Amperometric glucose biosensor based on entrapment of glucose oxidase in a poly(3,4-ethylenedioxythiophene) film

被引:99
|
作者
Nien, Po-Chin
Tung, Tsai-Shih
Ho, Kuo-Chuan [1 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
关键词
biosensor; ferrocene; glucose; glucose oxidase; poly(3,4-ethylenedioxythiophene);
D O I
10.1002/elan.200603552
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, conducting polymer, poly (3,4-ethyl enedioxythiophene) (PEDOT), is used as a matrix for the entrapment of glucose oxidase (GOD) and served as the working electrode for sensing glucose. The monomer, EDOT, is electropolymerized onto the platinum electrode by the cyclic voltammetric (CV) technique, scanned between 0.2 and 1.2 V (vs. Ag/AgCl/saturated KCl) in a phosphate buffer solution (PBS) containing GOD, which is entrapped into the PEDOT film simultaneously. The biosensor senses the reoxidative current of the mediator, ferricinium ions, with a constant applied potential of 0.35 V in the sensing system containing a phosphate buffer solution, ferricinium ions, and glucose. The indirect electrochemical method can efficiently reduce the sensing potential of the glucose. The sensing results show that the linear range of the calibration curve for the glucose concentration lies between 0.1 and 10.0 mM, which is a suitable level in the human body. Besides, the limit of detection and sensing sensitivity on glucose for the biosensor are 0.13 mM and 12.42 mA cm(-2) M-1, respectively. The response time of the biosensor, which is defined as the reaction current reaching 95% of the steady-state current, is about 4 - 10 s. In the aspects of interferences on ascorbic acid (AA) and uric acid (UA), the sensing currents increased about 9.7% and 39.1%, respectively, when compared to the sensing current of glucose. Moreover, the biosensor shows a good stability in which the sensing current of the electrode retains 80% of its original one over a period of 18 days.
引用
收藏
页码:1408 / 1415
页数:8
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