用环糊精胶束电动毛细管色谱法分离单萜烯异构体

Maria Regina A. Rodrigues, Elina B. Caramão, Lourdes Arce, Angel Rios, Miguel Valcárcel
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引用次数: 3

摘要

建立了测定樟烯、α-蒎烯、β-蒎烯、γ-萜烯、α-萜烯、萜烯和对伞花烃等单萜烯的胶束电动毛细管色谱法。在缓冲溶液中加入环糊精(CDs)可以分离这些单萜烯。环糊精的分离取决于CD的类型,在本方法中-CD是最有效的环糊精。该方法允许对低浓度的单萜烯进行分离和检测。在缓冲液中加入有机溶剂(乙腈)作为改性剂(10 mM NaH2PO4, 6 mM Na2B4O7, 50 mM SDS, 7 mM de γ-CD)实现了分离。分析是在温度为25°C的20 kV正电源下进行的。将样品静压(5 s)引入毛细管的阳极端,在200 nm处记录电泳图。该方法可高度适用于实际样品中叶精油、马角兰花和牛至花中单萜的分离和测定。©2001 John Wiley &[J] .中国机械工程,2001
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of cyclodextrins for the separation of monoterpene isomers by micellar electrokinetic capillary chromatography

The micellar electrokinetic capillary chromatographic method for the determination of monoterpenes such as camphene, α-pinene, β-pinene, γ-terpinene, α-terpinene, terpinolene and p-cymene was established. Addition of cyclodextrins (CDs) to the buffer solution permits the separation of these monoterpenes. The separation is dependent on the type of CD, and gamma-CD was the most effective cyclodextrin, in the method here developed. The method permits low concentrations of monoterpenes to be separated and detected. The addition of an organic solvent (acetonitrile) as modifier in the buffer (10 mM NaH2PO4, 6 mM Na2B4O7, 50 mM SDS, 7 mM de γ-CD) allowed this separation. The analysis was performed with a positive power supply of 20 kV at a temperature of 25°C. The samples were hydrostatically (5 s) introduced into the anodic end of the capillary and electropherograms were recorded at 200 nm. This method could be highly suitable for the separation and determination of monoterpenes in essential oils of leaves, and the flowers of marjoram and oregano among other real samples. © 2001 John Wiley & Sons, Inc. J Micro Sep 13: 293–299, 2001

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