Length-dependent toxicity of TiO₂ nanofibers: mitigation via shortening

Abstract

Length and aspect ratio represent important toxicity determinants of fibrous nanomaterials. We have previously shown that anatase TiO₂ nanofibers (TiO₂ NF) cause a dose-dependent decrease of cell viability as well as the loss of epithelial barrier integrity in polarized airway cell monolayers. Herein we have investigated the impact of fiber shortening, obtained by ball-milling, on the biological effects of TiO₂ NF of industrial origin. Long TiO₂ NF (L-TiO₂ NF) were more cytotoxic than their shortened counterparts (S-TiO₂ NF) toward alveolar A549 cells and bronchial 16HBE cells. Moreover, L-TiO₂ NF increased the permeability of 16HBE monolayers and perturbed the distribution of tight-junction proteins, an effect also mitigated by fiber shortening. Raw264.7 macrophages efficiently internalized shortened but not long NF, which caused cell stretching and deformation. Compared with L-TiO₂ NF, S-TiO₂ NF triggered a more evident macrophage activation, an effect suppressed by the phagocytosis inhibitor cytochalasin B. Conversely, a significant increase of inflammatory markers was detected in either the lungs or the peritoneal cavity of mice exposed to L-TiO₂ NF but not to S-TiO₂ NF, suggesting that short-term macrophage activation in vitro may not be always a reliable indicator of persistent inflammation in vivo. It is concluded that fiber shortening mitigates NF detrimental effects on cell viability and epithelial barrier competence in vitro as well as inflammation development in vivo. These data suggest that fiber shortening may represent an effective safe-by-design strategy for mitigating TiO₂ NF toxic effects.

Keywords:

• Aspect ratio
• macrophages
• nanofibers
• safety-by-design
• titanium dioxide

Acknowledgements

The confocal images were obtained in the Laboratory of Confocal Microscopy of the Department of Medicine and Surgery of the University of Parma.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by the EU FP7 SANOWORK Project (Grant agreement n. 280716, http://sanowork.eu/) to EB and ALC and by EU Horizon 2020 BIORIMA Project (Grant agreement n. 760928) to EB. CAP and RD are funded by the Colt Foundation (Grant n. CF/01/17). MC is supported by a fellowship of “Associazione Italiana per la Ricerca sul Cancro” (AIRC, no. 19272).