Determination of the urinary concentrations of six bisphenols in public servants by online solid-phase extraction-liquid chromatography tandem mass spectrometry

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Analítica, Nutrición e Bromatoloxíaes_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Acuiculturaes_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Investigación e Análises Alimentariases_ES
dc.contributor.authorEstévez-Danta, Andrea
dc.contributor.authorRodil Rodríguez, María del Rosario
dc.contributor.authorQuintana Álvarez, José Benito
dc.contributor.authorMontes Goyanes, Rosa
dc.date.accessioned2024-08-05T06:41:23Z
dc.date.available2024-08-05T06:41:23Z
dc.date.issued2024-06-18
dc.description.abstractBisphenols are widely used as monomers and additives in plastic production. Thus, bisphenol A (BPA) and its most prominent substitutes have been detected in many environmental and human samples. This study proposes an online solid-phase extraction analytical methodology coupled to liquid chromatography with tandem mass spectrometry for the determination of six bisphenols (BPA and bisphenols F (BPF), S (BPS), AF (BPAF), B (BPB), and E (BPE)) in urine samples as an efficient and automated methodology. The method was developed and validated for all bisphenols with good recoveries (92–112%) and repeatability (RSD ≤ 10%) despite the variable matrix effects, except BPAF (which would require a dedicated internal standard), achieving method quantification limits in the 0.05–2.2 ng mL−1 range. The methodology was subsequently applied to 435 urine samples from a non-occupational exposure population (civil servants for the regional government) from Santiago de Compostela (Galicia, Spain). Only BPA, BPF, and BPS were positively detected; the last two presented higher detection frequencies than BPA. When the urinary concentrations are extrapolated to human intake and compared to the European Food Safety Agency (EFSA) tolerable daily intake (TDI) of 2 × 10−4 µg kg−1 day−1 (TDI), all BPA positively identified samples would surpass this threshold. Although no TDI exists currently for the other two identified bisphenols, it is evident that human exposure to bisphenols should be limited. Finally, the results stratification by gender revealed higher levels of exposure to BPF in the women group.es_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipOpen Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This work was funded by the Spanish Agencia Estatal de Investigación MCIN/AEI/10.13039/501100011033 (ref. PID2020-117686RB-C32) and Consellería de Cultura, Educación y Universidades da Xunta de Galicia (ref. ED481A-2020/258 and ED431C 2021/06).es_ES
dc.identifier.citationEstévez-Danta et al. Determination of the urinary concentrations of six bisphenols in public servants by online solid-phase extraction-liquid chromatography tandem mass spectrometry. Analytical and Bioanalytical Chemistry 416 (2024) 4469–4480es_ES
dc.identifier.doi10.1007/s00216-024-05386-7
dc.identifier.essn1618-2650
dc.identifier.urihttp://hdl.handle.net/10347/34592
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-117686RB-C32/ES/EVALUACION DE LA EXPOSICION HUMANA Y AMBIENTAL A CONTAMINANTES QUIMICOS DE ESPECIAL RELEVANCIA/es_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s00216-024-05386-7es_ES
dc.rights© The Author(s) 2024. This article is licensed under a Creative Commons Attribution 4.0 International Licensees_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPlastic-related additiveses_ES
dc.subjectChemical exposurees_ES
dc.subjectHuman biomonitoringes_ES
dc.subjectHazardous substanceses_ES
dc.titleDetermination of the urinary concentrations of six bisphenols in public servants by online solid-phase extraction-liquid chromatography tandem mass spectrometryes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication3137e088-95ac-4ef1-bc9c-de760fd18a7a
relation.isAuthorOfPublicationf9079fd6-969f-404b-bf70-98c2489c9ed7
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relation.isAuthorOfPublicationa4157885-4219-4fe9-8eac-48d5a4d5945d
relation.isAuthorOfPublication.latestForDiscovery3137e088-95ac-4ef1-bc9c-de760fd18a7a

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