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机构地区:[1]中国人民解放军第三军医大学第三附属医院药学部,重庆400042 [2]重庆医科大学,重庆400016
出 处:《中国药业》2013年第23期27-28,共2页China Pharmaceuticals
摘 要:目的考察维生素C注射液与门冬氨酸钾镁注射液在0.9%氯化钠注射液中配伍的稳定性。方法考察常温下24 h内维生素C注射液与门冬氨酸钾镁注射液在0.9%氯化钠注射液中配伍后,其配伍液的外观、pH及药物的含量。结果与结论维生素C注射液和门冬氨酸钾镁注射液在0.9%氯化钠注射液中配伍后,24 h内药物的含量、pH及外观均无明显变化。Objective To investigate the compatible stability of Vitamin C Injection and Potassium Magnesium Aspartate Injection in 0.9% Sodium Chloride Injection. Methods The changes of appearance, pH value and the content of drugs in the mixture within 24 h at normal temperature were observed after Vitamin C Injection combined with Potassium Magnesium Aspartate Injection in 0. 9% Sodium Chloride Injection. Results and Conclusion No significant changes were found in the content, pH value and appearance in 24 h after Vitamin C Injection combined with Potassium Magnesium Aspartate Iniection in 0. 9% Sodium Chloride Iniection.
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