摘要
目的 考察乳酸环丙沙星注射液与地塞米松磷酸钠注射液配伍稳定性 ,为临床联合用药提供依据。方法 分别用紫外分光光度法和高效液相色谱法测定配伍后药物的含量。结果 在室温条件下 ,3h内两药配伍后外观与 pH无明显变化 ,但含量变化明显。
AIM The compatible stability of ciprofloxacin lactate injection with dexamethasone sodium phosphate injection was strictly checked in order to provide a basis for clinical drugs. Methods A dual wavelength spectrophotometry was described for the determination of ciprofloxacin lactate injection with dexamethasone sodium phosphate injection. Results The result showed that there was no evident variation in the surface and the value of pH. But there was an evident variation in the content during three hours at room temperature. Conclusion The two injections should not be in the compatible solution.
出处
《安徽医药》
CAS
2002年第4期59-60,共2页
Anhui Medical and Pharmaceutical Journal
关键词
环丙沙星
地塞米松
配伍
稳定性
ciprofloxacin lactate injection
dexamethasone sodium phosphate injection
compatible stability
