Dispersions of geometric TiO2 nanomaterials and their toxicity to RPMI 2650 nasal epithelial cells

• Published in: Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2014-11, Vol.16 (11), p.1, Article 2695
• Main Authors: Tilly, Trevor B., Kerr, Lei L., Braydich-Stolle, Laura K., Schlager, John J., Hussain, Saber M.
• Format: Article
• Language: English
• Subjects: Asbestos; Biological and medical sciences; Biotechnology; Characterization and Evaluation of Materials; Chemistry and Materials Science; Cross-disciplinary physics: materials science; rheology; Exact sciences and technology; Fundamental and applied biological sciences. Psychology; Inorganic Chemistry; Lasers; Materials Science; Methods. Procedures. Technologies; Nanocrystalline materials; Nanoparticles; Nanoscale materials and structures: fabrication and characterization; Nanotechnology; Nanotubes; Optical Devices; Optics; Others; Photonics; Physical Chemistry; Physics; Quantum wires; Research Paper; Respiratory system; Titanium dioxide; Toxicity; Various methods and equipments
• ISSN: 1388-0764; 1572-896X
• DOI: 10.1007/s11051-014-2695-5

Titanium dioxide (TiO 2 ) based nanofilaments—nanotube, nanowire, nanorod—have gained interest for industrial, electrical, and as of recent, medical applications due to their superior performance over TiO 2 nanoparticles. Safety assessment of these nanomaterials is critical to protect workers, patients, and bystanders as these technologies become widely implemented. Additionally, TiO 2 based nanofilaments can easily be inhaled by humans and their high aspect ratio, much like asbestos fibers, may make them toxic in the respiratory system. The tendency of TiO 2 nanofilaments to aggregate makes evaluating their nanotoxicity difficult and the results controversial, because incomplete dispersion results in larger particle sizes that are no longer in the nano dimensional size range. TiO 2 nanofilaments are aggregated and difficult to disperse homogeneously in solution by conventional methods, such as sonication and vortexing. In this study, a microfluidic device was utilized to produce stable, homogeneous dosing solutions necessary for in vitro toxicity evaluation by eliminating any toxicity caused by aggregated TiO 2 nanomaterials. The toxicity results could then be directly correlated to the TiO 2 nanostructure itself. The toxicity of four TiO 2 nanogeometries—nanotube, nanowire, nanorod, and nanoparticle—were assessed in RPMI 2650 human nasal epithelial cells at representative day, week, and month in vitro exposure dosages of 10, 50, 100 μg/ml, respectively. All TiO 2 based nanomaterials dispersed by the microfluidic method were nontoxic to RPMI 2650 cells at the concentrations tested, whereas higher concentrations of 100 μg/ml of nanowires and nanotubes dispersed by sonication reduced viability up to 27 %, indicating that in vitro toxicity results may be controlled by the dispersion of dosing solutions.