Titanium dioxide (titania) nanoparticle aggregation is an important factor in understanding cytotoxicity. However, the effect of the aggregate size of nanoparticles on cells is unclear. We prepared two sizes of titania aggregate particles and investigated their biological activity by analyzing biomarker expression based on mRNA expression analysis. The aggregate particle sizes of small and large aggregated titania were 166 nm (PDI = 0.291) and 596 nm (PDI = 0.417), respectively. These two size groups were separated by centrifugation from the same initial nanoparticle sample. We analyzed the gene expression of biomarkers focused on stress, inflammation, and cytotoxicity. Large titania aggregates show a larger effect on cell viability and gene expression when compared with the small aggregates. This suggests that particle aggregate size is related to cellular effects.
With recent developments in nanoscience and nanotechnology, carbon-based nanomaterials, such as carbon nanotubes or Fullerene nanowhiskers (FNWs), are attracting a great deal of interest. However, nanomaterials have novel properties that may cause safety problems in biological systems. Although the toxic effects of multiwall carbon nanotubes (MWCNTs) in vitro and in vivo have been well described, the effect of FNWs on cells remains unclear. In the present study, we analyzed the gene expression and cytotoxicity of FNWs-treated cells. The results of cell viabil-ity and gene expression analysis indicate that FNWs has a relatively smaller ability to induce cellular gene expression as compared with MWCNTs or titania nanoparticles. Our results suggest that FNWs have weak cytotoxic effects as compared to the effects of MWCNTs and tita-nia nanoparticles
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