A reagentless biosensor of nitric oxide based on direct electron transfer process of cytochrome C on multi-walled carbon nanotube

被引:13
|
作者
Zhao, GC [1 ]
Yin, ZZ [1 ]
Wei, XW [1 ]
机构
[1] Anhui Normal Univ, Sch Chem & Mat Sci, Anhui Key Lab Funct Mol Solids, Wuhu 241000, Peoples R China
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2005年 / 10卷
关键词
cytochrome c; multi-walled carbon nanotube; direct electron- transfer; biosensor;
D O I
10.2741/1675
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Direct electron transfer between Cytochrome c (Cyt.c) and electrode can be achieved through immobilizing Cyt.c on the surface of multi-walled carbon nanotubes (MWNTs). Under the condition of cyclic potential scans, Cyt.c can be adsorbed on the surface of MWNTs that were modified on a glassy carbon (GC) electrode to form an approximate monolayer. The redox characteristic and bioactivity of Cyt.c could be remained after it was adsorbed on MWNTs' surface. This provides a way to construct a new biosenser based on the activity of Cyt.c. Further investigation displayed that Cyt.c adsorbed on MWNTs showed an enzyme-like activity to catalyze the reduction of nitric oxide (NO). Due to catalyzing by Cyt.c, the reduction of NO in aqueous solution was achieved, which reductive potential appeared at -0.747V (vs. SCE). The peak currents were linearly proportional to concentration of NO in the range from 2 to 48 mu mol/l with a limit of detection of 1.3 mu M. The biosensor showed a good stability and excellent repeatability.
引用
收藏
页码:2005 / 2010
页数:6
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