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2 for another 3 h without changing the culture medium. Then 20 μL of the MTT solution (5 mg/mL) was added into each well. After incubation for 4 h at 37 °C, the cells were finally lysed with 150 μL of DMSO. The absorbance was measured at 490 nm with a microplate reader (ELX 800, Bio-tek, USA). The value for cell viability was expressed as the percentage of the control value. The results were expressed as means ± SD of the indicated numbers from three independent experiments. Statistical analysis was performed by one-way analysis of variance (ANOVA) and Student's Dunnett test using SPSS 16.0 statistical software.
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2 for another 3 h without changing the culture medium. Then 20 μL of the MTT solution (5 mg/mL) was added into each well. After incubation for 4 h at 37 °C, the cells were finally lysed with 150 μL of DMSO. The absorbance was measured at 490 nm with a microplate reader (ELX 800, Bio-tek, USA). The value for cell viability was expressed as the percentage of the control value. The results were expressed as means ± SD of the indicated numbers from three independent experiments. Statistical analysis was performed by one-way analysis of variance (ANOVA) and Student's Dunnett test using SPSS 16.0 statistical software.
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