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Evaluation of metabolic parameters in vitro as a model for testing the cytotoxicity of antiviral drugs

机译:以体外代谢参数评价为试验抗病毒药物细胞毒性的模型

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摘要

A new test system based on in vitro assessment of the cellular viability and/or metabolism is proposed, which offers an informative approach to the screening of antiviral drugs. Cytotoxic effects of the antiviral drugs rimantadine and polyrem were studied on the cultures of some mammalian cells. The results of short-term (2 h) exposures with the drugs tested were close to their LD50 values in mammals, which makes the proposed test system promising for the assessment of drug toxicity in vivo for the whole organism. A study of the state of cell metabolism after a long-term (48 h) exposure showed that the system of endocytosis is more sensitive than other indices with respect to antiviral drugs. Is was demonstrated on the cell level that the binding of drugs into polymeric complexes can decrease the degree of its cytotoxicity: the toxicity of polyrem (a polymeric complex of rimantadine) was lower as compared to that of the equimolar concentration of rimantadine or a mixture of rimantadine with a polymeric carrier.
机译:提出了一种基于体外评估细胞活力和/或代谢的新测试系统,其提供了抗病毒药物筛查的信息方法。在一些哺乳动物细胞的培养上研究了抗病毒药物rimantadine和多月份的细胞毒性作用。试验药物的短期(2小时)曝光的结果接近其哺乳动物中的LD50值,这使得提出的测试系统对整个生物体体内的药物毒性进行了承诺。长期(48小时)暴露后细胞代谢状态的研究表明,内吞作用的系统比其他抗病毒药物的其他指数更敏感。在细胞水平上证明了药物将药物与聚合物复合物的结合可以降低其细胞毒性的程度:与rimantadine的等摩尔浓度或混合物的相比rimantadine用聚合物载体。

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