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黄连琥珀清心丸质量标准研究

张潇丹 赵渤年 贺晓东 高燕 杨龙飞 张冠群 于子翔 柳明君 王雅菲 更藏加

山东科学2024,Vol.37Issue(4):17-25,9.
山东科学2024,Vol.37Issue(4):17-25,9.DOI:10.3976/j.issn.1002-4026.20230165

黄连琥珀清心丸质量标准研究

A study on the quality standards of Huanglian Hupo Qingxin pills

张潇丹 1赵渤年 1贺晓东 2高燕 1杨龙飞 1张冠群 1于子翔 1柳明君 1王雅菲 3更藏加4

作者信息

  • 1. 山东中医药大学 药物研究院黄河流域特色中药生态保护和高质量发展协同创新中心,山东 济南 250355
  • 2. 青岛上和中医医院,山东 青岛 266200
  • 3. 山东中医药大学 针灸推拿学院,山东 济南 250355
  • 4. 西南民族大学 药学院,四川 成都 610041
  • 折叠

摘要

Abstract

To establish a method for the qualitative and quantitative assay of Huanglian Hupo Qingxin pills and provide abasis for the subsequent establishment of quality standards,the six ingredients in the formula(Aquilariae Lignum Resinatum,Fructus Choerospondiatis,Terminalia Chebula,CoptidisRhizoma,Flos Gossampini,and Semen Myristicae)were identified through microscopical observation.Thin-layer chromatography was used to identify Terminalia Chebula.Berberine hydrochloride concentration was assessed using high-performance liquid chromatography.Microscopical and thin-layer identifications of Huanglian Hupo Qingxin pills were conducted,which revealed a berberine hydrochloride concentration of 0.018 0~0.902 0 mg/mL,exhibiting a good linear relationship.The assay method was found to bescientific,sensitive,and reproducible,with relative standard deviations(RSDs)for precision,stability,and reproducibility tests all below 3.0%.The average recovery rate from spike-and-recovery testing was 101.29%,with an RSD of 2.30%.The established quality standardis simple and reproducible and can be used for studying the quality standards of Huanglian Hupo Qingxin pills.

关键词

黄连琥珀清心丸/质量标准/显微鉴别/薄层色谱/高效液相色谱法

Key words

Huanglian Hupo Qingxin pills/quality standards/microscopical identification/thin-layer chromatography/high-performance liquid chromatography

分类

中医学

引用本文复制引用

张潇丹,赵渤年,贺晓东,高燕,杨龙飞,张冠群,于子翔,柳明君,王雅菲,更藏加..黄连琥珀清心丸质量标准研究[J].山东科学,2024,37(4):17-25,9.

基金项目

山东省重点研发计划项目(2021CXGC010511) (2021CXGC010511)

山东科学

OACSTPCD

1002-4026

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