山西医科大学学报2011，Vol.42Issue(7)：551-553,3.DOI:10.3969/J.ISSN.1007-6611.2011.07.008
替米沙坦片的质量和稳定性研究
Study on quality control and stability of telmisartan tablets
李晓红1
作者信息
- 1. 山西省太原晋阳制药厂,太原,030031
- 折叠
摘要
Abstract
Objective To study the quality and stability of telmisartan tablets. Methods The HPLC method was used to determine the contents,the dissolution and the stability of telmisartan tablets. Results The dissolution of telmisartan tablets in 45 min was beyond 80％ . Homogeneity of dissolution within the same batch or between different batches was fine. The contents in the three samples were 100. 3％,100. 4％ and 99. 89％ , which meel the standard requirement. The stability test showed that the drug was stable in 2 years. Conclusion The unifonnity of content,the reproducibility of dissolution and the stability of telmisartan tablets are well.关键词
替米沙坦片/质量控制/稳定性Key words
telmisartan tablets/ quality contml/ stability分类
医药卫生引用本文复制引用
李晓红..替米沙坦片的质量和稳定性研究[J].山西医科大学学报,2011,42(7):551-553,3.
