Herráez-Hernández R, Campíns-Falcó P
Department of Analytical Chemistry, University of Valencia, Spain.
J Chromatogr B Biomed Sci Appl. 2000 Apr 14;740(2):169-77. doi: 10.1016/s0378-4347(00)00103-1.
Different beta-cyclodextrins have been tested as chiral additives in the mobile phase for the chromatographic analysis of chlorthalidone enantiomers in a C18 LiChrospher (125 x 4 mm I.D.) column. The effect on enantioresolution of different parameters was studied: composition of the mobile phase (percentage of organic solvent, type of buffer and pH), mobile phase flow-rate, and type and concentration of beta-cyclodextrin. A 25:75 mixture of methanol and 0.1 M phosphate buffer, pH 4, containing 2% triethylamine (v/v), and 12.5 mM beta-cyclodextrin, at a flow-rate of 0.8 ml/min, was found to be the best option for the resolution of chlorthalidone enantiomers. Under such conditions, linear calibration curves were obtained in the 0.5-20-microg/ml interval using UV detection at 230 nm. The limit of detection for both isomers was 50 ng/ml. The utility of the described assay has been tested by analyzing chlorthalidone in different pharmaceutical preparations. Examples of application to biological samples are also given.
在C18 LiChrospher(125×4 mm内径)柱上,已对不同的β-环糊精作为手性添加剂用于氯噻酮对映体的色谱分析流动相进行了测试。研究了不同参数对映体拆分的影响:流动相组成(有机溶剂百分比、缓冲液类型和pH值)、流动相流速以及β-环糊精的类型和浓度。发现甲醇与0.1 M磷酸盐缓冲液(pH 4)以25:75的比例混合,含有2%三乙胺(v/v)以及12.5 mMβ-环糊精,流速为0.8 ml/min,是拆分氯噻酮对映体的最佳选择。在此条件下,使用230 nm紫外检测在0.5 - 20μg/ml区间获得了线性校准曲线。两种异构体的检测限均为50 ng/ml。通过分析不同药物制剂中的氯噻酮,测试了所述测定方法的实用性。还给出了应用于生物样品的示例。