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首页> 外文期刊>Journal of infection and chemotherapy: official journal of the Japan Society of Chemotherapy >Anti-multidrug-resistant Acinetobacter baumannii activity of DS-8587: In vitro activity and in vivo efficacy in a murine calf muscle infection model
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Anti-multidrug-resistant Acinetobacter baumannii activity of DS-8587: In vitro activity and in vivo efficacy in a murine calf muscle infection model

机译:DS-8587的抗多重耐药鲍曼不动杆菌活性:在鼠小腿肌肉感染模型中的体外活性和体内功效

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摘要

DS-8587 is a novel broad-spectrum fluoroquinolone with extended antimicrobial activity against both Gram-positive and Gram-negative pathogens. In this study, we evaluated the in vitro and in vivo antibacterial activity of DS-8587 against multidrug-resistant (MDR) Acinetobacter baumannii. The MIC range of DS-8587 against MDR A. baumannii was 0.25-2 mg/L. These DS-8587 MICs were a minimum of 16-fold or 8-fold more potent than ciprofloxacin or levofloxacin, respectively. Bactericidal activity, a 3 log10 reduction from the initial bacterial counts, was observed within 2 h for 1593644 and 4 h for 1593684 after exposure to DS-8587. Therapeutic efficacy of DS-8587 in the murine calf muscle model was observed at 256 mg/kg. The analysis of the pharmacokinetic and pharmacodynamic index revealed that the AUC/MIC ratio showed the best correlation with efficacy. The total and free drug AUC/MIC value required for a static effect was 29.4 and 14.1, respectively. These data indicate DS-8587 would be an effective agent against MDR A. baumannii infection.
机译:DS-8587是一种新型广谱氟喹诺酮,对革兰氏阳性和革兰氏阴性病原体均具有扩展的抗菌活性。在这项研究中,我们评估了DS-8587对多重耐药(MDR)鲍曼不动杆菌的体外和体内抗菌活性。 DS-8587对MDR鲍曼不动杆菌的MIC范围是0.25-2 mg / L。这些DS-8587 MIC的效价分别比环丙沙星或左氧氟沙星至少强16倍或8倍。暴露于DS-8587后,在2小时内对1593644和1593684观察到了杀菌活性(比初始细菌数减少3 log10)。观察到DS-8587在鼠小腿肌肉模型中的治疗功效为256mg / kg。药代动力学和药效学指数的分析表明,AUC / MIC比与药效关系最佳。达到静态效果所需的总药物和游离药物AUC / MIC值分别为29.4和14.1。这些数据表明DS-8587将是抗MDR鲍曼不动杆菌感染的有效剂。

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