Ishiyama M, Tominaga H, Shiga M, Sasamoto K, Ohkura Y, Ueno K
Dojindo Laboratories, Kumamoto, Japan.
Biol Pharm Bull. 1996 Nov;19(11):1518-20. doi: 10.1248/bpb.19.1518.
Cell viability and in vitro cytotoxicity assay methods were developed using a combination of dyes, 4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate (WST-1), neutral red (NR) and crystal violet (CV), with HeLa cells as a bioindicatior. As WST-1 produces a highly water soluble and non-cytotoxic formazan dye, ti allows each assay to be carried out in one culture dish. The combined cell viability assay using WST-1, NR and CV gave an absorbance that correlated linearly with the number of cells over the range 1000 to 50,000 cells/well. The combined assay was applied to the evaluation of IC50 values for sodium dodecyl sulfate as a model toxicant, which yielded similar values to those obtained with each assay independently.
利用染料4-[3-(4-碘苯基)-2-(4-硝基苯基)-2H-5-四氮唑]-1,3-苯二磺酸盐(WST-1)、中性红(NR)和结晶紫(CV)的组合,并以HeLa细胞作为生物指示剂,开发了细胞活力和体外细胞毒性测定方法。由于WST-1产生一种高度水溶性且无细胞毒性的甲臜染料,因此每次测定都可以在一个培养皿中进行。使用WST-1、NR和CV的联合细胞活力测定所得到的吸光度在每孔1000至50000个细胞的范围内与细胞数量呈线性相关。该联合测定法被应用于评估作为模型毒物的十二烷基硫酸钠的半数抑制浓度(IC50)值,所得结果与单独使用每种测定法获得的结果相似。