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20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

We report the synthesis of a novel looped enzyme-polyamidoamine nanocomposite with high enzyme loading density and long-term retention of bioactivity. The horseradish peroxidase (HRP) is first immobilized on fourth-grade (G4) poly(amidoamine) (PAMAM) dendrimer to form relatively a small enzyme-PAMAM composite, which is allowed to grow up into a larger one. The looped horseradish peroxidase-polyamidoamine (HRP-PAMAM) nanohybrid was characterized by TEM. The material obtained shows promising features as applied to the fabrication of high sensitive and long lifetime biosensors. In the presence of the hydroquinone mediator in the solution, the immobilized HRP exhibited excellent electro-catalytical response to H2O2. Under the optimal conditions, the resulting biosensor showed a linear response to H2O2 over a concentration range from 3.1x10(-6) to 2.0x10(-3) mol L(-1) with a sensitivity of 0.36 A L mol(-1) cm(-2) and a detection limit of 8.0x10(-7) mol L(-1). The sensitivity of the sensor response maintained over 70% of the original over 10 weeks. The catalytic activity of the looped enzyme-PAMAM nanohybrid form of HRP enzyme was obviously stabilized. As an extension, bienzyme sensor modified with glucose oxidase and HRP enzymatic PAMAM nanocomposites was constructed. The sensor exhibited improved performance and can be applied to the detection of glucose in real samples.
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PMID:Novel looped enzyme-polyamidoamine dendrimer nanohybrids used as biosensor matrix. 1799 39

The catalytic inactivation of Escherichia coli in water by a cerium (Ce)-promoted silver-loaded aluminum phosphate (Ag/ AlPO4) catalyst using molecular oxygen was investigated. With optimum Ce content, the Ag(Ce)/AlPO4 catalyst exhibited strong bactericidal activity. The process of decomposition of the cell wall and cell membrane was directly observed by TEM. The different morphological changes of E. coli cells treated with the Ag(Ce)/AlPO4 catalyst and those treated with Ag+ suggested that the Ag+ eluted from the catalyst surface did not play an important role during the bactericidal process. Results of DMPO spin-trapping measurements by electron spin resonance (ESR) indicated the formation of the reactive oxygen species (ROS) *OH and *O2-, which caused the considerable bactericidal activity. The formation of H2O2 acted as an important intermediate; this was confirmed by addition of catalase as the scavenger. A possible catalytic oxidation bactericidal mechanism using molecular oxygen was proposed for the Ag(Ce)/AlPO4 catalyst.
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PMID:Bactericidal activity of a Ce-promoted Ag/AlPO4 catalyst using molecular oxygen in water. 1844 23

A novel method for duplicating the hierarchical structures of biological substances at nanometer resolution in manganese oxides has been developed. This innovation uses natural biomorphic specimens, such as butterfly wing, cotton, and wood as templates. The biotemplates were first treated with either HCl/NaOH or HCl/H2O2/NaOH and then mixed with an aqueous solution of KMnO4. The treated biological materials were then ultrasonically irradiated, and finally, the biological templates were removed by calcination in air at temperatures between 500 and 800 degrees C. The structures of the resulting manganese oxides were characterized by a combination of XRD, FE-SEM, TEM and EDS. It was found that the fine hierarchical structures of the biological templates down to the nanometer scale were faithfully duplicated, and the duplication was positive. A mechanism for the positive replication is proposed and discussed in terms of the effects of the sonochemical reaction as well as the surface modification prior to the sonochemical reaction. The same sonochemical method can be extended to the duplication of intricate hierarchical structures of other biological forms in a large range of metal oxides.
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PMID:Precision replication of hierarchical biological structures by metal oxides using a sonochemical method. 1848 91

Small atomic gold clusters in solution, Au n , stabilized by tetrabutyl ammonium bromide (TBABr), have been synthesized by a simple electrochemical technique, based on the anodic dissolution of a gold electrode in the presence of TBABr salt, and using acetronitrile as solvent. The presence of clusters in the range Au3-Au11 were detected by MALDI-TOF spectroscopy, and further characterized by UV-vis absorption spectroscopy, TEM, AFM, X-ray diffraction, and cyclic voltammetry. Clusters display a semiconductor behavior with a band edge of approximately 2.5 eV. We report here their extraordinarily high electrocatalytic activity toward the O2 reduction reaction in acid solutions, which can explain Zhang's results, showing that a four-electron mechanism seems to occur because of the facile reduction of H2O2 on gold clusters compared to bulk gold or larger gold nanoparticles.
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PMID:Synthesis of atomic gold clusters with strong electrocatalytic activities. 1885 Jun 89

An effective and facile in situ electroless deposition approach for the fabrication of multi-walled carbon nanotube-supported Prussian blue nanoparticle (MWNTs/PB NP) composite nanomaterials is demonstrated in this article. The coverage of PB NPs on MWNTs is tunable by varying the experimental parameters, such as the initial molar concentration of FeCl3 + K3[Fe(CN)6], the relative concentration of FeCl3 + K3[Fe(CN)6] to MWNTs, and the temperature and duration of the heat treatment. This method involves a simple mixing process followed by a mild heating process and does not need the exhaustive surface oxidation process of MWNTs. TEM, FTIR, UV, and XRD are all used to characterize the MWNTs/PB composite materials. In addition, the electrochemical behavior of PB and catalysis of the reduction of H2O2, are investigated. The novel method is expected to be applicable for preparation of other coordination polymer/MWNTs composites and finds use in applications for electronic nanodevices.
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PMID:In situ synthesis and characterization of multi-walled carbon nanotube/Prussian blue nanocomposite materials and application. 1904 40

