Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/14905
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dc.contributor.authorVasquez Christodoulou, Marlen-
dc.contributor.authorTarapoulouzi, Maria-
dc.contributor.authorLambrianides, Nancy-
dc.contributor.authorHapeshi, Evroula-
dc.contributor.authorFelekkis, Kyriakos-
dc.contributor.authorSaile, Maria-
dc.contributor.authorSticht, Carsten-
dc.contributor.authorGretz, Norbert-
dc.contributor.authorFatta-Kassinos, Despo-
dc.date.accessioned2019-08-09T08:37:13Z-
dc.date.available2019-08-09T08:37:13Z-
dc.date.issued2016-11-
dc.identifier.citationEnvironmental Toxicology and Chemistry, 2016, vol. 35 , no.11, pp. 2753–2764en_US
dc.identifier.issn15528618-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/14905-
dc.description.abstractThe selection and prioritization of pharmaceuticals and their transformation products for evaluating effects on the environment and human health is a challenging task. One common approach is based on compounds (e.g., mixture composition, concentrations), and another on biology (e.g., relevant endpoint, biological organizational level). Both of these approaches often resemble a Lernaean Hydra-they can create more questions than answers. The present study embraces this complexity, providing an integrated approach toward assessing the potential effects of transformation products of pharmaceuticals by means of mutagenicity, estrogenicity, and differences in the gene expression profiles. Mutagenicity using the tk kinase assay was applied to assess a list of 11 priority pharmaceuticals, namely, atenolol, azithromycin, carbamazepine, diclofenac, ibuprofen, erythromycin, metoprolol, ofloxacin, propranolol, sulfamethoxazole, and trimethoprim. The most mutagenic compounds were found to be β-blockers. In parallel, the photolabile pharmaceuticals were assessed for their mixture effects on mutagenicity (tk assay), estrogenicity (T47D- KBluc assay), and gene expression (microarrays). Interestingly, the mixtures were mutagenic at the µg/L level, indicating a synergistic effect. None of the photolysed mixtures were statistically significantly estrogenic. Gene expression profiling revealed effects related mainly to certain pathways, those of the p53 gene, mitogen-activated protein kinase, alanine, aspartate, and glutamate metabolism, and translation-related (spliceosome). Fourteen phototransformation products are proposed based on the m/z values found through ultra-performance liquid chromatography-tandem mass spectrometry analysis. The transformation routes of the photolysed mixtures indicate a strong similarity with those obtained for each pharmaceutical separately. This finding reinforces the view that transformation products are to be expected in naturally occurring mixtures.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofEnvironmental Toxicology and Chemistryen_US
dc.rights© SETACen_US
dc.subjectGene expressionen_US
dc.subjectMammalian toxicologyen_US
dc.subjectMixture toxicityen_US
dc.subjectMutagenicityen_US
dc.subjectTransformation producten_US
dc.subjectPharmaceuticalen_US
dc.titleAssessing the potential of pharmaceuticals and their transformation products to cause mutagenic effects: Implications for gene expression profilingen_US
dc.typeArticleen_US
dc.collaborationUniversity of Cyprusen_US
dc.collaborationThe Cyprus Institute of Neurology and Geneticsen_US
dc.collaborationUniversity of Nicosiaen_US
dc.collaborationHeidelberg Universityen_US
dc.subject.categoryChemical Sciencesen_US
dc.journalsSubscriptionen_US
dc.countryCyprusen_US
dc.countryGermanyen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1002/etc.3444en_US
dc.relation.issue11en_US
dc.relation.volume35en_US
cut.common.academicyear2016-2017en_US
dc.identifier.spage2753en_US
dc.identifier.epage2764en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.fulltextNo Fulltext-
crisitem.journal.journalissn1552-8618-
crisitem.journal.publisherWiley-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0002-9849-5616-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
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