Petty R D, Sutherland L A, Hunter E M, Cree I A
Department of Pathology, University of Dundee, Ninewells Hospital and Medical School, Scotland.
J Biolumin Chemilumin. 1995 Jan-Feb;10(1):29-34. doi: 10.1002/bio.1170100105.
Cell viability assays are widely used to assess the effect chemotherapeutic drugs and other agents on cell lines and have shown promise for the prediction of tumour chemosensitivity. In this study we have compared two viability assays using Daudi and CCRF-CEM cell lines over a range of 1500-100,000 cells/well of a microplate. The ATP assay was able to detect the lower limit of 1563 cells/well with luminescence values at least 100 x background readings, while the MTT assay could not detect less than 25,000 cells/well above background readings. The ATP assay also showed better reproducibility and sensitivity when cells were grown in microtitre plates over several days, and is particularly useful for the measurement of viability with low cell numbers.
细胞活力测定法被广泛用于评估化疗药物和其他试剂对细胞系的影响,并已显示出在预测肿瘤化疗敏感性方面的前景。在本研究中,我们使用Daudi和CCRF - CEM细胞系,在微孔板每孔1500 - 100,000个细胞的范围内比较了两种活力测定法。ATP测定法能够检测到每孔1563个细胞的下限,发光值至少是背景读数的100倍,而MTT测定法在高于背景读数时无法检测到每孔少于25,000个细胞。当细胞在微量滴定板中培养数天时,ATP测定法还显示出更好的重现性和敏感性,并且对于低细胞数的活力测量特别有用。