[体外抗生素敏感性评估:MIC的关键特征]。

A Malcangi, C Mineccia, P Martinetto
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引用次数: 0

摘要

目前用于抗生素活性“体外”研究的方法,如最低抑制浓度,将细菌暴露于恒定浓度的抗生素中。“体内”情况明显不同,因为抗生素浓度随时间变化。药代动力学模型是“体外”实验系统,旨在模拟细菌暴露于血液和组织中存在的抗菌剂的条件。所有这些系统都是复杂的结构。描述了一种新的基于固相生长的简单“体外”动力学模型。
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[Evaluation of in vitro antibiotic sensitivity: critical features of the MIC].

Current methods for the "in vitro" study of antibiotic activity, as minimum inhibitory concentration, expose bacteria to constant concentrations of antibiotics. The "in vivo" situation is significantly different, since the antibiotic concentration changes with time. Pharmacokinetic models are "in vitro" experimental systems that seek to simulate conditions of exposure of bacteria to antimicrobial agents that exist in blood and tissues. All of these systems are complicated constructions. A new simple "in vitro" kinetic model, based on solid phase growth, is described.

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