摘要
目的:考察咽喉炎合剂的稳定性。方法:采用经典恒温加速试验法和留样观察法,以黄芩苷的含量作为考察指标,采用高效液相色谱(HPLC)法测定其含量的变化。结果:咽喉炎合剂中黄芩苷的含量变化符合一级动力学过程,2种考察方法的结果基本一致。在室温(25℃)条件下,咽喉炎合剂的有效期为1.06a。结论:建议咽喉炎合剂质量标准中有效期订为室温保存1a。
OBJECTIVE:To investigate the stability of Yanhouyan mixture(for pharyngolaryngitis).METHODS: The stability of Yanhouyan mixture was investigated by classic constant temperature accelerated test method and sample observation method taking the content of Baicalin as index which was determined by HPLC.RESULTS: The content change of Bacilin in Yanghouyan mixture was in line with the first order kinetics, and the test results for both methods were similar.Under room temperature(25 ℃ ), the validity duration of Yanhouyan mixture was 1.06 years.CONCLUSION: In establishing the quality standard for Yanhouyan mixture, the advisable storage life of 1 year for which should be considered .
出处
《中国药房》
CAS
CSCD
北大核心
2008年第36期2845-2846,共2页
China Pharmacy
关键词
咽喉炎合剂
黄芩苷
经典恒温加速试验法
留样观察法
稳定性
高效液相色谱法
Yanhouyan mixture
Baicalin
Classic constant temperature accelerated test method
Sample observation method
Stability
HPLC