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Comparison of ultra-high performance supercritical fluid chromatography and ultra-high performance liquid chromatography for the separation of spirostanol saponins

[Display omitted] •UHPSFC is a good automatic chromatographic technique and has little in common with normal phase HPLC.•UHPSFC separates spirostanol saponins varying only in sugar chains or in hydroxyls of aglycones well.•UHPLC with C18 column separates spirostanol saponins varying only in aglycone...

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Published in:Journal of pharmaceutical and biomedical analysis 2016-02, Vol.120, p.72-78
Main Authors: Zhu, Ling-ling, Zhao, Yang, Xu, Yong-wei, Sun, Qing-long, Sun, Xin-guang, Kang, Li-ping, Yan, Ren-yi, Zhang, Jie, Liu, Chao, Ma, Bai-ping
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cited_by cdi_FETCH-LOGICAL-c422t-8b44fea320a4d6d268b4e3c731fe3c6f7e50db39d6276334ac85051c6b2623593
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creator Zhu, Ling-ling
Zhao, Yang
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Liu, Chao
Ma, Bai-ping
description [Display omitted] •UHPSFC is a good automatic chromatographic technique and has little in common with normal phase HPLC.•UHPSFC separates spirostanol saponins varying only in sugar chains or in hydroxyls of aglycones well.•UHPLC with C18 column separates spirostanol saponins varying only in aglycones well, especially with different double bonds.•UHPSFC and UHPLC are complementary and could be applied together in separating spirostanol saponins. Spirostanol saponins are important active components of some herb medicines, and their isolation and purification are crucial for the research and development of traditional Chinese medicines. We aimed to compare the separation of spirostanol saponins by ultra-high performance supercritical fluid chromatography (UHPSFC) and ultra-high performance liquid chromatography (UHPLC). Four groups of spirostanol saponins were separated respectively by UHPSFC and UHPLC. After optimization, UHPSFC was performed with a HSS C18 SB column or a Diol column and with methanol as the co-solvent. A BEH C18 column and mobile phase containing water (with 0.1% formic acid) and acetonitrile were used in UHPLC. We found that UHPSFC could be performed automatically and quickly. It is effective in separating the spirostanol saponins which share the same aglycone and vary in sugar chains, and is very sensitive to the number and the position of hydroxyl groups in aglycones. However, the resolution of spirostanol saponins with different aglycones and the same sugar moiety by UHPSFC was not ideal and could be resolved by UHPLC instead. UHPLC is good at differentiating the variation in aglycones, and is influenced by double bonds in aglycones. Therefore, UHPLC and UHPSFC are complementary in separating spirostanol saponins. Considering the naturally produced spirostanol saponins in herb medicines are different both in aglycones and in sugar chains, a better separation can be achieved by combination of UHPLC and UHPSFC. UHPSFC is a powerful technique for improving the resolution when UHPLC cannot resolve a mixture of spirostanol saponins and vice versa.
doi_str_mv 10.1016/j.jpba.2015.12.002
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Spirostanol saponins are important active components of some herb medicines, and their isolation and purification are crucial for the research and development of traditional Chinese medicines. We aimed to compare the separation of spirostanol saponins by ultra-high performance supercritical fluid chromatography (UHPSFC) and ultra-high performance liquid chromatography (UHPLC). Four groups of spirostanol saponins were separated respectively by UHPSFC and UHPLC. After optimization, UHPSFC was performed with a HSS C18 SB column or a Diol column and with methanol as the co-solvent. A BEH C18 column and mobile phase containing water (with 0.1% formic acid) and acetonitrile were used in UHPLC. We found that UHPSFC could be performed automatically and quickly. It is effective in separating the spirostanol saponins which share the same aglycone and vary in sugar chains, and is very sensitive to the number and the position of hydroxyl groups in aglycones. However, the resolution of spirostanol saponins with different aglycones and the same sugar moiety by UHPSFC was not ideal and could be resolved by UHPLC instead. UHPLC is good at differentiating the variation in aglycones, and is influenced by double bonds in aglycones. Therefore, UHPLC and UHPSFC are complementary in separating spirostanol saponins. Considering the naturally produced spirostanol saponins in herb medicines are different both in aglycones and in sugar chains, a better separation can be achieved by combination of UHPLC and UHPSFC. 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However, the resolution of spirostanol saponins with different aglycones and the same sugar moiety by UHPSFC was not ideal and could be resolved by UHPLC instead. UHPLC is good at differentiating the variation in aglycones, and is influenced by double bonds in aglycones. Therefore, UHPLC and UHPSFC are complementary in separating spirostanol saponins. Considering the naturally produced spirostanol saponins in herb medicines are different both in aglycones and in sugar chains, a better separation can be achieved by combination of UHPLC and UHPSFC. 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Spirostanol saponins are important active components of some herb medicines, and their isolation and purification are crucial for the research and development of traditional Chinese medicines. We aimed to compare the separation of spirostanol saponins by ultra-high performance supercritical fluid chromatography (UHPSFC) and ultra-high performance liquid chromatography (UHPLC). Four groups of spirostanol saponins were separated respectively by UHPSFC and UHPLC. After optimization, UHPSFC was performed with a HSS C18 SB column or a Diol column and with methanol as the co-solvent. A BEH C18 column and mobile phase containing water (with 0.1% formic acid) and acetonitrile were used in UHPLC. We found that UHPSFC could be performed automatically and quickly. It is effective in separating the spirostanol saponins which share the same aglycone and vary in sugar chains, and is very sensitive to the number and the position of hydroxyl groups in aglycones. However, the resolution of spirostanol saponins with different aglycones and the same sugar moiety by UHPSFC was not ideal and could be resolved by UHPLC instead. UHPLC is good at differentiating the variation in aglycones, and is influenced by double bonds in aglycones. Therefore, UHPLC and UHPSFC are complementary in separating spirostanol saponins. Considering the naturally produced spirostanol saponins in herb medicines are different both in aglycones and in sugar chains, a better separation can be achieved by combination of UHPLC and UHPSFC. UHPSFC is a powerful technique for improving the resolution when UHPLC cannot resolve a mixture of spirostanol saponins and vice versa.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>26707085</pmid><doi>10.1016/j.jpba.2015.12.002</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0810-0466</orcidid></addata></record>
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subjects Chromatographic behavior
Chromatography, High Pressure Liquid - methods
Chromatography, Supercritical Fluid - methods
Methanol - chemistry
Natural products
Plants, Medicinal - chemistry
Saponins - chemistry
Spirostanol saponins
Spirostans - chemistry
Ultra-high performance liquid chromatography
Ultra-high performance supercritical fluid chromatography
Water - chemistry
title Comparison of ultra-high performance supercritical fluid chromatography and ultra-high performance liquid chromatography for the separation of spirostanol saponins
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