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Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles

Nanoparticles (NPs) of zinc oxide (ZnO) and titanium dioxide (TiO(2)) are receiving increasing attention due to their widespread applications. The aim of this study was to evaluate the toxic effect of ZnO and TiO(2) NPs at different concentrations (50, 100, 250 and 500 ppm) and compare them with the...

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Autores principales: Khan, Maryam, Naqvi, Alim Husain, Ahmad, Masood
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598137/
https://www.ncbi.nlm.nih.gov/pubmed/28962412
http://dx.doi.org/10.1016/j.toxrep.2015.02.004
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author Khan, Maryam
Naqvi, Alim Husain
Ahmad, Masood
author_facet Khan, Maryam
Naqvi, Alim Husain
Ahmad, Masood
author_sort Khan, Maryam
collection PubMed
description Nanoparticles (NPs) of zinc oxide (ZnO) and titanium dioxide (TiO(2)) are receiving increasing attention due to their widespread applications. The aim of this study was to evaluate the toxic effect of ZnO and TiO(2) NPs at different concentrations (50, 100, 250 and 500 ppm) and compare them with their respective salts using a battery of cytotoxicity, and genotoxicity parameters. To evaluate cytotoxicity, we have used human erythrocytes and for genotoxic studies human lymphocytes have been used as in vitro model species. Concentration dependent hemolytic activity to RBC's was obtained for both NPs. ZnO and TiO(2) NPs resulted in 65.2% and 52.5% hemolysis at 250 ppm respectively indicating that both are cytotoxic to human RBCs. Antioxidant enzymes assays were also carried out in their respective hemolysates. Both nanoparticles were found to generate reactive oxygen species (ROS) concomitant with depletion of glutathione and GST levels and increased SOD, CAT and lipid peroxidation in dose dependent manner. ZnO and TiO(2) NPs exerted roughly equal oxidative stress in terms of aforementioned stress markers. Genotoxic potential of both the NPs was investigated by in vitro alkaline comet assay. DNA damage induced by the NPs was concentration dependent and was significantly greater than their ionic forms at 250 and 500 ppm concentrations. Moreover, the nanoparticles of ZnO were significantly more genotoxic than those of TiO(2) at higher concentrations. The toxicity of these NPs is due to the generation of ROS thereby causing oxidative stress.
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spelling pubmed-55981372017-09-28 Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles Khan, Maryam Naqvi, Alim Husain Ahmad, Masood Toxicol Rep Article Nanoparticles (NPs) of zinc oxide (ZnO) and titanium dioxide (TiO(2)) are receiving increasing attention due to their widespread applications. The aim of this study was to evaluate the toxic effect of ZnO and TiO(2) NPs at different concentrations (50, 100, 250 and 500 ppm) and compare them with their respective salts using a battery of cytotoxicity, and genotoxicity parameters. To evaluate cytotoxicity, we have used human erythrocytes and for genotoxic studies human lymphocytes have been used as in vitro model species. Concentration dependent hemolytic activity to RBC's was obtained for both NPs. ZnO and TiO(2) NPs resulted in 65.2% and 52.5% hemolysis at 250 ppm respectively indicating that both are cytotoxic to human RBCs. Antioxidant enzymes assays were also carried out in their respective hemolysates. Both nanoparticles were found to generate reactive oxygen species (ROS) concomitant with depletion of glutathione and GST levels and increased SOD, CAT and lipid peroxidation in dose dependent manner. ZnO and TiO(2) NPs exerted roughly equal oxidative stress in terms of aforementioned stress markers. Genotoxic potential of both the NPs was investigated by in vitro alkaline comet assay. DNA damage induced by the NPs was concentration dependent and was significantly greater than their ionic forms at 250 and 500 ppm concentrations. Moreover, the nanoparticles of ZnO were significantly more genotoxic than those of TiO(2) at higher concentrations. The toxicity of these NPs is due to the generation of ROS thereby causing oxidative stress. Elsevier 2015-02-19 /pmc/articles/PMC5598137/ /pubmed/28962412 http://dx.doi.org/10.1016/j.toxrep.2015.02.004 Text en © 2015 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Khan, Maryam
Naqvi, Alim Husain
Ahmad, Masood
Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title_full Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title_fullStr Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title_full_unstemmed Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title_short Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
title_sort comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598137/
https://www.ncbi.nlm.nih.gov/pubmed/28962412
http://dx.doi.org/10.1016/j.toxrep.2015.02.004
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