人体生物体液内源性成分的电化学SERS研究

N. E. Markina, A. Zakharevich, A. Markin
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摘要

本文描述了一种适合于制备铜电极的电化学(EC)方法,这种铜电极可以用作表面增强拉曼光谱(SERS)的衬底。这些SERS活性电极已被用于基于电化学和SERS分析(EC-SRS分析)相结合的电谱研究。本研究选择了几种内源性体液成分(尿素、肌酐、尿酸、胆红素),因为它们可以显著影响基于sers的体液中其他分析物(例如药物)的测定。研究了SERS活性电极极化(外加电位)和分析溶液的pH值对SERS信号和电流值的影响。所有分析物的最大SERS信号对应的极化值均为负值(低于- 0.2 V vs.铜伪参比电极)。大多数分析物在中性介质(在SERS活性电极的最佳极化值时)中SERS信号最大,在碱性介质中SERS信号最弱。高pH值下EC-SERS信号减弱的原因是分析物分子的去质子化使分析物在负极化的sers活性电极上的吸附恶化。通过分析电流-电压曲线来估计所研究分子EC变化对其EC- sers信号可能产生的影响。本工作的结果将有助于EC-SERS系统的发展,适用于测定人体生物体液中的各种内和外源性化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical SERS study of some endogenous components of human biofluids
The work describes electrochemical (EC) protocol suitable for preparation of copper electrodes which can be used as substrates in surface-enhanced Raman spectroscopy (SERS). These SERS-active electrodes have been used for electrospectral studies based on the combination of electrochemical and SERS analysis (EC-SRS analysis). Several endogenous bodyfluid components (urea, creatinine, uric acid, bilirubin) have been selected for the study because they can significantly affect the SERS-based determination of other analytes in bodyfluids (for example, drugs). The influence of the SERS-active electrode polarization (applied potential) and the pH level of the analyte solutions on the SERS signal and current value have been investigated. The polarization values corresponded to the maximum SERS signal are observed at negative values for all analytes (below −0.2 V vs. copper pseudo-reference electrode). The maximal SERS signal has been observed for most of the analytes in a neutral medium (at the optimum polarization value of the SERS-active electrode), and the weakest signal has been in an alkaline medium. The diminishing of EC-SERS signal at high pH values is explained by deprotonation of analyte molecules that deteriorates analyte adsorption onto the negatively polarized SERS-active electrodes. Analysis of the current-voltage curves has been used to estimate the possible influence of EC changes of the studied molecules on their EC-SERS signal. The results obtained in this work will be useful for the development of EC-SERS systems suitable for the determination of various endo- and exogenous compounds in human biofluids.
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