浅谈中国药典起草与基础研究工作

A Brief Discussion on Drafting and Basic Research of Chinese Pharmacopoeia

本文从TLC鉴别对照药材的确定、含量测定指标的选择及限度制订等方面,指出了中国药典起草与实际应用的相关性,并就毒性药材中毒性成分的量效关系的研究、成分与药效的研究、加快指纹谱基础研究的进度等基础研究工作方面,以及如何更深入地完善中药质量标准提出了设想。

This article points out the relatianship between the drafting and the application of Chinese pharmacopoeia on the basis of the comparison of TLC identification criteria of drugs with the definition of medicinal materials as well as the selection and the formulation of the limits of identification criteria of medicinal material contents.It makes also suggestions on how to strengthen such basic researches as the relationship between quantity and effectiveness of toxic contents in toxic medicinal materials,the constituents and their effectiveness and the acceleration of the fingerprint of Chinese materia medica so as to further improve the standard of the quality of Chinese drugs.