SW480 and HeLa cells (4.5 × 103 cells per well) were seeded into 96-well plates. After 24 h, the media was changed to non-serum RPMI 1640, and after a further 24 h, the cells were treated withJC-Fe3O4 and CT-Fe3O4 NPs at different concentrations. The treated cells were incubated for 48 h, washed with cold PBS, and then exposed to MTT with media for 4 h. The media was changed to DMSO, and the dissolved formazan dye was quantified by measuring the absorbance at 540 nm. As a control, untreated cells were examined in the same manner.
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