摘要
目的:研究苦参散主要成份的分离鉴定,为该药建立企业质量标准提供实验依据。方法:胶束薄层层析。结果:CTAB、SDS胶束水溶液浓度分别为0.006mol·L ̄(-10).04mol·L ̄(-1)时,甘草的Rf值为0.50,0.52;黄芩的Rf值为0.72,0.69;苦参的Rf值为0.30,0.37。分离效果最好。结论:胶束薄层层析法,可做为苦参散中各主要成份含量的分离方法。
Objective:To study main composition of kurainone powder medicine which is separated Methods:Using micellarthin Layer Chromatography ReSults: Surface active agent CTAB concentration is 0.006mol. L^(-1), SDS concentration is 0.04mol. L^(-1),Licorice root Rf CTAB= 0.50 Rf SDS=0.52, Baicalein Rf CTAB=0.72 Rf SDS=0.69,kurainoe Rf CTAB=0.30, Rf SDS=0.37 It's separate ettection was batter than other method .Conclusions: Micellar thin layer chromatography may be to ma-jor method which kurainone Powder medicine's main conpeition. Such condtision Provied a strong experimented evidencefor kurainone Powder medicine on quality standard of enterprise.
出处
《兰州医学院学报》
1997年第4期17-18,共2页
Journal of Lanzhou Medical College
关键词
胶束
薄层层析
苦参散
micellar
thin layer chromatography
separation