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阐述仿制药逍遥丸(浓缩丸)在质量标准提高研究过程中,采用高效液相色谱法对其芍药苷含量测定的研究,并与市售产品进行比对,结果证明其工艺稳定、含量可控,弥补了现行逍遥丸(浓缩丸)质量标准没有含量测定的不足。
This paper expounds the research on the determination of paeoniflorin in high-performance liquid chromatography (HPLC) in the process of improving the quality standard of the Xiaoyao Pill (Concentrated Pill) which is a generic drug, and compares it with the commercially available products. The result shows that the process is stable and the content is controllable , To make up for the current Xiaoyao Wan (Pill) quality standards without the determination of the lack of content.