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A parallel dual-electrode detector for capillary electrophoresis

机译:用于毛细管电泳的平行双电极检测器

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摘要

An approach to on-capillary dual-electrode detection for CE using a parallel electrode configuration has been developed. The parallel configuration provides two operating modes. In the first mode, one working electrode is held at an oxidizing potential and the second working electrode is held at a reducing potential. This results in redox cycling of analytes between the oxidized and reduced forms, enhancing sensitivity compared to single-electrode detection. In the second mode, both working electrodes are held at different oxidizing potentials. This mode provides electrochemical characterization of electrophoretic peaks. In the redox cyclying mode, signal enhancement of up to twofold was observed for the dual-electrode detection of phenolic acid standards compared to single-electrode detection. Variation in response of less than 10% from electrode to electrode was determined (at a concentration of 60 nM) indicating reproducible fabrication. LODs were determined to be as low as 5.0 nM for dual-electrode configuration. Using the dual-potential mode peak identification of targeted phenolic acids in whiskey samples were confirmed based on both migration time and current ratios.
机译:已经开发出一种使用平行电极配置对CE进行毛细管上双电极检测的方法。并行配置提供两种操作模式。在第一模式中,一个工作电极被保持在氧化电势,而第二工作电极被保持在还原电势。与单电极检测相比,这导致分析物在氧化形式和还原形式之间的氧化还原循环,从而提高了灵敏度。在第二模式中,两个工作电极被保持在不同的氧化电势。该模式提供了电泳峰的电化学表征。在氧化还原循环模式下,与单电极检测相比,酚酸标准品的双电极检测可观察到高达两倍的信号增强。确定电极之间的响应变化小于10%(浓度为60 nM),表明可重复制造。对于双电极配置,LOD被确定为低至5.0 nM。使用双电势模式,根据迁移时间和电流比,可确定威士忌样品中目标酚酸的峰鉴定。

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