An amperometric urea biosensor based on covalently immobilized urease on an electrode made of hyperbranched polyester functionalized gold nanoparticles

被引:91
|
作者
Tiwari, Ashutosh [1 ]
Aryal, Santosh [1 ]
Pilla, Srikanth [1 ]
Gong, Shaoqin [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Mech Engn, Milwaukee, WI 53211 USA
[2] Univ Wisconsin, Dept Mat, Milwaukee, WI 53211 USA
基金
美国国家科学基金会;
关键词
Urea biosensor; Amperometric detection; Covalent immobilization; Boltron (R) H40; Gold nanoparticles; ENZYME-ELECTRODE; ELECTROCHEMICAL DETECTION; BLOOD-SAMPLES;
D O I
10.1016/j.talanta.2009.02.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An amperometric biosensor was fabricated for the quantitative determination of urea in aqueous medium using hematein, a pH-sensitive natural dye. The urease(Urs) was covalently immobilized onto an electrode made of gold nanoparticles functionalized with hyperbranched polyester-Boltron (R) H40 (H40-Au) coated onto an indium-tin oxide (ITO) covered glass substrate. The covalent linkage between the Urs enzyme and H40-Au nanoparticles provided the resulting enzyme electrode (Urs/H40-Au/ITO) with a high level of enzyme immobilization and excellent lifetime stability. The response studies were carried out as a function of urea concentration with amperometric and photometric measurements. The biosensor based on Urs/H40-Au/ITO as the working electrode showed a linear current response to the urea concentration ranging from 0.01 to 35 mM. The urea biosensor exhibited a sensitivity of 7.48 nA/mM with a response time of 3s. The Michaelis-Menten constant for the Urs/H40-Au/ITO biosensor was calculated to be 0.96 mM, indicating the Urs enzyme immobilized on the electrode surface had a high affinity to Urea. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1401 / 1407
页数:7
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