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KMID : 0365220120490010021
Korean Journal of Public Health
2012 Volume.49 No. 1 p.21 ~ p.31
Cyto-genotoxicity of metal oxide nanoparticles (CuO, Al©üO©ý, CuAl©üO©þ) in A549 cells
Ha Tae-Kyung

Kim Yang-Jee
Choi Young-Joo
Lee Joong-Won
Lee Young-Hyun
Lee Sun-Yeong
Chung Hai-Won
Abstract
Objectives: Recently, growing nanotechnology industry leads to concerns about unknown health effects of nanoparticles in humans. Metal and metal oxide nanomaterials are used in skin care products, abrasives, and polishers. However, the toxicity of these nanoparticles is not fully understood. The purpose of this study is to assess the toxicity of three kinds of metal oxide nanoparticles (CuO, Al©üO©ý, and CuAl©üO©þ).

Methods: To evaluate cell death induced by the metal oxide nanoparticles, we performed MTT assay in the carcinomic human lung epithelial cell line (A549). We examined the genotoxic effects of the nanoparticles in A549 cells using alkaline single cell gel electrophoresis (Comet) assay. The level of reactive oxygen species (ROS) generation induced by the metal oxide nanoparticlesinA549 cells was determined by flow cytometry using the fluorescent dye, 2", 7¡¯-dichlorofluorescin diacetate (DCF-DA).

Results: Dose-dependent decrease in cell survival was observed after treatment of CuO, Al©üO©þ and CuAl©üO©þ. Dose-response trend in the nanoparticles induced DNA damage could be seen in A549 cells treated with CuO, Al©üO©ý, and CuAl©üO©þ. The relative levels of intracellular ROS induced by nanoparticles treatment were significantly augmented. DCF fluorescence intensity in the 50§¶/§¢of CuO, Al©üO©ý, and CuAl©üO©þ treated cells was increased by 441, 176 and 235 %, respectively, as compared to the control group.

Conclusion: Taken together, CuO, Al©üO©ý, and CuAl©üO©þ nanoparticles induced DNA damage and generation of intracellular ROS, eventually, triggering the cell death.
KEYWORD
Copper oxide nanoparticle, Aluminum oxide nanoparticle, Copper-aluminum oxide nanoparticle, mixed metal oxide nanoparticle, Cytotoxicity, Reactive oxygen species(ROS), DNA damage
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