Direct electrochemistry and electrocatalysis of catalase immobilized on a SWNT-nanocomposite film

被引:44
|
作者
Jiang, Hui-Jun [1 ,2 ]
Yang, Hui [3 ]
Akins, D. L. [1 ]
机构
[1] CUNY City Coll, CASI, Dept Chem, New York, NY 10031 USA
[2] Nanjing Med Univ, Sch Pharm, Nanjing 210029, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Catalase; Single-walled carbon nanotubes; Chitosan; Direct electrochemistry; Electrocatalysis;
D O I
10.1016/j.jelechem.2008.07.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Investigations are reported regarding the electrochemical performance of catalase (CAT) immobilized on a film composed of chitosan-wrapped single-walled carbon nanotubes (SWNTs), and the use of such a system as a biosensor. The immobilized CAT displays a pair of well-defined and quasi-reversible redox peaks, with a formal potential (E-01) of -0.476 V vs. SCE in 0.1 M, pH 7.0 phosphate buffer solution: also the electrochemical response indicates a surface-controlled electrode process. The dependence of formal potential on solution pH indicated that the direct electron transfer reaction of CAT is a one-electron transfer coupled with a one-proton transfer reaction. The heterogeneous electron transfer rate constant was measured as 118 s(-1), indicating electron transfer between catalase and the modified electrode surface is greatly improved over that which is typically reported in the literature. This result is likely attributed to close contacts between the electroactive centers and the SWNTs. Experimental results demonstrate that absorbed CAT exhibits remarkable electrocatalytic activities toward the reduction of oxygen, hydrogen peroxide and nitrite. Also, the modified electrode exhibited good analytical performance for the amperometric determination of hydrogen peroxide and nitrite, and might find use as a third-generation biosensor based on the direct electrochemistry of catalase. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 186
页数:6
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