Discrimination of Regioisomeric and Stereoisomeric Saponins from Aesculus hippocastanum Seeds by Ion Mobility Mass Spectrometry.
Cyclic ion mobility
Escin
Ion mobility
Natural products
Regioisomers
Saponins
Stereoisomers
TWIMS
Journal
Journal of the American Society for Mass Spectrometry
ISSN: 1879-1123
Titre abrégé: J Am Soc Mass Spectrom
Pays: United States
ID NLM: 9010412
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
26
03
2019
accepted:
08
08
2019
revised:
01
08
2019
pubmed:
28
8
2019
medline:
28
8
2019
entrez:
28
8
2019
Statut:
ppublish
Résumé
Modern mass spectrometry methods provide a huge benefit to saponin structural characterization, especially when combined with collision-induced dissociation experiments to obtain a partial description of the saponin (ion) structure. However, the complete description of the structures of these ubiquitous secondary metabolites remain challenging, especially since isomeric saponins presenting small differences are often present in a single extract. As a typical example, the horse chestnut triterpene glycosides, the so-called escins, comprise isomeric saponins containing subtle differences such as cis-trans ethylenic configuration (stereoisomers) of a side chain or distinct positions of an acetyl group (regioisomers) on the aglycone. In the present paper, the coupling of liquid chromatography and ion mobility mass spectrometry has been used to distinguish regioisomeric and stereoisomeric saponins. Ion mobility arrival time distributions (ATDs) were recorded for the stereoisomeric and regioisomeric saponin ions demonstrating that isomeric saponins can be partially separated using ion mobility on a commercially available traveling wave ion mobility (TWIMS) mass spectrometer. Small differences in the ATD can only be monitored when the isomeric saponins are separated with liquid chromatography prior to the IM-MS analysis. However, gas phase separation between stereoisomeric and regioisomeric saponin ions can be successfully realized, without any LC separation, on a cyclic ion mobility-enabled quadrupole time-of-flight (Q-cIM-oaToF) mass spectrometer. The main outcome of the present paper is that the structural analysis of regioisomeric and stereoisomeric natural compounds that represents a real challenge can take huge advantages of ion mobility experiments but only if increased ion mobility resolution is attainable.
Identifiants
pubmed: 31452089
doi: 10.1007/s13361-019-02310-7
pii: 10.1007/s13361-019-02310-7
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2228-2237Références
Eur J Mass Spectrom (Chichester). 2009;15(2):113-30
pubmed: 19423898
Rapid Commun Mass Spectrom. 2018 Jun 6;:null
pubmed: 29873851
Adv Pharm Bull. 2015 Nov;5(4):587-91
pubmed: 26819933
J Nat Prod. 1996 Apr;59(4):348-54
pubmed: 8699179
J Am Soc Mass Spectrom. 2014 Sep;25(9):1600-9
pubmed: 25001382
Mar Drugs. 2010 Jan 21;8(1):173-89
pubmed: 20161976
Phytochem Rev. 2010 Sep;9(3):425-474
pubmed: 20835386
Anal Chem. 2019 Jul 2;91(13):8564-8573
pubmed: 31141659
Anal Chem. 2017 Nov 21;89(22):12176-12184
pubmed: 29039942
Chem Pharm Bull (Tokyo). 1998 Nov;46(11):1764-9
pubmed: 9845957
Chem Pharm Bull (Tokyo). 1994 Jun;42(6):1357-9
pubmed: 8069982
J Am Soc Mass Spectrom. 2006 Jun;17(6):795-806
pubmed: 16603377
Arch Microbiol. 1975 Jun 22;104(2):147-50
pubmed: 1171670
J Ethnopharmacol. 2004 Oct;94(2-3):219-43
pubmed: 15325725
Chem Pharm Bull (Tokyo). 1996 Aug;44(8):1454-64
pubmed: 8795266
J Am Soc Mass Spectrom. 2017 Nov;28(11):2483-2491
pubmed: 28762031
Mar Drugs. 2018 Nov 01;16(11):null
pubmed: 30388793
Comp Biochem Physiol B Biochem Mol Biol. 2009 Feb;152(2):124-34
pubmed: 19036349
Biol Pharm Bull. 1997 Oct;20(10):1092-5
pubmed: 9353571
Org Biomol Chem. 2014 Nov 28;12(44):8803-22
pubmed: 25295776
Comp Biochem Physiol B Biochem Mol Biol. 2014 Feb;168:1-11
pubmed: 24177147
Phytochemistry. 2007 Feb;68(3):275-97
pubmed: 17141815
Rapid Commun Mass Spectrom. 2011 Jun 15;25(11):1559-66
pubmed: 21594930
Anal Bioanal Chem. 2017 May;409(12):3115-3126
pubmed: 28251290