Study of the Mechanism of Antiviral Activity of Cytovir®-3 Against Respiratory Viruses In Vitro

V. Zarubaev, V. S. Smirnov, T. A. Kudryavtseva, S. Petlenko, A. V. Slita, H. Minh, V. Zaplutanov
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Abstract

Introduction. The requirements of modern clinical guidelines for the treatment of respiratory viral infections suggest the possibility of identifying a specific viral pathogen. In this regard, the search for drugs with selective activity against respiratory syncytial virus and parainfluenza virus is relevant. The purpose of the work is to study the antiviral activity of the drug Cytovir®-3 in vitro in relation to the cytopathogenic effect of respiratory viruses (parainfluenza virus and respiratory syncytial virus). Material and methods. The antiviral effect of Cytovir®-3 in comparison with Umifenovir against parainfluenza virus and respiratory syncytial virus was studied on Vero cell culture. Drugs were administered 1 hour before (prophylactic regimen) and 1 hour after (treatment regimen) infection of the cell culture with respiratory viruses. The working range of concentrations of the studied drugs was calculated based on the values of 50% cytotoxic concentration calculated based on the results of a quantitative microtetrazole test. Results and discussion. The drug Cytovir®-3 in two schemes of application (therapeutic or prophylactic) showed its antiviral efficacy in vitro against respiratory syncytial virus and parainfluenza virus due in the non-toxic range (0–794 µg/ml). At the same time, the suppressive effect of the drug Cytovir®-3 against the parainfluenza virus begins at lower concentrations of the drug with its early (preventive) introduction into cell culture (250 mcg/ml). Conclusion. Antiviral activity of Cytovir®-3 has been proven in vitro against parainfluenza virus and respiratory syncytial virus. At the same time, in all series of experiments, Cytovir®-3 had a higher index of selectivity of antiviral action than that of the comparison drug Umifenovir.
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Cytovir®-3体外抗呼吸道病毒作用机制的研究
介绍。现代临床指南的要求,呼吸道病毒感染的治疗建议的可能性,以确定一个特定的病毒病原体。在这方面,寻找对呼吸道合胞病毒和副流感病毒具有选择性活性的药物是相关的。本研究的目的是在体外研究药物Cytovir®-3的抗病毒活性与呼吸道病毒(副流感病毒和呼吸道合胞病毒)的细胞致病性的关系。材料和方法。在Vero细胞培养上研究了Cytovir®-3与Umifenovir对副流感病毒和呼吸道合胞病毒的抗病毒作用。在细胞培养物感染呼吸道病毒前1小时(预防方案)和后1小时(治疗方案)给药。所研究药物的工作浓度范围是根据微四唑定量试验结果计算的50%细胞毒浓度值计算得出的。结果和讨论。药物Cytovir®-3在治疗和预防两种应用方案下,对呼吸道合胞病毒和副流感病毒的体外抗病毒效果在无毒范围内(0-794µg/ml)。同时,药物Cytovir®-3对副流感病毒的抑制作用开始于较低浓度的药物,早期(预防性)引入细胞培养(250微克/毫升)。结论。在体外对副流感病毒和呼吸道合胞病毒的抗病毒活性已被证实。同时,在所有系列实验中,Cytovir®-3抗病毒作用的选择性指数均高于对照药物umifenvir。
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