首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >In-capillary derivatization and analysis of ephedrine and pseudoephedrine by micellar electrokinetic chromatography with laser-induced fluorescence detection
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In-capillary derivatization and analysis of ephedrine and pseudoephedrine by micellar electrokinetic chromatography with laser-induced fluorescence detection

机译:胶束电动色谱-激光诱导荧光检测法进行麻黄碱和伪麻黄碱的毛细管内衍生化和分析

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This paper describes an automatic rapid approach for in-capillary derivatization of ephedrine (E) and pseudoephedrine (PE) and subsequent sensitive determination of the derivatives by micellar electrokinetic chromatography (MEKC) with laser-induced fluorescence (LIF) detection using 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) as fluorescent reagent. The unique feature of this method is the capillary being used as a small reaction chamber, in which the sample, derivatization buffer and reagent solutions were injected directly into the capillary by tandem mode, followed by an electrokinetic step (5 W, 15 s) to enhance the mixing efficiency of analytes and reagent plugs. Standing a specified time of 1 min for reaction, the derivatives were then immediately separated and determined. Several parameters for in-capillary derivatization and subsequent MEKC separation were systematically investigated. Under these optimized conditions, a baseline separation of the two analytes was achieved within 10 min and the derivatization concentration limits of detection were found to be 4.8 ng mL(-1) for E and 1.6 ng mL(-1) for PE, respectively. The method was validated in terms of precision, linearity, accuracy and successfully applied for the determination of the two alkaloids in ephedra herb and its preparations. (C) 2008 Elsevier B.V. All rights reserved.
机译:本文介绍了一种自动快速的方法,用于麻黄碱(E)和伪麻黄碱(PE)的毛细管内衍生化,以及随后通过胶束电动色谱(MEKC)和使用4-氟甲基苯甲酸酯的激光诱导荧光(LIF)检测对衍生物进行灵敏测定。 7-硝基-2,1,3-苯并恶二唑(NBD-F)作为荧光试剂。该方法的独特之处在于毛细管被用作小型反应室,其中样品,衍生化缓冲液和试剂溶液通过串联模式直接注入毛细管中,随后进行电动步骤(5 W,15 s)提高分析物和试剂塞的混合效率。在指定的1分钟时间进行反应后,立即分离并确定衍生物。系统地研究了毛细管内衍生化和随后的MEKC分离的几个参数。在这些优化的条件下,两种分析物的基线分离在10分钟内实现,E的衍生化浓度极限分别为E和PE分别为4.8 ng mL(-1)和1.6 ng mL(-1)。该方法在精密度,线性,准确性方面均得到验证,并成功应用于麻黄及其制剂中两种生物碱的测定。 (C)2008 Elsevier B.V.保留所有权利。

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