Effects of structural characteristics of (un)conjugated steroid metabolites in their collision cross section value
View/ Open
Impact
Scholar |
Other documents of the author: Bressan, Claudia; Celma, Alberto; Alechaga Silva, Élida; Monfort, Nuria; Ventura, Rosa; Sancho, Juan V
Metadata
Show full item recordcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/33596
comunitat-uji-handle3:10234/33597
comunitat-uji-handle4:
INVESTIGACIONMetadata
Title
Effects of structural characteristics of (un)conjugated steroid metabolites in their collision cross section valueAuthor (s)
Date
2023-05-08Publisher
ElsevierISSN
0003-2670Bibliographic citation
Bressan, C., Celma, A., Alechaga, É., Monfort, N., Ventura, R., Sancho, J. V. Effects of structural characteristics of (un)conjugated steroid metabolites in their collision cross section value, Anal Chim Acta. 1254 (2023) 341128. 10.1016/j.aca.2023.341128Type
info:eu-repo/semantics/articlePublisher version
https://www.sciencedirect.com/science/article/pii/S0003267023003495?casa_token=j ...Version
info:eu-repo/semantics/submittedVersionSubject
Abstract
In this work, the collision cross section (CCS) value of 103 steroids (including unconjugated metabolites and phase II metabolites conjugated with sulfate and glucuronide groups) was determined by liquid chromatography ... [+]
In this work, the collision cross section (CCS) value of 103 steroids (including unconjugated metabolites and phase II metabolites conjugated with sulfate and glucuronide groups) was determined by liquid chromatography coupled to traveling wave ion mobility spectrometry (LC-TWIMS). A time of flight (QTOF) mass analyzer was used to perform the analytes determination at high-resolution mass spectrometry. An electrospray ionization source (ESI) was used to generate [M+H]+, [M + NH4]+ and/or [M − H]- ions. High reproducibility was observed for the CCS determination in both urine and standard solutions, obtaining RSD lower than 0.3% and 0.5% in all cases respectively. CCS determination in matrix was in accordance with the CCS measured in standards solution showing deviations below 2%. In general, CCS values were directly correlated with the ion mass and allowed differentiating between glucuronides, sulfates and free steroids although differences among steroids of the same group were less significant. However, more specific information was obtained for phase II metabolites observing differences in the CCS value of isomeric pairs concerning the conjugation position or the α/β configuration, which could be useful in the structural elucidation of new steroid metabolites in the anti-doping field. Finally, the potential of IMS reducing interferences from the sample matrix was also tested for the analysis of a glucuronide metabolite of bolasterone (5β-androstan-7α,17α-dimethyl-3α,17β-diol-3-glucuronide) in urine samples. [-]
Is part of
Analytica Chimica Acta, 2023, vol. 1254Funder Name
Ministerio de Economía y Competitividad (España) | University Jaume I | Generalitat de Catalunya
Funder ID
http://dx.doi.org/10.13039/501100003329
Project code
MINECO/ICTI2013-2016/CTQ2015-63968-C2-2-P | UJI-B2020-19 | 2021SGR0040
Project title or grant
Aplicación de los avances recientes en espectrometría de masas al análisis de drogas y fármacos en fluidos biológicos
Rights
Copyright © Elsevier B.V. All rights reserved.
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
This item appears in the folowing collection(s)
- IUPA_Articles [310]