School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Arch Toxicol. 2013 Jan;87(1):99-109. doi: 10.1007/s00204-012-0912-5. Epub 2012 Aug 11.
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.
为了揭示 TiO(2) 纳米粒子的尺寸对其潜在毒性的影响,测试了不同尺寸的 TiO(2) 纳米粒子在光照激活和非光照激活条件下的细胞毒性。结果表明,在非光照激活条件下,TiO(2)纳米粒子的浓度高达 100μg/ml 时仍保持惰性。相反,在光照激活条件下,TiO(2)纳米粒子的毒性显著增加,这与颗粒的比表面积密切相关。我们的研究结果还表明,光照激活后 TiO(2)纳米粒子产生的羟基自由基和活性氧物质(ROS)介导的对表面吸附生物分子的损伤可能是其细胞毒性的两个主要原因。在生物和非生物条件下,更小的颗粒产生了更高水平的 ROS。更小的颗粒可以吸附更多的蛋白质,这一点通过热重分析得到了证实。为了进一步研究羟基自由基的生成和蛋白质吸附的影响,使用聚(乙烯-共-马来酸酐)(PEMA)和壳聚糖对 TiO(2) 纳米粒子进行了包覆。结果证实,通过在光照激活过程中阻碍生物分子的吸附和羟基自由基(·OH)的生成,TiO(2)纳米粒子的表面包覆可以降低光照激活后的这种毒性。