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Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape

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...

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Autores principales: Breisch, Marina, Olejnik, Mateusz, Loza, Kateryna, Prymak, Oleg, Rosenkranz, Nina, Bünger, Jürgen, Sengstock, Christina, Köller, Manfred, Westphal, Götz, Epple, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221891/
https://www.ncbi.nlm.nih.gov/pubmed/37242038
http://dx.doi.org/10.3390/nano13101621
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author Breisch, Marina
Olejnik, Mateusz
Loza, Kateryna
Prymak, Oleg
Rosenkranz, Nina
Bünger, Jürgen
Sengstock, Christina
Köller, Manfred
Westphal, Götz
Epple, Matthias
author_facet Breisch, Marina
Olejnik, Mateusz
Loza, Kateryna
Prymak, Oleg
Rosenkranz, Nina
Bünger, Jürgen
Sengstock, Christina
Köller, Manfred
Westphal, Götz
Epple, Matthias
author_sort Breisch, Marina
collection PubMed
description 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.
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spelling pubmed-102218912023-05-28 Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape Breisch, Marina Olejnik, Mateusz Loza, Kateryna Prymak, Oleg Rosenkranz, Nina Bünger, Jürgen Sengstock, Christina Köller, Manfred Westphal, Götz Epple, Matthias Nanomaterials (Basel) Article 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. MDPI 2023-05-12 /pmc/articles/PMC10221891/ /pubmed/37242038 http://dx.doi.org/10.3390/nano13101621 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Breisch, Marina
Olejnik, Mateusz
Loza, Kateryna
Prymak, Oleg
Rosenkranz, Nina
Bünger, Jürgen
Sengstock, Christina
Köller, Manfred
Westphal, Götz
Epple, Matthias
Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title_full Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title_fullStr Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title_full_unstemmed Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title_short Cell-Biological Response and Sub-Toxic Inflammatory Effects of Titanium Dioxide Particles with Defined Polymorphic Phase, Size, and Shape
title_sort cell-biological response and sub-toxic inflammatory effects of titanium dioxide particles with defined polymorphic phase, size, and shape
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221891/
https://www.ncbi.nlm.nih.gov/pubmed/37242038
http://dx.doi.org/10.3390/nano13101621
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