A novel protocol for covalent immobilization of thionine on glassy carbon electrode and its application in hydrogen peroxide biosensor

被引:43
|
作者
Xu, Xingyong [2 ]
Feng, Yan [1 ]
Li, Jingjing [1 ]
Li, Feng [1 ]
Yu, Hongjun [2 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Minist Educ, Key Lab Ecochem Engn, Qingdao 266042, Peoples R China
[2] State Ocean Adm, Inst Oceanog 1, Key Lab Marine Sediment & Environm Geol, Qingdao 266061, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2010年 / 25卷 / 10期
基金
中国国家自然科学基金;
关键词
Thionine; Covalent immobilization; Potentiostatic activation; Mediator; Biosensor; HORSERADISH-PEROXIDASE; DIRECT ELECTROCHEMISTRY; AMPEROMETRIC IMMUNOSENSOR; GLUCOSE BIOSENSOR; MULTILAYER FILMS; GOLD; ELECTROCATALYSIS; NANOPARTICLES; NANOTUBES; GLUTARALDEHYDE;
D O I
10.1016/j.bios.2010.03.027
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel protocol for effectively covalent immobilization of thionine (Th) was proposed, which was based on Schiff-base reaction between -NH2 of Th and -COH which was in situ generated on glassy carbon electrode (GCE) via simple potentiostatic activation in diluted nitric acid. GCE pretreated by potentiostatic activation possessed CHO-riched surface and microporous structure with high distribution density of electron transfer sites, and thus it became a good candidate for effective immobilization of Th through imine bond with high stability. The application of the resulting Th modified electrode in hydrogen peroxide biosensor was also investigated and it exhibited rapid response to H2O2 within 3s. The linear calibration ranged from 5.0 x 10(-7) to 5.8 x 10(-3)M with a detection limit of 1.0 x 10(-7)M. The effective immobilization of Th on potentiostatically activated GCE surface has deep significance in mediator immobilization, on which further researches based are under way. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2324 / 2328
页数:5
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