首页> 外文期刊>Environmental toxicology and pharmacology >Correlation among the toxicity profiling (28-days repeated oral dose toxicity), toxicokinetics and tissue distribution data of ulifloxacin, the active metabolite of prulifloxacin in Wistar albino rats
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Correlation among the toxicity profiling (28-days repeated oral dose toxicity), toxicokinetics and tissue distribution data of ulifloxacin, the active metabolite of prulifloxacin in Wistar albino rats

机译:Wistar白化病大鼠毒性谱(28天重复口服剂量毒性),奥利沙星的毒性动力学和组织分布数据之间的相关性;普利沙星的活性代谢产物

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摘要

This experiment was designed to investigate correlation among 28-days repeated oral dose toxicity, toxicokinetics and tissue distribution data of ulifloxacin (active metabolite of prulifloxacin) in Wistar albino rats. Prulifloxacin was administered for 28-days in rats at 0,100, 200,400 mg/kg/day followed by 14-days recovery period. Simultaneously different toxicokinetic parameters and tissue distributions of ulifloxacin was examined by LC-MS/MS method. Plasma levels and tissue concentrations of ulifloxacin were increased with dose-related manner. Ulifloxacin was also distributed to many tissues, and concentration in lungs nearly equivalent to the plasma concentration. Based on these results it was concluded that long-term repeated dose of prulifloxacin may produce different blood parameters abnormality, liver damage, stomach ulcer, joint damage and dysfunction of lungs in rats which relates to high tissue distribution and accumulation of ulifloxacin in these tissues. These findings help in management of prulifloxacin induced adverse effects by appropriate dose selection in clinical practice.
机译:本实验旨在研究Wistar白化病大鼠28天重复口服剂量毒性,毒物动力学和奥利沙星(普鲁沙星的活性代谢产物)的组织分布数据之间的相关性。在大鼠中以0,100,200,400 mg / kg /天的剂量给予普利沙星28天,然后恢复14天。同时采用LC-MS / MS方法检测了奥利沙星的不同毒理动力学参数和组织分布。奥利沙星的血浆水平和组织浓度随剂量相关的方式增加。 Ulifloxacin也分布于许多组织,并且在肺中的浓度几乎等于血浆浓度。根据这些结果,得出结论,长期重复服用普利沙星可能会导致大鼠不同的血液参数异常,肝损伤,胃溃疡,关节损伤和肺功能异常,这与这些组织中奥利沙星的高组织分布和累积有关。这些发现有助于通过临床实践中适当的剂量选择来控制普鲁沙星引起的不良反应。

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