A1 Refereed original research article in a scientific journal

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




AuthorsSaha Sanjib, Imran Iqbal Bin

PublisherJohn Wiley & Sons Ltd.

Publication year2021

JournalRapid Communications in Mass Spectrometry

Article numbere9005

Volume35

Issue5

eISSN1097-0231

DOIhttps://doi.org/10.1002/rcm.9005

Web address https://doi.org/10.1002/rcm.9005

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/50029316


Abstract

RATIONALE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.


Downloadable publication

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.





Last updated on 2024-26-11 at 20:09