Third-generation superoxide anion sensor based on superoxide dismutase directly immobilized by sol-gel thin film on gold electrode

被引:91
作者
Di, JW
Bi, SP [1 ]
Zhang, M
机构
[1] Nanjing Univ, Dept Chem, State Key Lab Coordinat Chem China, Nanjing 210093, Peoples R China
[2] Suzhou Univ, Dept Chem, Suzhou 215006, Peoples R China
关键词
duperoxide (O-2(center dot-)) sensor; duperoxide dismutase (SOD); electrochemical detection; sol-gel method;
D O I
10.1016/j.bios.2003.12.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A third-generation biosensor for superoxide anion (O-2(.-)) was developed based on superoxide dismutase (SOD) immobilized by thin silica-PVA sol-gel film on gold electrode surface. A rapid and direct electron transfer of SOD in the thin sol-gel film at the gold electrode was realized without any mediators or promoters. The characterization of the SOD electrodes showed a quasi-reversible electrochemical redox behavior with a formal potential of 80 + 5 mV (versus SCE) in 50 mmol 1(-1) phosphate buffer solution (PBS), pH 7.0. The heterogeneous electron transfer rate constant was evaluated to be about 2.1 s(-1). The anodic and cathodic transfer coefficients are 0.6 and 0.4, respectively. Based on biomolecular recognition for specific reactivity of SOD toward O-2(.-), the SOD electrode was applied to a sensitive and selective measurement Of 02*- with the low operation potential (-0.15 V versus SCE) in phosphate buffer solution, pH 7.0. The amperometric response was proportional to O-2(.-) concentration in the range of 0.2-1.6 mumol 1(-1) and the detection limit was 0.1 mumol 1(-1) at a signal-to-noise ration of 3. The preparation of SOD electrode is easy and simple. The uniform porous structure of the silica-PVA sol-gel matrix results in a fast response rate of immobilized SOD and is very efficient for stabilizing the enzyme activity. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:1479 / 1486
页数:8
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