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. 2014 Nov 15;7(2):89–92. doi: 10.2478/intox-2014-0012

Figure 1.

Figure 1

Inhibitory effect of UPE on melanin content (A) and cell viability (B) of B16F10 cells. B16F10 cells (2.0×104 µg/mL) were pre-incubated for 18 h and the melanin content was assayed after incubation of the B16F10 cells treated with α-MSH (100 nM), melasolv (40 µM), and UPE (3.125, 6.25 and 12.5 µg/mL) for 72 h at 37°C in a 5% CO2 atmosphere. The absorbance was measured at 405 nm by ELISA. MTT assay was performed after incubation of the B16F10 cells treated with varying concentrations of UPE (3.125, 6.25 and 12.5 µg/mL) for 24 h at 37°C in a 5% CO2 atmosphere. The absorbance was measured at 570 nm with a spectrophotometer (Power Wave; Bio-tek, Winooski, VT). Values are the mean ± SEM of triplicate experiments. *p<0.05; **p<0.01.