McKinlay M A, Frank J A, Benziger D P, Steinberg B A
J Infect Dis. 1986 Oct;154(4):676-81. doi: 10.1093/infdis/154.4.676.
The systemic efficacy of the antipicornavirus agent WIN 51711 was assessed in suckling mice infected with echovirus type 9 (Barty strain). Single, daily intraperitoneal doses of WIN 51711 as low as 10 mg/kg significantly (P less than .01) slowed the rate of onset of echovirus-induced paralysis and reduced the number of paralyzed animals. Intraperitoneal administration beginning 2 hr before infection or 48 hr after infection was equally effective in preventing paralysis. Oral administration of WIN 51711 twice daily beginning 72 hr after infection was the most-effective dosage regimen, with doses as low as 3 mg/kg preventing paralysis in 75% of the animals. Titers of virus in asymptomatic mice on day 6 after infection were reduced by up to 4.75 log pfu in WIN 51711-medicated mice when compared with placebo. Maximal concentrations of WIN 51711 in adult mice after oral medication with a 100 mg/kg dose were 24.3, 21.5, 10.4, 9.8, 6.9, and 4.1 micrograms/g in heart, kidney, brain, liver, serum (micrograms/ml), and muscle, respectively at 0.5-1.0 hr after medication.
在感染埃可病毒9型(巴尔蒂毒株)的乳鼠中评估了抗微小核糖核酸病毒药物WIN 51711的全身疗效。每日单次腹腔注射低至10 mg/kg的WIN 51711能显著(P小于0.01)延缓埃可病毒诱导的麻痹发作速度,并减少麻痹动物的数量。在感染前2小时或感染后48小时开始腹腔给药在预防麻痹方面同样有效。在感染后72小时开始每日口服两次WIN 51711是最有效的给药方案,低至3 mg/kg的剂量可使75%的动物预防麻痹。与安慰剂相比,感染后第6天,WIN 51711给药小鼠无症状小鼠的病毒滴度降低了高达4.75 log pfu。以100 mg/kg剂量口服给药后,成年小鼠在给药后0.5 - 1.0小时心脏、肾脏、大脑、肝脏、血清(微克/毫升)和肌肉中WIN 51711的最大浓度分别为24.3、21.5、10.4、9.8、6.9和4.1微克/克。