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. 2018 May 17;13:2907–2919. doi: 10.2147/IJN.S159388

Figure 4.

Figure 4

GO induces ROS generation in MG-63 and K7M2 cells.

Notes: (A) MG-63 and K7M2 cells were treated with 0, 25, and 50 µg/mL GO for 2 h. Then, DHE analyses were applied to detect ROS generation. (B) Fluorescence analysis of ROS content. MG-63 and K7M2 cells were treated with 0, 25, and 50 µg/mL GO for 0.5, 2, 4, and 8 h. Fluorescence intensity was calculated compared to untreated control cells. Values are presented as mean±SD and compared with untreated control (*P<0.05, #P<0.01). (C) Cell viability assay was conducted by MTT. MG-63 and K7M2 cells were treated with 0, 25, and 50 µg/mL GO with or without NAC (10 mmol/L) for 8 h. #P<0.01 (compared with GO treatment alone).

Abbreviations: DHE, dihydroethidium; GO, graphene oxide; NAC, N-acetylcysteine; ROS, reactive oxygen species.