Significant ROS production capability of bare iron oxide nanoparticles in safe doses for healthy cells offers an interesting therapeutic window for cancer. In this context, the aim of the current study is to investigate therapeutic potential of the synthesized magnetite (Fe₃O₄) nanoparticles (~80 nm) as attractive vehicles for biomedical applications on hepatocellular carcinoma cells (HepG2). To investigate their time (0-72 h) and dose (0-100 μg/ml) dependent effect on physiological state (proliferation/ cytotoxicity) and mitochondrial activity of the tumor cells, xCELLigence system and MTT assay were used, respectively. Both 50 and 100 μg/ml of nanoparticle treatment induced significant (p < 0.01) increases in ROS production in HepG2 cells; however, ~4-day real-time cell analysis illustrated that all concentrations of the nanoparticles caused significant (p < 0.01) increases in proliferation of the tumor cells from 4 h after the treatment to the end of the analysis. While 50 and 100 μg/ml of nanoparticles caused significant deteriorations in the mitochondrial activity of the tumor cells in the case of 24 h-(p < 0.05 and p < 0.01, respectively) and 72 h-treatment (p < 0.01); 24 h-treatment of 100 μg/ml of nanoparticles and 72 h-treatment of 50 and 100 μg/ml of nanoparticles caused significant increases in the mitochondrial activity of the tumor cells (p < 0.01) under static magnetic field (1.35 T). Although the synthesized magnetite nanoparticles have not therapeutic potential alone on HepG2 cells in doses safe for healthy cells, the results of the current study are illuminating for future magnetite nanoparticle-based biomedical applications and combination cancer therapy containing magnetite nanoparticles.

#	Concept	H-Index	Publications	Citations
1	Engineering	1	1	36
2	Chemical Engineering	1	1	36
3	Chemistry	1	1	36
4	Inorganic Chemistry	1	1	36

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