首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Separation of a triterpenoid saponin mixture from Maesa lanceolata: semipreparative reversed-phase wide pore high performance liquid chromatography with temperature control.
【24h】

Separation of a triterpenoid saponin mixture from Maesa lanceolata: semipreparative reversed-phase wide pore high performance liquid chromatography with temperature control.

机译:一种从三叶毛毛树中分离出三萜皂苷混合物的方法:具有温度控制功能的半制备反相广孔高效液相色谱仪。

获取原文
获取原文并翻译 | 示例
           

摘要

A mixture of triterpenoid saponins derived from the dried leaves of Maesa lanceolata was separated, without structure deterioration, in its components. Seven fractions (I-VII) of high molecular weight (1234-1358) saponins were obtained on a semipreparative scale using wide pore reversed-phase high performance liquid chromatography with an acetonitrile trifluoroacetic acid (500:0.3 w/w)-water-trifluoroacetic acid (391:0.3, w/w) gradient from 35 to 56% in 30 min. The mobile phase was cooled in an ice bath (0 degrees C) during chromatography in order to prevent bubble formation and to improve the quality of the separation. Freeze-dried fractions IV, V, VI and VII were further separated using solvent systems developed for each of the fractions. Fourteen pure triterpenoid saponins were isolated in this way and their molar weight determined.
机译:分离了从毛叶前茅(Maesa lanceolata)的干燥叶片中得到的三萜皂苷的混合物,其成分没有结构变质。使用宽孔反相高效液相色谱和乙腈三氟乙酸(500:0.3 w / w)-水-三氟乙酸,半制备规模获得高分子量(1234-1358)皂苷的七个馏分(I-VII) 30分钟内从35%到56%的酸(391:0.3,w / w)梯度。在色谱过程中,将流动相在冰浴(0摄氏度)中冷却,以防止气泡形成并提高分离质量。使用针对每种馏分开发的溶剂系统进一步分离冻干的馏分IV,V,VI和VII。用这种方法分离了十四个纯三萜皂苷,并确定了它们的摩尔重量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号