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[不同药物对牛疱疹病毒和瘟病毒的抗病毒活性研究]

[Study of antiviral activity of different drugs against bovine herpes virus and pestivirus].

作者信息

Glotov A G, Glotova T I, Sergeev A A, Sergeev A N

出版信息

Antibiot Khimioter. 2004;49(6):6-9.

Abstract

In vitro antiviral activity of 11 different drugs against the viruses of infectious bovine rhionotracheitis (IBR) and bovine viral diarrhea (BVD) was studied. The ID50 of the drugs were determined in monolayers of cell cultures MDBK and KCT: 20 mcg/ml for anandin, 25 mcg/ml for polyprenole, 50 mcg/ml for bromuridin, methisazone, aciclovir, gossypole, ribavirin and liposomal ribavirin, 100 mcg/ml for eracond, and 200 mcg/ml for phosprenil and argovit. Phosprenil was the only drug that showed virucidal activity against the IBR virus. All the drugs inhibited reproduction of the IBR virus in sensitive cell culture MDBK: 100,000-fold inhibition by bromuridin, aciclovir, ribavirin and methisazone, 1000-10000-fold inhibition by liposomal ribavirin, gossypole, anandin, polyprenole and phosprenil, 100-fold inhibition by eracond and argovit. As for the BVD virus, bromuridin, phosprenil, polyprenole, methisazone, aciclovir, gossypole, argovit, ribavirin and liposomal ribavirin also showed their activity in cell culture KCT (100-10,000-fold inhibition). The other drugs were ineffective.

摘要

研究了11种不同药物对牛传染性鼻气管炎(IBR)病毒和牛病毒性腹泻(BVD)病毒的体外抗病毒活性。在MDBK和KCT细胞培养单层中测定了这些药物的半数感染剂量(ID50):阿南定的ID50为20微克/毫升,聚戊烯醇为25微克/毫升,溴尿苷、甲吲噻腙、阿昔洛韦、棉酚、利巴韦林和脂质体利巴韦林为50微克/毫升,埃拉康为100微克/毫升,磷丙酯和阿戈维他为200微克/毫升。磷丙酯是唯一对IBR病毒表现出杀病毒活性的药物。所有药物均抑制IBR病毒在敏感细胞培养物MDBK中的繁殖:溴尿苷、阿昔洛韦、利巴韦林和甲吲噻腙的抑制倍数为100,000倍,脂质体利巴韦林、棉酚、阿南定、聚戊烯醇和磷丙酯的抑制倍数为1000 - 10000倍,埃拉康和阿戈维他的抑制倍数为100倍。至于BVD病毒,溴尿苷、磷丙酯、聚戊烯醇、甲吲噻腙、阿昔洛韦、棉酚、阿戈维他、利巴韦林和脂质体利巴韦林在KCT细胞培养中也表现出活性(抑制倍数为100 - 10,000倍)。其他药物无效。

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