biodiesel Production

    PubMed Central

    Dumri, Kanchana; Hung Anh, Dau

    2014-01-01

    Biodiesel production technology is competitive in terms of low cost and alternative source of energy which should be not only sustainable but also environmentally friendly. Designing of the lipase immobilization for biodiesel production has a remarkable impact and is still challenging. In this work, biodiesel production from soybean oil was enhanced and facilitated by using a novel biocatalyst consisting of commercial lipase (EC 3.1.1.3), silver nanoparticles, and polydopamine. Silver nanoparticles (AgNPs) were synthesized with a size range of 10–20 nm. Polydopamine (PD) was delivered by the self-polymerization of dopamine in 10 mM Tris-HCl pH 8.5 and simultaneously coated the AgNPs to form a PD/AgNPs complex. Lipase was immobilized on the PD/AgNPs complex surface via covalent bonds to form a tailor-made biocatalyst consisting of immobilized lipase/PD/AgNPs complex (LPA). The formation and morphology of each composition were characterized by UV-Vis spectroscopy and scanning electron microscope (SEM). Significantly, gas chromatography analysis showed a remarkable biodiesel production yield of 95% by using the LPA complex at 40°C for 6-hours reaction time, whereas the yield was 86% when using free lyophilized lipase. The LPA complex was apparently reusable after 7 batches and the latter conversion rate of soybean oil was decreased by only 27%. PMID:25328685

  2. A novel electrochemical DNA biosensor construction based on layered CuS-graphene composite and Au nanoparticles.

    PubMed

    Xu, Chun-Xuan; Zhai, Qiu-Ge; Liu, Yu-Jie; Huang, Ke-Jing; Lu, Lu; Li, Ke-Xin

    2014-11-01

    A novel CuS-graphene (CuS-Gr) composite was synthesized to achieve excellent electrochemical properties for application as a DNA electrochemical biosensor. CuS-Gr composite was prepared by a hydrothermal method, in which two-dimensional graphene served as a two-dimensional conductive skeleton to support CuS nanoparticles. A sensitive electrochemical DNA biosensor was fabricated by immobilizing single-stranded DNA (ss-DNA) labeled at the 5' end using 6-mercapto-1-hexane (HS-ssDNA) on the surface of Au nanoparticles (AuNPs) to form ssDNA-S-AuNPs/CuS-Gr, and hybridization sensing was done in phosphate buffer. Cyclic voltammetry and electrochemical impedance spectroscopy were performed for the characterization of the modified electrodes. Differential pulse voltammetry was applied to monitor the DNA hybridization using an [Fe(CN)6](3-/4-) solution as a probe. Under optimum conditions, the biosensor developed exhibited a good linear relationship between the current and the logarithm of the target DNA concentration ranging from 0.001 to 1 nM, with a low detection limit of 0.1 pM (3σ/S). The biosensor exhibited high selectivity to differentiate one-base-mismatched DNA and three-base-mismatched DNA. The results indicated that the sensing platform based on CuS-Gr provides a stable and conductive interface for electrochemical detection of DNA hybridization, and could easily be extended to the detection of other nucleic acids. PMID:24894519

  3. Interaction of Mesotetrakis (2,6,dimethoxyphenol) Porphyrin with AuTiO2 Nanoparticles: A Spectroscopic Approach.

    PubMed

    Revathi, R; Rameshkumar, A; Sivasudha, T

    2016-06-01

    The combination of nanoparticles with the photosensitizing molecules will assist in developing new approach for their biological applications. In this paper work, we have studied the interaction of photosensitising mesotetrakis (2,6,dimethoxyphenol) porphyrin molecule (P1) with AuTiO2 nanoparticles using absorption, fluorescence and time resolved measurements. An isosbestic point is appeared in the absorption spectrum of P1 on increasing the concentration of AuTiO2 nanoparticles indicates the interaction of P1 with AuTiO2 nanoparticles. Static type of quenching is observed in the fluorescence quenching measurement which is confirmed through lifetime measurements. Energy level calculations and Rehm Weller methods confirms the electron transfer mechanism from the excited P1 to the AuTiO2 nanoparticles. The observed effective binding and electron transfer property of porphyrin with AuTiO2 nanoparticles has great potential to be applied in the field of photodynamic therapy. PMID:27427692

