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基于膜-大孔树脂联用工艺及质量控制研究从蝙蝠渣中富集总黄酮和蝙蝠葛碱 A

Enrichment of Total Flavonoids and Licochalcone A from Bat. Residue Based on a Combined Membrane-Macroporous Resin Process and a Quality-Control Study.

机构信息

Key Laboratory of Xinjiang Phytomedicine Resource and Utilisation, Ministry of Education, School of Pharmaceutical Sciences, Shihezi University, Shihezi 832002, China.

出版信息

Molecules. 2024 May 12;29(10):2282. doi: 10.3390/molecules29102282.

Abstract

Bat. produces a lot of licorice waste after water extraction, which also retains abundant total flavonoids (TFs) and licochalcone A. However, licorice residue is often wasted due to the lack of good utilization of resources in practical applications. This study first screened the optimal membrane pore size and resin type and then explored the mechanism and conditions of the adsorption of TFs on the resin. Then, different combinations and sequences of membrane and macroporous resin (MR) methods were investigated. It was found that using the membrane method for initial purification, followed by the MR method for further purification, yielded the best purification results. Next, response surface methodology was utilized to investigate the resin's dynamic desorption conditions for TFs. Finally, the TF purity increased from 32.9% to 78.2% (2.38-fold) after purification by a combined membrane-MR process; the purity of licochalcone A increased from 11.63 mg·g to 22.70 mg·g (1.95-fold). This study verified the feasibility of enriching TFs and licochalcone A from licorice residue using a membrane-MR coupling method. In addition, a quality-control method was established using a fingerprinting method on the basis of ultrahigh-performance liquid chromatography (UPLC) to ensure the stability of the enrichment process.

摘要

从水提后剩余的废渣中仍可提取出大量甘草,其中还保留了丰富的总黄酮(TFs)和甘草查尔酮 A。但由于实际应用中资源缺乏良好的利用,甘草废渣通常被浪费掉。本研究首先筛选出最佳的膜孔径和树脂类型,然后探索 TFs 在树脂上吸附的机制和条件。接着,考察了不同的膜-大孔树脂(MR)组合和序列方法。结果发现,采用膜法进行初步纯化,然后再用 MR 法进行进一步的纯化,可获得最佳的纯化效果。然后,利用响应面法研究了树脂对 TFs 的动态解吸条件。最后,经膜-MR 联合工艺纯化后,TFs 的纯度从 32.9%提高到 78.2%(提高了 2.38 倍);甘草查尔酮 A 的纯度从 11.63mg·g提高到 22.70mg·g(提高了 1.95 倍)。该研究验证了采用膜-MR 耦合方法从甘草废渣中富集 TFs 和甘草查尔酮 A 的可行性。此外,还基于超高效液相色谱(UPLC)建立了一种指纹图谱法质量控制方法,以确保富集过程的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ccc/11124024/16ad4c8b183b/molecules-29-02282-g001.jpg

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