pH-, Sugar-, and Temperature-Sensitive Electrochemical Switch Amplified by Enzymatic Reaction and Controlled by Logic Gates Based on Semi-Interpenetrating Polymer Networks

被引:48
|
作者
Liu, Dan [1 ]
Liu, Hongyun [1 ]
Hu, Naifei [1 ]
机构
[1] Beijing Normal Univ, Dept Chem, Beijing 100875, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2012年 / 116卷 / 05期
基金
中国国家自然科学基金;
关键词
SEMI-IPN; CONFORMATIONAL BEHAVIOR; BINARY ARCHITECTURE; FILMS; BIOELECTROCATALYSIS; SURFACES; POLYELECTROLYTE; BRUSHES; POLY(N; N-DIETHYLACRYLAMIDE); POLY(N-ISOPROPYLACRYLAMIDE);
D O I
10.1021/jp209788g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Phenylboronic acid (PBA) moieties are grafted onto the backbone of poly(acrylic acid) (PAA), forming the PAA-PBA polyelectrolyte. The semi-interpenetrating polymer network (semi-IPN) films composed of PAA-PBA and poly(N,N-diethylacrylamide) (PDEA) were then synthesized on electrode surface with entrapped horseradish peroxidase (HRP), designated as PDEA-(PAA-PBA)-HRP. The films demonstrated reversible pH-, fructose-, and thermo-responsive on-off behavior toward electroactive probe K3Fe(CN)(6) in its cyclic voltammetric (CV) response. This multiswitchable CV behavior of the system could be further employed to control and modulate the electrochemical reduction of H2O2 catalyzed by HRP immobilized in the films with K3Fe(CN)(6) as the mediator in solution. The responsive mechanism of the system was also explored and discussed. The pH-sensitive property was attributed to the electrostatic interaction between the PAA component of the films and the probe at different pH; the thermo-responsive behavior originated from the structure change of PDEA hydrogel component of the films with temperature; the fructose-sensitive property was ascribed to the structure change of the films induced by the complexation between the PBA constituent and the sugar. This smart system could be used as a 3-input logic network composed of enabled OR (EnOR) gates in chemical or biomolecular computing by combining the multiresponsive property of the films and the amplification effect of bioelectrocatalysis and demonstrated the potential perspective for fabricating novel multiswitchable electrochemical biosensors and bioelectronic devices.
引用
收藏
页码:1700 / 1708
页数:9
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