  4. Photoluminescence enhancement in few-layer WS{sub 2} films via Au nanoparticles

    SciTech Connect

    Choi, Sin Yuk; Yip, Cho Tung; Li, Guang-Can; Lei, Dang Yuan; Fung, Kin Hung; Yu, Siu Fung E-mail: jh.hao@polyu.edu.hk; Hao, Jianhua E-mail: jh.hao@polyu.edu.hk

    2015-06-15

    Nano-composites of two-dimensional atomic layered WS{sub 2} and Au nanoparticles (AuNPs) have been fabricated by sulfurization of sputtered W films followed by immersing into HAuCl{sub 4} aqueous solution. The morphology, structure and AuNPs distribution have been characterized by electron microscopy. The decorated AuNPs can be more densely formed on the edge and defective sites of triangle WS{sub 2}. We have compared the optical absorption and photoluminescence of bare WS{sub 2} and Au-decorated WS{sub 2} layers. Enhancement in the photoluminescence is observed in the Au-WS{sub 2} nano-composites, attributed to localized surface plasmonic effect. This work provides the possibility to develop photonic application in two-dimensional materials.

  5. Effects of the proximity of Au nanoparticles on magnetic and transport properties of LSMO ultrathin layers

    SciTech Connect

    Brivio, S.; Magen Dominguez, Cesar; Sidorenko, A; Petti, D.; Cantoni, M.; Finazzi, M; Ciccacci, F; Renzi, R; Varela del Arco, Maria; Picozzi, S.; Bertacco, R.

    2010-01-01

    The effect of the proximity of Au nanoparticles on the transport and magnetic properties of ultrathin La2/3Sr1/3MnO3 (LSMO) films has been investigated. We find a huge increase of the resistivity of the manganite (by four orders of magnitude for a Au nominal thickness of 2 nm), which is accompanied by a strong decrease of the Curie temperature. A combined scanning transmission electron microscopy and electron energy loss spectroscopy (STEM-EELS) analysis shows that interfaces are coherent and atomically sharp, and that the structural quality is very high. On the other end, a strong reduction of the Mn oxidation state is seen upon Au capping. NMR data show a strong attenuation of the double exchange signal upon formation of Au nanoparticles. Ab-initio calculations indicate a negligible influence of Au on LSMO at an ideal interface, with the LSMO surface magnetic and electronic properties essentially unchanged upon creation of the Au/LSMO interface. In view of these calculations, the experimental results cannot be explained in terms of purely electrostatic effects induced by the proximity of a noble metal. Here we propose that the main driving force underlying the observed change in physical properties is the high reactivity of Au nanoparticles which can locally pump oxygen from the manganite, thus favouring a phase separation ensuing from O inhomogeneity which deteriorates the transport and electrical properties.

  6. Immobilization and surface functionalization of gold nanoparticles monitored via streaming current/potential measurements.

    PubMed

    Greben, Kyrylo; Li, Pinggui; Mayer, Dirk; Offenhäusser, Andreas; Wördenweber, Roger

    2015-05-14

    A streaming current/potential method is optimized and used for the analysis of the variation of the surface potential upon chemical modifications of a complex interface consisting of different organic molecules and gold nanoparticles (AuNPs). The surfaces of Si/SiO2 substrates modified with 3-aminopropyltriethoxysilane (APTES), AuNPs, and 11-amino-1-undecanethiol (aminothiols) are analyzed via pH and time dependent ζ potential measurements that reveal the stability and modification of the surface and identify crucial parameters for each individual preparation step. For instance, surface activation and especially molecular adsorbate layers tend not to be stable in time, whereas the substrate and the AuNPs provide a stable surface potential as long as impurities are avoided. It is shown that the streaming potential/current technique represents an ideal tool to analyze and monitor the complex surfaces and their modification. PMID:25905436

