A new hydrogen peroxide biosensor based on synergy of Au@Au2S2O3 core-shell nanomaterials and multi-walled carbon nanotubes towards hemoglobin

被引:19
|
作者
Li, Yuanjun [1 ]
Huang, Fuying [1 ]
Luo, Zhuanxi [2 ]
Xu, Bin [2 ]
Wang, Xinxing [1 ]
Li, Feiming [1 ]
Wang, Fei [1 ]
Huang, Lixia [1 ]
Li, Shunxing [1 ]
Li, Yancai [1 ]
机构
[1] Zhangzhou Normal Univ, Dept Chem, Zhangzhou 363000, Peoples R China
[2] Chinese Acad Sci, Inst Urban Environm, Xiamen 361021, Peoples R China
基金
中国国家自然科学基金;
关键词
H2O2; biosensor; Au@Au2S2O3; Core@shell nanomaterials; Hemoglobin; Multi-walled carbon nanotubes; DIRECT ELECTRON-TRANSFER; BY-LAYER FILMS; DIRECT ELECTROCHEMISTRY; COMPOSITE FILM; GOLD NANORODS; OPTICAL-PROPERTIES; NANOPARTICLES; MYOGLOBIN; ELECTROCATALYSIS; FABRICATION;
D O I
10.1016/j.electacta.2012.04.097
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A new H2O2 biosensor was constructed by immobilizing Hb in the Chit-MWNTs/Au@Au2S2O3 composite membrane. Owing to the superior performance of novel Au@Au2S2O3 core-shell nanomaterials and its synergy with multi-walled carbon nanotubes (MWNTs), the direct electron transfer of Hb in composite membrane was easily achieved. The Chit-MWNTs/Hb/Au@Au2S2O3/CCE displayed a pair of well-defined and reversible redox peaks in 0.1 M pH 7.0 PBS. The electrocatalytic reduction to H2O2 of Chit-MWNTs/Hb/Au@Au2S2O3/GCE was also studied. Its apparent Michaelis-Menten constant for H2O2 was 0.014 mM, showing a good affinity. The experimental results showed that the linear dependence of the biosensor was from 4.0 x 10(-5) to 7.2 x 10(-4) M, and the detection limit of the sensor was 3.2 x 10(-6) M (S/N = 3). Moreover, the biosensor showed a rapid response to H2O2, a good stability and reproducibility. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:280 / 286
页数:7
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