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Size of TiO(2) Nanoparticles Influences Their Phototoxicity: an in Vitro Investigation

Overview
Journal Arch Toxicol
Specialty Toxicology
Date 2012 Aug 14
PMID 22885792
Citations 13
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Abstract

To uncover the size influence of TiO(2) nanoparticles on their potential toxicity, the cytotoxicity of different-sized TiO(2) nanoparticles with and without photoactivation was tested. It was demonstrated that without photoactivation, TiO(2) nanoparticles were inert up to 100 μg/ml. On the contrary, with photoactivation, the toxicity of TiO(2) nanoparticles significantly increased, which correlated well with the specific surface area of the particles. Our results also suggest that the generation of hydroxyl radicals and reactive oxygen species (ROS)-mediated damage to the surface-adsorbed biomolecules could be the two major reasons for the cytotoxicity of TiO(2) nanoparticles after photoactivation. Higher ROS generation from smaller particles was detected under both biotic and abiotic conditions. Smaller particles could adsorb more proteins, which was confirmed by thermogravimetric analysis. To further investigate the influence of the generation of hydroxyl radicals and adsorption of protein, poly (ethylene-alt-maleic anhydride) (PEMA) and chitosan were used to coat TiO(2) nanoparticles. The results confirmed that surface coating of TiO(2) nanoparticles could reduce such toxicity after photoactivation, by hindering adsorption of biomolecules and generation of hydroxyl radical (·OH) during photoactivation.

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References
1.
Nel A, Xia T, Madler L, Li N . Toxic potential of materials at the nanolevel. Science. 2006; 311(5761):622-7. DOI: 10.1126/science.1114397. View

2.
George S, Xia T, Rallo R, Zhao Y, Ji Z, Lin S . Use of a high-throughput screening approach coupled with in vivo zebrafish embryo screening to develop hazard ranking for engineered nanomaterials. ACS Nano. 2011; 5(3):1805-17. PMC: 3896549. DOI: 10.1021/nn102734s. View

3.
Ophus E, Rode L, Gylseth B, Nicholson D, Saeed K . Analysis of titanium pigments in human lung tissue. Scand J Work Environ Health. 2010; 5(3):290-6. DOI: 10.5271/sjweh.3104. View

4.
Nakagawa Y, Wakuri S, Sakamoto K, Tanaka N . The photogenotoxicity of titanium dioxide particles. Mutat Res. 1998; 394(1-3):125-32. DOI: 10.1016/s1383-5718(97)00126-5. View

5.
Xia T, Kovochich M, Brant J, Hotze M, Sempf J, Oberley T . Comparison of the abilities of ambient and manufactured nanoparticles to induce cellular toxicity according to an oxidative stress paradigm. Nano Lett. 2006; 6(8):1794-807. DOI: 10.1021/nl061025k. View