3种碱性药物在手性柱上的对映体分离  

Enantioseparation of Three Basic Drugs on (S, S)-Whelk-O 1 Chiral Column

作　　者：何红梅[1] 蔡小军[1] 徐秀珠[1] 潘春秀[1] 张雪君[1] 陈娟娟[1] 

机构地区：[1]浙江大学化学系,杭州310027

出　　处：《分析化学》2005年第6期861-864,共4页Chinese Journal of Analytical Chemistry

基　　金：浙江省科技计划(No.2004C33050);分析测试基金(No.03111)资助项目

摘　　要：在(S,S)WhelkO1手性柱上对去甲羟基安定、扁桃酰胺和氯噻酮3种碱性药物进行了对映体分离研究。考察了流动相正己烷体系中不同种类和浓度的醇类添加剂、不同浓度乙酸对3种碱性药物对映体分离的影响,并初步探讨了其手性分离机理。结果表明,去甲羟基安定和扁桃酰胺在正己烷/异丙醇/乙酸为80∶20∶0.1(V/V)条件下都获得了很好的分离,其最佳分离度分别为2.59和3.63,氯噻酮则未获得分离。Enantioseparations of oxazepam, mandelic acidamide and chlorthalidone on (S, S)-Whelk-O 1 column were investigated. The influences of the concentration and kind of alcohols, concentration of acetic acid on enantioseparation of three basic drugs were studied. Besides, chiral separation mechanism of these drugs was also discussed. The results showed that oxazepam and mandelic acidamide were separated successfully. In the mobile phase of n-hexane,iso-propanol and acetic acid (80∶20∶0.1, V/V) , the ~resolution of ~oxazepam′s and mandelic acidamiale′s were 2.59 and 3.63, respectively. But chlorthalidone was not got chiral separation.

关 键 词：对映体分离 碱性药物 手性柱 分离机理 正己烷 添加剂 流动相 分离度 安定 羟基 酰胺 扁桃 浓度 乙酸 醇类 酮 

分 类 号：TQ460.6[化学工程—制药化工]