Publication | Closed Access
Comparative cytotoxicity and genotoxicity of cobalt (II, III) oxide, iron (III) oxide, silicon dioxide, and aluminum oxide nanoparticles on human lymphocytes in vitro
126
Citations
52
References
2015
Year
NanotherapeuticsEngineeringImmunotoxicologyIron MetabolismAluminum Oxide NanoparticlesImmunologyComparative CytotoxicityNanotoxicologyRedox BiologyOxidative StressChemical EngineeringToxicologyEcotoxicologyReactive Oxygen SpeciePharmacologyAl 2Bioactive MetalChromosomal AberrationMetal ToxicityEnvironmental ToxicologyMedicineSilicon Dioxide
Despite the extensive use of nanoparticles (NPs) in various fields, adequate knowledge of human health risk and potential toxicity is still lacking. The human lymphocytes play a major role in the immune system, and it can alter the antioxidant level when exposed to NPs. Identification of the hazardous NPs was done using in vitro toxicity tests and this study mainly focuses on the comparative in vitro cytotoxicity and genotoxicity of four different NPs including cobalt (II, III) oxide (Co 3 O 4 ), iron (III) oxide (Fe 2 O 3 ), silicon dioxide (SiO 2 ), and aluminum oxide (Al 2 O 3 ) on human lymphocytes. The Co 3 O 4 NPs showed decrease in cellular viability and increase in cell membrane damage followed by Fe 2 O 3 , SiO 2 , and Al 2 O 3 NPs in a dose-dependent manner after 24 h of exposure to human lymphocytes. The oxidative stress was evidenced in human lymphocytes by the induction of reactive oxygen species, lipid peroxidation, and depletion of catalase, reduced glutathione, and superoxide dismutase. The Al 2 O 3 NPs showed the least DNA damage when compared with all the other NPs. Chromosomal aberration was observed at 100 µg/ml when exposed to Co 3 O 4 NPs and Fe 2 O 3 NPs. The alteration in the level of antioxidant caused DNA damage and chromosomal aberration in human lymphocytes.
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