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Cytotoxic, genotoxic and the hemolytic effect of titanium dioxide (TiO2) nanoparticles on human erythrocyte and lymphocyte cells in vitro.

Authors :
Ghosh, Manosij
Chakraborty, Anirban
Mukherjee, Anita
Source :
Journal of Applied Toxicology; Oct2013, Vol. 33 Issue 10, p1097-1110, 14p
Publication Year :
2013

Abstract

ABSTRACT With the increasing clinical use of titanium dioxide (TiO<subscript>2</subscript>) nanoparticles, a better understanding of their safety in the blood stream is required. The present study evaluates the toxic effect of commercially available TiO<subscript>2</subscript> nanoparticles (~100 nm) using a battery of cytotoxic, genotoxic, hemolytic and morphological parameters. The cytotoxic effects of TiO<subscript>2</subscript> nanoparticles in human lymphocyte cells were studied with respect to membrane damage, mitochondrial function, metabolic activity and lysosomal membrane stability. Genotoxicity in lymphocyte cells was quantitated using a comet assay. The mode of cell death (apoptosis/necrosis) was evaluated using PI/Annexin V staining. TiO<subscript>2</subscript> nanoparticles were also evaluated for their hemolytic properties, osmotic fragility and interaction with hemoglobin. Human erythrocyte cells were studied for morphological alterations using atomic force microscopy (AFM). Results suggest that the particles could induce a significant reduction in mitochondrial dehydrogenase activity in human lymphocyte cells. Membrane integrity remained unaffected by nanoparticle treatment. DNA damage and apoptosis were induced by TiO<subscript>2</subscript> nanoparticles in a dose-dependent manner. A study on human erythrocyte cells revealed a hemolytic property of TiO<subscript>2</subscript> nanoparticles characterized by spherocytosis and echinocytosis. Spectral analysis revealed a hemoglobin TiO<subscript>2</subscript> nanoparticle interaction. Our in vitro study results suggest that commercially available blood contacting nanoparticles (TiO<subscript>2</subscript> nanoparticle) should be carefully evaluated for their toxic potential. Copyright © 2013 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0260437X
Volume :
33
Issue :
10
Database :
Complementary Index
Journal :
Journal of Applied Toxicology
Publication Type :
Academic Journal
Accession number :
89399242
Full Text :
https://doi.org/10.1002/jat.2863