Tian Kan, Wang Yushang, Chen Yonglei, Chen Xingguo, Hu Zhide
Department of Chemistry, Lanzhou University, Lanzhou, China; State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.
Talanta. 2007 Apr 30;72(2):587-93. doi: 10.1016/j.talanta.2006.11.027. Epub 2006 Dec 28.
A capillary zone electrophoresis method using only 1-alkyl-3-methylimidazolium-based ionic liquids as background electrolyte for the simultaneous determination of five anthraquinone derivatives including aloe-emodin, emodin, chrysophanol, physcion and rhein in Rhubarb species was described. Ion association constants, K(ass), between anthraquinone anions and imidazolium cations were determined by analyzing the electrophoretic mobility change of anthraquinone anions using a non-linear least-squares method and factors contributing to ion associability were systematically clarified. For method optimization, several parameters such as ionic liquids concentration, background electrolyte pH and applied voltage, on the separation were evaluated and the optimum conditions were obtained as follows: 90mM 1-butyl-3-methylimidazolium tetrafluoroborate (pH 11.0) with an applied voltage of 20kV. Under these conditions, the method has been successfully applied to the determination of anthraquinones in extracts of two kinds of Rhubarb plants (R. palmatum and R. hotaoense) within 12min. The method proposed herein was shown to be much simpler than the previously reported methods.
描述了一种毛细管区带电泳方法,该方法仅使用基于1-烷基-3-甲基咪唑鎓的离子液体作为背景电解质,用于同时测定大黄属植物中包括芦荟大黄素、大黄素、大黄酚、大黄素甲醚和大黄酸在内的五种蒽醌衍生物。通过使用非线性最小二乘法分析蒽醌阴离子的电泳迁移率变化,确定了蒽醌阴离子与咪唑鎓阳离子之间的离子缔合常数K(ass),并系统地阐明了影响离子缔合性的因素。为了优化方法,评估了离子液体浓度、背景电解质pH值和施加电压等几个参数对分离的影响,并获得了如下最佳条件:90mM四氟硼酸1-丁基-3-甲基咪唑鎓(pH 11.0),施加电压20kV。在这些条件下,该方法已成功应用于在12分钟内测定两种大黄植物(掌叶大黄和河套大黄)提取物中的蒽醌。本文提出的方法比先前报道的方法要简单得多。