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一种用于测定尿酸的安培型生物传感器,由固定在聚吡咯膜中的尿酸酶制备而成。

An amperometric biosensor for uric acid determination prepared from uricase immobilized in polypyrrole film.

作者信息

Cete Servet, Yaşar Ahmet, Arslan Fatma

机构信息

Department of Chemistry, Faculty of Arts and Sciences, Gazi University, Ankara, Turkey.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 2006;34(3):367-80. doi: 10.1080/10731190600684116.

Abstract

In order to prepare a biosensor for the determination of uric acid, electropolymerization of pyrrole on Pt surface was carried out with an electrochemical cell containing pyrrole, ferrocene (as a electron mediator) and tetrabutylammonium tetrafluoroborat in acetonitrile by cyclic voltammetry between 0.0 and 1.0 V (vs. Ag/AgCl) at a scan rate of 50 mV/s upon Pt electrode. Uricase was immobilized by a glutaraldehyde/gelatine croslinking procedure on to polypyrrole film after the electropolymerization processes. The response of the biosensor against uric acid was measured after 330 seconds following the application of a constant potential of +0.7 V (vs. Ag/AgCl). The resulting biosensor exhibits excellent electrocatalysis for the uric acid. The amperometric determination is based on the electrochemical detection of H2O2, which is generated in enzymatic reaction of uric acid. The sensor responds to uric acid with a detection limit of 5.0 x 10(-7) M. The sensor remains relatively stable for 5 weeks. Interference effect were investigated on the amperometric response of the biosensor. Determination of uric acid was carried out in the biological fluids by biosensor.

摘要

为了制备用于测定尿酸的生物传感器,在含有吡咯、二茂铁(作为电子媒介体)和四氟硼酸四丁铵的乙腈电化学池中,采用循环伏安法在铂电极上于0.0至1.0 V(相对于Ag/AgCl)、扫描速率为50 mV/s的条件下进行吡咯在铂表面的电聚合。在电聚合过程之后,通过戊二醛/明胶交联程序将尿酸酶固定在聚吡咯膜上。在施加 +0.7 V(相对于Ag/AgCl)的恒定电位330秒后,测量生物传感器对尿酸的响应。所得生物传感器对尿酸表现出优异的电催化作用。安培测定法基于对尿酸酶促反应中产生的H2O2的电化学检测。该传感器对尿酸的响应检测限为5.0×10(-7) M。该传感器在5周内保持相对稳定。研究了干扰对生物传感器安培响应的影响。通过生物传感器在生物体液中进行尿酸的测定。

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