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为了确定消渴胶囊的制备工艺,使用了检索法和浏览法对中国期刊数据库中部分相关资料进行查阅。将水提取工艺确定以加12倍水煎煮出膏率较高,干燥温度控制60℃以下,压力0.08~0.095Mpa,粉碎出粉率91%以上。得出其制备工艺在原有药物消渴丸基础上有所提高,质量标准有较大提高,为消渴胶囊产品的申报奠定了基础。
In order to determine the preparation process of Xiaoke Capsule, the retrieval method and browsing method were used to check some relevant information in the Chinese Journal Database. The water extraction process to determine the increase of 12 times the water decoction rate is higher, the drying temperature control below 60 ℃, pressure 0.08 ~ 0.095Mpa, pulverized powder rate of 91% or more. The result shows that the preparation process has been improved on the basis of the existing drug Xiao Ke Pills, the quality standard has been greatly improved, which has laid the foundation for the declaration of Xiaoke Capsule products.