Muldoon R L, Mezny L, Jackson G G
Antimicrob Agents Chemother. 1972 Sep;2(3):224-8. doi: 10.1128/AAC.2.3.224.
The antiviral activity of isoprinosine was tested in tissue cultures and mice. In tissue cultures, concentrations of 25 to 100 mug/ml inhibited the infectivity of influenza and herpes hominis viruses but not parainfluenza virus, rhinovirus, or adenovirus. Among different strains of influenza A, there was considerable variability in the inhibitory concentration of isoprinosine. For influenza B, a zone effect was observed in the inhibitory drug concentration. Oral prophylactic administration of isoprinosine beginning 24 hr before infection with an intermediate challenge dose of influenza A and continued as treatment for 5 days produced a significant reduction in mortality. No protection was provided against a high dose challenge. Oral or intraperitoneal treatment of mice beginning 24 hr after infection with influenza A or B viruses significantly delayed or prevented death when the drug was administered for 10 days, but not when treatment was limited to 4 days. An increased fatality rate which occurred in treated mice given a virus dose of low lethality could not be attributed to drug toxicity.
在组织培养和小鼠中测试了异丙肌苷的抗病毒活性。在组织培养中,25至100微克/毫升的浓度可抑制流感病毒和人疱疹病毒的感染性,但对副流感病毒、鼻病毒或腺病毒无抑制作用。在不同的甲型流感病毒株中,异丙肌苷的抑制浓度存在相当大的差异。对于乙型流感,在抑制药物浓度方面观察到一种区域效应。在感染中等剂量甲型流感病毒前24小时开始口服预防性给予异丙肌苷,并持续治疗5天,可显著降低死亡率。对高剂量攻击无保护作用。在感染甲型或乙型流感病毒后24小时开始对小鼠进行口服或腹腔注射治疗,当给药10天时可显著延迟或预防死亡,但治疗限于4天时则不能。给予低致死性病毒剂量的治疗小鼠中出现的死亡率增加不能归因于药物毒性。