16 results on '"Chen, Hong-Yuan"'
Search Results
2. The study of redox mechanism of dobutamine at different pH media by electrochemical and in situ spectroelectrochemical methods
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Yang, Gong-Jun, Xu, Jing-Juan, and Chen, Hong-Yuan
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DOBUTAMINE , *CATECHOLAMINES , *ELECTROCHEMICAL analysis , *CHEMICAL reactions , *ABSORPTION spectra - Abstract
Based on the comprehensive analyses of the experimental results of the electrochemical methods, in situ UV-Vis absorption spectra, in situ electron spin resonance (ESR), and attenuated total-internal reflection (ATR) as well as the calculation of UV-Vis absorption data by PM3 Semi-Empirical method, a reaction mechanism for the redox processes of dobutamine was presented. When the anodic sweep is carried out, dobutamine firstly undergoes a free radical reaction with one-electron and one-proton to form semi-quinone free radicals, which will continuously convert to its corresponding quinone form by further electrochemical oxidation reaction. The formed quinone cannot only undergo a cyclization process by chemical reaction to produce a new compound, which can be reduced at more negative potential, but also be reduced to form dobutamine again when subsequent cathodic sweep is followed. The cyclization rate is depended upon pH values, and it increases with the increase of pH. In neutral medium, the corresponding oxidation form of the cyclization reaction product is easy to convert to melanin. [Copyright &y& Elsevier]
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- 2004
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3. Ion current rectification-nanopipette technique for single-cell analysis.
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Xu, Yi-Tong, Ruan, Yi-Fan, Zhang, Tian-Yang, Shi, Xiao-Mei, Wang, Hai-Yan, Zhao, Wei-Wei, Chen, Hong-Yuan, and Xu, Jing-Juan
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IONS , *ELECTROCHEMICAL analysis - Abstract
Single-cell analysis (SCA) could provide in-depth understanding of cell biology yet is of great challenge. Many attempts have been made to develop novel techniques for SCA. Nanopipette-based ion current rectification (ICR) electroanalysis represents an emerging methodology to combat in this arena. In this review, the working rationale of ICR and its key regulation factors are discussed, followed by the sensing strategies established for SCA using illustrative examples. Future perspectives in this field are also proposed. • Ion current rectification (ICR)-nanopipette technique for single-cell analysis (SCA) is reviewed. • The fundamentals, operation rationales, and the state of the art are discussed. • Trends and prospects of this field are presented. [ABSTRACT FROM AUTHOR]
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- 2023
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4. Dual-biomarker-based logic-controlled electrochemical diagnosis for prostate cancers.
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Liu, Jing, Zhou, Hong, Xu, Jing-Juan, and Chen, Hong-Yuan
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BIOMARKERS , *DIAGNOSIS , *PROSTATE cancer , *ELECTROCHEMICAL analysis , *LOGIC devices , *SURVIVIN (Protein) , *FARADAIC current , *MESSENGER RNA - Abstract
Abstract: As single biomarker often has inadequate predictive value in clinical examination, we designed a dual-biomarker “AND” logic device that defines the concentration of prostate-specific antigen (PSA) and survivin mRNA as inputs and the increase in faradaic current from intercalation agent Co(phen)3 3+ as output for prostate cancer (CaP) diagnosis on Au nano-film covered gold electrode surfaces. Primary capture antibody (Ab1) was first immobilized on AuNP electrode, then while both PSA and survivin mRNA exist, current of Co(phen)3 3+ observably increased due to the formation of dsDNA structure between survivin antisensoligonucleotide connected secondary detection antibody (Ab2) and survivin mRNA. And when one of the two biomarkers was absent, no obvious current increment was found. Thus the designed “AND” logic gate greatly reduced the possibility of false-positive assay from non-cancerous prostate diseases such as prostatic hyperplasia and prostatitis in diagnosis of CaPs. [Copyright &y& Elsevier]
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- 2013
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5. Simultaneous electrochemical immunoassay using CdS/DNA and PbS/DNA nanochains as labels
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Kong, Fen-Ying, Xu, Bi-Yi, Xu, Jing-Juan, and Chen, Hong-Yuan
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ELECTROCHEMICAL analysis , *IMMUNOASSAY , *CADMIUM sulfide , *LEAD sulfide , *DNA microarrays , *ALPHA fetoproteins - Abstract
