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dc.rights.licensehttp://creativecommons.org/licenses/by-nc-sa/3.0/ve/
dc.contributor.authorEljarrat, E.es_VE
dc.contributor.authorOliveros Bastidas, Albertoes_VE
dc.contributor.authorMacías, Francisco A.es_VE
dc.contributor.authorGuillamón, M.es_VE
dc.contributor.authorSeuma, J.es_VE
dc.contributor.authorMogensen, B. B.es_VE
dc.contributor.authorFomsgaard, I. S.es_VE
dc.contributor.authorStochmal, A.es_VE
dc.contributor.authorOleszek, W.es_VE
dc.contributor.authorShakaliene, O.es_VE
dc.contributor.authorBarceló, D.es_VE
dc.date2008-07-02es_VE
dc.date.accessioned2008-07-02T09:00:00Z
dc.date.available2008-07-02T09:00:00Z
dc.date.created2008-07-02es_VE
dc.date.issued2008-07-02T09:00:00Zes_VE
dc.identifier.otherT016300002117/0es_VE
dc.identifier.urihttp://www.saber.ula.ve/handle/123456789/16844
dc.description.abstractFirst European interlaboratory study of the analysis of benzoxazinone derivatives in plants by liquid chromatography (Eljarrat, E.; Guillamón, M.; Seuma, J.; Mogensen, B. B.; Fomsgaard, I. S.; Oliveros Bastidas, Alberto; Macías, F. A.; Stochmal, A.; Oleszek, W.; Shakaliene, O.; Barceló, D.) Abstract Six laboratories from four different countries participated in the first European interlaboratory comparison exercise within the framework of the "Fate and toxicity of allelochemicals (natural plant toxins) in relation to environment and consumer" (FATEALLCHEM) European Union Project. The study, organized between November 2002 and March 2003, involved the analyses of seven benzoxazinone derivatives in two standard solutions and one purified extract of root material. Results are reported from the first phase of the study that examined the variability associated with different detection methods and different laboratories. The analytical strategies were based on liquid chromatography (LC) with diode array detection, LC coupled to mass spectrometry (MS) and LC coupled to tandem MS. When data from all laboratories were pooled, the relative standard deviation values ranged from 2 to 14% for the determination of target compounds in standard solutions, and between 19 and 47% for the analysis in root material. Comparison of the three detection techniques leads to the conclusion that MS approaches are the most accurate and precise techniques for the determination of benzoxazinone derivatives at ng/µL level in plant material. © 2004 Elsevier B.V. All rights reserved. This article was presented at the 3rd Meeting of the Spanish Association of Chromatography and Related Techniques and the EuropeanWorkshop: 3rdWasteWater Cluster, Aguadulce (Almeria), 19-21 November, 2003.es_VE
dc.language.isoeses_VE
dc.publisherSABER ULAes_VE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleFirst European interlaboratory study of the analysis of benzoxazinone.es_VE
dc.typeinfo:eu-repo/semantics/article
dc.description.emaileeeqam@cid.csic.eses_VE
dc.description.emailaloliver@ula.vees_VE
dc.description.emailfamacias@uca.eses_VE
dc.description.tiponivelNivel monográficoes_VE
dc.subject.Mots-clesQuímicaes_VE
dc.subject.facultadFacultad de Ciencias.es_VE
dc.subject.idiomaIngléses_VE
dc.subject.keywordsInterlaboratory studieses_VE
dc.subject.keywordsPlant materiales_VE
dc.subject.keywordsBenzoxazinoneses_VE
dc.subject.tipoArtículoses_VE


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