摘要
目的:模拟临床应用,将华蟾素注射液与常用输液配伍,观察配伍后的外观、pH值变化及含量测定。采用紫外分光光度法进行光谱扫描和测定。结果:在室温26℃,6h内各混合液均澄明,无颜色改变,pH值无明显变化,吸收光谱和含量基本无变化。
he stability of cinobufacin injection in commonly used intravenous solutions was studied.Solution appearance and pH were assessed,Ultraviolet spectrophotometry was used to determined the drug concentration.The result stated that:at room temperature 26 ℃,none of the admixtures changed in clarity,colour and pH.The spectrum of absorption and drug concentration did not change either,in 6 hours.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
1998年第5期215-216,共2页
Chinese Journal of Hospital Pharmacy
关键词
华蟾素
注射液
配伍
紫外分光光度法
cinobufacin,injection ,compatibility,ultraviolet spectrophotometry