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注射用无菌粉末质量控制要点

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摘要 目的:了解注射用无菌粉末的质量控制要点,为临床提供高质量的制剂。方法:参考文献,从原辅料的选择和用量、玻璃化转变温度的确定、生产过程中的各个环节以及贮藏的要点进行综述。结果与结论:注射用无菌粉末需达到以下要求:原辅料选择应恰当,配比应合理,玻璃化温度适宜,生产工艺严格,贮藏应在干燥和低温条件下。整个生产过程需进行严格控制,以保证制剂的质量和临床疗效。
出处 《中国药房》 CAS CSCD 2012年第41期3921-3923,共3页 China Pharmacy
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