A study on the preparation and quality standard of Saifula granules

M. Aisha, Atikanmu Wahafu, Yilifanjiang Kuerban, Akenmujiang Aierken, Refuhati Saimaiti, Maimaitiaili Kadi, Ainiwaer Talifu
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Abstract

Objective: To establish the decocting and formulation technology of Saifula granules, and establish a reliable TLC identification quality control standard. Methods: Orthogonal test was used to optimize the water extraction process and TLC was used for qualitative identification. Results: To optimize the process parameters of SFL granules, first, the content of total flavonoids and the total extraction rate were taken as the indexes. Through single factor and orthogonal test, the optimal extraction process was determined as follows: extraction time 1 h, solvent multiple 1:10, extract three times. After the process parameters were determined, in order to further explain the chemical composition of SFL extract, 15 compounds in SFL extract were identified by UHPLC-Q-Orbitrap-MS, 13 batches of SFL extracts were prepared, and their fingerprints were analyzed. The results showed that there were 28 common characteristic peaks in the 13 batches of SFL extracts. The similarity evaluation results of fingerprints showed that the similarities of 13 batches of SFL extracts were greater than 0.9. An HPLC-DAD method for the simultaneous determination of gallic acid, corilagin, and ellagic acid was established. The method has good repeatability, stability, and accurate results. Conclusion: The standard can comprehensively reflect the material basis of SFL granules, and the above methods are accurate, easy to operate, stable and feasible, and provide scientific basis and basis for the development, promotion, and clinical application of SFL granules.
赛富拉颗粒的制备及质量标准研究
目的:建立赛福拉颗粒煎煮配方工艺,并建立可靠的薄层色谱鉴别质量控制标准。方法:采用正交试验优化水提工艺,采用薄层色谱法进行定性鉴别。结果:首先以总黄酮的含量和总提取率为指标,对三叶莲叶颗粒剂的工艺参数进行优化。通过单因素和正交试验,确定最佳提取工艺为:提取时间1 h,溶剂倍数1:10,提取3次。在确定工艺参数后,为了进一步解释SFL提取物的化学成分,采用UHPLC-Q-Orbitrap-MS对SFL提取物中的15个化合物进行了鉴定,制备了13批SFL提取物,并对其指纹图谱进行了分析。结果表明,13批药材提取物共有28个共同特征峰。指纹图谱相似度评价结果表明,13批药材提取物相似度均大于0.9。建立了HPLC-DAD同时测定没食子酸、纤毛素和鞣花酸的方法。该方法重复性好,稳定性好,结果准确。结论:该标准能全面反映SFL颗粒的物质基础,上述方法准确、操作简便、稳定可行,为SFL颗粒的开发、推广和临床应用提供了科学依据和依据。
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