Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/47124
Campo DC Valoridioma
dc.contributor.authorAufartová, Janaen_US
dc.contributor.authorEsther Torres-Padron, Mariaen_US
dc.contributor.authorSosa-Ferrera, Zoraidaen_US
dc.contributor.authorNováková, Lucieen_US
dc.contributor.authorSolich, Petren_US
dc.contributor.authorSantana-Rodríguez, José Juanen_US
dc.contributor.otherNovakova, Lucie-
dc.contributor.otherZoraida, Sosa-Ferrera-
dc.contributor.otherTorres-Padron, Maria Esther-
dc.contributor.otherSolich, Petr-
dc.date.accessioned2018-11-23T11:02:16Z-
dc.date.available2018-11-23T11:02:16Z-
dc.date.issued2014en_US
dc.identifier.issn1082-6076en_US
dc.identifier.urihttp://hdl.handle.net/10553/47124-
dc.description.abstractAn innovative methodology based on in-tube SPME using micellar desorption coupled to liquid chromatography combined with diode array (DAD) and fluorescence (FD) detection is proposed for the determination of five endocrine disruptors compounds (EDCs) (estriol, bisphenol A, norethisterone, 17α-ethynylestradiol, and D-norgestrel) in environmental samples. For the first time, in the present study, a micellar desorption was used with a GC Supel-Q capillary column with a length of 80 cm to optimize the in-tube SPME method. To identify the optimal extraction conditions, several parameters, including the extraction time, desorption time, column length, desorption volume, sample volume, and number of injections, were investigated. Under the optimal extraction conditions, micellar desorption was studied as an alternative to organic eluents. Using a DAD, the limits of detection (LODs) and quantification (LOQs) for the proposed method were 0.03–1.95 ng mL−1 and 0.09–5.95 ng mL−1, respectively. In contrast, using a FD detector, the LODs and LOQs were 0.02–0.14 ng mL−1and 0.06–0.42 ng mL−1, respectively, for estriol, bisphenol A, and 17α-ethynylestradiol. The proposed method was successfully applied to environmental matrices (seawater and wastewater from a treatment plant) and relative recoveries greater than 86% were obtained in all cases.en_US
dc.languageengen_US
dc.publisher1082-6076-
dc.relationDesarrollo de Nuevas Estrategias de Extracción en El Análisis de Residuos Farmacéuticos.Implementación en Muestras Reales de Interés Medioambiental.en_US
dc.relation.ispartofJournal of Liquid Chromatography and Related Technologiesen_US
dc.sourceJournal Of Liquid Chromatography & Related Technologies [ISSN 1082-6076], v. 37 (12), p. 1654-1672en_US
dc.subject2301 química analíticaen_US
dc.subject330810 Tecnología de aguas residualesen_US
dc.subject.otherEndocrine disruptor compounds (EDCs)en_US
dc.subject.otherEnvironmental liquid samplesen_US
dc.subject.otherIn-tube solid phase microextractionen_US
dc.subject.otherLiquid chromatographyen_US
dc.subject.otherMicellar desorptionen_US
dc.subject.otherWastewateren_US
dc.titleDevelopment of a novel in-tube solid phase microextraction based on micellar desorption followed by LC-DAD-FD for the determination of some endocrine disruptor compounds in environmental liquid samplesen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1080/10826076.2013.807461
dc.identifier.scopus84896911921-
dc.identifier.isi000334042700003-
dcterms.isPartOfJournal Of Liquid Chromatography & Related Technologies-
dcterms.sourceJournal Of Liquid Chromatography & Related Technologies[ISSN 1082-6076],v. 37 (12), p. 1654-1672-
dc.contributor.authorscopusid36187944300-
dc.contributor.authorscopusid8452532700-
dc.contributor.authorscopusid6602897915-
dc.contributor.authorscopusid6603839921-
dc.contributor.authorscopusid7003997787-
dc.contributor.authorscopusid56248783900-
dc.description.lastpage1672-
dc.description.firstpage1654-
dc.relation.volume37-
dc.investigacionCienciasen_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000334042700003-
dc.contributor.daisngid3089112-
dc.contributor.daisngid22437017
dc.contributor.daisngid2812385-
dc.contributor.daisngid770178-
dc.contributor.daisngid133166-
dc.contributor.daisngid88909-
dc.contributor.daisngid745012-
dc.contributor.daisngid10914640
dc.identifier.investigatorRIDS-6604-2017-
dc.identifier.investigatorRIDN-1602-2014-
dc.identifier.investigatorRIDE-9038-2012-
dc.identifier.investigatorRIDB-1851-2009-
dc.identifier.externalWOS:000334042700003-
dc.identifier.externalWOS:000334042700003-
dc.contributor.wosstandardWOS:Aufartova, J
dc.contributor.wosstandardWOS:Torres-Padron, ME
dc.contributor.wosstandardWOS:Sosa-Ferrera, Z
dc.contributor.wosstandardWOS:Novakova, L
dc.contributor.wosstandardWOS:Solich, P
dc.contributor.wosstandardWOS:Santana-Rodriguez, JJ
dc.date.coverdateJulio 2014
dc.identifier.ulpgces
dc.description.sjr0,297
dc.description.jcr0,606
dc.description.sjrqQ2
dc.description.jcrqQ4
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.project.principalinvestigatorSosa Ferrera, María Zoraida-
crisitem.author.deptGIR IUNAT: Análisis Químico Medioambiental-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.deptGIR IUNAT: Análisis Químico Medioambiental-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.deptGIR IUNAT: Análisis Químico Medioambiental-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.orcid0000-0001-7000-4419-
crisitem.author.orcid0000-0003-3003-3607-
crisitem.author.orcid0000-0002-5635-7215-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.fullNameTorres Padrón, María Esther-
crisitem.author.fullNameSosa Ferrera, María Zoraida-
crisitem.author.fullNameSantana Rodríguez, José Juan-
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