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dc.creatorSantigosa, Eliaes
dc.creatorPedersen-Bjergaard, Stiges
dc.creatorGiménez Gómez, Pabloes
dc.creatorMuñoz, Maríaes
dc.creatorRamos Payán, María Doloreses
dc.date.accessioned2022-05-16T13:24:16Z
dc.date.available2022-05-16T13:24:16Z
dc.date.issued2022
dc.identifier.citationSantigosa, E., Pedersen-Bjergaard, S., Giménez Gómez, P., Muñoz, M. y Ramos Payán, M.D. (2022). A rapid and versatile microfluidic method for the simultaneous extraction of polar and non-polar basic pharmaceuticals from human urine. Analytica Chimica Acta, 1208, 339829.
dc.identifier.issn0003-2670es
dc.identifier.issn1873-4324es
dc.identifier.urihttps://hdl.handle.net/11441/133343
dc.description.abstractIn sample preparation, simultaneous extraction of analytes of very different polarity from biological matrixes represents a challenge. In this work, verapamil hydrochloride (VRP), amitriptyline (AMP), tyramine (TYR), atenolol (ATN), metopropol (MTP) and nortriptyline (NRP) were used as basic model analytes and simultaneously extracted from urine samples by liquid-phase microextraction (LPME) in a microfluidic device. The model analytes (target compounds) were pharmaceuticals with 0.4 < log P < 5. Different organic solvents and mixtures of them were investigated as supported liquid membrane (SLM), and a mixture of 2:1 (v/v) tributyl phosphate (TBP) and dihexyl ether (DHE) was found to be highly efficient for the simultaneous extraction of the non-polar and polar model analytes. TBP reduced the intrinsic hydrophobicity of the SLM and facilitated extraction of polar analytes, while DHE served to minimize trapping of non-polar analytes. Sample and acceptor phase composition were adjusted to pH 12 and pH 1.5, respectively. Urine samples were pumped into the microfluidic system at 1 μL min-1 and the extraction was completed in 7 min. Recoveries exceeded 78% for the target analytes, and the relative standard deviation (n = 4) was below 7% in all cases. Using five microliters of SLM, the microfluidic extraction system showed good long-term stability, and the same SLM was used for more than 18 consecutive extractions.es
dc.description.sponsorshipAgencia de Gestió d'Ajusts Universitaris i the Recerca 2017-SGR-329es
dc.description.sponsorshipMinisterio de Ciencia e Innovación PGC2018-096608-B-C21es
dc.formatapplication/pdfes
dc.format.extent9 p.es
dc.language.isoenges
dc.publisherElsevieres
dc.relation.ispartofAnalytica Chimica Acta, 1208, 339829.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBasic drugses
dc.subjectLiquid phase microextractiones
dc.subjectMicrofluidices
dc.subjectSupported liquid membranees
dc.subjectUrine sampleses
dc.titleA rapid and versatile microfluidic method for the simultaneous extraction of polar and non-polar basic pharmaceuticals from human urinees
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química Analíticaes
dc.relation.projectID2017-SGR-329es
dc.relation.projectIDPGC2018-096608-B-C21es
dc.relation.publisherversionhttps://doi.org/10.1016/j.aca.2022.339829es
dc.identifier.doi10.1016/j.aca.2022.339829es
dc.journaltitleAnalytica Chimica Actaes
dc.publication.volumen1208es
dc.publication.initialPage339829es
dc.contributor.funderAgencia de Gestió d'Ajusts Universitaris i the Recercaes
dc.contributor.funderAgencia Estatal de Investigación. Españaes
dc.description.awardwinningPremio Mensual Publicación Científica Destacada de la US. Facultad de Química

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