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Pentacyanoammineferrate-Based Non-Enzymatic Electrochemical Biosensing Platform for Selective Uric Acid Measurement

机译:基于戊酰胺的非酶促电化学生物传感平台用于选择性尿酸测量

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摘要

The electrochemical-based detection of uric acid (UA) is widely used for diagnostic purposes. However, various interfering species such as ascorbic acid, dopamine, and glucose can affect electrochemical signals, and hence there is an outstanding need to develop improved sensing platforms to detect UA with high selectivity. Herein, we report a pentagonal mediator-based non-enzymatic electrochemical biosensing platform to selectively measure UA in the presence of interfering species. The working electrode was fabricated by electrodepositing polymerized 1-vinylimidazole (PVI), which has an imidazole ligand, onto indium tin oxide (ITO), and then conjugating nickel ions to the PVI-coated ITO electrode. Electrode performance was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements and integrated together with pentacyanoammineferrate, which can bind to the amine groups of UA and function as an electron transferring mediator. The experimental results showed a wide linear range of UA concentration-dependent responses and the multi-potential step (MPS) technique facilitated selective detection of UA in the presence of physiologically relevant interfering species. Altogether, these findings support that pentacyanoammineferrate-based non-enzymatic electrodes are suitable biosensing platforms for the selective measurement of UA, and such approaches could potentially be extended to other bioanalytes as well.
机译:尿酸(UA)的电化学检测广泛用于诊断目的。然而,各种干扰物种如抗坏血酸,多巴胺和葡萄糖可以影响电化学信号,因此有优异的需要开发改进的传感平台以检测具有高选择性的UA。在此,我们报告了一种基于五边形介质的非酶促电化学生物传感平台,以在干扰物种存在下选择性地测量UA。通过电沉积的聚合的1-乙烯基咪唑(PVI)制造工作电极,其具有咪唑配体,在氧化铟锡(ITO)上,然后将镍离子缀合至PVI涂覆的ITO电极。电极性能的特征在于循环伏安法(CV)和电化学阻抗光谱(EIS)测量并与五环素萌生酸盐一起集成,其可以与UA的胺基结合并用作电子转移介体的功能。实验结果表明,在生理相关的干扰物种存在下,多电位步骤(MPS)技术有助于UA的选择性检测,具有宽的UA浓度依赖性响应和多电位步骤(MPS)技术。总共,这些发现支持基于五环素的非酶促电极是适合于UA的选择性测量的合适的生物传感平台,并且这些方法也可能延伸到其他生物分析。

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