A novel conducting polymer based platform for ethanol sensing

被引:19
|
作者
Kekec, Nur Cicek [1 ]
Kanik, Fulya Ekiz [2 ]
Udum, Yasemin Arslan [3 ]
Hizliates, Cevher Gundogdu [4 ]
Ergun, Yavuz [4 ]
Toppare, Levent [1 ,2 ,5 ,6 ]
机构
[1] Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey
[2] Middle E Tech Univ, Dept Biotechnol, TR-06800 Ankara, Turkey
[3] Gazi Univ, Inst Sci & Technol, Dept Adv Technol, TR-06570 Ankara, Turkey
[4] Dokuz Eylul Univ, Fac Sci, Dept Chem, TR-35160 Izmir, Turkey
[5] Middle E Tech Univ, Dept Polymer Sci & Technol, TR-06800 Ankara, Turkey
[6] Middle E Tech Univ, Ctr Solar Energy Res & Applicat GUNAM, TR-06800 Ankara, Turkey
来源
关键词
Conducting polymer; Ethanol biosensor; Alcohol oxidase; Covalent immobilization; ALCOHOL OXIDASE; AMPEROMETRIC BIOSENSOR; POLYPYRROLE; MATRIX; ACID;
D O I
10.1016/j.snb.2013.12.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Anew amperometric ethanol biosensor was fabricated for sensitive and rapid analysis of ethanol. For this purpose, a novel monomer, 9-methyl-9H-carbazole-3-carbohydrazine (MCCH), was designed and electrochemically polymerized on a graphite electrode to achieve a conducting and effective immobilization matrix for enzyme immobilization. Due to the presence of amino groups in the structure of conducting polymer, alcohol oxidase molecules were covalently immobilized onto the functional polymer which brought an effective and long-life analysis of the substrate, ethanol. N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC)/N-hydroxysuccinimide (NHS) chemistry was used for linking carboxylic acid groups of the enzyme molecules with amino groups of the polymer. After successful immobilization, amperometric biosensor responses were recorded at 0.7V vs. Ag/AgCl in phosphate buffer (pH 7.0). K-M(app) (8.74 mM), I-max (5.94 mu A), LOD (0.131 mM) and sensitivity (4.79 mu A mM(-1) cm(-2)) values were determined. Finally, the prepared biosensor was successfully applied for determination of ethanol content in alcoholic beverages. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:306 / 314
页数:9
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