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羧甲基-β-环糊精为手性剂拆分3种碱性药物对映体 被引量:4

Enantiomeric Separation of Three Basic Drugs Using Carboxymethyl-β-cyclodextrin as the Chiral Selector
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摘要 目的:建立高效毛细管电泳法分离3种碱性药物对映体。方法:采用未涂层熔融石英毛细管柱,30 mmol·L-1NaH2PO4缓冲溶液中加入羧甲基-β-糊精(CM-β-CD)作为背景电解质,可使3种碱性药物的对映体得到较好的分离。结果:在最佳条件下,吲达帕胺、盐酸异丙嗪和盐酸普萘洛尔的分离度(R)分别为4.79,2.45和6.90。结论:CM-β-CD对吲达帕胺、盐酸异丙嗪和盐酸普萘洛尔有很高的对映体选择性。该方法重现性好,简便、快捷。 Objective: To establish a high performance capillary electrophoresis method for the chiral separation of indapamide, promethazine hydrochloride and propranolol hydrochloride. Method : The separations of the enantiomers were performed in an untreated fused-silica capillary tube with earboxymethyl-β-cyclodextrin (CM-β-CD) in 30 mmol · L-1 NaH2PO4 buffer as the chiral selector and a high voltage of 20 kV. Result : Under the optimal conditions, the resolution of indapamide, promethazine hydrochloride and prop- ranolol hydrochloride was 4.79, 2.45 and 6.90, respectively. Conclusion: CM-β-CD is highly enantioselective for indapamide, promethazine hydrochloride and propranolol hydrochloride. The method is simple and fast with an improved reproducibility.
出处 《中国药师》 CAS 2012年第6期772-774,共3页 China Pharmacist
关键词 毛细管电泳 吲达帕胺 盐酸异丙嗪 盐酸普萘洛尔 手性分离 Capillary eletrophoresis Indapamide Promethazine hydrochloride Propranolol hydrochloride Chiral separation
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