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头孢西丁钠在葡萄糖氯化钠钾注射液中的稳定性考察
引用本文:翁小红,储蓉.头孢西丁钠在葡萄糖氯化钠钾注射液中的稳定性考察[J].抗感染药学,2010,7(2):113-114.
作者姓名:翁小红  储蓉
作者单位:1. 苏州市立医院,药剂科,江苏,苏州,215002
2. 苏州药品检验所,江苏,苏州,215002
摘    要:目的:考察室温(25℃)下注射用头孢西丁钠在葡萄糖氯化钠钾注射液中的稳定性。方法:采用高效液相色谱法测定配伍液中头孢西丁钠的质量浓度,并考察配伍液外观、pH值及不溶性微粒的变化。结果:头孢西丁钠与葡萄糖氯化钠钾注射液配伍后8h内其外观、pH值及质量浓度均无明显变化,不溶性微粒符合药典规定。结论:注射用头孢西丁钠室温(25℃)下可与葡萄糖氯化钠钾注射液配伍,8h内使用。

关 键 词:头孢西丁钠  葡萄糖  氯化钠  氯化钾  配伍稳定性  高效液相色谱法

Stability of Cefoxitin Sodium for Injection Mixed with Glucose and Sodium Chloride Potassium Chloride Injection
WENG Xiao-hong,CHU Rong.Stability of Cefoxitin Sodium for Injection Mixed with Glucose and Sodium Chloride Potassium Chloride Injection[J].Anti-infection Pharmacy,2010,7(2):113-114.
Authors:WENG Xiao-hong  CHU Rong
Institution:1 Municipal Hospital of Suzhou,Suzhou Jiangsu 215002,China;2Suzhou Institute for Drug Control,Suzhou Jiangsu 215002,China
Abstract:Objective:To study the stability of cefoxitin sodium for injection mixed with glucose and sodium chloride-potassium chloride injection(GNK) at room temperature(25 ℃).Methods:The mass concentration of cefoxitin was determined by HPLC,the appearance of the solution was observed and its pH value and particles were tested.Results:There were no significant changes in appearance,pH value and mass concentration of the mixed solution within eight hours,and the particles met the pharmacopoeia requirements.Conclusion:Cefoxitin sodium for injection mixed with GNK at room temperature(25 ℃ )was compatible and it should be used within 8 hours.
Keywords:Cefoxitin sodium  glucose  sodium chloride  potassium chloride  compatible stability  HPLC
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