评估聚合物电解质衍生物类药物对多种病毒的抗病毒活性

D. N. Razgulyaeva, A. M. Klabukov, A. V. Galochkina, A. V. Garshinina, O. N. Zhuravskaya, I. I. Gavrilova, V. A. Manakhov, N. Nesterova, A. Shtro, E. F. Panarin
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引用次数: 0

摘要

背景。现代医疗保健系统正在不断改进和引入新的措施来保护人们免受病毒性疾病的侵袭,但 COVID-19 大流行的经验表明,感染并不总是能在全球范围内得到控制。本研究旨在研究不同化学结构的苯乙烯磺酸钠和乙烯基单体共聚物的抗病毒活性和细胞毒性,并确定有希望开发新型抗病毒药物的聚合物。合成了 14 种苯乙烯磺酸钠(NaSS)与各种功能共聚单体的共聚物。选择了三种具有不同繁殖策略和传播方式的病毒--呼吸道合胞病毒、流感病毒和疱疹病毒--进行抗病毒活性评估。筛选结果表明,共聚物对这三种病毒都具有很高的活性。结果发现,在 NaSS 结构中引入各种官能团不会降低抗病毒活性,但会显著降低细胞毒性。分子量对活性也有明显影响。病毒和细胞对所研究聚合物的敏感性不同,这可能与病毒外壳和细胞壁的结构特征有关。研究结果表明,苯乙烯磺酸钠共聚物具有开发广谱抗病毒药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Antiviral Activity of Drugs from the Group of Polymer Electrolyte Derivatives against a Wide Range of Viruses
Background. The modern healthcare system is constantly improving and introducing new measures to protect the population from viral diseases, but the experience of the COVID-19 pandemic has shown that infections cannot always be controlled on global scale. In this regard, the development of new broad-spectrum antiviral drugs is more relevant than ever.The aim of the study was to investigate the antiviral activity and cytotoxicity of copolymers of sodium styrene sulfonate and vinyl monomers of various chemical structures, as well as to identify promising polymers for the development of new antiviral agents.Materials and methods. 14 copolymers of sodium styrene sulfonate (NaSS) with various functional comonomers were synthesized. Three viruses with different reproduction strategies and transmission methods — respiratory syncytial virus, influenza virus, and herpes virus — were selected for the assessment of antiviral activity.Results. The screening identified copolymers that showed high activity against all three viruses. It was found that the introduction of various functional groups into the structure of NaSS did not decrease antiviral activity, but significantly reduced cytotoxicity. The molecular weight has also shown a noticeable effect on the activity. Different sensitivity of viruses and cells to the studied polymers was revealed, likely due to the structural features of the virus shell and cell wall.Conclusions. The results demonstrate the potential of sodium styrene sulfonate copolymers as a model for developing a broad-spectrum antiviral drug.
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