摘要
目的考察头孢哌酮他唑巴坦在含果糖的0.9%氯化钠溶液中的稳定性。方法观察配伍液室温放置6h内的外观并测定pH,采用高效液相色谱法测定配伍液的含量变化。结果配伍液放置6h内的外观、色泽均无明显变化,pH略有变化,头孢哌酮、他唑巴坦含量均保持在95%以上,无新物质产生。结论头孢哌酮他唑巴坦在含果糖氯化钠溶液中配伍后于室温放置6h内性质基本稳定。
Objective To study the compatible stability of Cefoperazone Tazobactam for Injection in 0. 9% Sodium Chloride Injection containing fructose. Methods The content of the compatible solution in 0.9% Sodium Chloride Injection was determined at different time by HPLC; the appearance of the solution was observed and its pH value was determined. Results No significant differences were noted for the compatible solution in appearance, pH value and contents within 6 h after mixing. The content of CefoperazoneTazobactam was more than 95%. No new substance was produced. Conclusion The compatible solution of CefoperazoneTazobactam for Injection and 0. 9% Sodium Chloride Injection containing fructose can be used within 6h under room temperature.
出处
《中国药业》
CAS
2009年第10期24-25,共2页
China Pharmaceuticals
关键词
头孢哌酮他唑巴坦
果糖
配伍
稳定性
HPLC
cefoperazonetazobactam
fructose
compatibility
stability