A comparison of different purification procedures for single walled carbon nanotubes (SWCNTs) synthesized by laser-vapourization has been presented. The methods involved gas-phase oxidation by calcination, liquid-phase oxidation by H2O2, hydrothermal treatment and acid refluxing in HCI. Sample purity is documented with Raman spectroscopy, Transmission electron microscopy, Scanning electron microscopy and thermogravimetric analysis. Multi-spot analyses were done to check the homogeneity of the purified samples. Different purification processes produced SWCNT material with purity in the range of 48-78%. Raman and TEM results suggested that prolonged calcination results in selective etching of larger diameter nanotubes. SEM and TGA analyses showed increase in density of SWCNTs with better oxidation resistance after purification.
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PMID:Purification of laser synthesized SWCNTs by different methods: a comparative study. 1919 41

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 degrees C and pH 7.2 of the reaction mixture before addition of H2O2 (3% w/w), 2% (w/v) PEG(6000) and 0.062:1 molar ratio of PEG to FeCl2 x 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.
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PMID:Polymer-assisted iron oxide magnetic nanoparticle immobilized keratinase. 1943 67

A simple and unique route to synthesize nanosize Pd particles using a zeolite support including a single-site Ti oxide moiety (TS-1) under UV-light irradiation has been developed. By the photoassisted deposition (PAD) method, a Pd precursor can be deposited directly on the photoexcited tetrahedrally coordinated Ti oxide moiety within the zeolite frameworks from an aqueous solution of Pd. The subsequent reduction with H2 generates the nanosized Pd metal particles with a narrow size distribution (PAD-Pd/TS-1). Characterization by XAFS and TEM analysis revealed that the size of the metal particles depends on the preparation methods and that the smaller sizes of Pd nanoparticles were formed on the photodeposited catalysts compared with the conventionally prepared impregnated catalysts. PAD also provides PdAu bimetallic nanoparticles from an aqueous solution of mixture of PdCl2 and HAuCl4. The catalytic activities in the direct synthesis of hydrogen peroxide (H2O2) using H2 and O2 gases under atmospheric pressure were strongly dependent on the preparation method and the presence of Au atoms. Here, both deposition of PdAu onto the TS-1 moiety under UV-light irradiation was the most efficient for the above reaction. The applicability of the present catalytic system is highlighted by the one-pot reaction of phenol using PAD-Pd/TS-1 in the presence of H2 and O2, in which both Pd nanoparticles and isolated Ti oxide moieties within the frameworks participate in the formation of H2O2 and oxidation of phenol, respectively.
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PMID:New route for the preparation of Pd and PdAu nanoparticles using photoexcited Ti-containing zeolite as an efficient support material and investigation of their catalytic properties. 1960 70

The abilities of Keggin type polyoxometalate, silicotungstic acid (STA) to reduce metal ions by electron transfer and to modify carbon surface by strong adsorption have been explored for the preparation of Pt nanoparticles supported on carbon composites (20% Pt/STA-C). The prepared composites were characterized by Transmission electron microscopy (TEM and HRTEM)), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The electrocatalytic activities of the prepared nanocomposites were examined by using Cyclic voltammetry (CV) for oxygen reduction reaction which takes place at cathode in fuel cells. The prepared composite (20% Pt/STA-C) proved efficient compared to STA free 20% Pt/C, prepared by hydrogen reduction method. H2O2 intermediate formation is a serious concern as it reduces the activity of Pt sites during oxygen reduction. The composites prepared by polyoxometalate reduction method (20% Pt/STA-C) showed better reduction ability towards H2O2 compared to STA free 20% Pt/C composite and thus showed better performance as cathode electrocatalyst for fuel cells.
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PMID:Electrochemical oxygen reduction reaction by Pt nanoparticles on carbon support stabilized by polyoxometalates. 1992

We report photocatalytic degradation studies on Navy Blue HE2R (NB) dye on significant details as a representative from the class of azo dyes using functional nanosystems specifically designed to allow a strong photocatalytic activity. A modified sol-gel route was employed to synthesize Au and gamma-Fe2O3 modified TiO2 nanoparticles (NPs) at low temperature. The attachment strategy is better because it allows clear surface of TiO2 to remain open for photo-catalysis. X-ray diffraction, Raman and UV-VIS spectroscopy studies showed the presence of gold and iron oxide phases along-with the anatase TiO2 phase. TEM studies showed TiO2 nanocomposite particles of size approximately 10-12 nm. A detailed investigation on heterogeneous photocatalytic performance for Navy Blue HE2R dye was done using the as-synthesized catalysts Au:TiO2 and gamma-Fe2O3:TiO2 in aqueous suspension under 8 W low-pressure mercury vapour lamp irradiation. Also, the photocatalytic degradation of Amranth and Orange G azo dyes were studied. The surface modified TiO2 NPs showed significantly improved photocatalytic activity as compared to pure TiO2. Exposure of the dye to the UV light in the presence of pure and gold NPs attached TiO2 catalysts caused dye degradation of about approximately 20% and approximately 80%, respectively, in the first couple of hours. In the presence of gamma-Fe2O3 NPs attached TiO2, a remarkable approximately 95% degradation of the azo dye was observed only in the first 15 min of UV exposure. The process parameters for the optimum catalytic activity are established which lead to a complete decoloration and substantial dye degradation, supported by the values of the Chemical Oxygen Demand (COD) approximately 93% and Total Organic Carbon (TOC) approximately 65% of the treated dye solution after 5 hours on the employment of the UV/Au:TiO2/H2O2 photocatalytic process.
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PMID:Photocatalytic degradation of azo dyes using Au:TiO2, gamma-Fe2O3:TiO2 functional nanosystems. 2262 74


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