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최성득

Choi, Sung-Deuk
Environmental Analytical Chemistry Lab.
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dc.citation.startPage 31 -
dc.citation.title PARTICLE AND FIBRE TOXICOLOGY -
dc.citation.volume 16 -
dc.contributor.author Lee, Jinsoo -
dc.contributor.author Jeong, Ji-Seong -
dc.contributor.author Kim, Sang Yun -
dc.contributor.author Park, Min-Kyu -
dc.contributor.author Choi, Sung-Deuk -
dc.contributor.author Kim, Un-Jung -
dc.contributor.author Park, Kwangsik -
dc.contributor.author Jeong, Eun Ju -
dc.contributor.author Nam, Sang-Yoon -
dc.contributor.author Yu, Wook-Joon -
dc.date.accessioned 2023-12-21T18:58:48Z -
dc.date.available 2023-12-21T18:58:48Z -
dc.date.created 2019-08-14 -
dc.date.issued 2019-07 -
dc.description.abstract Background: Titanium dioxide (TiO2) nanoparticles are among the most manufactured nanomaterials in the industry, and are used in food products, toothpastes, cosmetics and paints. Pregnant women as well as their conceptuses may be exposed to TiO2 nanoparticles; however, the potential effects of these nanoparticles during pregnancy are controversial, and their internal distribution has not been investigated. Therefore, in this study, we investigated the potential effects of oral exposure to TiO2 nanoparticles and their distribution during pregnancy. TiO2 nanoparticles were orally administered to pregnant Sprague-Dawley rats (12 females per group) from gestation days (GDs) 6 to 19 at dosage levels of 0, 100, 300 and 1000 mg/kg/day, and then cesarean sections were conducted on GD 20. Results: In the maternal and embryo-fetal examinations, there were no marked toxicities in terms of general clinical signs, body weight, food consumption, organ weights, macroscopic findings, cesarean section parameters and fetal morphological examinations. In the distribution analysis, titanium contents were increased in the maternal liver, maternal brain and placenta after exposure to high doses of TiO2 nanoparticles. Conclusion: Oral exposure to TiO2 during pregnancy increased the titanium concentrations in the maternal liver, maternal brain and placenta, but these levels did not induce marked toxicities in maternal animals or affect embryo-fetal development. These results could be used to evaluate the human risk assessment of TiO2 nanoparticle oral exposure during pregnancy, and additional comprehensive toxicity studies are deemed necessary considering the possibility of complex exposure scenarios and the various sizes of TiO2 nanoparticles. -
dc.identifier.bibliographicCitation PARTICLE AND FIBRE TOXICOLOGY, v.16, pp.31 -
dc.identifier.doi 10.1186/s12989-019-0313-5 -
dc.identifier.issn 1743-8977 -
dc.identifier.scopusid 2-s2.0-85070091462 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/27827 -
dc.identifier.url https://particleandfibretoxicology.biomedcentral.com/articles/10.1186/s12989-019-0313-5 -
dc.identifier.wosid 000476527300001 -
dc.language 영어 -
dc.publisher BMC -
dc.title Titanium dioxide nanoparticles oral exposure to pregnant rats and its distribution -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Toxicology -
dc.relation.journalResearchArea Toxicology -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Titanium dioxide nanoparticles -
dc.subject.keywordAuthor Developmental toxicity -
dc.subject.keywordAuthor Maternal and fetal distribution -
dc.subject.keywordAuthor Nanotoxicity -
dc.subject.keywordPlus DEVELOPMENTAL TOXICITY -
dc.subject.keywordPlus INTRATRACHEAL INSTILLATION -
dc.subject.keywordPlus QUANTITATIVE BIOKINETICS -
dc.subject.keywordPlus TIO2 PARTICLES -
dc.subject.keywordPlus MICE -
dc.subject.keywordPlus ZEBRAFISH -
dc.subject.keywordPlus DAMAGE -

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