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dc.contributor.authorÁlvarez Escalante, Iván Alejandro
dc.contributor.authorMartínez Páramo, Sonia 
dc.contributor.authorIrusta Mata, Rubén 
dc.date.accessioned2025-03-03T12:59:01Z
dc.date.available2025-03-03T12:59:01Z
dc.date.issued2024
dc.identifier.citationEcotoxicology,2024,vol.33, n.7, p.722-736es
dc.identifier.issn0963-9292es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/75205
dc.descriptionProducción Científicaes
dc.description.abstractIn recent years, the presence of Pharmaceutical Active Compounds (PhACs) in ecosystems has become a serious environmental problem due to their capacity to induce harmful effects at extremely low concentrations in both humans and wildlife. Water treatment plants have not been designed to remove these types of compounds efficiently. Thus, the detection of these pollutants is essential to evaluate their negative impacts and is one of the emerging issues in environmental chemistry. The main objective of this study is to determine the bacterial toxicity of two PhACs (both individually and as a mixture) through the quantification of bioluminescence inhibition in the marine bacteria Aliivibrio fischeri, a commonly used method in short-term toxicity tests. In this work, Acetaminophen and Edaravone, two drugs approved by the Food and Drug Administration, have been studied. The acute toxicity of these PhACs has been tested at two exposure times (5 and 15 min) and different concentrations, by estimation of the median effective concentration (EC 50) for each individual compound or in combination at different concentrations. Moreover, the EC 50 of the binary mixtures Acetaminophen/Edaravone have been forecast using two traditional predictive models, Concentration Addition and Independent Action. The results show that toxicity decreases with exposure time and depends on the concentration tested. Furthermore, a novel semi-empirical Van Laar-based model has been proposed and validated with the experimental data from this study and literature data, obtaining satisfactory estimations of the EC 50 for binary mixtureses
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherSpringeres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classificationMicrotoxes
dc.subject.classificationPharmaceuticalses
dc.subject.classificationBinary mixtureses
dc.subject.classificationConcentration Additiones
dc.subject.classificationIndependent Actiones
dc.subject.classificationVan Laar-based modeles
dc.titleBacterial toxicity of Acetaminophen and Edaravone, and their binary mixtures: experimental and predicted values using traditional and novel Van Laar-based modelses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2024 The Author(s)es
dc.identifier.doi10.1007/s10646-024-02772-wes
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s10646-024-02772-wes
dc.identifier.publicationfirstpage722es
dc.identifier.publicationissue7es
dc.identifier.publicationlastpage736es
dc.identifier.publicationtitleEcotoxicologyes
dc.identifier.publicationvolume33es
dc.peerreviewedSIes
dc.description.projectPublicación en abierto financiada por el Consorcio de Bibliotecas Universitarias de Castilla y León (BUCLE), con cargo al Programa Operativo 2014ES16RFOP009 FEDER 2014-2020 DE CASTILLA Y LEÓN, Actuación:20007-CL - Apoyo Consorcio BUCLEes
dc.description.projectMinisterio de Ciencia, Innovación y Universidades (CTQ2017-84006-C3- 1-R)es
dc.description.projectJunta de Castilla y León (UIC 071, and VA080G18) and the EU-FEDER (CLU 2017-09 and CTQ2017-84006-C3-1-R)es
dc.identifier.essn1573-3017es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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