Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/45333
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dc.contributor.authorGonzález-Antuña, Anaen_US
dc.contributor.authorRodríguez-González, Pabloen_US
dc.contributor.authorLavandera, Ivánen_US
dc.contributor.authorCentineo, Giuseppeen_US
dc.contributor.authorGotor, Vicenteen_US
dc.contributor.authorGarcía Alonso, J. Ignacioen_US
dc.date.accessioned2018-11-22T09:01:21Z-
dc.date.available2018-11-22T09:01:21Z-
dc.date.issued2012en_US
dc.identifier.issn1618-2642en_US
dc.identifier.urihttp://hdl.handle.net/10553/45333-
dc.description.abstractA novel and fast routine method for the simultaneous determination and confirmation of clenbuterol in bovine and human urine samples by gas chromatography electron ionization mass spectrometry (GC-EI-MS) has been developed. The method employs isotope dilution mass spectrometry (IDMS) and is based on a combination of minimal labeling (a single (13)C label in the molecule) and isotope pattern deconvolution (IPD). This new methodology does not require the construction of a methodological calibration graph, and was compared with the classical IDMS procedure employed in clenbuterol analysis based on the use of a deuterated compound as internal standard (d(9)-clenbuterol) and a calibration curve. The sample preparation consists of simple extraction with dichloromethane, which was dried and derivatized with chloro(chloromethyl)dimethylsilane, generating a cyclic dimethylsilamorpholine (DMS) derivative suitable for GC(EI)MS detection and identification. This compound produces five intense ions in the electron ionization source, which allow the presence of clenbuterol to be confirmed in just one analysis, as demanded by European Union directives. The accuracy of the method was studied by performing recovery experiments at different concentration levels (from 0.3 to 5 ng g(-1)) in 5 mL bovine urine samples using two labeled compounds: an in-house-synthesized (13)C(1)-clenbuterol and a commercially available d(9)-clenbuterol. The detection limit of the method in human urine was 0.050 ng g(-1) with a sample volume of 10 mL, and is thus suitable for antidoping control purposes. Finally, the (13)C(1)-clenbuterol standard was employed for the determination of clenbuterol in two reference materials, BCR-503 and BCR-504 (lyophilized bovine urine). The concentrations obtained were in agreement with the certified values, with a reproducibility of below 1% RSD.en_US
dc.languageengen_US
dc.relation.ispartofAnalytical and Bioanalytical Chemistryen_US
dc.sourceAnalytical and Bioanalytical Chemistry [ISSN 1618-2642], v. 402, p. 1879-1888 (Febrero 2012)en_US
dc.subject32 Ciencias médicasen_US
dc.subject230103 Análisis cromatográficoen_US
dc.subject230110 Espectroscopia de masasen_US
dc.subject.otherClenbuterolen_US
dc.subject.otherMinimal labelingen_US
dc.subject.otherIsotope dilutionen_US
dc.subject.otherFood safetyen_US
dc.subject.otherDoping controlen_US
dc.titleDevelopment of a routine method for the simultaneous confirmation and determination of clenbuterol in urine by minimal labeling isotope pattern deconvolution and GC-EI-MSen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00216-011-5611-1en_US
dc.identifier.scopus84858698239-
dc.contributor.authorscopusid36058862700-
dc.contributor.authorscopusid6603228633-
dc.contributor.authorscopusid6505871917-
dc.contributor.authorscopusid35557054000-
dc.contributor.authorscopusid7005873573-
dc.contributor.authorscopusid7005508838-
dc.description.lastpage1888en_US
dc.description.firstpage1879en_US
dc.relation.volume402en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages10en_US
dc.utils.revisionen_US
dc.date.coverdateFebrero 2012en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,347
dc.description.jcr3,659
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.fullNameGonzález Antuña, Ana-
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