On the basis of definite active extraction and quality controlled of the semifinished products. the preparetion technology is fixed. The overall quality evaluation on the reliability "effectiveness" controllable character and stability of Fugan capsule was performed.
在有效浸出物药效确切、半成品质量可控的基础上，确定了复肝胶囊制剂的制备工艺，对复肝胶囊的安全性、有效性、可控性及稳定性进行了质量综合评价，研制出安全、有效、稳定、可控的复肝胶囊新制剂，供临床应用。
参考来源 - 复肝胶囊制剂的研究·2,447,543篇论文数据，部分数据来源于NoteExpress
目的：制备复肝灵胶囊，并对其稳定性进行考察。
Objective: To prepare the Fuganling capsule and investigate its stability.
方法以出膏率和绿原酸含量为指标，采用正交试验法和HPLC，优选复肝宁胶囊的提取工艺。
Methods the quantity of chlorogenic acid and the extraction yield of solid extracts were chosen as indexes, the orthogonal test and HPLC was used to optimize the process conditions.
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