Shipkowitz N L, Bower R R, Schleicher J B, Aquino F, Appell R N, Roderick W R
Appl Microbiol. 1972 Jan;23(1):117-22. doi: 10.1128/am.23.1.117-122.1972.
The marked antiviral activity of (S,S-1,2-bis(5-methoxy-2-benzimidazolyl)-1,2-ethanediol (Abbott 36683) against rhinoviruses in tissue culture warranted investigation of its antiviral activity in vivo. Antiviral levels in mouse sera were attained with an oral dose as small as 10 mg/kg and detectable antiviral levels of drug were also found in lung, liver, kidney, intestinal contents, and urine of mice given a single 300 mg/kg oral dose. Antiviral serum levels were also obtained when monkeys were given a single oral dose of Abbott 36683. Six chimpanzees were infected with 100 median tissue culture infective dose units (TCID(50)) of rhinovirus 30. Three of the animals were treated with Abbott 36683, 100 mg/kg daily for 4 consecutive days. Virus shedding occurred in the infected controls but could not be demonstrated in the treated animals from postinfection days 1 to 8. Two of the treated animals did, however, shed virus on day 9. The compound was retested in chimpanzees at dosage levels of 15 and 50 mg/kg daily for 4 days. Each animal was challenged with 100 TCID(50) of rhinovirus 49. Partial protection was obtained. In a third trial, a single 100 mg/kg dose of the compound was administered to chimpanzees infected with rhinovirus 44. Virus was isolated from all throat smears taken from treated animals, indicating that at the lowest drug level no protection occurred.
(S,S-1,2-双(5-甲氧基-2-苯并咪唑基)-1,2-乙二醇(雅培36683)在组织培养中对鼻病毒具有显著的抗病毒活性,这使得对其体内抗病毒活性进行研究成为必要。口服剂量低至10毫克/千克时,小鼠血清中就能达到抗病毒水平,在给予单次300毫克/千克口服剂量的小鼠的肺、肝、肾、肠内容物和尿液中也发现了可检测到的药物抗病毒水平。给猴子单次口服雅培36683后,也能获得抗病毒血清水平。六只黑猩猩感染了100个鼻病毒30的半数组织培养感染剂量单位(TCID50)。其中三只动物用雅培36683治疗,每天100毫克/千克,连续治疗4天。感染的对照组出现了病毒排出,但在感染后第1天至第8天,治疗组动物中未检测到病毒排出。然而,有两只治疗组动物在第9天排出了病毒。该化合物在黑猩猩中以每天15毫克/千克和50毫克/千克的剂量水平重新进行了4天的测试。每只动物用100个鼻病毒49的TCID50进行攻击。获得了部分保护。在第三次试验中,给感染鼻病毒44的黑猩猩单次施用100毫克/千克剂量的该化合物。从治疗组动物的所有咽喉涂片样本中都分离出了病毒,这表明在最低药物水平下没有产生保护作用。