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http://hdl.handle.net/11452/28490
Başlık: | Evaluation of in vitro cytotoxicity and genotoxicity of copper-zinc alloy nanoparticles in human lung epithelial cells |
Yazarlar: | Kumbıçak, Ümit Kumbıçak, Zübeyde Akan Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Bölümü. 0000-0003-1620-1918 0000-0002-7687-3284 0000-0002-3595-6286 Çavaş, Tolga Çinkılıç, Nilüfer Vatan, Özgür Yılmaz, Dilek AAH-3508-2021 O-7508-2015 AAH-5296-2021 6602989548 26533892300 16235098100 6701369462 |
Anahtar kelimeler: | Nanotoxicology Copper-zinc alloy nanoparticles BEAS-2B cells Cytotoxicity Genotoxicity Metal-oxide nanoparticles Zno nanoparticles DNA-damage Toxicity Nanomaterials Release Nickel CUO Food science & technology Toxicology |
Yayın Tarihi: | Kas-2014 |
Yayıncı: | Pergamon-Elsevier Science |
Atıf: | Kumbıçak, Ü. vd. (2014). "Evaluation of in vitro cytotoxicity and genotoxicity of copper-zinc alloy nanoparticles in human lung epithelial cells". Food and Chemical Toxicology, 73, 105-112. |
Özet: | In the present study, in vitro cytotoxic and genotoxic effect of copper-zinc alloy nanoparticles (Cu-Zn ANPs) on human lung epithelial cells (BEAS-2B) were investigated. XTT test and clonogenic assay were used to determine cytotoxic effects. Cell death mode and intracellular reactive oxygen species formations were analyzed using M30, M65 and ROS Elisa assays. Genotoxic effects were evaluated using micronucleus, comet and gamma-H2AX foci assays. Cu-Zn ANPs were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential measurements. Characterization of Cu-Zn ANPs showed an average size of 200 nm and zeta potential of -22 mV. TEM analyses further revealed the intracellular localization of Cu-Zn ANPs in cytoplasm within 24 h. Analysis of micronucleus, comet and gamma-H2AX foci counts showed that exposure to Cu-Zn ANPs significantly induced chromosomal damage as well as single and double stranded DNA damage in BEAS-2B cells. Our results further indicated that exposure to Cu-Zn ANPs significantly induced intracellular ROS formation. Evaluation of M30:M65 ratios suggested that cell death was predominantly due to necrosis. |
URI: | https://doi.org/10.1016/j.fct.2014.07.040 https://www.sciencedirect.com/science/article/pii/S027869151400372X http://hdl.handle.net/11452/28490 |
ISSN: | 0278-6915 1873-6351 |
Koleksiyonlarda Görünür: | Scopus Web of Science |
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