MTT Assay for Cytotoxic Drugs on Experimental Study of L2 Cells
Bing Li
Abstract
Bing Li
Abstract
Objective:To evaluate the reliability of toxic effects of drugs using MTT assay.Methods:The rat alveolar epithelial L2 cells exposure to TBHQ 10-100 μM,BSO 1-10 mM,respectively,using MTT assay to detect the activity of cells,JC-1 fluorescent dye to detect the changes in mitochondrial potential,trypan blue exclusion to detect the prevalence.Results:In the treatment dose range,the OD values detected by MTT assay failed to meet generally determine the IC 50 level,and the highest inhibition rate is around 30%;trypan blue exclusion assay data indicate that the LC 50 value of TBHQ is 50 μM,BSO to 5 mM;using of JC-1 fluorescent dye to determine the half dose is 50 μM and 7 mM,respectively.Conclusion:MTT assay is the most common means to detect the cell growth inhibition,but it may not objectively reflect the activity of cells in a given experiment.We suggest to use a variety of methods in conjunction.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To evaluate the reliability of toxic effects of drugs using MTT assay.Methods:The rat alveolar epithelial L2 cells exposure to TBHQ 10-100 μM,BSO 1-10 mM,respectively,using MTT assay to detect the activity of cells,JC-1 fluorescent dye to detect the changes in mitochondrial potential,trypan blue exclusion to detect the prevalence.Results:In the treatment dose range,the OD values detected by MTT assay failed to meet generally determine the IC 50 level,and the highest inhibition rate is around 30%;trypan blue exclusion assay data indicate that the LC 50 value of TBHQ is 50 μM,BSO to 5 mM;using of JC-1 fluorescent dye to determine the half dose is 50 μM and 7 mM,respectively.Conclusion:MTT assay is the most common means to detect the cell growth inhibition,but it may not objectively reflect the activity of cells in a given experiment.We suggest to use a variety of methods in conjunction.
Key concepts: Trypan blue, MTT assay, Cytotoxicity, Molecular biology, Chemistry, Cytotoxic T cell, Fluorescence, In vitro