Abstract: An electrochemical method for the simultaneous detection of two different tumor markers, carcinoembryonic antigen (CEA) and α-fetoprotein (AFP), in one-pot, using CdS/DNA and PbS/DNA nanochains as labels was developed. Herein, magnetic beads (MBs) as bimolecule immobilizing carriers, were used for co-immobilization of primary anti-CEA and anti-AFP antibodies. The distinguishable signal labels were synthesized by in situ growth of CdS and PbS nanoparticles on DNA chains, respectively, which were further employed to label the corresponding secondary antibodies. A sandwich-type immunoassay format was formed by the biorecognition of the antigens and corresponding antibodies. The assay was based on the peak currents of Cd2+ and Pb2+ dissolved from CdS and PbS nanoparticles by HNO3 using square wave stripping voltammetry. Experimental results show that the multiplexed electrochemical immunoassay has enabled the simultaneous monitoring of CEA and AFP in a single run with wide working ranges of 0.1–100ngmL−1 for CEA and 0.5–200ngmL−1 for AFP. The detection limits reach to 3.3pgmL−1 for CEA and 7.8pgmL−1 for AFP. [Copyright &y& Elsevier]
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- 2013
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6. DNAzyme-functionalized Pt nanoparticles/carbon nanotubes for amplified sandwich electrochemical DNA analysis
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Dong, Xiao-Ya, Mi, Xiao-Na, Zhang, Long, Liang, Tong-Ming, Xu, Jing-Juan, and Chen, Hong-Yuan
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PLATINUM nanoparticles , *CARBON nanotubes , *ELECTROCHEMICAL analysis , *DNA , *BIOCONJUGATES , *MICROFABRICATION , *MOLECULAR self-assembly , *ELECTROCHEMICAL sensors - Abstract
Abstract: A novel DNAzyme-functionalized Pt nanoparticles/carbon nanotubes (DNAzyme/Pt NPs/CNTs) bioconjugate was fabricated as trace tag for ultrasensitive sandwich DNA detection. The Pt NPs/CNTs were prepared via layer-by-layer (LBL) assembly of the Pt NPs and polyelectrolyte on the carboxylated CNTs, followed by the functionalization with the DNAzyme and reporter probe DNA through the platinum—sulfur bonding. The subsequent sandwich-type DNA specific reaction would confine numerous DNAzyme/Pt NPs/CNTs bioconjugate onto the gold electrode surface for amplifying the signal. In the presence of 3,3′,5,5′ tetramethylbenzidine (TMB) which could be oxidized by the DNAzyme, electrochemical signals could be generated by chronoamperometry via the interrogation of reduction electrochemical signal of oxidized TMB. The constructed DNA sensor exhibited a wide linear response to target DNA ranging from 1.0fM to 10pM with the detection limit down to 0.6fM and exhibited excellent selectivity against even a single base mismatch. In addition, this novel DNA sensor showed fairly good reproducibility, stability, and reusability. [Copyright &y& Elsevier]
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- 2012
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7. Double-probe signal enhancing strategy for toxin aptasensing based on rolling circle amplification
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Tong, Ping, Zhao, Wei-Wei, Zhang, Lan, Xu, Jing-Juan, and Chen, Hong-Yuan
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GENE amplification , *APTAMERS , *ELECTROCHEMICAL analysis , *BIOSENSORS , *QUANTUM dots , *BIOCONJUGATES , *DNA probes , *CELLULAR signal transduction - Abstract
Abstract: On the basis of aptamer-based rolling circle amplification (RCA) and magnetic beads (MBs), a highly sensitive electrochemical method was developed for the determination of Ochratoxin A (OTA). Initially, an amino-modified capture DNA was immobilized onto MBs for the following hybridization with an OTA aptamer and a phosphate labeled padlock DNA. In the presence of OTA, the aptamer would dissociate from the bioconjugate, and the padlock DNA would subsequently hybridize with the capture DNA to form a circular template with the aid of the T4 ligase. Next, capture DNA would act as primer to initiate a linear RCA reaction and hence generate a long tandem repeated sequences by phi29 DNA polymerase and dNTPs. Then, two quantum dots (QDs) labeled DNA probes were tagged on the resulted RCA product to indicate the OTA recognition event by electrochemical readout. This strategy, based on the novel design of OTA-mediated DNA circularization, the combination of RCA and double signal probes introduction, could detect OTA down to the level of 0.2pgmL−1 with a dynamic range spanning more than 4 orders of magnitude. The proposed approach is tested to determine OTA in red wines and shows good application potential in real samples. [Copyright &y& Elsevier]
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- 2012
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8. Gold nanoparticles-coated magnetic microspheres as affinity matrix for detection of hemoglobin A1c in blood by microfluidic immunoassay
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Chen, Shao-Peng, Yu, Xiao-Dong, Xu, Jing-Juan, and Chen, Hong-Yuan
