Screening for Astragalus hamosus Triterpenoid Saponins Using HPTLC Methods: Prior Identification of Azukisaponin Isomers
Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from and, more precisely, the saponins. Subsequent purificati...
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Published in | Molecules (Basel, Switzerland) Vol. 27; no. 17; p. 5376 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Abstract | Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from
and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the
saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed. |
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AbstractList | Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from Astragalus hamosus and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the Astragalus hamosus saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed.Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from Astragalus hamosus and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the Astragalus hamosus saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed. Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from Astragalus hamosus and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the Astragalus hamosus saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from Astragalus hamosus and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the Astragalus hamosus saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed. Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed. Due to their particular structural characteristics, the extraction and isolation of saponins from plants present a serious challenge. In this study, specific extraction protocols were first implemented to extract the secondary metabolites from Astragalus hamosus and, more precisely, the saponins. Subsequent purification of the extracts was based on a single chromatographic technique, high-performance thin-layer chromatography, applying two development systems: a one-step system that separated molecules according to their polarity and a multiple development system that made it possible to detect the triterpenoid saponins, azukisaponin or soyasapogenol at a retarded Rf of 0.2. The difficulties of detecting the Astragalus hamosus saponins encountered during the extraction and purification of the extracts have been highlighted and the strategy carried out to isolate the saponins has been discussed. |
Author | Raynaud, Christine Delgado Marghali, Sonia Giacinti, Geraldine Nafti, Khouloud |
AuthorAffiliation | 1 Laboratoire de Chimie Ago-Industrielle (LCA), Université de Toulouse, INRAe, 4 Allée Emile Monso, 31030 Toulouse, France 3 Centre d’Application et de Traitement des Agro-Ressources (CATAR), Toulouse-INP, ENSIACET, 4 Allée Emile Monso, 31030 Toulouse, France 2 Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Tunis 1068, Tunisia |
AuthorAffiliation_xml | – name: 2 Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Tunis 1068, Tunisia – name: 3 Centre d’Application et de Traitement des Agro-Ressources (CATAR), Toulouse-INP, ENSIACET, 4 Allée Emile Monso, 31030 Toulouse, France – name: 1 Laboratoire de Chimie Ago-Industrielle (LCA), Université de Toulouse, INRAe, 4 Allée Emile Monso, 31030 Toulouse, France |
Author_xml | – sequence: 1 givenname: Khouloud surname: Nafti fullname: Nafti, Khouloud organization: Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Tunis 1068, Tunisia – sequence: 2 givenname: Geraldine surname: Giacinti fullname: Giacinti, Geraldine organization: Centre d'Application et de Traitement des Agro-Ressources (CATAR), Toulouse-INP, ENSIACET, 4 Allée Emile Monso, 31030 Toulouse, France – sequence: 3 givenname: Sonia orcidid: 0000-0002-3090-1454 surname: Marghali fullname: Marghali, Sonia organization: Laboratoire de Génétique Moléculaire, Immunologie et Biotechnologie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Tunis 1068, Tunisia – sequence: 4 givenname: Christine Delgado surname: Raynaud fullname: Raynaud, Christine Delgado organization: Centre d'Application et de Traitement des Agro-Ressources (CATAR), Toulouse-INP, ENSIACET, 4 Allée Emile Monso, 31030 Toulouse, France |
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Keywords | azukisaponin triterpenoid saponin Astragalus hamosus soyasaponin HPTLC |
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SubjectTerms | Alzheimer's disease Astragalus hamosus Astragalus Plant - chemistry azukisaponin Biological activity Breast cancer Chromatography Chromatography, Thin Layer - methods Development systems HPTLC Isomers Life Sciences Metabolites Plant Extracts - chemistry Polarity Purification Saponins Saponins - chemistry Secondary metabolites Seeds Solvents soyasaponin Thin layer chromatography Triterpenes - chemistry triterpenoid saponin |
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Title | Screening for Astragalus hamosus Triterpenoid Saponins Using HPTLC Methods: Prior Identification of Azukisaponin Isomers |
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