Toxicity of binary mixtures of Al2O3 and ZnO nanoparticles toward fibroblast and bronchial epithelium cells.
Jéssica Schveitzer KöerichDiego José NogueiraVitor Pereira VazCarmen SimioniMarlon Luiz Neves Da SilvaLuciane Cristina OuriquesDenice Schulz VicentiniWilliam Gerson MatiasPublished in: Journal of toxicology and environmental health. Part A (2020)
The objective of this study was to examine the cytotoxic effects of binary mixtures of Al2O3 and ZnO NPs using mouse fibroblast cells (L929) and human bronchial epithelial cells (BEAS-2B) as biological test systems. The synergistic, additive, or antagonistic behavior of the binary mixture was also investigated. In toxicity experiments, cellular morphology, mitochondrial function (MTT assay), apoptosis, nuclear size and shape, clonogenic assays, and damage based upon oxidative stress parameters were assessed under control and NPs exposure conditions. Although Abbott modeling results provided no clear evidence of the binary mixture of Al2O3 and ZnO NPs exhibiting synergistic toxicity, some specific assays such as apoptosis, nuclear size and shape, clonogenic assay, activities of antioxidant enzymatic enzymes catalase, superoxide dismutase, and levels of glutathione resulted in enhanced toxicity for the mixtures with 1 and 1.75 toxic units (TU) toward both cell types. Data demonstrated that co-presence of Al2O3 and ZnO NPs in the same environment might lead to more realistic environmental conditions. Our findings indicate cytotoxicity of binary mixtures of Al2O3 and ZnO NPs produced greater effects compared to toxicity of either individual compound.
Keyphrases
- oxidative stress
- ionic liquid
- induced apoptosis
- room temperature
- oxide nanoparticles
- cell cycle arrest
- quantum dots
- high throughput
- ischemia reperfusion injury
- dna damage
- diabetic rats
- reduced graphene oxide
- endoplasmic reticulum stress
- cell death
- visible light
- endothelial cells
- light emitting
- stem cells
- pi k akt
- signaling pathway
- cancer therapy
- cell therapy
- data analysis
- mesenchymal stem cells
- drug delivery
- induced pluripotent stem cells
- risk assessment
- anti inflammatory
- human health