4.7 Article

An on-off biosensor based on multistimuli-responsive polymer films with a binary architecture and bioelectrocatalysis

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 173, 期 -, 页码 367-376

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2012.07.016

关键词

Multi-sensitive films; Binary architecture; Biosensor; Poly(4-vinylpyridine); Poly(N,N '-diethylacrylamide); Glucose oxidase

资金

  1. National Natural Science Foundation of China [NSFC 21105004]
  2. Fundamental Research Funds for the Central Universities [2010105561]

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The films with binary architecture combining electropolymerized poly(4-vinylpyridine) (P4VP) as the inner layers and chemically polymerized poly(N,N'-diethylacrylamide) (PDEA) hydrogels containing glucose oxidase (GOD) as the outer layers were successfully prepared on electrode surface, designated as P4VP/PDEA-GOD. Cyclic voltammetric response of ferrocenedicarboxylic acid (Fc(COOH)2) at P4VP/PDEA-GOD film electrodes showed reversible on-off behaviors to environmental pH, temperature, ClO4-, and SO42- concentration. In particular, the films exhibited a very sensitive ClO4--responsive behavior toward Fc(COOH)(2) with the critical concentration as low as 0.01 M. The responsive mechanism of the films to different stimuli was discussed and explored by comparative experiments. The pH- and ClO4--sensitive properties were mainly attributed to the electrostatic interaction between P4VP inner layers and Fc(COOH)2 under different conditions, and the thermo- and SO42--responsive behaviors should be ascribed to the structure change of PDEA hydrogels in PDEA-GOD outermost layers under different conditions. The multiple stimuli-responsive films could be further used to realize multiply switchable electrochemical oxidization of glucose catalyzed by GOD immobilized in the films with Fc(COOH)(2) in solution as the mediator. The films with the unique binary architecture may open a new way to establish a foundation for fabricating a novel type of multi-controllable biosensors based on bioelectrocatalysis with immobilized enzymes. (c) 2012 Elsevier B.V. All rights reserved.

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