Herrmann J E, Bruns M, West K, Ennis F A
Division of Infectious Diseases, University of Massachusetts Medical School, Worcester 01655.
Antiviral Res. 1989 Apr;11(3):127-35. doi: 10.1016/0166-3542(89)90024-7.
Rimantadine HCl was assessed for its effect on influenza A virus titer in lungs of infected BALB/c mice. Rimantadine administered orally via drinking water, with and without an intraperitoneal prophylactic loading dose, was compared to intraperitoneal administration. Mice were infected with a non-lethal dose of influenza A/Port Chalmers/H3N2 virus and the pulmonary virus titers were determined at intervals over a 21 day period. Prophylactic treatment with rimantadine followed by oral administration resulted in up to a 4 log10 reduction in pulmonary virus titer. The oral doses given to the mice were comparable on a mg/kg/day basis to those recommended for treatment of human infections. Reductions in pulmonary virus titers also occurred after intraperitoneal rimantadine treatment which included a prophylactic dose, but the reductions in pulmonary virus titers were less striking and not consistent over the course of infection. There were no significant reductions in pulmonary virus titers by either route if treatment was started 8 h after exposure to virus.
对盐酸金刚乙胺在感染甲型流感病毒的BALB/c小鼠肺中的病毒滴度影响进行了评估。将通过饮用水口服给予盐酸金刚乙胺(有无腹腔内预防性负荷剂量)的情况与腹腔内给药进行了比较。用非致死剂量的甲型/查尔姆斯港/H3N2流感病毒感染小鼠,并在21天内定期测定肺部病毒滴度。先进行预防性治疗然后口服金刚乙胺,可使肺部病毒滴度降低多达4个对数10。按毫克/千克/天计算,给予小鼠的口服剂量与推荐用于治疗人类感染的剂量相当。腹腔内给予金刚乙胺(包括预防性剂量)后,肺部病毒滴度也有所降低,但肺部病毒滴度的降低不太显著,且在感染过程中不一致。如果在接触病毒8小时后开始治疗,两种给药途径的肺部病毒滴度均无显著降低。