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Cited 3 time in webofscience Cited 4 time in scopus
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Intrinsic toxicity of stable nanosized titanium dioxide using polyacrylate in human keratinocytes

Authors
Koedrithu, PreeyapornKim, Yeo JinKim, YounghunKang, Joo-HyonSeo, Young Rok
Issue Date
Jul-2018
Publisher
KOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT
Keywords
Dispersing stabilizer; Cytotoxicity; Genotoxicity; Human keratinocytes; Titanium dioxide nanoparticles
Citation
MOLECULAR & CELLULAR TOXICOLOGY, v.14, no.3, pp 273 - 282
Pages
10
Indexed
SCIE
SCOPUS
KCI
Journal Title
MOLECULAR & CELLULAR TOXICOLOGY
Volume
14
Number
3
Start Page
273
End Page
282
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/9341
DOI
10.1007/s13273-018-0030-4
ISSN
1738-642X
2092-8467
Abstract
Backgrounds: 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.
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