Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape.
Marina BreischMateusz OlejnikKateryna LozaOleg PrymakNina RosenkranzJürgen BüngerChristina SengstockManfred KöllerGötz WestphalMatthias EpplePublished in: Nanomaterials (Basel, Switzerland) (2023)
Six types of titanium dioxide particles with defined size, shape, and crystal structure (polymorphic form) were prepared: nanorods (70 × 25 nm 2 ), rutile sub-microrods (190 × 40 nm 2 ), rutile microspheres (620 nm), anatase nanospheres (100 nm), anatase microspheres (510 nm), and amorphous titania microspheres (620 nm). All particles were characterized by scanning electron microscopy, X-ray powder diffraction, dynamic light scattering, infrared spectroscopy, and UV spectroscopy. The sub-toxic cell-biological response to these particles by NR8383 macrophages was assessed. All particle types were taken up well by the cells. The cytotoxicity and the induction of reactive oxygen species (ROS) were negligible for all particles up to a dose of 100 µg mL -1 , except for rutile microspheres which had a very rough surface in contrast to anatase and amorphous titania microspheres. The particle-induced cell migration assay (PICMA; based on chemotaxis) of all titanium dioxide particles was comparable to the effect of control silica nanoparticles (50 nm, uncoated, agglomerated) but did not show a trend with respect to particle size, shape, or crystal structure. The coating with carboxymethylcellulose (CMC) had no significant biological effect. However, the rough surface of rutile microspheres clearly induced pro-inflammatory cell reactions that were not predictable by the primary particle size alone.
Keyphrases
- crystal structure
- photodynamic therapy
- electron microscopy
- reactive oxygen species
- molecularly imprinted
- single cell
- cell migration
- cell therapy
- high resolution
- diabetic rats
- light emitting
- cell death
- high glucose
- oxidative stress
- magnetic resonance imaging
- stem cells
- high throughput
- gold nanoparticles
- drug induced
- mesenchymal stem cells
- bone marrow
- computed tomography
- dna damage
- cell cycle arrest
- endothelial cells
- solid state
- solid phase extraction