Affiliations 

  • 1 Univ Angers, SONAS, SFR QUASAV, F-49000, Angers, France
  • 2 Technical University of Munich, TUM School of Natural Sciences, Werner Siemens-Chair of Synthetic Biotechnology (WSSB), Lichtenbergstraße 4, 85748, Garching, Germany
  • 3 University of Malaya, Faculty of Sciences, Department of Chemistry, Malaysia
  • 4 Institut de Chimie des Substances Naturelles, CNRS-ICSN, UPR 2301, Université Paris-Saclay, 91198, Gif-sur-Yvette, France
  • 5 Univ Angers, LERIA, SFR MATHSTIC, F-49000, Angers, France
  • 6 Univ Angers, SONAS, SFR QUASAV, F-49000, Angers, France. Electronic address: severine.derbre@univ-angers.fr
  • 7 Univ Angers, SONAS, SFR QUASAV, F-49000, Angers, France. Electronic address: andreas.schinkovitz@univ-angers.fr
Talanta, 2025 Jan 23;287:127626.
PMID: 39893730 DOI: 10.1016/j.talanta.2025.127626

Abstract

The chemical profiling of complex mixtures of natural products (NPs) is a major challenge in analytical chemistry and generally addressed by liquid chromatography coupled to mass spectrometry (LC-MS). In recent years also matrix free laser desorption ionization-mass spectrometry (LDI-MS) has become a versatile and time efficient complement to LC-MS. However, the absence of chromatographic separation in LDI-MS does not permit the differentiation of isomers. Providing a potential solution to this problem, the current work presents a combined LDI-Ion mobility spectrometry-tandem mass spectrometry (LDI-IMS-MS2) approach, which facilitated the successful differentiation of four constitutional xanthone isomers namely butyraxanthone D, cratoxylone, garcinone D and parvixanthone G. In addition, the experimental collision cross section (CCS) distribution values of nine unreported xanthones are described. Based on these results, a proof of concept for the so far unexplored concept of a LDI-IMS-MS2 based molecular network is being presented.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.