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基于固定在胶体金修饰碳糊电极上的葡萄糖氧化酶直接电子转移的无试剂葡萄糖生物传感器。

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

作者信息

Liu Songqin, Ju Huangxian

机构信息

Department of Chemistry, Institute of Analytical Science, State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, China.

出版信息

Biosens Bioelectron. 2003 Nov 30;19(3):177-83. doi: 10.1016/s0956-5663(03)00172-6.

DOI:10.1016/s0956-5663(03)00172-6
PMID:14611752
Abstract

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 microA/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.

摘要

研究了吸附在胶体金修饰碳糊电极上的葡萄糖氧化酶(GOD)的直接电化学。在0.1 M pH 5.0磷酸盐缓冲溶液中,吸附的GOD呈现出一对形式电位为-(449±1) mV的氧化还原峰。该响应显示为表面控制的电极过程,在10至100 mV/s的扫描速率范围内测定的电子转移速率常数为(38.9±5.3)/s。吸附在金胶体纳米颗粒上的GOD保持其生物活性和稳定性。固定化的GOD可电催化溶解氧的还原,并导致还原峰电流大幅增加。加入葡萄糖后,还原峰电流降低,可用于高灵敏度(8.4 μA/mM)的葡萄糖检测,线性范围为0.04至0.28 mM,在信噪比为3σ时检测限为0.01 mM。该传感器可排除常见共存尿酸和抗坏血酸的干扰。

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