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  Indian J Med Microbiol
 

Figure 2: Effect of toxicity activity of aqueous extract of Caralluma europaea in vitro spleen cells from mice were cultured in RPMI supplemented with 10% heat inactivated fetal calf serum, 4 mM glutamine, 100 μg/mL gentamicin, and penicillin–streptomycin (200U/mL and 200 μg/mL) and 100 μl of the plant extract at 0.5 or 2 mg/ml. The cells were maintained in continuous culture in a humid atmosphere at 37°C for 24 h. In vitro cytotoxicity assay was carried using Trypan blue (dye exclusion) method for mortality rate determination

Figure 2: Effect of toxicity activity of aqueous extract of <i>Caralluma europaea in vitro</i> spleen cells from mice were cultured in RPMI supplemented with 10% heat inactivated fetal calf serum, 4 mM glutamine, 100 μg/mL gentamicin, and penicillin–streptomycin (200U/mL and 200 μg/mL) and 100 μl of the plant extract at 0.5 or 2 mg/ml. The cells were maintained in continuous culture in a humid atmosphere at 37°C for 24 h. <i>In vitro</i> cytotoxicity assay was carried using Trypan blue (dye exclusion) method for mortality rate determination