Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/41387
Campo DC Valoridioma
dc.contributor.authorGarcía-Guerra, R.B.en_US
dc.contributor.authorMontesdeoca-Esponda, Sarahen_US
dc.contributor.authorSosa-Ferrera, Zoraidaen_US
dc.contributor.authorKabir, A.en_US
dc.contributor.authorFurton, K.G.en_US
dc.contributor.authorSantana-Rodríguez, José Juanen_US
dc.contributor.otherZoraida, Sosa-Ferrera
dc.contributor.otherKabir, Abuzar
dc.contributor.otherSANTANA RODRIGUEZ, JOSE JUAN
dc.date.accessioned2018-06-27T08:59:29Z-
dc.date.available2018-06-27T08:59:29Z-
dc.date.issued2016en_US
dc.identifier.issn0045-6535en_US
dc.identifier.urihttp://hdl.handle.net/10553/41387-
dc.description.abstractBenzotriazole UV stabilizers (BUVSs) are a group of compounds added to personal care products such as sunscreens, hair dyes, make up formulations, soaps or shampoos, among others. Direct input from beaches or another aquatic recreational areas is the main source of BUVSs incorporation to the environment, where they can be mutagenic, toxic, pseudo-persistent and bioaccumulative. Due to the low levels of concentration of these compounds found in environmental samples, an extraction process is required prior to their determination. Fabric phase sorptive extraction integrates the advanced material properties of sol-gel hybrid inorganic-organic sorbents with flexible, permeable and functionally active fabric substrates, being a highly responsive, efficient and cheap device that also can be reused. In this paper, we applied fabric phase sorptive extraction methodology to analyse six BUVSs in twenty-four seawater samples from different coastal areas of Gran Canaria Island (Spain). It was coupled to ultra high performance liquid chromatography with tandem mass spectrometry in order to achieve a fast, reliable and sensitive separation and determination of the analytes from different simple matrices, regardless of its complexity and composition. Under the optimum conditions, the proposed method provided enrichment factors of 25 times with limits of detection from 1.06 to 8.96 ng L−1 and limits of quantification from 3.54 to 29.9 ng L−1 for the analytes under study in spiked samples. Intra and inter-day relative standard deviations were between 3.97 and 20.8% for all compounds. The application of the optimized methodology to non-spiked seawater samples allows detecting and quantifying the UV 360 in the range from 41.12 to 544.9 ng L−1.en_US
dc.languageengen_US
dc.relation.ispartofChemosphereen_US
dc.sourceChemosphere[ISSN 0045-6535],v. 164, p. 201-207en_US
dc.subject251002 Oceanografía químicaen_US
dc.subject.otherBenzotriazole UV stabilizersen_US
dc.subject.otherFabric phase sorptive extractionen_US
dc.subject.otherMass spectrometry detectionen_US
dc.subject.otherSeawateren_US
dc.subject.otherUltra-high performance liquid chromatographyen_US
dc.titleRapid monitoring of residual UV-stabilizers in seawater samples from beaches using fabric phase sorptive extraction and UHPLC-MS/MSen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.chemosphere.2016.08.102
dc.identifier.scopus84984645832-
dc.identifier.isi000385318200024
dcterms.isPartOfChemosphere
dcterms.sourceChemosphere[ISSN 0045-6535],v. 164, p. 201-207
dc.contributor.authorscopusid57190950442
dc.contributor.authorscopusid57201412739
dc.contributor.authorscopusid6602897915
dc.contributor.authorscopusid7005744830
dc.contributor.authorscopusid7004543580
dc.contributor.authorscopusid56248783900
dc.description.lastpage207-
dc.description.firstpage201-
dc.relation.volume164-
dc.investigacionCienciasen_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000385318200024-
dc.contributor.daisngid11698015
dc.contributor.daisngid2366921
dc.contributor.daisngid770178
dc.contributor.daisngid29952453
dc.contributor.daisngid1163455
dc.contributor.daisngid141262
dc.contributor.daisngid10914640
dc.identifier.investigatorRIDN-1602-2014
dc.identifier.investigatorRIDNo ID
dc.identifier.investigatorRIDNo ID
dc.contributor.wosstandardWOS:Garcia-Guerra, RB
dc.contributor.wosstandardWOS:Montesdeoca-Esponda, S
dc.contributor.wosstandardWOS:Sosa-Ferrera, Z
dc.contributor.wosstandardWOS:Kabir, A
dc.contributor.wosstandardWOS:Furton, KG
dc.contributor.wosstandardWOS:Santana-Rodriguez, JJ
dc.date.coverdateDiciembre 2016
dc.identifier.ulpgces
dc.description.sjr1,417
dc.description.jcr4,208
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
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.orcid0000-0001-9872-5293-
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.fullNameMontesdeoca Esponda, Sarah-
crisitem.author.fullNameSosa Ferrera, María Zoraida-
crisitem.author.fullNameSantana Rodríguez, José Juan-
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