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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/12795
Title: Genotoxic and cytotoxic of biosynthesized titanium dioxide nanoparticles against CaCO2 and MDA-MB-231 cell lines
Authors: Ganash, Magdah
Keywords: Biosynthesis
titanium dioxide nanoparticles
cytotoxicity
genotoxicity
Issue Date: 3-Jan-2020
Publisher: Karachi:Pakistan Journal of Pharmaceutical Sciences, university of Karachi.
Citation: Ganash, M. (2020). Genotoxic and cytotoxic of biosynthesized titanium dioxide nanoparticles against CaCO2 and MDA-MB-231 cell lines. PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 33(3), 1199-1207.
Abstract: Till now there is a general lack of information concerning the genotoxic and cytotoxic effects of nanoparticles. Titanium dioxide nanoparticles (TiO2NPs) were synthesized using Trichoderma harzianum and characterized by Fourier Transmission Infrared spectroscopy, Ultra-Violet visible spectroscopy and Transmission Electron Microscope. The 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay revealed the concentration-dependent cytotoxic effects of TiO2NPs in a concentration range of 7.8 to 500 μg/ml. The reduction in proliferation of CaCO2 and MDA-MB-231 cell lines was observed in a concentration dependent manner which became more clear especially at higher (500 μg/ml) concentrations of TiO2NPs. The anti-proliferative effect of TiO2NPs treatment was more potent on CaCO2 than MDAMB-231 cells, where the IC50 was 124 and 107 µg/ml respectively. Exposure of CaCO2 cell line to 7.80, 15.60, 31.25, 62.50, 125, 250 and 500 µg/ml of TiO2NPs showed an increase by 1.10, 1.54, 1.83, 2.64, 3.76, 4.76 and 5.21 fold respectively in SOD activity with respect to untreated control. The effect of low concentrations of TiO2NPs up to 62.5 µg/ml was weakly induced the release of LDH, while followed these concentrations become high. DNA “laddering” pattern in CaCO2 cells treated with TiO2NP is one of the reasons for cell death.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/12795
ISSN: 1011-601X
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