Khamitov R A, Loginova S Ia, Shchukina V N, Borisevich S V, Maksimov V A, Shuster A M
Vopr Virusol. 2008 Jul-Aug;53(4):9-13.
Experimental studies of arbidol and arbidol mesylate versus ribavirin suggest that insertion of these agents into the nutrient medium of the cultured cells GMK-AH-1 (D) after infection at concentrations of 50, 25, and 100 microg/ml, respectively, is effective in suppressing the reproduction of severe acute respiratory syndrome (SARS) virus. Arbidol and arbidol mesylate were shown to have a direct antiviral effect in early viral replication in the cultured cells. The promising antiviral agent is arbidol mesylate that is nearly 5 times as effective as arbidol in reducing the reproduction of SARS virus in the cultured cells. Insertion of arbidol, arbidol mesylate, and ribavirin into the nutrient medium 2 hours after infection of porcine embryonic renal cells caused a reduction in the accumulation of the pathogen by 2.5, 2.1, and 2.6 Ig, respectively.
阿比朵尔和甲磺酸阿比朵尔与利巴韦林的实验研究表明,在感染后分别以50、25和100微克/毫升的浓度将这些药物加入培养细胞GMK-AH-1 (D)的营养培养基中,可有效抑制严重急性呼吸综合征(SARS)病毒的繁殖。阿比朵尔和甲磺酸阿比朵尔在培养细胞的病毒早期复制中具有直接抗病毒作用。有前景的抗病毒药物是甲磺酸阿比朵尔,其在减少培养细胞中SARS病毒繁殖方面的效果几乎是阿比朵尔的5倍。在猪胚胎肾细胞感染后2小时将阿比朵尔、甲磺酸阿比朵尔和利巴韦林加入营养培养基中,病原体的积累分别减少了2.5、2.1和2.6 Ig。