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  Indian J Med Microbiol
 

Figure 3: (a) Effect of condurangogenin A (ConA) on the viability of H460 cells. Cells were exposed to ConA for 12 h, 18 h, 24 h and 48 h, at different concentrations (30-45 µg/ml) and the cell viability was determined by diphenyltetrazolium bromide (MTT) assay. 6% alcohol (6% Alc.) was used as vehicle control. Results were expressed as percentage of cell viability and each expressed as mean ± standard division (N = 6). Significance, *P < 0.05 versus untreated (UT) and #P < 0.05 versus 6% Alc.-treated groups. Significance, P < 0.001 versus UT. (b) Effect of 6% Alc. (0.4 µl/ml) and ConA (32 µg/ml) on peripheral blood mononuclear cells (PBMC) by MTT assay. PBMCs were incubated for 12 h, 18 h and 24 h with 6% Alc. and ConA

Figure 3: (a) Effect of condurangogenin A (ConA) on the viability of H460 cells. Cells were exposed to ConA for 12 h, 18 h, 24 h and 48 h, at different concentrations (30-45 µg/ml) and the cell viability was determined by diphenyltetrazolium bromide (MTT) assay. 6% alcohol (6% Alc.) was used as vehicle control. Results were expressed as percentage of cell viability and each expressed as mean ± standard division (<i>N</i> = 6). Significance, *<i>P</i> < 0.05 versus untreated (UT) and #<i>P</i> < 0.05 versus 6% Alc.-treated groups. Significance, <i>P</i> < 0.001 versus UT. (b) Effect of 6% Alc. (0.4 µl/ml) and ConA (32 µg/ml) on peripheral blood mononuclear cells (PBMC) by MTT assay. PBMCs were incubated for 12 h, 18 h and 24 h with 6% Alc. and ConA