A novel nanobiocomposite based glucose biosensor using neutral red functionalized carbon nanotubes

被引:95
作者
Jeykumari, D. R. Shobha [1 ]
Narayanan, S. Sriman [1 ]
机构
[1] Univ Madras, Sch Chem Sci, Dept Analyt Chem, Madras 600025, Tamil Nadu, India
关键词
multiwalled carbon nanotubes; nanobiocomposite; Nafion; glucose biosensor;
D O I
10.1016/j.bios.2007.12.007
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The performance of a new glucose biosensor based on the combination of biocatalytic activity of glucose oxidase (GOx) with the electrocatalytic properties of CNTs and neutral red (NR) for the determination of glucose is described. This sensor is comprised of a multiwalled carbon nanotubes (MWNTs) conduit functionalized with NR and Nafion (Nf) as a binder and glucose oxidase as a biocatalyst. Neutral red was covalently immobilized on carboxylic acid groups of the CNTs via carbodiimide reaction. The functionalized MWNTs were characterized by microscopic, spectroscopic and thermal methods. The MWNT-NR-GOx-Nf nanobiocomposite was prepared by mixing the GOx solution with NR functionalized CNTs followed by mixing homogeneously with Nation. The performance of the MWNT-NR-GOx-Nf nanobiocomposite modified electrode was examined by electrochemical impedance spectroscopy and cyclic voltammetry. The catalytic reduction of hydrogen peroxide liberated from the enzymatic reaction of glucose oxidase upon glucose with NR functionalized CNTs leads to the selective detection of glucose. The excellent electrocatalytic activity and the influence of nanobiocomposite film result in good characteristics such as low potential detection of glucose with a large determination range from 1 x 10(-8) to 1 x 10(-3) M with a detection limit of 3 x 10(-9) M glucose, a short response time (with 4 s), good stability and anti-interferent ability. The improved electrocatalytic activity and stability made the MWNT-NR-GOx-Nf nanobiocomposite biosensor system a potential platform to immobilize different enzymes for other bioelectrochemical applications. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:1404 / 1411
页数:8
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