A versatile strategy for electrochemical detection of hydrogen peroxide as well as related enzymes and substrates based on selective hydrogen peroxide-mediated boronate deprotection

被引:28
作者
Hu, Lianzhe [1 ,2 ]
Han, Shuang [1 ,2 ]
Liu, Zhongyuan [1 ]
Parveen, Sairna [1 ,2 ,3 ]
Yuan, Yali [1 ,2 ]
Xu, Guobao [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Changchun 130022, Jilin, Peoples R China
[3] Islamia Univ Bahawalpur, Dept Chem, Bahawalpur, Pakistan
基金
中国国家自然科学基金;
关键词
Electrochemistry; Borates; Biosensors; Glucose; Peroxides; GLUCOSE-OXIDASE; ELECTRODES; NANOPARTICLES; IMMUNOASSAY; BIOSENSORS;
D O I
10.1016/j.elecom.2011.10.016
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We reported a versatile strategy for electrochemical determination of H(2)O(2) as well as related enzymes and substrates by combining the advantages of H(2)O(2)-mediated selective boronate deprotection and p-aminophenol for the first time. H(2)O(2) is selectively detected through the determination of p-aminophenol generated from H(2)O(2)-mediated boronate deprotection of p-aminophenylboronic acid. This method allows H(2)O(2) detection in the range from 1 mu M to 1 mM with a detection limit of 0.8 mu M. Since many enzymes and their substrates can be detected through the determination of H(2)O(2), we extend this method to detect related enzymes and their substrates using glucose and glucose oxidase as representative analytes. There is a good linear relationship between the current responses and GOx activity from 0.01 U/mL to 0.8 U/mL with a detection limit of 0.01 U/mL. The method is promising for broad and important applications, such as driver alcohol detection as well as clinical analysis of glucose, uric acid, lactate, glutamate, and so on. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1536 / 1538
页数:3
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