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dc.contributor.authorRaro Macián, Montserrat
dc.contributor.authorIbáñez, Maria
dc.contributor.authorGil Solsona, Ruben
dc.contributor.authorFabregat, Andreu
dc.contributor.authorTudela, Eva
dc.contributor.authorDeventer, Koen
dc.contributor.authorVentura, Rosa
dc.contributor.authorSegura, Jordi
dc.contributor.authorMarcos, Josep
dc.contributor.authorKotronoulas, Aristotelis
dc.contributor.authorJoglar, Jesús
dc.contributor.authorFarré, Magi
dc.contributor.authorYang, Sheng
dc.contributor.authorXing, Yanyi
dc.contributor.authorVan Eenoo, Peter
dc.contributor.authorPitarch, Elena
dc.contributor.authorHernandez, Felix
dc.contributor.authorSancho, Juan V
dc.contributor.authorPozo, Óscar J.
dc.date.accessioned2015-12-16T11:16:23Z
dc.date.available2015-12-16T11:16:23Z
dc.date.issued2015
dc.identifier.issn0003-2700
dc.identifier.issn1520-6882
dc.identifier.urihttp://hdl.handle.net/10234/143752
dc.description.abstractThe use of untargeted metabolomics for the discovery of markers is a promising and virtually unexplored tool in the doping control field. Hybrid quadrupole time-of- flight (QTOF) and hybrid quadrupole Orbitrap (Q Exactive) mass spectrometers, coupled to ultrahigh pressure liquid chromatography, are excellent tools for this purpose. In the present work, QTOF and Q Exactive have been used to look for markers for testosterone cypionate misuse by means of untargeted metabolomics. Two different groups of urine samples were analyzed, collected before and after the intramuscular administration of testosterone cypionate. In order to avoid analyte losses in the sample treatment, samples were just 2-fold diluted with water and directly injected into the chromatographic system. Samples were analyzed in both positive and negative ionization modes. Data from both systems were treated under untargeted metabolomic strategies using XCMS application and multivariate analysis. Results from the two mass spectrometers differed in the number of detected features, but both led to the same potential marker for the particular testosterone ester misuse. The in-depth study of the MS and MS/MS behavior of this marker allowed for the establishment of 1-cyclopentenoylglycine as a feasible structure. The putative structure was confirmed by comparison with synthesized material. This potential marker seems to come from the metabolism of the cypionic acid release after hydrolysis of the administered ester. Its suitability for doping control has been evaluated.ca_CA
dc.description.sponsorShipMinistry of Education and Science, Spain: DEP2011-­‐28573-­‐C02-­‐01/02; WADA: project 14A29OP; Generalitat Valenciana: Prometeo/2009/054; PrometeoII/2014/023; ISIC EnviFood 2012/016ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relation.isPartOfAnalytical Chemistry , vol. 87. núm. 16ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/CNE/1.0/*
dc.subjectUHPLC-­‐(Q)TOF MSca_CA
dc.subjectOrbitrapca_CA
dc.subjectTestosteroneca_CA
dc.subjectdopingca_CA
dc.subjectmetabolomicsca_CA
dc.subjectmultivariate analysisca_CA
dc.titleUntargeted Metabolomics in Doping Control: Detection of New Markers of Testosterone Misuse by Ultrahigh Performance Liquid Chromatography Coupled to High-Resolution Mass Spectrometryca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/acs.analchem.5b02254
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/pdf/10.1021/acs.analchem.5b02254ca_CA
dc.editionpostprint del autorca_CA
dc.type.versioninfo:eu-repo/semantics/acceptedVersion


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