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电化学检测谷胱甘肽:一种吸附溶出伏安法方法。

Voltammetric detection of glutathione: an adsorptive stripping voltammetry approach.

机构信息

Departamento de Química Fundamental, Centro de Ciências Exatas e da Natureza, Universidade Federal de Pernambuco, Av. Jornalista Anibal Fernandes, s/no Cidade Universitária - Recife, PE, Brazil - CEP 50.740-560.

Department of Chemistry, Physical and Theoretical Chemistry Laboratory, Oxford University, South Parks Road, Oxford, OX1 3QZ, UK.

出版信息

Analyst. 2016 May 10;141(10):2904-10. doi: 10.1039/c6an00550k.

Abstract

A simple, sensitive, and rapid detection of glutathione by cyclic voltammetry using a bare glassy carbon electrode is reported in which glutathione forms a 1 : 1 complex compound with copper(ii) ions. This complex compound is adsorbed onto the electrode surface and undergoes electrochemical oxidation at a characteristic oxidation potential of ca. -0.20 V vs. the standard mercury/mercurous sulphate reference electrode, which is used to detect the glutathione concentration. The linear dynamic range is obtained for a glutathione concentration from 1 μM to 12.5 μM, and the sensitivity is found to be 0.1 ± 0.002 μA μM(-1). A low limit of detection (n = 3) of 0.14 μM and a precision of 1.8% are achieved using a simple, unmodified electrode. The robustness of the present methodology is demonstrated by the successful quantitative analysis of glutathione in the presence of cysteine.

摘要

本文报道了一种利用裸玻碳电极通过循环伏安法简单、灵敏、快速检测谷胱甘肽的方法,其中谷胱甘肽与铜(ii)离子形成 1:1 络合物。该络合物被吸附到电极表面,并在特征氧化电位约为-0.20 V(相对于标准汞/硫酸亚汞参比电极)下发生电化学氧化,用于检测谷胱甘肽浓度。谷胱甘肽浓度在 1 μM 至 12.5 μM 范围内呈线性动态范围,灵敏度为 0.1±0.002 μA μM(-1)。使用简单的未经修饰的电极,检测限(n=3)低至 0.14 μM,精密度为 1.8%。本方法的稳健性通过在半胱氨酸存在下成功定量分析谷胱甘肽得到了证明。

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