“…After 24 h drug exposure durations, the medium was substituted with 200 lL fresh RPMI-1640 medium for 24 h. The cells were incubated with 50 lL of 2 mg/ml MTT which dissolved in PBS, for 4 h. Then, the content of all wells was replaced with 200 lL pure DMSO and 25 lL Sorensen's glycine buffer. Finally, in a reference wavelength of 630 nm, an ELISA-reader was used to estimate the absorbance measurement at 570 nm (Baviskar et al 2012, C amara et al 2014, Cervadoro et al 2013, Gudoshnikov et al 2012, 2013, Martinez-Boubeta et al 2013, Thakor et al 2013.…”