...
首页> 外文期刊>Journal of separation science. >High-performance purification of quaternary alkaloids from Corydalis yanhusuo W. T. Wang using a new polar-copolymerized stationary phase
【24h】

High-performance purification of quaternary alkaloids from Corydalis yanhusuo W. T. Wang using a new polar-copolymerized stationary phase

机译:使用新型极性共聚固定相从延胡索中高效提取季生物碱

获取原文
获取原文并翻译 | 示例

摘要

An efficient method for purification of alkaloids from Corydalis yanhusuo W. T. Wang using HPLC was developed, featuring a polar-copolymerized stationary phase named C18HCE. As ionizable solutes, the crude alkaloid sample often suffered from serious peak tailing problem on conventional RP-LC columns, and the separation would rapidly became destroyed with the increasing of load amount. However, on the new stationary phase, good peak shapes (asymmetry factor <1.5) as well as good loadability were easily obtained in a commonly used acidic mobile phase condition. The loading amount could reach 10 mg per injection on an analytical C18HCE column for laboratory-scale purification. About 6.8 mg of palmatine (HPLC purity >98%) and 44.4 mg of dehydrocorydaline (HPLC purity >98%) were rapidly derived from 200 mg of the crude alkaloid sample, and the recoveries of these two compounds were 76.5 and 81.7%, respectively. The purified alkaloids were characterized by comparing retention times with standard compounds as well as 1H-NMR data. The new method is simple and high yielding, and it may provide a promising tool for purification of alkaloids as well as other alkaline compounds.
机译:开发了一种高效液相色谱法从延胡索中提取生物碱的有效方法,该方法具有极性共聚的固定相C18HCE。作为可离子化的溶质,粗生物碱样品在常规RP-LC色谱柱上经常会遇到严重的峰拖尾问题,并且随着负载量的增加,分离会迅速被破坏。但是,在新的固定相上,在常用的酸性流动相条件下,很容易获得良好的峰形(不对称因子<1.5)和良好的负载能力。在用于实验室规模纯化的分析性C18HCE色谱柱上,每次进样的上样量可达到10 mg。从200 mg粗生物碱样品中快速衍生出约6.8 mg的棕榈碱(HPLC纯度> 98%)和44.4 mg的去氢羟脯氨酸(HPLC纯度> 98%),这两种化合物的回收率分别为76.5和81.7%。 。通过与标准化合物比较保留时间以及1H-NMR数据来表征纯化的生物碱。该新方法简单,收率高,为纯化生物碱及其他碱性化合物提供了有希望的工具。

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