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IMMUNOASSAY , *HEMOGLOBINOMETRY , *MICROFLUIDIC devices , *GOLD coatings , *NANOPARTICLES , *MICROSPHERES , *MAGNETIC materials , *ELECTROCHEMICAL analysis , *COLLOIDAL gold , *BIOCHIPS - Abstract
Abstract: A novel microfluidic immunoassay system for specific detection of hemoglobin A1c (HbA1c) was developed based on a three-component shell/shell/core structured magnetic nanocomposite Au/chitosan/Fe3O4, which was synthesized with easy handling feature of Fe3O4 by magnet, high affinity for gold nanoparticles of chitosan and good immobilization ability for anti-human hemoglobin-A1c antibody (HbA1c mAb) of assembled colloidal gold nanoparticles. The resulting HbA1c mAb/Au/chitosan/Fe3O4 magnetic nanoparticles were then introduced into microfluidic devices coupled with a gold nanoband microelectrode as electrochemical detector. After that, three-step rapid immunoreactions were carried out in the sequence of HbA1c, anti-human hemoglobin antibodies (Hb mAb) and the secondary alkaline phosphatase (AP)-conjugated antibody within 20min. The current response of 1-naphtol obtained from the reaction between the secondary AP-conjugated antibody and 1-naphthyl phosphate (1-NP) increased proportionally to the HbA1c concentration. Under optimized electrophoresis and detection conditions, HbA1c responded linearly in the concentration of 0.05–1.5μgmL−1, with the detection limit of 0.025μgmL−1. This system was successfully employed for detection of HbA1c in blood with good accuracy and renewable ability. The proposed method proved its potential use in clinical immunoassay of HbA1c. [Copyright &y& Elsevier]
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- 2011
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9. An electrochemical immunosensing method based on silver nanoparticles
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Hao, Nan, Li, Hui, long, Yitao, Zhang, Lei, Zhao, Xirui, Xu, Danke, and Chen, Hong-Yuan
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COLLOIDAL silver , *GLUTATHIONE , *ELECTROCHEMICAL analysis , *THIOLS , *GLUTARALDEHYDE , *AMINO group , *DETECTORS , *OXIDATION , *ELECTROCHEMICAL sensors - Abstract
Abstract: In this article, an electrochemically direct stripping approach based on silver nanoparticles (AgNPs) labeled with antibody was proposed. To prepare AgNPs labels, glutathione (GSH) was chemically absorbed on the surface of AgNPs through its free thiol groups. Glutaraldehyde was used as a coupling reagent, its two aldehyde groups reacted with the amino group of GSH absorbed on the AgNPs surfaces and the amino groups of antibodies, respectively. The resulting labeled electrochemical active nanoparticles could recognize the proteins specifically via the immobilized antibody. To prove the electrochemical property of labeled AgNPs, human IgG was used as a model protein sample to be immobilized on a screen printed electrode (SPE) and the goat-anti-human IgG labeled AgNPs was added onto the surface of the SPE, followed by differential pulse voltammetric (DPV) method. With the oxidation of AgNPs labels coupled on the electrodes, the concentration of hIgG could be assayed directly and calculated. The dynamic concentration was in the range of 1–1000ng/mL and the detection limit was 0.4ng/mL (S/N =3). In addition, the presented method was also compared to indirect electrochemical stripping detection by dissolving AgNPs labels with nitric acids and the results showed advantages such as lower detection limit, rapidity and simplicity. [Copyright &y& Elsevier]
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- 2011
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10. Electrochemically deposited boronate affinity extracting phase for covalent solid phase microextraction of cis-diol biomolecules
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He, Jiangang, Liu, Zhen, Dou, Peng, Liu, Jing, Ren, Lianbing, and Chen, Hong-Yuan
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ELECTROCHEMICAL analysis , *SOLID phase extraction , *BIOMOLECULES , *DISSOCIATION (Chemistry) , *HYDROGEN-ion concentration , *HIGH performance liquid chromatography , *AFFINITY chromatography - Abstract
Abstract: A new format of solid phase microextraction (SPME), boronate affinity SPME, was proposed for the first time for covalent extraction of cis-diol containing biomolecules. This new SPME format is based on the reversible complex formation between boronic acids and 1,2- and 1,3-cis-diols. The complex formation and dissociation can be facilely controlled by changing pH. An extracting phase of poly-3-aminophenylboronate (polyAPBA) electrochemically deposited on a metal wire was employed to demonstrate the concept of this new methodology. Catechol and riboflavin were used as the test analytes, and the SPME extraction was combined off-line with high-performance liquid chromatographic (HPLC) separation followed by UV absorbance or fluorescence detection. Fundamental aspects, such as selectivity, extraction/desorption equilibrium, linearity, effect of competing compounds, reproducibility and life-time, were first investigated. Then the developed method was applied to beer samples since the content of riboflavin plays an important role in the flavor stability of beverages. Excellent performance of the SPME fibers was observed for both standard and real samples. Particularly, the expected excellent features of the polyAPBA extracting phase were experimentally verified, which include specific selectivity, eliminated matrix effect and manipulable capture/release. The new methodology of SPME can be a promising tool since a lot of 1,2- and 1,3-cis-diol-containing compounds are of great biological importance. [Copyright &y& Elsevier]
