节点文献

氟哌酸前药IMB—85210的药效与毒理

PHARMACOLOGICAL STUDY OF NORFLOCACIN PRODRUG-IMB-85210

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 林赴田余兰香许嘉齐于锋熊雁琼宋坤改刘京芳

【Author】 Lin Fu-tian, Yu Lian-xiang, Xu jia-qt, Yu Feng, ’ ?Xiong Yan-qiong, Song Kun-gai and Liu Jin^-fang(Department of Pharmacology, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences, Beijing 100050)

【机构】 中国医学科学院医药生物技术研究所中国医学科学院医药生物技术研究所 北京 100050北京 100050北京 100050

【摘要】 氟哌酸前药IMB-85210的药效学和毒理学研究表明,在体外对革兰氏阴性菌和革兰氏阳性菌的活性比氟哌酸和甲氟哌酸为弱,但对感染肺炎杆菌和金葡球菌小鼠的效果(ED50)比氟哌酸强1.7倍和2.4倍;对感染大肠杆菌和绿脓杆菌小鼠的效果比氟哌酸强1.4倍,小鼠和大鼠口服LD50>400mg/kg;致畸胎试验和致突变试经均为阴性。结果表示,IMB-85210的动物保护效果明显强于氟哌酸,而毒性低,是值得进一步研究的新药。

【Abstract】 IMB-85210 is a new norfloxacin prodrug with in vitro and in vivo activities. In vitro activity of IMB-85210 was less than norfloxacin and pefloxacin against gram-negative and gram-positive bacteria. In the experimental infected Mice, the efficacy of IMB-85210 was similar with pefloxacin and more effective than norfloxacin. The LD50 values in mice and rats were >4000 mg/kg (po), respectively. Teratogenity test and dominant lethal test in mice were negative. These results suggest that IMB-85210 would be worthy to study further.

【关键词】 氟哌酸前药IMB-85210抗菌活性毒性
【Key words】 NorfloxaeinProdrugIMB-85210ActivityToxicity
  • 【文献出处】 中国抗生素杂志 ,Chinese Journal of Antibiotics , 编辑部邮箱 ,1991年01期
  • 【被引频次】2
  • 【下载频次】46
节点文献中: 

本文链接的文献网络图示:

本文的引文网络