Graphene/polyaniline/gold nanoparticles nanocomposite for the direct electron transfer of glucose oxidase and glucose biosensing

被引:152
作者
Xu, Qin [1 ]
Gu, Sai-Xi [1 ,2 ]
Jin, Longyun [1 ]
Zhou, Yue-e [1 ]
Yang, Zhanjun [1 ]
Wang, Wei [2 ]
Hu, Xiaoya [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Peoples R China
[2] Yancheng Inst Technol, Sch Chem & Biol Engn, Yancheng 224051, Peoples R China
关键词
Graphene/polyaniline/AuNPs; Glucose oxidase; Direct electrochemistry; Biosensor; DIRECT ELECTROCHEMISTRY; CARBON NANOTUBES; HYDROGEN-PEROXIDE; ELECTROCATALYTIC ACTIVITY; ENZYME; FABRICATION; IMMOBILIZATION; LAYER; FILM;
D O I
10.1016/j.snb.2013.09.049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel glucose biosensor was developed based on the direct electrochemistry of glucose oxidase (GOD) adsorbed in graphene/polyaniline/gold nanoparticles (AuNPs) nanocomposite modified glassy carbon electrode (GCE). Compared with graphene, polyanilline (PANI) or graphene/PANI, the graphene/PANI/AuNPs nanocomposite was more biocompatible and it offered a favorable microenvironment for facilitating the direct electron transfer between GOD and electrode. The adsorbed GOD displayed a pair of well-defined quasi-reversible redox peaks with a formal potential of -0.477 V (vs. SCE) and an apparent electron transfer rate constant (k(s)) of 4.8 s(-1) in 0.1 M pH 7.0 PBS solution. The apparent Michaelis-Menten constant of the adsorbed GOD was 0.60 mM, implying a fabulous catalytic activity and a remarkable affinity of the adsorbed GOD for glucose. The amperometric response of GOD-graphene/PANI/AuNPs modified electrode was linearly proportional to the concentration of glucose in the range of 4.0 mu M to 1.12 mM with a low detection limit of 0.6 mu M at signal-to-noise of 3. The combination of the direct electron transfer character of GOD and the promising feature of graphene/PANI/AuNPs nanocomposite favors the selective and sensitive determination of glucose with improved analytical capabilities. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:562 / 569
页数:8
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