首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Field-amplified sample injection in capillary electrophoresis with amperometric detection for the ultratrace analysis of diastereomeric ephedrine alkaloids
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Field-amplified sample injection in capillary electrophoresis with amperometric detection for the ultratrace analysis of diastereomeric ephedrine alkaloids

机译:非安定麻黄碱生物碱超痕量分析中毛细管电泳-安培检测的场放大样品进样

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摘要

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.
机译:开发了一种场放大样品进样(FASI)CE与安培检测的耦合方法,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10 s到充满高导电背景电解质(BGE)的毛细管中,引入FASI。通过使用高离子强度的硼酸盐缓冲液作为BGE,提高了非对映异构体的选择性和检测灵敏度。研究了影响FASI和CE分离的参数以达到最佳条件。在15分钟内,使用200 mmol / L硼酸盐缓冲液(pH 9.5)和+18 kV分离电压分离了四种分析物,检测电势为+1.0 V(vs. Ag / AgCl),碳盘电极为工作电极。在峰值电流和分析物浓度之间的0.1-100 ng / mL范围内观察到极好的线性。 (-)-麻黄碱,(+)-伪麻黄碱,(-)-N-甲基麻黄碱和(+)-N-甲基伪麻黄碱的LOD(S / N = 3)为39.3、54.9、30.8和44.1 pg / mL,分别。该方法成功用于麻黄中生物碱的测定,结果与HPLC法吻合良好。发现平均回收率为102.1-109.7%,RSD小于6%。并且已经证明了高灵敏度和选择性以及简单和稳定操作的优点。

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