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机构地区:[1]中山大学药学院药物分析实验室,广州510006 [2]中国农村技术开发中心,北京100045
出 处:《天然产物研究与开发》2011年第5期878-881,945,共5页Natural Product Research and Development
基 金:2005年度广东省中医药管理局计划项目(1050163);2005年度珠海市科技计划项目项(PC20051072)
摘 要:首次采用反相中压制备色谱从芦荟中一次分离制备得到芦荟苷A、B以及异芦荟色苷D。以库拉索芦荟丙酮粗提物为原料,采用中压制备色谱系统:SCO色谱柱(40 cm×26 cm,30~50μm),流动相甲醇-0.5%乙酸水(33∶67,V/V),流速20 mL/min,等度洗脱方式,柱温室温,检测波长254 nm,收集波长356 nm对芦荟样品进行分离制备,得到三种化合物单体。经高效液相色谱、紫外、红外、质谱及核磁共振等方法分析表明所得到的三种化合物分别是异芦荟色苷D、芦荟苷A和芦荟苷B,其纯度分别达到了98.0%,96.0%和98.9%。该方法简便,产品质量高,一次制备可以得到多种单体,为芦荟成分的测定与药理活性的研究提供了条件。A medium pressure preparative liquid chromatography (MPLC) was used to isolate the aloins A and B and isoaloeresin D from Aloe vera simultaneously for the first time. The crude material extracted by acetone, was performed with ODS column (40 cm ×26 cm,30-50 μm) by using isoeratie elution with methanol-0.5% acetic water (33:67 ,v/ v) as the mobile phase at a flow rate of 20 mL/min. The detecting and collecting wavelengths were set at 254 nm and 356 nm,respectively, and the column temperature was room temperature. Three compounds were identified as aloins A and B and isoaloeresin D by using UV,IR,MS and NMR,and their purities were 98.0% ,96.0% and 98.9% ,respectively. The method was convenient, and active constituents with high purity could be obtained simultaneously,which provided conditions to investigate the constituents and their activities of Aloe vera.
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