Indian J Pharm Close
 

Figure 3: Survival inhibition of hepatocellular carcinoma Bel-7402 cells by EtOH extract n-butyl-β-D-fructofuranoside assessed via MTT proliferation assay. (a) Cells were treated with n-butyl-β-D-fructofuranoside at concentrations 0.47, 2.95, 5.90, 11.8, 17.7 and 23.6μg/ml for 24, 48 and 72 hours. Nontreated and 0.1% DMSO-treated cells were used as control. n-butyl-β-D-fructofuranoside suppressed proliferation of Bel-7402 cells in both time- and dose-dependent manner. Each value represents means ± SD in three different experiments. The IC50 could be calculated via logistic curve fitting of cell viabilities for 24 (b), 48 (c) and 72 hours (d)

Figure 3: Survival inhibition of hepatocellular carcinoma Bel-7402 cells by EtOH extract n-butyl-β-D-fructofuranoside assessed via MTT proliferation assay. (a) Cells were treated with n-butyl-β-D-fructofuranoside at concentrations 0.47, 2.95, 5.90, 11.8, 17.7 and 23.6μg/ml for 24, 48 and 72 hours. Nontreated and 0.1% DMSO-treated cells were used as control. n-butyl-β-D-fructofuranoside suppressed proliferation of Bel-7402 cells in both time- and dose-dependent manner. Each value represents means ± SD in three different experiments. The IC50 could be calculated via logistic curve fitting of cell viabilities for 24 (b), 48 (c) and 72 hours (d)