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

机译:评估体外代谢参数,作为测试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:提出了一种基于细胞活力和/或代谢的体外评估的新测试系统,该系统为筛选抗病毒药物提供了有益的方法。研究了抗病毒药物金刚乙胺和多菌灵对某些哺乳动物细胞培养的细胞毒性作用。在哺乳动物中短期(2 h)接触药物的结果接近其LD50值,这使得拟议的测试系统有望在整个生物体内评估药物毒性。长期(48小时)暴露后细胞代谢状态的研究表明,就抗病毒药物而言,内吞作用系统比其他指标更敏感。在细胞水平上已证明药物与聚合物复合物的结合可降低其细胞毒性程度:与等摩尔浓度的金刚乙胺或其混合物相比,polyrem(金刚烷胺的聚合物复合物)的毒性较低。金刚烷胺与聚合物载体。

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