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Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells

Titanium dioxide nanoparticles (TiO(2) NPs) are widely used in sunscreens, cosmetics and body implants, and this raises toxicity concerns. Although a large number of reports claim that they are safe to use, others claim that they induce reactive oxygen species formation and can be carcinogenic. In t...

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Detalles Bibliográficos
Autores principales: Kuku, Gamze, Culha, Mustafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408175/
https://www.ncbi.nlm.nih.gov/pubmed/28398241
http://dx.doi.org/10.3390/nano7040083
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author Kuku, Gamze
Culha, Mustafa
author_facet Kuku, Gamze
Culha, Mustafa
author_sort Kuku, Gamze
collection PubMed
description Titanium dioxide nanoparticles (TiO(2) NPs) are widely used in sunscreens, cosmetics and body implants, and this raises toxicity concerns. Although a large number of reports claim that they are safe to use, others claim that they induce reactive oxygen species formation and can be carcinogenic. In this study, the origins of toxic response to TiO(2) NPs were investigated by using Surface-enhanced Raman spectroscopy (SERS) which provides multidimensional information on the cellular dynamics at single cell level without any requirement for cell fixation. Three cell lines of vein (HUVEC), lung carcinoma (A549) and skin (L929) origin were tested for their toxic response upon exposure to 20, 40, 80 and 160 µg/mL anatase-TiO(2) NPs for 24 h. It was demonstrated that the level of toxic response is both cell line and dose-dependent. L929 fibroblasts were the most resistant cell line to oxidative stress whereas in HUVEC and A549, cell lines collagen and lipid deformation were observed, respectively.
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spelling pubmed-54081752017-05-03 Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells Kuku, Gamze Culha, Mustafa Nanomaterials (Basel) Article Titanium dioxide nanoparticles (TiO(2) NPs) are widely used in sunscreens, cosmetics and body implants, and this raises toxicity concerns. Although a large number of reports claim that they are safe to use, others claim that they induce reactive oxygen species formation and can be carcinogenic. In this study, the origins of toxic response to TiO(2) NPs were investigated by using Surface-enhanced Raman spectroscopy (SERS) which provides multidimensional information on the cellular dynamics at single cell level without any requirement for cell fixation. Three cell lines of vein (HUVEC), lung carcinoma (A549) and skin (L929) origin were tested for their toxic response upon exposure to 20, 40, 80 and 160 µg/mL anatase-TiO(2) NPs for 24 h. It was demonstrated that the level of toxic response is both cell line and dose-dependent. L929 fibroblasts were the most resistant cell line to oxidative stress whereas in HUVEC and A549, cell lines collagen and lipid deformation were observed, respectively. MDPI 2017-04-11 /pmc/articles/PMC5408175/ /pubmed/28398241 http://dx.doi.org/10.3390/nano7040083 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kuku, Gamze
Culha, Mustafa
Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title_full Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title_fullStr Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title_full_unstemmed Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title_short Investigating the Origins of Toxic Response in TiO(2) Nanoparticle-Treated Cells
title_sort investigating the origins of toxic response in tio(2) nanoparticle-treated cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408175/
https://www.ncbi.nlm.nih.gov/pubmed/28398241
http://dx.doi.org/10.3390/nano7040083
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