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头孢他啶在体外药代动力学模型中的抗菌活性研究。

Study on the antibacterial activity of ceftazidime in an in vitro pharmacokinetic model.

作者信息

Xerri L, Broggio R

出版信息

Drugs Exp Clin Res. 1985;11(1):49-54.

PMID:3915274
Abstract

A kinetic model was used to evaluate the activity of ceftazidime against recently isolated bacterial strains. The microorganisms were subjected in vitro to drug concentrations simulating the serum kinetics of ceftazidime after i.v. administration of 1 g of the drug. In these conditions ceftazidime showed a bactericidal effect lasting up to 12 h, even at concentrations below the MICs for some strains. In no case did resistant populations develop after exposure to the drug.

摘要

采用动力学模型评估头孢他啶对近期分离的细菌菌株的活性。将这些微生物在体外置于模拟静脉注射1克该药物后头孢他啶血清动力学的药物浓度下。在这些条件下,头孢他啶即使在某些菌株的浓度低于最低抑菌浓度时也显示出长达12小时的杀菌效果。在接触该药物后,均未出现耐药菌群体。

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