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用于研究人体模拟抗生素浓度对细菌生物膜影响的新型体外模型。

New in vitro model to study the effect of human simulated antibiotic concentrations on bacterial biofilms.

作者信息

Haagensen Janus A J, Verotta Davide, Huang Liusheng, Spormann Alfred, Yang Katherine

机构信息

Department of Civil and Environmental Engineering, Stanford University, Stanford, California, USA.

Department of Bioengineering and Therapeutic Sciences, University of California San Francisco School of Pharmacy, San Francisco, California, USA.

出版信息

Antimicrob Agents Chemother. 2015 Jul;59(7):4074-81. doi: 10.1128/AAC.05037-14. Epub 2015 Apr 27.

Abstract

A new in vitro pharmacokinetic/pharmacodynamic simulator for bacterial biofilms utilizing flow cell technology and confocal laser scanning microscopy is described. The device has the ability to simulate the changing antibiotic concentrations in humans associated with intravenous dosing on bacterial biofilms grown under continuous culture conditions. The free drug concentrations of a single 2-g meropenem intravenous bolus dose and first-order elimination utilizing a half-life of 0.895 h (elimination rate constant, 0.776 h(-1)) were simulated. The antibacterial activity of meropenem against biofilms of Pseudomonas aeruginosa PAO1 and three clinical strains isolated from patients with cystic fibrosis was investigated. Additionally, the effect of meropenem on PAO1 biofilms cultured for 24 h versus that on biofilms cultured for 72 h was examined. Using confocal laser scanning microscopy, rapid biofilm killing was observed in the first hour of the dosing interval for all biofilms. However, for PAO1 biofilms cultured for 72 h, only bacterial subpopulations at the periphery of the biofilm were affected, with subpopulations at the substratum remaining viable, even at the conclusion of the dosing interval. The described model is a novel method to investigate antimicrobial killing of bacterial biofilms using human simulated concentrations.

摘要

描述了一种利用流动细胞技术和共聚焦激光扫描显微镜的新型细菌生物膜体外药代动力学/药效学模拟器。该装置能够模拟与静脉给药相关的人体中不断变化的抗生素浓度对在连续培养条件下生长的细菌生物膜的影响。模拟了单次2克美罗培南静脉推注剂量的游离药物浓度以及利用半衰期0.895小时(消除速率常数,0.776小时⁻¹)的一级消除过程。研究了美罗培南对铜绿假单胞菌PAO1生物膜以及从囊性纤维化患者中分离出的三株临床菌株生物膜的抗菌活性。此外,还考察了美罗培南对培养24小时的PAO1生物膜与培养72小时的生物膜的作用效果。使用共聚焦激光扫描显微镜观察到,在给药间隔的第一个小时内,所有生物膜均出现了快速的生物膜杀灭现象。然而,对于培养72小时的PAO1生物膜,即使在给药间隔结束时,仅生物膜周边的细菌亚群受到影响,而基质处的亚群仍保持存活。所描述的模型是一种利用人体模拟浓度研究抗菌药物对细菌生物膜杀灭作用的新方法。

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