Fabrication of GNPs/CDSH-Fc/nafion modified electrode for the detection of dopamine in the presence of ascorbic acid

被引:12
作者
Chen, Ming
Wei, Xiujuan
Qian, Hui
Diao, Guowang [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2011年 / 31卷 / 07期
基金
中国国家自然科学基金;
关键词
Cyclodextrin; Ferrocene; Gold nanoparticles; Dopamine; Ascorbic acid; GLASSY-CARBON ELECTRODE; SIMULTANEOUS ELECTROCHEMICAL DETERMINATION; SIMULTANEOUS VOLTAMMETRIC DETECTION; URIC-ACID; GOLD NANOPARTICLES; SELECTIVE DETERMINATION; COMPOSITE; CYCLODEXTRIN; BIOSENSOR; COMPLEX;
D O I
10.1016/j.msec.2011.04.002
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A novel dopamine sensor was fabricated by forming the inclusion complex between mono-6-thio-beta-cyclodextrin (CD-SH) and ferrocene (Fe) functionalized gold nanoparticles (GNPs) films on a platinum electrode. The properties of the GNPs/CDSH-Fc nanocomposite were characterized by Fourier transform infrared spectra, UV-visible absorption spectroscopy, transmission electron microscopy and cyclic voltammetry. The electrochemistry of dopamine (DA) was investigated by cyclic voltammetry (CV) and differential pulse voltammograms (DPV). The electrooxidation of dopamine could be catalyzed by Fc/Fc(+) couple as a mediator and had a higher electrochemical response due to the unique performance of GNPs/CDSH-Fc. The anodic peaks of DA and ascorbic acid (AA) in their mixture can be well separated by the prepared electrode. Under optimum conditions linear calibration graphs were obtained over the DA concentration range 2.0 x 10(-6) to 5.0 x 10(-5) M with a correlation coefficient of 0.998 and a detection limit of 9.0 x 10(-8) M (S/N = 3). The modified electrode had been effectively applied for the assay of DA in dopamine hydrochloride injections. This work provides a simple and easy approach to selectively detect DA in the presence of AA. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1271 / 1277
页数:7
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