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机构地区:[1]山东大学药学院,济南市250012 [2]山东省立医院药剂科,济南市250021
出 处:《中国药房》2005年第18期1419-1420,共2页China Pharmacy
摘 要:目的:考察多索茶碱注射液与地塞米松磷酸钠注射液的配伍稳定性。方法:观察及测定多索茶碱注射液与地塞米松磷酸钠注射液在5%葡萄糖注射液中配伍后于25℃放置6h内的外观及pH值,并采用高效液相色谱法测定配伍液的含量。结果:与配伍后0h比较,配伍液放置6h内的外观色泽、澄明度及含量均无明显变化,而pH值有所升高。结论:多索茶碱注射液与地塞米松磷酸钠注射液在5%葡萄糖注射液中配伍后于25℃放置6h内质量稳定。OBJECTIVE: To study the compatible stability of doxofylline injection and dexmethasone sodium phosphate injection. METHODS: The changes in appearance and pH value of the mixture of doxofylline injection and dexmethasone sodium phosphate injection in 5% glucose injection within 6 hours at 2512 were observed and determined, the content of which was determined by HPLC. RESULTS: Compared with the solution at 0b of mixing, no significant changes were noted in color, clarity and content within 6 hours' mixing, however, there was an increase in its pH value. CONCLUSION: The mixture of doxophylline and dexmethasone in 5% glucose injection is stable in quality within 6 hours' mixing at 25℃.
关 键 词:多索茶碱注射液 地塞米松磷酸钠注射液 配伍 稳定性 高效液相色谱法
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