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Procedure for determination of individual sensitivity to antitumor drugs

机译:测定抗肿瘤药物个体敏感性的程序

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The present paper proposes to employ the cultured tumor cells of the breast and chick fibroblasts after long-term cultivation (for above 24 days) to determine their individual drug sensitivity and, as a criterion of cell damage, to use the percent of destruction of the cell layer formed in the wells 24 hours after drug insertion. It also presents the comparative results of tests of 2 cellular models that have been used to determine the in vitro sensitivity of the cells of breast cancer and chick fibroblasts to melfalan and its complex compound with copper acetylacetonate - MOK*M. At the same time, the cytotoxic activity of MOK*M and melfalan against tumor cells has been not shown to differ greatly (16.02+/-1.85 and 15.71+/-0.65% cell layer destruction, respectively), but the same activity of MOK*M against the model of intact cells (chick fibroblasts) was much less (15.23+/-1.97%) than that of melfalan (95.39+/-1.11%). The test system proposed by the authors is of certain informative value and it may beused for the determination of the individual sensitivity of tumor cells to antitumor drugs.
机译:本文提出在长期培养后使用乳腺和鸡肉成纤维细胞的培养肿瘤细胞(64天)来确定其个体药物敏感性,作为细胞损伤的标准,使用损坏的百分比在药物插入后24小时形成细胞层。它还介绍了2种细胞模型的测试的比较结果,该模型已被用于确定乳腺癌细胞的体外敏感性,并用乙酰乙酰丙酯 - MOK * M与氯酰丙酯铜和其复杂的化合物。同时,Mok * M和Melfalan对肿瘤细胞的细胞毒性活性未显示出很大(16.02 +/- 1.85和15.71 +/- 0.65%的细胞层破坏),但Mok的相同活动*抗完整细胞模型(小鸡成纤维细胞)比Melfalan(95.39 +/- 1.11%)更少(15.23 +/- 1.97%)。作者提出的测试系统具有一定的信息价值,并且可能被派去确定肿瘤细胞对抗肿瘤药物的个体敏感性。

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