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机构地区:[1]南京药物研究所
出 处:《中国药学杂志》1990年第3期164-166,共3页Chinese Pharmaceutical Journal
摘 要:蛇床子样品粉碎,在脂肪提取器中用乙醇提取,点于硅胶板上,以甲苯-乙酸乙酯(9:1)为展开剂。相应部分刮下后,用甲醇洗脱,蛇床子素于λ322nm测定,总线性呋喃香豆素于λ249nm测定。在20~100μg范围内获得良好线性。本法结果与HPLC法相比是一致的。The osthol and total linearfuranocumarin inShechuangzi (Cnidium monnieri) were determi-ned by TLC-spectrophotome tric method. Sam-ple was pulverized and extracted with ethanolin Soxhlet extractor. The extracted solutionwas spotted on silica gel plate with toluene-ethylacetate (9:1) as a developing agent. Therelevant parts of the silica gel were scrapedoff, and extracted with methanol (or ethanol)Osthol was determined at 322nm, and the to-tal linearfuranocumarin at 249nm. The linearrelation was obtained between 20~100μg. Theresults were in agreement with those byHPLC method.
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