Inflammatory and genotoxic effects of nanoparticles designed for inclusion in paints and lacquers
2011; Taylor & Francis; Volume: 6; Issue: 5 Linguagem: Inglês
10.3109/17435390.2011.587900
ISSN1743-5404
AutoresAnne Thoustrup Saber, Keld Alstrup Jensen, Nicklas Raun Jacobsen, Renie Birkedal, Lone Mikkelsen, Peter Möller, Steffen Loft, Håkan Wallin, Ulla Vogel,
Tópico(s)Heavy Metal Exposure and Toxicity
ResumoManufactured nanomaterials are projected to be used on a large scale in paints and lacquers. We selected seven commercially interesting materials: Three titanium dioxide-based (two coated rutile; one uncoated anatase), one carbon black (Flamrüss 101), one kaolinite clay, and two silica products, whereas carbon black, Printex 90, was used as reference material. DNA damaging activity and inflammogenicity (pulmonary cell composition and mRNAs) were determined 24 h after intratracheal instillation of a single dose of 54 μg in mice. Greatest inflammation was induced by Printex 90 and uncoated titanium dioxide. The inflammatory potency correlated with instilled surface area (R2 = 0.94) but not with material volume (R2 = 0.17). The coated titanium dioxides induced DNA damage in lung lining fluid cells. The uncoated titanium dioxide was not DNA damaging by the comet assay 24 h after exposure despite being highly inflammogenic. This suggests that inflammation is not a prerequisite to DNA damage in titanium dioxide-based products.
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