Cargando…

Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography

In this work, pH-zone-refining countercurrent chromatography was investigated in the preparative separation of two bioactive components, oleanolic acid and ursolic acid, from three different natural products, Aralia chinensis, apple peels and Eriobotrya japonica Thunb. Oleanolic acid and ursolic aci...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Chaoyue, Wang, Xiang, Zhao, Shanshan, Sun, Wenyu, Tong, Shengqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076006/
https://www.ncbi.nlm.nih.gov/pubmed/35540200
http://dx.doi.org/10.1039/c9ra06082k
_version_ 1784701814507044864
author Wang, Chaoyue
Wang, Xiang
Zhao, Shanshan
Sun, Wenyu
Tong, Shengqiang
author_facet Wang, Chaoyue
Wang, Xiang
Zhao, Shanshan
Sun, Wenyu
Tong, Shengqiang
author_sort Wang, Chaoyue
collection PubMed
description In this work, pH-zone-refining countercurrent chromatography was investigated in the preparative separation of two bioactive components, oleanolic acid and ursolic acid, from three different natural products, Aralia chinensis, apple peels and Eriobotrya japonica Thunb. Oleanolic acid and ursolic acid are structurally isomeric pentacyclic triterpene acids that are widely distributed in many natural products. However, it was difficult to separate these components with high purity by conventional methods. A biphasic solvent system composed of n-hexane–dichloromethane–methanol–water (7 : 3 : 2 : 8, v/v) was selected, in which an optimized concentration of 10 mmol L(−1) trifluoroacetic acid was added in the upper phase as the retainer and 10 mmol L(−1) ammonia (with 25–28% NH(3)) was added in the aqueous phase as the eluter. Consequently, 38.56 mg of oleanolic acid with 99.01% purity was separated from 100 mg of the crude extract of Aralia chinensis, while 65.6 mg of a mixture of ursolic acid (90.98%) and oleanolic acid (6.51%) and 46.6 mg of a mixture of ursolic acid (74.35%) and oleanolic acid (23.61%) were separated from 100 mg of the crude extract of apple peels and 100 mg of the crude extract of Eriobotrya japonica Thunb., respectively, by pH-zone-refining countercurrent chromatography using the above selected biphasic solvent system. The results showed that pH-zone-refining countercurrent chromatography is an efficient method for the preparative separation of pentacyclic triterpene acids from natural products.
format Online
Article
Text
id pubmed-9076006
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90760062022-05-09 Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography Wang, Chaoyue Wang, Xiang Zhao, Shanshan Sun, Wenyu Tong, Shengqiang RSC Adv Chemistry In this work, pH-zone-refining countercurrent chromatography was investigated in the preparative separation of two bioactive components, oleanolic acid and ursolic acid, from three different natural products, Aralia chinensis, apple peels and Eriobotrya japonica Thunb. Oleanolic acid and ursolic acid are structurally isomeric pentacyclic triterpene acids that are widely distributed in many natural products. However, it was difficult to separate these components with high purity by conventional methods. A biphasic solvent system composed of n-hexane–dichloromethane–methanol–water (7 : 3 : 2 : 8, v/v) was selected, in which an optimized concentration of 10 mmol L(−1) trifluoroacetic acid was added in the upper phase as the retainer and 10 mmol L(−1) ammonia (with 25–28% NH(3)) was added in the aqueous phase as the eluter. Consequently, 38.56 mg of oleanolic acid with 99.01% purity was separated from 100 mg of the crude extract of Aralia chinensis, while 65.6 mg of a mixture of ursolic acid (90.98%) and oleanolic acid (6.51%) and 46.6 mg of a mixture of ursolic acid (74.35%) and oleanolic acid (23.61%) were separated from 100 mg of the crude extract of apple peels and 100 mg of the crude extract of Eriobotrya japonica Thunb., respectively, by pH-zone-refining countercurrent chromatography using the above selected biphasic solvent system. The results showed that pH-zone-refining countercurrent chromatography is an efficient method for the preparative separation of pentacyclic triterpene acids from natural products. The Royal Society of Chemistry 2019-11-27 /pmc/articles/PMC9076006/ /pubmed/35540200 http://dx.doi.org/10.1039/c9ra06082k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Chaoyue
Wang, Xiang
Zhao, Shanshan
Sun, Wenyu
Tong, Shengqiang
Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title_full Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title_fullStr Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title_full_unstemmed Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title_short Preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by pH-zone-refining countercurrent chromatography
title_sort preparative separation of structural isomeric pentacyclic triterpene oleanolic acid and ursolic acid from natural products by ph-zone-refining countercurrent chromatography
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076006/
https://www.ncbi.nlm.nih.gov/pubmed/35540200
http://dx.doi.org/10.1039/c9ra06082k
work_keys_str_mv AT wangchaoyue preparativeseparationofstructuralisomericpentacyclictriterpeneoleanolicacidandursolicacidfromnaturalproductsbyphzonerefiningcountercurrentchromatography
AT wangxiang preparativeseparationofstructuralisomericpentacyclictriterpeneoleanolicacidandursolicacidfromnaturalproductsbyphzonerefiningcountercurrentchromatography
AT zhaoshanshan preparativeseparationofstructuralisomericpentacyclictriterpeneoleanolicacidandursolicacidfromnaturalproductsbyphzonerefiningcountercurrentchromatography
AT sunwenyu preparativeseparationofstructuralisomericpentacyclictriterpeneoleanolicacidandursolicacidfromnaturalproductsbyphzonerefiningcountercurrentchromatography
AT tongshengqiang preparativeseparationofstructuralisomericpentacyclictriterpeneoleanolicacidandursolicacidfromnaturalproductsbyphzonerefiningcountercurrentchromatography