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酞丁安对单纯疱疹病毒在细胞培养内复制的影响

EFFECT OF TAI-DING-AN ON HERPES SIMPLEX VIRUS REPLICATION IN CELL CULTURE

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【作者】 尹明标; 高雅君; 夏丽娟; 李占荣; 王琳; 赵知中;

【Author】 YIN Ming-biao, GAO Ya-jun, XIA Li-juan, LI Zhan-rong, WANG Lin and ZHAO Zhi-zhong (Institute of Virology and Institute of Materia Medica, Chinese Academy of Medical Sciences, Beijing)

【机构】 中国医学科学院病毒研究所; 中国医学科学院药物研究所; 中国医学科学院药物研究所 北京; 北京; 北京;

【摘要】 <正> 酞丁安(3-phthalimido-2-oxo-butyraldchyde-bis-thiosemicarbazone,V6133)是我们自己设计合成的一种缩氨基硫脲类化合物。实验室及临床研究证明有抗沙眼衣原体活性的作用,对其生产工艺和临床疗效已进行了鉴定。最近临床试用认为,对带状疱疹及单纯疱疹有一定的疗效,但目前尚未见实验室的研究报道。为了探索酞丁安的抗病毒活性,我们用组织培养细胞研究了对HSV-1及HSV-2复制的抑制作用,及其对正常细胞的毒性。结果报道如下。

【Abstract】 PR assay, YR assay and CPE inhibition assay were used to determine the effect of Tai-Ding-An (3-phthalimido-2-oxo-butyraldehyde-bis-thiosemicarbazone, V 6133) against HSV-1 and HSV-2 in vitro. The results of PR assay showed that the ratio of the plaque number was near to zero in the presence of drug concentrations of more than 50μg/ml in comparison with DMSO control. Dose-response curve obtained by YR assay revealed that Tai-Ding-An markedly inhibited replication of both HSV-1 and HSV-2. PRK cells were treated with 100 μg/ml of Tai-Ding-An and incubated for 2 days, no HSV-induced CPE was observed while CPE was very evident in the control. No CPE was observed for up to 5 days when the PRK cells were treated continuously with the media containing 100 μg/ml of the drug and changed daily. From these results it would appear that Tai-Ding-An is an effective agent against HSV-1 and HSV-2.In vitro experiments also showed that the toxic effect was mild when the concentration of Tai-Ding-An was less than 100 μg/ml.

  • 【文献出处】 药学学报 ,Acta Pharmaceutica Sinica , 编辑部邮箱 ,1984年05期
  • 【被引频次】26
  • 【下载频次】57
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