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Intrinsic toxicity of stable nanosized titanium dioxide using polyacrylate in human keratinocytes

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dc.contributor.authorKoedrithu, Preeyaporn-
dc.contributor.authorKim, Yeo Jin-
dc.contributor.authorKim, Younghun-
dc.contributor.authorKang, Joo-Hyon-
dc.contributor.authorSeo, Young Rok-
dc.date.accessioned2023-04-28T08:41:04Z-
dc.date.available2023-04-28T08:41:04Z-
dc.date.issued2018-07-
dc.identifier.issn1738-642X-
dc.identifier.issn2092-8467-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/9341-
dc.description.abstractBackgrounds: Trends in the use of an anticoagulant as a dispersing stabilizer are addressed. An effective approach to preparing stable nanosized titanium dioxide (nTiO(2)) for accurate and systematic assessment of nano- toxicity has not been established. Methods: Among the dispersants tested here, it was found that sodium polyacrylate (PAA) was the most effective dispersant for nTiO(2) in culture media. Our study was the first to demonstrate that a stable PAA-dispersed nTiO(2) (nTiO(2)/PAA) suspension showed more toxic than nTiO(2) without PAA in human HaCaT keratinocytes. Results: Initially, MTT results showed that the stable nTiO(2)/PAA dispersion exhibited significantly greater cytotoxicity than nTiO(2) without PAA. In addition, the stable nTiO(2)/PAA dispersion induced markedly more oxidative stress than nTiO(2) without PAA. Importantly, the stable nTiO(2)/PAA dispersion caused DNA breakage to a greater extent than nTiO(2) without PAA. Conclusion: Our findings indicated that the anti-coagulant PAA is suitable for preparing homologous dispersed nTiO(2) under realistic physiological culture test conditions.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT-
dc.titleIntrinsic toxicity of stable nanosized titanium dioxide using polyacrylate in human keratinocytes-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s13273-018-0030-4-
dc.identifier.scopusid2-s2.0-85060332500-
dc.identifier.wosid000436131600004-
dc.identifier.bibliographicCitationMOLECULAR & CELLULAR TOXICOLOGY, v.14, no.3, pp 273 - 282-
dc.citation.titleMOLECULAR & CELLULAR TOXICOLOGY-
dc.citation.volume14-
dc.citation.number3-
dc.citation.startPage273-
dc.citation.endPage282-
dc.type.docTypeArticle-
dc.identifier.kciidART002362447-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusTHIOREDOXIN REDUCTASE 1-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordPlusCARBON-BLACK-
dc.subject.keywordPlusHACAT CELLS-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusPARTICLES-
dc.subject.keywordPlusULTRAFINE-
dc.subject.keywordPlusVALIDATION-
dc.subject.keywordPlusSKIN-
dc.subject.keywordAuthorDispersing stabilizer-
dc.subject.keywordAuthorCytotoxicity-
dc.subject.keywordAuthorGenotoxicity-
dc.subject.keywordAuthorHuman keratinocytes-
dc.subject.keywordAuthorTitanium dioxide nanoparticles-
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