Efficient preparation of hyperoside and quercitrin from Zanthoxylum bungeanum Maxim leaves using an integrated surfactant-based aqueous two-phase system, back-extraction and adsorption separation

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2024-09-16 DOI:10.1080/14786419.2023.2219822
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Abstract

Zanthoxylum bungeanum leaves (ZBL) are of great medicinal value for being rich in hyperoside and quercitrin. In this study, a novel, efficient and economical continuous process was established. First, aqueous two-phase system (ATPS) composed of Triton X-100/(NH4)2SO4 was employed to enrich hyperoside and quercitrin from ZBL extracts and the recoveries reached 98.53% and 99.12%. Then back-extraction with dichloromethane-water system was adopted to separate hyperoside and quercitrin from Triton X-100 micelles which were recycled and the recoveries reached 86.58% and 85.19%. Finally, S-8 macroporous resin was used for removing the salt introduced in ATPS and the final recoveries reached 82.38% and 81.81%, much higher than the total flavonoids recovery as 69.08%. Furthermore, scale-up experiment certified that the continuous process was feasible for industrial production. Efficiently and economically, this method achieved a great breakthrough in purity and provided a novel reference for further purification and phase-forming component recycle.
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利用基于表面活性剂的综合水基两相体系、反萃取和吸附分离,从 Zanthoxylum bungeanum Maxim 叶子中高效制备金丝桃苷和槲皮素。
黄樟叶(Zanthoxylum bungeanum,ZBL)富含金丝桃苷和槲皮素,具有极高的药用价值。本研究建立了一种新颖、高效、经济的连续生产工艺。首先,采用Triton X-100/(NH4)2SO4组成的水相两相体系(ATPS)富集ZBL提取物中的金丝桃苷和槲皮素,回收率分别达到98.53%和99.12%。然后采用二氯甲烷-水体系反萃取,从回收的 Triton X-100 胶束中分离出金丝桃苷和槲皮苷,回收率分别达到 86.58% 和 85.19%。最后,使用 S-8 大孔树脂去除 ATPS 中引入的盐分,最终回收率分别达到 82.38% 和 81.81%,远高于总黄酮回收率 69.08%。此外,放大实验证明该连续工艺可用于工业生产。该方法高效、经济,在纯度方面实现了重大突破,为进一步纯化和回收相形成成分提供了新的参考。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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