Electrochemical sensing platform based on covalent immobilization of thionine onto gold electrode surface via diazotization-coupling reaction

被引:7
作者
Li, Feng [1 ]
Feng, Yan [1 ]
Yang, Limin [1 ]
Liu, Shufeng [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Shandong Prov Key Lab Biochem Anal, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Thionine; Covalent immobilization; Diazotization-coupling reaction; 4; Aminothiophenol; Sensor; GLASSY-CARBON ELECTRODE; LAYER ASSEMBLY FILMS; HORSERADISH-PEROXIDASE; HYDROGEN-PEROXIDE; AMPEROMETRIC IMMUNOSENSOR; BIOSENSOR; NANOPARTICLES; MULTILAYER; MONOLAYER; NANOTUBES;
D O I
10.1016/j.talanta.2010.09.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel electrochemical sensing platform by modification of electroactive thionine (Th) onto gold electrode surface was constructed which was realized by diazotization of 4-aminothiophenol (ATP) self-assembled monolayer followed by coupling of Th with the diazonium group to form a covalent diazo bond A pair of well-defined redox peaks of Th was observed in the cyclic voltammetric measurement The resulting diazo-ATP monolayer displayed superior electrical conductivity which contributed to I he sensitive detection of hydrogen peroxide (H(2)O(2)) The immobilized Th also showed a remarkable stability which may benefit from the pi-pi stacking force and the covalent diazo bond between diazo-ATP and Th molecules Under the optimized experimental conditions the current fabricated non-enzyme and reagentless sensor could show a rapid response to H(2)O(2) within 3s and a linear calibration plot ranged from 1 0 x 10(-6) to 638 x 10(-3) M with a detection limit of 67 x 10(-7) M The current fabrication strategy of electroactive interface is expected to be used as a versatile route for the immobilization of more electroactive molecules and offer more opportunities for the applications in electrochemical sew or biosensor electrocatalysis etc (C) 2010 Elsevier 8 V All rights reserved
引用
收藏
页码:205 / 209
页数:5
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