Literature DB >> 26551537

Identification, characterization and distribution of monoterpene indole alkaloids in Rauwolfia species by Orbitrap Velos Pro mass spectrometer.

Sunil Kumar1, Awantika Singh2, Vikas Bajpai2, Brijesh Kumar3.   

Abstract

Monoterpene indole alkaloids (MIAs) are medicinally important class of compounds abundant in the roots of Rauwolfia species (Apocynaceae). MIAs such as yohimbine (aphrodisiac agent) and reserpine (antihypertensive, tranquilizer) are the official drugs included in Model List of Essential Drugs of World Health Organization (WHO). Therefore, we have attempt to identify and characterize the MIAs in the crude extracts of six Rauwolfia species using ultrahigh-performance liquid chromatography coupled with Orbitrap Velos Pro hybrid mass spectrometer. The identity of the MIAs were construed using the high resolution tandem mass spectrometry (HRMS/MS) spectra of standard compounds 'yohimbine' and 'reserpine' in higher energy collisional dissociation (HCD) and collision-induced dissociation (CID) modes. The diagnostic fragment ions found in HCD mode was highly affected by variation of normalized collision energy (NCE) and gave few product ions ('C-F') while CID produced intense and more diagnostic product ions ('A-F'). Consequently, CID-MS/MS mode provided significantly more structural information about basic skeleton and therefore the recommended mode for analysis of MIAs. Furthermore, six diagnostic fragmentation pathways were established by multi-stage mass analysis (MS(n) (n=5)) analysis which gave information regarding the substitution. Fragment ions 'A-F' revealed the number and position of substituents on indole and terpene moieties. The proposed diagnostic fragmentation pathways have been successfully applied for identification and characterization of MIAs in crude root extracts of six Rauwolfia species. Ten bioactive reserpine class of MIAs were tentatively identified and characterized on the basis of chromatographic and mass spectrometric features as well as HRMS/MS an MS(n) (n=4) analysis.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Collision-induced dissociation; Higher energy collisional dissociation; Monoterpene indole alkaloids; Orbitrap Velos Pro; Rauwolfia species

Mesh:

Substances:

Year:  2015        PMID: 26551537     DOI: 10.1016/j.jpba.2015.10.037

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  4 in total

1.  Structural characterization of monoterpene indole alkaloids in ethanolic extracts of Rauwolfia species by liquid chromatography with quadrupole time-of-flight mass spectrometry.

Authors:  Sunil Kumar; Awantika Singh; Vikas Bajpai; Mukesh Srivastava; Bhim Pratap Singh; Brijesh Kumar
Journal:  J Pharm Anal       Date:  2016-05-07

2.  Analysis of isoquinoline alkaloids from Mahonia leschenaultia and Mahonia napaulensis roots using UHPLC-Orbitrap-MSn and UHPLC-QqQLIT-MS/MS.

Authors:  Awantika Singh; Vikas Bajpai; Sunil Kumar; Ajay Kumar Singh Rawat; Brijesh Kumar
Journal:  J Pharm Anal       Date:  2016-10-18

3.  On-the-fly investigation of XUV excited large molecular ions using a high harmonic generation light source.

Authors:  Marius Hervé; Alexie Boyer; Richard Brédy; Abdul-Rahman Allouche; Isabelle Compagnon; Franck Lépine
Journal:  Sci Rep       Date:  2022-08-01       Impact factor: 4.996

4.  Identification of alkaloids and related intermediates of Dendrobium officinale by solid-phase extraction coupled with high-performance liquid chromatography tandem mass spectrometry.

Authors:  Cheng Song; Yunpeng Zhang; Muhammad Aamir Manzoor; Guohui Li
Journal:  Front Plant Sci       Date:  2022-08-04       Impact factor: 6.627

  4 in total

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