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Distribution and Antimicrobial Activity of Fosfomycin in the Interstitial Fluid of Human Soft Tissues

机译:磷霉素在人软组织间质液中的分布及抗菌活性

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摘要

Fosfomycin is a broad-spectrum antibiotic which is established as therapy for uncomplicated lower urinary tract infections. In addition, preliminary data indicate that fosfomycin has a potential role in the treatment of soft tissue infections. However, the use of fosfomycin has not been established for this condition, and it is unclear whether the level of fosfomycin penetration into human soft tissues is high enough to eradicate relevant pathogens. To better characterize the antibiotic potential of fosfomycin, we applied a combined in vivo pharmacokinetic-in vitro pharmacodynamic model to human volunteers. For this purpose fosfomycin concentrations in vivo in the fluid of the interstitial space of human soft tissues were measured by microdialysis following intravenous infusion of 4 or 8 g of fosfomycin (n = 6). Subsequently, bacterial isolates with relevance for soft tissue infections were exposed to concentrations according to the in vivo pharmacokinetic profile in the interstitial space fluid obtained by microdialysis. Our experiments indicated a high degree of soft tissue penetration for fosfomycin, with ratios of the area under the concentration-time curve from 0 to 8 h for muscle (AUC0–8muscle)/AUC0–8serum of 0.48 ± 0.08 and 0.53 ± 0.04 and ratios of AUC0–8adipose tissue/AUC0–8serum of 0.74 ± 0.12 and 0.71 ± 0.11 following administration of 4 and 8 g, respectively. In corresponding in vitro simulation experiments with selected isolates of Staphylococcus aureus, Enterobacter cloacae, and Serratia marcescens for which MICs were 16 μg/ml, organisms were undetectable after a single dosing interval. Fosfomycin exhibits a strong ability to penetrate into the fluid of the interstitial space of soft tissues and reaches levels sufficient to substantially inhibit the growth of relevant bacteria at the target site. We therefore conclude that fosfomycin might qualify as an alternative candidate for the therapy of soft tissue infections.
机译:磷霉素是一种广谱抗生素,已被确立为对简单的下尿路感染的治疗方法。此外,初步数据表明,磷霉素在软组织感染的治疗中具有潜在作用。然而,尚未针对这种情况使用磷霉素,并且尚不清楚磷霉素渗透至人软组织的水平是否足够高以根除相关病原体。为了更好地表征磷霉素的抗生素潜力,我们将组合的体内药代动力学-体外药效学模型应用于人类志愿者。为此,在静脉输注4或8 g磷霉素(n = 6)后,通过微透析法测定人软组织间质液中体内磷霉素的浓度。随后,将与软组织感染相关的细菌分离株暴露于根据通过微透析获得的组织间隙液中的体内药代动力学特征的浓度。我们的实验表明磷霉素具有很高的软组织渗透率,肌肉(AUC0–8肌肉)/ AUC0–8血清在0至8 h浓度-时间曲线下的面积比为0.48±0.08和0.53±0.04,并且比率分别施用4和8 g后,AUC0-8脂肪组织/ AUC0-8血清的浓度分别为0.74±0.12和0.71±0.11。在相应的体外模拟实验中,选择的金黄色葡萄球菌,阴沟肠杆菌和粘质沙雷氏菌的分离株的MIC为16μg/ ml,在单个给药间隔后无法检测到生物。磷霉素具有很强的渗透到软组织间质液中的能力,并达到足以基本上抑制相关细菌在靶部位生长的水平。因此,我们得出结论,磷霉素可能有资格作为治疗软组织感染的替代药物。

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