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dc.contributor.authorPitarch-Motellón, Jorge
dc.contributor.authorRoig-Navarro, Antoni F.
dc.contributor.authorSancho, Juan V
dc.contributor.authorIbáñez, Maria
dc.contributor.authorFabregat-Cabello, Neus
dc.contributor.authorPozo, Óscar J.
dc.contributor.authorVentura, Rosa
dc.contributor.authorGarcía Alonso, J. Ignacio
dc.contributor.authorRodríguez González, Pablo
dc.contributor.authorGonzález Gago, Adriana
dc.contributor.authorEreño Artabe, Amaia
dc.contributor.authorVan Eenoo, Peter
dc.contributor.authorDeventer, Koen
dc.contributor.authorDehnes, Yvette
dc.contributor.authorRzeppa, Sebastian
dc.date.accessioned2017-06-06T10:39:35Z
dc.date.available2017-06-06T10:39:35Z
dc.date.issued2017-06
dc.identifier.urihttp://hdl.handle.net/10234/167880
dc.description.abstractThree quantification methodologies, namely calibration with internal standard (Cal-IS, non-weighted), weighted calibration with internal standard (wCal-IS) and isotope pattern deconvolution (IPD) have been used for the determination of testosterone in urine by LC-MS/MS. Uncertainty has been calculated and compared for the three methodologies through intra- and inter-laboratory reproducibility assays. IPD showed the best performance for the intra-laboratory reproducibility, with RSD and combined uncertainty values below 4% and 9% respectively. wCal-IS showed similar performance, while Cal-IS where not constant and clearly worse at the lowest concentration assayed (2 ng/mL) reaching RSD values up to 16%. The inter-laboratory assay indicated similar results although wCal-IS RSD (20%) was higher than IPD (10%) and Cal-IS get worse with RSD higher than 40% for the lowest concentration level. Uncertainty budgets calculated for the three procedures revealed that intercept and slope were the most important factors contributing to uncertainty for Cal-IS. The main factors for wCal-IS and IPD were the volumes of sample and/or standard measured.ca_CA
dc.description.sponsorShipThe authors acknowledge financial support from the Generalitat Valenciana (Research group of excellence Prometeo II 2014/023 and Collaborative Research on Environment and Food Safety ISIC/2012/016), as well as University Jaume I for project PB1-1B2013-55. Finally, the authors are grateful to the Serveis Centrals d'Instrumentació Científica (SCIC) of University Jaume I for using Acquity and TQD instruments.ca_CA
dc.format.extent18 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherElsevierca_CA
dc.relation.isPartOfJournal of Chromatography A, June 2017ca_CA
dc.rights© 2017 Elsevier B.V. All rights reserved.ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjecttestosteroneca_CA
dc.subjecturineca_CA
dc.subjectmass spectrometryca_CA
dc.subjectliquid chromatographyca_CA
dc.titleEvaluation of uncertainty sources in the determination of testosterone in urine by calibration-based and isotope dilution quantification using ultra high performance liquid chromatography tandem mass spectrometryca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttps://doi.org/10.1016/j.chroma.2017.05.072
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersionhttp://www.sciencedirect.com/science/article/pii/S0021967317308300ca_CA
dc.type.versioninfo:eu-repo/semantics/submittedVersion


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