摘要
目的研究咽炎颗粒的制备,建立该制剂的质量标准,并对其稳定性进行试验。方法确定处方组成,拟定该制剂的生产工艺流程,并进行性状检查等质量研究,采用薄层层析法对其中有效成分进行鉴别稳定性试验。结果确定该制剂生产工艺流程及质量标准。结论该制剂生产工艺流程合理,质量稳定。
Purpose Do research into the manufacture method of pharyngitis pellet , establish its quality specification and test its stability. Method Definite the composition of prescription, draw up the technical process of the prescription and do research into its performance and condition; carry on the distinction of its effective component with TLC and the experiment of its stability.Result Definite the production technical process of the pharnyngitis pellet and its quality specification. Conclusion The production technical process of the preparation pellet is reasonable and its quality is stable.
出处
《中国实用医药》
2007年第33期16-,共1页
China Practical Medicine
关键词
咽炎颗粒
生产工艺流程
质量标准
Pharyngitis pellet
Production technical process
Quality specification