首页> 美国卫生研究院文献>BMC Veterinary Research >Prediction of marbofloxacin dosage for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida by pharmacokinetic/pharmacodynamic modelling
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Prediction of marbofloxacin dosage for the pig pneumonia pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida by pharmacokinetic/pharmacodynamic modelling

机译:药代动力学/药效学模型预测猪肺炎病原菌肺炎放线杆菌和多杀巴斯德氏菌的马尔福沙星剂量

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摘要

BackgroundBacterial pneumonia in pigs occurs widely and requires antimicrobial therapy. It is commonly caused by the pathogens Actinobacillus pleuropneumoniae and Pasteurella multocida. Marbofloxacin is an antimicrobial drug of the fluoroquinolone class, licensed for use against these organisms in the pig. In recent years there have been major developments in dosage schedule design, based on integration and modelling of pharmacokinetic (PK) and pharmacodynamic (PD) data, with the objective of optimising efficacy and minimising the emergence of resistance. From in vitro time-kill curves in pig serum, PK/PD breakpoint Area under the curve (AUC) 24h /minimum inhibitory concentration (MIC) values were determined and used in conjunction with published PK, serum protein binding data and MIC distributions to predict dosages based on Monte Carlo simulation (MCS).
机译:背景猪中的细菌性肺炎广泛存在,需要抗菌治疗。它通常由病原体胸膜肺炎放线杆菌和多杀巴斯德氏菌引起。 Marbofloxacin是氟喹诺酮类的抗菌药物,已被许可用于猪中的这些生物。近年来,基于药代动力学(PK)和药效学(PD)数据的集成和建模,剂量方案设计有了重大发展,目的是优化功效并最大程度降低耐药性的出现。根据猪血清的体外时间杀灭曲线,确定PK / PD断点曲线下面积(AUC)24h /最小抑菌浓度(MIC)值,并与已发表的PK,血清蛋白结合数据和MIC分布一起用于预测剂量基于蒙特卡罗模拟(MCS)。

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