摘要
总结了注射剂灭菌工艺研究中存在的常见问题,如处方研究前未了解药物的稳定特性,忽视了附加剂和灭菌工艺的筛选、无菌保证值和F0值的考察以及工艺验证研究等,并针对上述问题提出了保证注射剂安全性和稳定性的若干建议。
This article summarized the common problems occurring in sterilization process of injection products, such as lacking sufficient knowledge of drug stability, ignoring screening of excipients and sterilization process, neglecting sterilizing ensuring level and F0 study and process validation. It also provided some considerations for ensuring the safety and stability of injection products.
出处
《中国新药杂志》
CAS
CSCD
北大核心
2009年第9期780-783,共4页
Chinese Journal of New Drugs
关键词
注射剂
无菌保证值
F0值
灭菌工艺
灭菌工艺验证
injection
sterilizing ensuring level
Fo value
sterilization process
sterilization process validation