The cell viability were measured using an MTT assay as described previously [43]. Briefly, a total of 25 µL of MTT (1 g/L in PBS) was added to each well before the conduction of incubation at 37 °C for 4 h. The assay was stopped by the addition of a 100 µL of lysis buffer (20% SDS in 50% N′N-dimethylformamide, pH 4.7). Optical density (OD) was measured at the 570 nm wavelength by the use of an ELX-800 microplate assay reader (Bio-tek, Winooski, VT, USA), and the results were expressed as a percentage of absorbance measured in the control cells.
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