Study on Antiviral Activity and Pharmacological Safety of Double-Stranded Ribonucleic Acid for Intranasal Administration

S. G. Gamaley, G. G. Shimina, E. S. Tsyplenkova, O. V. Simakova, M. Skarnovich, M. A. Skarnovich, L. Shishkina, O. Taranov, O. S. Ivanova, G. M. Levagina, E. Danilenko
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Abstract

Interferon inducers are of interest as the first line of defense against viral infections, including influenza. Double-stranded ribonucleic acid (dsRNA) for intranasal administration has been developed, the excipients and drug components were selected at the Institute of Medical Biotechnology, a branch of the State Research Center of Virology and Biotechnology «Vector». This work presents the results of the study on antiviral activity and pharmacological safety of a new form of dsRNA. The antiviral activity of the preparation was studied in BALB/c mice infected with influenza A/Aichi/2/68 (H3N2) or Bishkek/01/2009 (H1N1pdm09) viruses. A safety study was performed with a single administration of intranasal dsRNA into white outbred ICR mice. The study showed that the administration of therapeutic and prophylactic regimen of intranasal dsRNA at a dose of 2.5 mg/kg increases the survival and average life expectancy of mice infected with the mentioned strains of influenza virus. The protective effect of the preparation in mice infected with a lethal dose of Bishkek/01/2009 virus was comparable to the effect of Tamiflu. The absence of toxic effects of intranasal dsRNA at a pharmacological dose in laboratory mice, the functional state of their physiological systems, as well as main types of metabolism, established in the experiments, lead to a conclusion concerning pharmacological safety of the preparation and the prospects for further work to complete pharmaceutical development of a new antiviral drug.
鼻用双链核糖核酸抗病毒活性及药理安全性研究
干扰素诱导剂作为抵御病毒感染(包括流感)的第一道防线,引起了人们的兴趣。用于鼻内给药的双链核糖核酸(dsRNA)已经开发,赋形剂和药物成分是在国家病毒学和生物技术研究中心“载体”分支机构医学生物技术研究所选择的。本文介绍了一种新型dsRNA的抗病毒活性和药理安全性的研究结果。研究了该制剂对感染甲型流感病毒/爱知/2/68 (H3N2)和比什凯克/01/2009 (H1N1pdm09)的BALB/c小鼠的抗病毒活性。一项安全性研究通过单次给药鼻内dsRNA到白色杂交ICR小鼠。研究表明,治疗性和预防性的鼻内dsRNA剂量为2.5 mg/kg,可提高感染上述流感病毒株的小鼠的存活率和平均预期寿命。该制剂对感染致死剂量比什凯克/01/2009病毒的小鼠的保护作用与达菲的作用相当。实验小鼠鼻内dsRNA在药理学剂量下无毒性作用,实验确定了小鼠生理系统的功能状态以及主要代谢类型,得出了有关该制剂的药理学安全性的结论,并展望了进一步工作以完成新型抗病毒药物的药物开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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