Determination of isoproterenol and uric acid by voltammetric method using carbon nanotubes paste electrode and p-chloranil

被引:56
作者
Ensafi, Ali A. [1 ]
Dadkhah, Maryam [1 ]
Karimi-Maleh, H. [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran
关键词
Isoproterenol and uric acid determination; Carbon nanotubes paste electrode; p-Chloranil; Electrocatalytic effect; Voltammetry; PERFORMANCE LIQUID-CHROMATOGRAPHY; INJECTION SPECTROPHOTOMETRIC DETERMINATION; PHARMACEUTICAL DOSAGE FORMS; ELECTROCATALYTIC DETERMINATION; ASCORBIC-ACID; ELECTROCHEMICAL DETECTION; AMPEROMETRIC DETECTION; SILICA-GEL; CATECHOLAMINES; ISOPRENALINE;
D O I
10.1016/j.colsurfb.2010.12.028
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An electrochemical method is described for the voltammetric determination of isoproterenol in the presence of uric acid using p-chloranil-carbon nanotubes paste electrode. Cyclic voltammetric, chronoamperometric, and electrochemical impedance spectroscopic methods have used to investigate the suitability of p-chloranil as a mediator for the electrocatalytic oxidation of isoproterenol at pH = 10.5. Using differential pulse voltammetry, isoproterenol (ISPT) and uric acid (UA) in a mixture can be measured simultaneously and individually with a potential difference of 360 mV. The electrocatalytic currents increase linearly with ISPT and UA concentrations over the concentration ranges of 0.015-100 mu mol L(-1) ISPT and 3.0-310 mu mol L(-1) UA. The detection limits for ISPT and UA were equal to 0.009 and 2.3 mu mol L(-1), respectively. The diffusion coefficient and the kinetic parameters such as electron transfer coefficient and heterogeneous rate constant were determined for ISPT, using the electrochemical approaches. The proposed method was successfully applied to the determination of isoproterenol in both ampoule and urine samples. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:148 / 154
页数:7
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