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罗红霉素、克拉霉素和阿奇霉素对呼吸道病原体的抗生素后效应及抗生素后亚抑菌浓度效应

Postantibiotic effects and postantibiotic sub-MIC effects of roxithromycin, clarithromycin, and azithromycin on respiratory tract pathogens.

作者信息

Odenholt-Tornqvist I, Löwdin E, Cars O

机构信息

Department of Infectious Diseases, University Hospital, Uppsala, Sweden.

出版信息

Antimicrob Agents Chemother. 1995 Jan;39(1):221-6. doi: 10.1128/AAC.39.1.221.

Abstract

Pharmacodynamic parameters have become increasingly important for the determination of the optimal dosing schedules of antibiotics. In this study, the postantibiotic effects (PAEs), the postantibiotic sub-MIC effects (PA SMEs), and the sub-MIC effects (SMEs) of roxithromycin, clarithromycin, and azithromycin on reference strains of Streptococcus pyogenes group A, Streptococcus pneumoniae, and Haemophilus influenzae were investigated. The PAE was induced by 2x MICs (S. pneumoniae) or 10x MICs of the different drugs for 2 h, and the antibiotics were eliminated by washing and dilution. The PA SMEs were studied by addition of 0.1, 0.2, and 0.3x MICs during the postantibiotic phase of the bacteria, and the SMEs were studied by exposition of the bacteria to the drugs at the sub-MICs only. Growth curves were followed by viable counts for 24 h. The SMEs were generally very short. A PAE of 2.9 to 8 h was noted for all antibiotics against all strains. Clarithromycin induced a statistically significantly shorter PAE on S. pneumoniae than did roxithromycin and azithromycin and did so also against H. influenzae in comparison with azithromycin. The PA SMEs were long and varied at 0.3x MIC between 6.4 19.6 h. This pronounced suppression of regrowth of bacteria which are first treated with a suprainhibitory concentration of antibiotics and then reexposed to sub-MIC levels indicates that long dosing intervals for macrolides and azalides can be allowed.

摘要

药效学参数对于确定抗生素的最佳给药方案愈发重要。在本研究中,考察了罗红霉素、克拉霉素和阿奇霉素对A组化脓性链球菌、肺炎链球菌和流感嗜血杆菌参考菌株的抗生素后效应(PAEs)、抗生素后亚抑菌浓度效应(PA SMEs)及亚抑菌浓度效应(SMEs)。PAE通过用不同药物的2倍MIC(肺炎链球菌)或10倍MIC诱导2小时产生,抗生素通过洗涤和稀释去除。PA SMEs通过在细菌的抗生素后阶段添加0.1、0.2和0.3倍MIC进行研究,SMEs仅通过将细菌暴露于亚抑菌浓度的药物进行研究。通过活菌计数跟踪24小时的生长曲线。SMEs通常非常短。所有抗生素对所有菌株的PAE为2.9至8小时。克拉霉素对肺炎链球菌诱导的PAE在统计学上显著短于罗红霉素和阿奇霉素,与阿奇霉素相比,对流感嗜血杆菌也是如此。PA SMEs较长,在0.3倍MIC时为6.4至19.6小时不等。先用高于抑菌浓度的抗生素治疗细菌,然后再暴露于亚抑菌水平,这种对细菌再生长的明显抑制表明,大环内酯类和氮杂内酯类药物可以采用较长的给药间隔。

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