Immobilization of uricase on ZnO nanorods for a reagentless uric acid biosensor

被引:332
作者
Zhang, FF
Wang, XL
Ai, SY
Sun, ZD
Wan, Q
Zhu, ZQ
Xian, YZ
Jin, LT [1 ]
Yamamoto, K
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
[2] E China Normal Univ, Dept Elect Engn, Shanghai 200062, Peoples R China
[3] BAS Co Ltd, Sumida Ku, Tokyo 131, Japan
基金
中国国家自然科学基金;
关键词
reagentless biosensor; ZnO nanorods; uricase; uric acid;
D O I
10.1016/j.aca.2004.05.070
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A reagentless uric acid (UA) biosensor based on uricase immobilized on ZnO nanorods was developed. Direct electrochemistry and thermal stability of immobilized uricase were studied. The ZnO nanorods derived electrode retained the enzyme bioactivity and could enhance the electron transfer between the enzyme and the electrode. This sensor showed a high thermal stability up to 85 degreesC and an electrocatalytic activity to the oxidation of uric acid without the presence of an electron mediator. The electrocatalytic response showed a linear dependence on the uric acid concentration ranging from 5.0 x 10(-6) to 1.0 x 10(-3) mol L-1 with a detection limit of 2.0 x 10(-6) mol L-1 at 3sigma. The apparent K-M(app) value for the uric acid sensor was estimated to be 0.238 mM, showing a high affinity. (C) 2004 Published by Elsevier B.V.
引用
收藏
页码:155 / 160
页数:6
相关论文
共 35 条
[1]  
BOWERS LD, 1986, ANAL CHEM, V58, P513
[2]   Conductometric uric acid and urea biosensor prepared from electroconductive polyaniline-poly(n-butyl methacrylate) composites [J].
Castillo-Ortega, MM ;
Rodriguez, DE ;
Encinas, JC ;
Plascencia, M ;
Méndez-Velarde, FA ;
Olayo, R .
SENSORS AND ACTUATORS B-CHEMICAL, 2002, 85 (1-2) :19-25
[3]   ELECTRODE SYSTEMS FOR CONTINUOUS MONITORING IN CARDIOVASCULAR SURGERY [J].
CLARK, LC ;
LYONS, C .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1962, 102 (01) :29-&
[4]   DETECTION OF GALACTOSE AND LACTOSE BY A POLY(AMPHIPHILIC PYRROLE)-GALACTOSE OXIDASE ELECTRODE [J].
COSNIER, S ;
INNOCENT, C .
ANALYTICAL LETTERS, 1994, 27 (08) :1429-1442
[5]   DIRECT ELECTRICAL COMMUNICATION BETWEEN CHEMICALLY MODIFIED ENZYMES AND METAL-ELECTRODES .2. METHODS FOR BONDING ELECTRON-TRANSFER RELAYS TO GLUCOSE-OXIDASE AND D-AMINO-ACID OXIDASE [J].
DEGANI, Y ;
HELLER, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (08) :2615-2620
[6]  
FIRTIER G, 1992, ELECTROANAL, V4, P275
[7]   Enzyme-catalyzed direct electron transfer: Fundamentals and analytical applications [J].
Ghindilis, AL ;
Atanasov, P ;
Wilkins, E .
ELECTROANALYSIS, 1997, 9 (09) :661-674
[8]   Direct electron transfer between heme-containing enzymes and electrodes as basis for third generation biosensors [J].
Gorton, L ;
Lindgren, A ;
Larsson, T ;
Munteanu, FD ;
Ruzgas, T ;
Gazaryan, I .
ANALYTICA CHIMICA ACTA, 1999, 400 :91-108
[9]   Direct electron transfer and characterization of hemoglobin immobilized on a Au colloid-cysteamine-modified gold electrode [J].
Gu, HY ;
Yu, AM ;
Chen, HY .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 516 (1-2) :119-126
[10]   Regularly shaped, single-crystalline ZnO nanorods with wurtzite structure [J].
Guo, L ;
Ji, YL ;
Xu, HB ;
Simon, P ;
Wu, ZY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (50) :14864-14865