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Contribution to hazard characterization of the Next-Generation Plasticizer DINCH®: cytotoxicity and genotoxicity assessment in human cells

dc.contributor.authorVasconcelos, Ana Luísa
dc.contributor.authorSilva, Maria João
dc.contributor.authorLouro, Henriqueta
dc.date.accessioned2020-05-23T11:10:06Z
dc.date.available2020-05-23T11:10:06Z
dc.date.issued2019-10-25
dc.description.abstractThe chemical diisononyl cyclohexane-1,2-dicarboxylate (Hexamoll® DINCH®), a cyclohexanoate plasticizer, has been employed as a safer alternative to restricted phthalates, to increase flexibility and elasticity of many consumer products made of PVC or polystyrene, namely food packaging, children’s toys, and medical devices. Concomitantly, the detection of DINCH in human surroundings and in biological matrices has increased during the last decade. This prompt the establishment of biomonitoring guidance values for DINCH metabolites in urine, as a measure of precaution; however, the studies about potential adverse effects of DINCH in humans are still scarce. DINCH is not classified as reprotoxic nor genotoxic and mutagenic however, there are limited data available regarding safety assessment, especially regarding cytotoxic and genotoxic effects. Since liver and kidney are DINCH target organs in animal models, the aim of this study was to assess DINCH cytotoxic and genotoxic effects in a human liver (HepG2) and kidney cell lines (HK-2). The methodology included the MTT cell viability, micronucleus, conventional and FPG-modified comet assays to detect cytotoxicity and genotoxicity. The results showed that DINCH was moderately cytotoxic for kidney cells exposed for 48h, but not for liver cells. No chromosomal damage was induced after short-term or longer exposures of both cell lines. However, DINCH was able to induce oxidative DNA damage in liver cells exposed for 3h, which decreased after a more prolonged exposure. The occurrence of oxidative lesions, even transiently, implies that mutation fixation may occur leading to adverse effects in liver. Overall, the present work provides new insights into the potential toxicity of this next-generation plasticizer in kidney and liver cells, in spite of public reports in which DINCH is classified as non-genotoxic agent. On the other hand, human biomonitoring studies are fundamental to confirm the current levels of human internal exposure to DINCH, as well as to detect early biologic effects.pt_PT
dc.description.sponsorshipThis research was partially funded by INSA, Centre for Toxicogenomics and Human Health, ToxOmics (UID/MMIM/00009/2013). The authors thank BASF for kindly providing Hexamoll® DINCH for analysis.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6768
dc.language.isoengpt_PT
dc.peerreviewednopt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectPlasticizerpt_PT
dc.subjectLiver and Kidney Cellspt_PT
dc.subjectDINCHpt_PT
dc.subjectCytotoxicitypt_PT
dc.subjectEnvironmental Genotoxicitypt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleContribution to hazard characterization of the Next-Generation Plasticizer DINCH®: cytotoxicity and genotoxicity assessment in human cellspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FBIM%2F00009%2F2013/PT
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.title2nd HBM-PT Workshop on Human BioMonitoring in Portugal: HBM: assessing exposure for a healthier future in Portugal, Agência Portuguesa do Ambiente (APA), 25 outubro 2019pt_PT
oaire.fundingStream5876
person.familyNameSilva
person.familyNameLouro
person.givenNameMaria Joao
person.givenNameHenriqueta
person.identifier157627
person.identifier.ciencia-id7710-643D-97A3
person.identifier.ciencia-id721D-2BB1-7DB1
person.identifier.orcid0000-0002-6060-0716
person.identifier.orcid0000-0001-9744-7332
person.identifier.scopus-author-id55944437600
person.identifier.scopus-author-id6507971479
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT
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relation.isAuthorOfPublication2361a951-8b9a-4b90-92d6-f6384003a242
relation.isAuthorOfPublication.latestForDiscoverya7763685-7c34-468d-b958-9dd0aca66db4
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