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毛细管电泳中采用安培检测的场放大进样用于非对映异构麻黄碱生物碱的超痕量分析。

Field-amplified sample injection in capillary electrophoresis with amperometric detection for the ultratrace analysis of diastereomeric ephedrine alkaloids.

作者信息

Chen Xiaoyan, Tang Yanxia, Wang Shaoyun, Song Yunping, Tang Fengxiang, Wu Xiaoping

机构信息

Ministry of Education and Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, College of Chemistry, Fuzhou University, Fuzhou, Fujian, P. R. China.

Fujian Metrology Institute, Fuzhou, Fujian, P. R. China.

出版信息

Electrophoresis. 2015 Aug;36(16):1953-61. doi: 10.1002/elps.201500024.

DOI:10.1002/elps.201500024
PMID:25873262
Abstract

A coupling method of field-amplified sample injection (FASI) CE with amperometric detection is developed for ultratrace analysis of ephedrine alkaloids stereoisomers. FASI was introduced by injecting electrokinetically the sample solution for 10 s into the capillary filled with highly conductive background electrolyte (BGE). The diastereomeric selectivity and the detection sensitivity were improved by using borate buffer of high ionic strength as BGE. Parameters affecting FASI and CE separation were investigated to achieve the optimal conditions. Four analytes were separated within 15 min using 200 mmol/L borate buffer (pH 9.5) and separation voltage of +18 kV, with detection potential at +1.0 V (vs. Ag/AgCl) and carbon disc electrode as working electrode. Excellent linearity was observed between peak current and concentration of analytes in the range of 0.1-100 ng/mL. The LODs (S/N = 3) for (-)-ephedrine, (+)-pseudoephedrine, (-)-N-methylephedrine and (+)-N-methylpseudoephedrine were 39.3, 54.9, 30.8, and 44.1 pg/mL, respectively. The proposed method was successfully applied to the determination of alkaloids in Ephedra sinica, with results agreed well with HPLC method. Mean recoveries of 102.1-109.7% and RSDs less than 6% were found. And the merits of high sensitivity and selectivity, as well as a simple and stable operation, have been demonstrated.

摘要

建立了一种场放大进样(FASI)毛细管电泳与安培检测联用的方法,用于麻黄碱生物碱立体异构体的超痕量分析。通过将样品溶液电动注入充满高导电背景电解质(BGE)的毛细管中10 s来实现FASI。使用高离子强度的硼酸盐缓冲液作为BGE,提高了非对映体选择性和检测灵敏度。研究了影响FASI和毛细管电泳分离的参数,以实现最佳条件。使用200 mmol/L硼酸盐缓冲液(pH 9.5)和+18 kV的分离电压,在15分钟内分离出四种分析物,检测电位为+1.0 V(相对于Ag/AgCl),工作电极采用碳盘电极。在0.1 - 100 ng/mL范围内,分析物的峰电流与浓度之间呈现出良好的线性关系。(-)-麻黄碱、(+)-伪麻黄碱、(-)-N-甲基麻黄碱和(+)-N-甲基伪麻黄碱的检测限(S/N = 3)分别为39.3、54.9、30.8和44.1 pg/mL。该方法成功应用于麻黄中生物碱的测定,结果与高效液相色谱法吻合良好。平均回收率为102.1 - 109.7%,相对标准偏差小于6%。证明了该方法具有高灵敏度、高选择性以及操作简单稳定的优点。

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