Reagentless glucose biosensor based on direct electron transfer of glucose oxidase immobilized on colloidal gold modified carbon paste electrode

被引:439
作者
Liu, SQ [1 ]
Ju, HX [1 ]
机构
[1] Nanjing Univ, State Key Lab Coordinat Chem, Inst Analyt Sci, Dept Chem, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
biosensors; carbon paste electrode; glucose oxidase; electrocatalysis; colloidal gold; glucose;
D O I
10.1016/S0956-5663(03)00172-6
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The direct electrochemistry of glucose oxidase (GOD) adsorbed on a colloidal gold modified carbon paste electrode was investigated. The adsorbed GOD displayed a pair of redox peaks with a formal potential of -(449 +/- 1) mV in 0.1 M pH 5.0 phosphate buffer solution. The response showed a surface-controlled electrode process with an electron transfer rate constant of (38.9 +/- 5.3)/s determined in the scan rate range from 10 to 100 mV/s. GOD adsorbed on gold colloid nanoparticles maintained its bioactivity and stability. The immobilized GOD could electrocatalyze the reduction of dissolved oxygen and resulted in a great increase of the reduction peak current. Upon the addition of glucose, the reduction peak current decreased, which could be used for glucose detection with a high sensitivity (8.4 muA/mM), a linear range from 0.04 to 0.28 mM and a detection limit of 0.01 mM at a signal-to-noise ratio of 3sigma. The sensor could exclude the interference of commonly coexisted uric and ascorbic acid. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 183
页数:7
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