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Simultaneous determination of uric acid and ascorbic acid at a ferrocenium–thioglycollate modified electrode

机译:铈-巯基乙酸铁修饰电极同时测定尿酸和抗坏血酸

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摘要

Self-assembled monolayers (SAMS) of chemisorbed thioglycollate on a gold electrode surface have been used as a base interface for the electrostatic adsorption of ferrocenium ion. Electrochemical impedance spectra (EIS) and cyclic voltammetry (CV) were used to evaluate the electrochemical properties of the supramolecular film. The bare gold electrode failed to distinguish the oxidation peaks of ascorbic acid (AA) and uric acid (UA) in phosphate buffer solution (PBS, pH 7.0), while the ferricinium–thioglycollate modified electrode could separate them efficiently. In differiential pulse voltammetric measurements, the prepared gold electrode could separate AA and UA signals, allowing the simultaneous determination of AA and UA. Under optimal conditions and within the linear range of 1.0 × 10−6 to 5.0 × 10−4 M, the detection limits of AA and UA achieved were 2.0 × 10−7 and 1.0 × 10−7 M, respectively. The applicability of the prepared electrode was demonstrated by measuring AA and UA in human urine without any pretreatment.
机译:在金电极表面上化学吸附的巯基乙酸盐的自组装单层(SAMS)已用作静电吸附二茂铁离子的基础界面。电化学阻抗谱(EIS)和循环伏安法(CV)用于评估超分子膜的电化学性能。裸金电极未能区分磷酸盐缓冲溶液(PBS,pH 7.0)中抗坏血酸(AA)和尿酸(UA)的氧化峰,而硫代乙醇酸铁修饰的电极可以有效地将它们分离。在差分脉冲伏安法测量中,准备好的金电极可以分离AA和UA信号,从而可以同时测定AA和UA。在最佳条件下,并且在1.0×10−6 到5.0×10−4 M的线性范围内,AA和UA的检出限分别为2.0×10−7 和1.0 ×10−7 M。无需任何预处理即可通过测量人尿中的AA和UA来证明所制备电极的适用性。

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