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- 2009
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11. Selective detection of dopamine based on the unique property of gold nanofilm
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Ge, Pei-Yu, Du, Ying, Xu, Jing-Juan, and Chen, Hong-Yuan
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DOPAMINE , *GOLD films , *POROUS materials , *NANOSTRUCTURED materials , *ELECTROCHEMICAL analysis , *SURFACE energy , *CHARGE exchange , *CHEMICAL detectors - Abstract
Abstract: Gold nanofilm, with a nanoporous morphology, was found to have the unique property to catalyze the oxidization of ascorbic acid (AA) and dopamine (DA), resulting in the improved electrochemical behavior of the two species and a negative shift of the oxidization potential of AA for about 300mV. The catalytic oxidization of gold nanofilm to AA is mainly ascribed to its high surface energy, while the enhanced electron transfer ability of DA on the gold nanofilm is attributed to the strong interaction between DA and the electrode surface. Based on the peak separation of DA and AA, selective detection of DA was achieved on the gold nanofilm modified electrode. Differential pulse voltammetry (DPV) techniques and cyclic voltammetry (CV) were used to investigate the electrochemical behavior of AA and DA on the surface of the electrode. Afterwards, the obtained gold nanofilm was applied in selective detection of dopamine (DA) in the presence of ascorbic acid (AA) at near neutral pH by DPV in the optimized conditions. The linear range for DA was 1.5–27.5μM. The electrode also shows good stability during detection. [Copyright &y& Elsevier]
- Published
- 2009
- Full Text
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12. Electrochemical determination of arsenite in neutral media on reusable gold nanostructured films
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Du, Ying, Zhao, Wei, Xu, Jing-Juan, and Chen, Hong-Yuan
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ELECTROCHEMICAL analysis , *ARSENIC compounds , *BUFFER solutions , *GOLD films , *COLLOIDAL gold , *OXIDATION-reduction reaction , *ELECTRODES - Abstract
Abstract: We report a simple and novel method of stirring-only-driven accumulation and electrochemical determination of arsenite (As(III)) with both of the oxidation and reduction peaks associated with As(0)/As(III) using a gold nanofilm electrode in neutral solution. Under stirring, a large amount of As(III) was deposited on the modified electrode and the electrochemical response was greatly amplified. The accumulated As(III) on the electrode showed well-defined redox couple in 0.1M blank phosphate buffer solution (pH 7.0), which could be used for the measurement of As(III). Under optimal conditions, As(III) could be detected in the range from 0.20 to 375ppb with a detection limit of 0.04ppb. In particular, with the use of the reduction peak of As(III) the modified electrode exhibits excellent performance for As(III) determination even in the presence of abundant Cu(II). The regeneration of the electrodes is facile with good reproducibility. The electrochemical system was applied to analyze As(III) in lake water, As(III) spiked tap water and drinking water. [Copyright &y& Elsevier]
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- 2009
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13. Choline biosensors based on a bi-electrocatalytic property of MnO2 nanoparticles modified electrodes to H2O2
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Bai, Yu-Hui, Du, Ying, Xu, Jing-Juan, and Chen, Hong-Yuan
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BIOSENSORS , *CHOLINE , *NANOPARTICLES , *ELECTROCHEMICAL analysis - Abstract
Abstract: An interesting mode of reactivity of MnO2 nanoparticles modified electrode in the presence of H2O2 is reported. The MnO2 nanoparticles modified electrodes show a bi-direction electrocatalytic ability toward the reduction/oxidation of H2O2. Based on this property, a choline biosensor was fabricated via a direct and facile electrochemical deposition of a biocomposite that was made of chitosan hydrogel, choline oxidase (ChOx) and MnO2 nanoparticles onto a glassy carbon (GC) electrode. The biocomposite is homogeneous and easily prepared and provides a shelter for the enzyme to retain its bioactivity. The results of square wave voltammetry showed that the electrocatalytic reduction currents increased linearly with the increase of choline chloride concentration in the range of 1.0×10−5 –2.1×10−3 M and no obvious interference from ascorbic acid and uric acid was observed. Good reproducibility and stability were obtained. A possible reaction mechanism was proposed. [Copyright &y& Elsevier]
