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机构地区:[1]河南绿十字生物工程研究所,河南省分析测试中心
出 处:《中国医药工业杂志》1996年第12期531-533,共3页Chinese Journal of Pharmaceuticals
摘 要:以云南红豆杉树皮(或树叶)为原料,提取纯化紫杉醇。先经95%乙醇、二氯甲烷提取,再经硅藻土柱涂渍色谱、硅胶60中压快速柱色谱分离,收集含紫杉醇-cephalomannine的组分后以C_(18)制备型RP-HPLC分离,两次结晶后得到紫杉醇无色结晶固体,纯度≥98.8%,收率为树皮干重的0.028%,树叶干重的0.0088%。An improved method for the isolation and purification of Taxol from Taxus Yunnanensis is described. The bark(or needles) is extracted with 95% ethanol, the extract is partitioned between methylene chloride. The methylene chloride extract is dissolved in an ethyl acetate/methanol, and chromatographed on Celite 545 flash column, eluted with hexane, methylene chloride.Then, it is chromatographed on silica gel 60 medium-pressure flash column,the mobile Phase is gradually increased hexane/acetone. And it is further fractioned on a silica gel 60 medium pressure flash column, the mobile phase is methanol/ methylene chloride. Taxol was separated from cephalomannine by reversed-Phase C_(18) Preparative HPLC. The purity of product was≥98.8%, the yield(dry base) of taxol was 0.028% of the bark, and 0.0088% of the needles.
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