摘要
目的制备肝炎合剂并制定质量鉴别。方法药材按处方经水浸泡、煎煮、浓缩、纯化等后制备成肝炎合剂,用薄层色谱法和化学鉴别法对主要成分进行定性鉴别。结果该制剂制备工艺可行,质量可控,稳定性好。结论本制剂制备工艺简单,组方合理,无不良反应。
OBJECTIVE To Prepare Ganyan mixture and set standards for quality control. METHODS Medicinal materials were soaked, boiled, condensed, and purified according prescription. Then main gradients were qualitatively identified by means of thin layer chromatography and chemical analysis. RESULTS The technology of the preparation was mature with controllable quality and stability. simple and prescription reasonable with no adverse reaction. CONCLUSION The procession of this preparation is
出处
《海峡药学》
2014年第9期12-13,共2页
Strait Pharmaceutical Journal
关键词
肝炎合剂
制备
质量控制
Ganyan mixture
Preparation
Quality control
