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XIA Ting, TANG Meng, YIN Hai-rong, . Effect of Fe2O3 nanoparticles on cell viability and apoptosis in RAW264.7 cells[J]. Chinese Journal of Public Health, 2008, 24(9): 1074-1076. DOI: 10.11847/zgggws2008-24-09-27
Citation: XIA Ting, TANG Meng, YIN Hai-rong, . Effect of Fe2O3 nanoparticles on cell viability and apoptosis in RAW264.7 cells[J]. Chinese Journal of Public Health, 2008, 24(9): 1074-1076. DOI: 10.11847/zgggws2008-24-09-27

Effect of Fe2O3 nanoparticles on cell viability and apoptosis in RAW264.7 cells

  • Objective To study the effect of Fe2O3 nanopar ticles on proliferation and apoptosis and the oxidativ e damage of RA w264.7 cells.Methods The cy to toxicity and inter vening concentration of nanoparticles were detected by MTT assays.0.24,0.48 and 0.96 mg/ml Fe2O3 nanoparticles suspension-inter vened macrophages were set as Fe2O3 nanoparticle groups,and normal saline group was set as control group.The levels of LDH activity in medium were analyzed using the reagent kits.The mitochondrial membr ane potent(MMP)and cell apoptosis rate were analyzed by flow cytometry.Results The proliferations of RA w264.7 cells were suppr essed when exposed to Fe2O3 nanopart icles of 0.816~3.523 mg/ml.The IC50 of Fe2O3 nanoparticles on RAW 26417 cells was 11.76 mg/ml.The levels of LDH activity in Fe2O3 nanoparticle groups were higher than that of control group(P<0.05).Flow cytometry assay showed that the MMP decreased in different exposure groups and cell apoptosis rate of exposure groups were higher than that of the control(P<0.05).Conclusion Fe2O3 nanoparticles could cause cytotoxicity,increase cell membrane permeability and depress the activities of LDH.Fe2O3 nanoparticles could also reduce the MMP and lead to apoptosis in RAW 264.7 cells.
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