Isolation, detection, and quantification of hydrolyzable tannins of the biosynthetic pathway by liquid chromatography coupled with tandem mass spectrometry

dc.contributor.authorSaha Sanjib
dc.contributor.authorImran Iqbal Bin
dc.contributor.organizationfi=lääkekehityksen kemia|en=Pharmaseutical Chemistry|
dc.contributor.organization-code2606303
dc.converis.publication-id50029316
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/50029316
dc.date.accessioned2022-10-28T14:01:47Z
dc.date.available2022-10-28T14:01:47Z
dc.description.abstract<p>RATIONALE</p><p>Hydrolyzable tannins (HTs) are widely distributed complex secondary metabolites with potential bioactivities and health‐promoting benefits. A highly sensitive compound‐specific UHPLC/MS/MS method is required for their successful detection and quantification in order to advance the study of HTs.</p><p>METHODS</p><p>In this study, 36 HTs belonging to the HT biosynthetic pathway covering 13 major branches were extracted by cold extraction and fractioned by Sephadex LH‐20 size exclusion chromatography. Followed fractionation, the HTs were purified by semipreparative HPLC so that they could be used for the development of a UHPLC/QqQ‐MS/MS multiple reaction monitoring (MRM) method for their characterization. The cone voltage and collision energy for each HT were extensively optimized during the development of the MRM method.</p><p>RESULTS</p><p>The developed method was very useful for the detection and quantification of marker tannins with a low limit of detection (LOD) and limit of quantification (LOQ), depending on the size and complexity of the structures of HTs. Each isolated compound was successfully identified and characterized by UHPLC/ESI‐Orbitrap‐MS/MS analysis. In addition, a new methodology for cold extraction and fractionation by Sephadex LH‐20 chromatography has been developed for the targeted extraction of HTs.</p><p>CONCLUSIONS</p><p>This study has provided a compound‐specific MRM method for the detection and quantification of representative HTs from the diverse phytochemical samples, with higher sensitivity than the existing group‐specific MRM method.<br></p>
dc.identifier.eissn1097-0231
dc.identifier.jour-issn0951-4198
dc.identifier.olddbid185832
dc.identifier.oldhandle10024/168926
dc.identifier.urihttps://www.utupub.fi/handle/11111/42588
dc.identifier.urlhttps://doi.org/10.1002/rcm.9005
dc.identifier.urnURN:NBN:fi-fe2021042824752
dc.language.isoen
dc.okm.affiliatedauthorSaha, Sanjib
dc.okm.affiliatedauthorImran, Iqbal
dc.okm.discipline114 Physical sciencesen_GB
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline119 Other natural sciencesen_GB
dc.okm.discipline114 Fysiikkafi_FI
dc.okm.discipline116 Kemiafi_FI
dc.okm.discipline119 Muut luonnontieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherJohn Wiley & Sons Ltd.
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumbere9005
dc.relation.doi10.1002/rcm.9005
dc.relation.ispartofjournalRapid Communications in Mass Spectrometry
dc.relation.issue5
dc.relation.volume35
dc.source.identifierhttps://www.utupub.fi/handle/10024/168926
dc.titleIsolation, detection, and quantification of hydrolyzable tannins of the biosynthetic pathway by liquid chromatography coupled with tandem mass spectrometry
dc.year.issued2021

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