利用高度集成的非接触式电导检测器通过微芯片电泳快速测定人血浆中的加兰他敏

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Zhilei Li, Gangyuan Lin, Xiujuan Yang
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引用次数: 0

摘要

利用高度集成的非接触式电导检测器(CCD),采用微芯片电泳法测定了人体血浆中的加兰他敏。研究并优化了影响检测器响应的仪器参数,如激励频率和激励电压。系统研究了影响加兰他敏分离和检测的电泳条件,包括缓冲溶液组成、缓冲液pH值、缓冲液浓度、添加剂、进样时间和分离电压。在最佳条件下,峰高与人体血浆中10至160微克/升的加兰他敏浓度呈良好的线性关系,相关系数为0.9992,检出限为1.1微克/升。回收率为98.6%至102.1%。该方法灵敏、快速、简便,可替代现有的加兰他敏检测方法。此外,这种高度集成的 CCD 在临床生化分析中也大有可为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid Determination of Galantamine in Human Plasma by Microchip Electrophoresis With a Highly Integrated Contactless Conductivity Detector

A novel and rapid method was developed for the determination of galantamine in human plasma by microchip electrophoresis with a highly integrated contactless conductivity detector (CCD). The instrumental parameters affecting the response of the detector, such as excitation frequency and excitation voltage, were examined and optimized. The electrophoresis conditions that influenced the separation and detection of galantamine, including the composition of buffer solution, buffer pH, buffer concentration, additives, injection time, and separation voltage were systematically investigated. Under the optimal conditions, the peak height had a good linear relationship with the concentration of galantamine in human plasma from 10 to 160 µg/L, and the correlation coefficient was 0.9992, the limit of detection reached 1.1 µg/L. The recoveries were between 98.6% and 102.1%. This sensitive, rapid, and convenient method is a good alternative to existing methods for galantamine determination. Also, this highly integrated CCD holds great promise in clinical biochemical analysis.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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