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- 2007
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14. Separation of aminophenol isomers in polyelectrolyte multilayers modified PDMS microchip
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Xiao, Yan, Wang, Kai, Yu, Xiao-Dong, Xu, Jing-Juan, and Chen, Hong-Yuan
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NUCLEAR isomers , *INTEGRATED circuits , *ELECTROCHEMICAL analysis , *INFORMATION technology - Abstract
Abstract: The separation of three kinds of aminophenol isomers were achieved within 1min in polyelectrolytes multilayers modified PDMS microchips by layer-by-layer assembly with electrochemical detection (EC). Two polyelectrolytes, poly(dially dimethyl ammonium chloride) (PDDA) and poly(sodium-4-styrene-sulfonate) (PSS) were used to form polyelectrolyte multilayers (PEMs). The surface characteristic of the modified microchip was studied by XPS. The electroosmotic flow (EOF) on PEMs modified PDMS microchips was more stable than that of the native PDMS microchips and the adsorption of samples was greatly reduced on PEMs modified PDMS microchips during the electrophoretic process. The column efficiencies on PEMs modified microchip were increased by 100 times and the signals enhanced by 2 times compared with those of native microchips. The separation conditions such as running buffer pH, running buffer concentration and separation voltage were also optimized. [Copyright &y& Elsevier]
- Published
- 2007
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15. A simple method to fabricate a chitosan-gold nanoparticles film and its application in glucose biosensor
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Du, Ying, Luo, Xi-Liang, Xu, Jing-Juan, and Chen, Hong-Yuan
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NANOPARTICLES , *CARBON electrodes , *ELECTROCHEMICAL analysis , *DETECTORS - Abstract
Abstract: A novel film of chitosan-gold nanoparticles is fabricated by a direct and facile electrochemical deposition method and its application in glucose biosensor is investigated. HAuCl4 solution is mixed with chitosan and electrochemically reduced to gold nanoparticles, which can be stabilized by chitosan and electrodeposited onto glassy carbon electrode surfaces along with the electrodeposition of chitosan. Then a model enzyme, glucose oxidase (GOD) is immobilized onto the resulting film to construct a glucose biosensor through self-assembly. The resulting modified electrode surfaces are characterized with both AFM and cyclic voltammetry. Effects of chitosan and HAuCl4 concentration in the mixture together with the deposition time and the applied voltage on the amperometric response of the biosensor are also investigated. The linear range of the glucose biosensor is from 5.0×10−5 ∼1.30×10−3 M with a Michaelis–Menten constant of 3.5 mM and a detection limit of about 13 μM. [Copyright &y& Elsevier]
- Published
- 2007
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16. Electrochemically deposited chitosan hydrogel for horseradish peroxidase immobilization through gold nanoparticles self-assembly
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Luo, Xi-Liang, Xu, Jing-Juan, Zhang, Qing, Yang, Gong-Jun, and Chen, Hong-Yuan
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NANOPARTICLES , *METALLOENZYMES , *ATOMIC force microscopy , *ELECTROCHEMICAL analysis , *IMPEDANCE spectroscopy - Abstract
Abstract: A new strategy for immobilization of horseradish peroxidase (HRP) has been presented by self-assembling gold nanoparticles on chitosan hydrogel modified Au electrode. From a mildly acidic chitosan solution, a chitosan film is electrochemically deposited on Au electrode surface via a negative voltage bias. This process is accompanied by the hydrogen evolution reaction, and the released hydrogen gas made the deposited chitosan film with porous structure, which facilitates the assembly of gold nanoparticles and HRP. The resulting substrates were characterized by atomic force microscopy (AFM) and electrochemical impedance spectroscopy (EIS). The immobilized HRP displayed an excellent catalytic property to the reduction of H2O2 in the presence of methylene blue mediator. The resulting biosensor (HRP-modified electrode) showed a wide dynamic range of 8.0μM–15mM H2O2, and the linear ranges were 8.0μM–0.12mM and 0.50–12mM, with a detection limit of 2.4μM estimated at a signal-to-noise ratio of 3. Moreover, the biosensor remained about 85% of its original sensitivity after four weeks’ storage. [Copyright &y& Elsevier]
- Published
- 2005
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