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采用超滤法制备感冒康注射液,通过对质量进行控制来探究超滤法制备注射液的可行性,并对其制剂的澄明度、有效成分含量测定、pH值、杂质检查、无菌检查、安全试验进行检查.结果表明,所有试验均符合中国药典(2005年版)规定,所建立的超滤法可用于感冒康注射液的制备,且方法简便、快速.
The ultrafiltration method was used to prepare the fluconazole injection and the quality control was carried out to explore the feasibility of preparing the injection by ultrafiltration. The formulation of the injection was determined for its clarity, content of active ingredients, pH value, impurity test, sterility test, Safety test.The results show that all the tests are in accordance with the provisions of the Chinese Pharmacopoeia (2005 edition), the established ultrafiltration method can be used for the preparation of influenza virus injection, and the method is simple and fast.