  7. Synthesis of α-glucosidase-immobilized nanoparticles and their application in screening for α-glucosidase inhibitors.

    PubMed

    Xiong, Yejuan; Liu, Qingshan; Yin, Xiaoying

    2016-06-01

    In order to rapidly and accurately screen compounds present in Chinese herbal medicines for α-glucosidase inhibition activity, we have developed a screening strategy which couples the immobilized enzymes with HPLC analysis. First, the core-shell PMMA/CS nanoparticle carrier was prepared by graft polymerization method. Subsequently, α-glucosidase was loaded on the nanoparticles to prepare the immobilized enzyme and construct a screening model. Secondly, the morphology and structure of the core-shell PMMA/CS material were characterized by transmission electron microscopy (TEM) and infrared spectroscopy (IR). The results indicate that the size distribution was uniform for the α-glucosidase-immobilized nanoparticles, with an average particle size of about 239nm. Finally, the α-glucosidase-immobilized nanoparticles were used to screen α-glucosidase inhibitors from extracts of traditional Chinese medicine and from a mixture of pharmacologically active compounds. Extracts of traditional Chinese medicines were analyzed by HPLC method before and after incubation with the immobilized enzyme nanoparticles. Using this method, magnoflorine was selectively separated from methanol extracts of Magnoliae Officinalis Cortex and genistein was selectively separated from a mixture of isoflavone compounds. Both the two compounds have previously been reported to have α-glucosidase inhibitory activity. These results demonstrate that this screening strategy represents a rapid and highly efficient method for the identification of α-glucosidase inhibitors in complex extracts of Chinese herbal medicines. PMID:27085015

  8. Covalent Immobilization of Biotin on Magnetic Nanoparticles: Synthesis, Characterization, and Cytotoxicity Studies.

    PubMed

    Islam, Md Rafiqul; Bach, Long Giang; Vo, Thanh-Sang; Lim, Kwon Taek

    2015-01-01

    A simple protocol for covalent immobilization of biotin onto the surface of Fe3O4 magnetic nanoparticles (MNPs) for improving the biocompatibility of original MNPs has been realized. MNPs were first prepared by co-precipitation method which was subsequently anchored with functionalized biotin. The as-synthesized MNPs were observed to be monocrystalline as evidenced from XRD and TEM images. The covalent grafting of biotin to MNPs was confirmed by FT-IR. The XPS analysis suggested the successful preparation of Biotin-f-MNPs. The as-synthesized Biotin-f-MNPs were found to be superparamagnetic character as recorded by SQUID. Cell viability studies revealed that the biocompatibility of MNPs was improved upon Biotin immobilization. PMID:26328324

  9. Construction of glutamate biosensor based on covalent immobilization of glutamate oxidase on polypyrrole nanoparticles/polyaniline modified gold electrode.

    PubMed

    Batra, Bhawna; Kumari, Seema; Pundir, Chandra Shekhar

    2014-04-10

    A method is described for construction of a highly sensitive electrochemical biosensor for detection of glutamate. The biosensor is based on covalent immobilization of glutamate oxidase (GluOx) onto polypyrrole nanoparticles and polyaniline composite film (PPyNPs/PANI) electrodeposited onto Au electrode. The enzyme electrode was characterized by cyclic voltammetry (CV), scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infra-red spectroscopy (FTIR) and electrochemical impedance spectroscopy (EIS). The biosensor showed optimum response within 3s at pH 7.5 (0.1 M sodium phosphate) and 35 °C, when operated at 50 mV s⁻¹. It exhibited excellent sensitivity (detection limit as 0.1 nM), fast response time and wider linear range (from 0.02 to 400 μM). Analytical recovery of added glutamate (5 mM and 10 mM) was 95.56 and 97%, while within batch and between batch coefficients of variation were 3.2% and 3.35% respectively. The enzyme electrode was used 100 times over a period of 60 days, when stored at 4 °C. The biosensor measured glutamate level in food stuff, which correlated well with a standard colorimetric method (r=0.99). PMID:24629270

  10. Influence of the S-Au Bond Strength on the Magnetic Behavior of S-Capped Au Nanoparticles

    NASA Astrophysics Data System (ADS)

    Vázquez, María J. Rodríguez; Rivas, José; López-Quintela, M. Arturo; Mosquera, Antonio Mouriño; Torneiro, Mercedes

    Recently, large permanent atomic magnetic moments have been found in Au nanoparticles capped with thiols. It is assumed that the formation of localized Au-S bonds at the particle surface induces the damping of the surface plasmon resonance and the appearance of a ferromagnetic-like behavior. In this work we will show for the first time that thioethers can also induce both phenomena, i.e., the damping of the plasmon band and the appearance of permanent magnetic moments. Furthermore, we have studied the influence of the Au-S bond strength on both phenomena using two different synthesized thioether ligands. It will be shown that, although both ligands can induce a complete damping of the plasmon band, only with one of the ligands (the one corresponding to the stronger S-Au bond) the appearance of a ferromagnetic-like order is observed. This is an indication of the extreme sensitivity of the magnetism on the strength of the charge transfer at the S-Au bond.