Braga P C, Dal Sasso M, Woodnutt G
Center of Respiratory Pharmacology, Department of Pharmacology, School of Medicine, University of Milan, Italy.
J Chemother. 2002 Feb;14(1):41-6. doi: 10.1179/joc.2002.14.1.41.
This study was designed to investigate the capacity of subinhibitory concentrations of the newly developed fluoroquinolone antibiotic gemifloxacin to interfere with the mechanism of bacterial adhesion. Human buccal epithelial cells were incubated with Staphylococcus aureus and Escherichia coli, and grown in the presence of serial dilutions of gemifloxacin from 1/2 MIC to 1/128 MIC. A significant decrease in the adhesion of both S. aureus and E. coli was observed from 1/2 MIC to 1/32 MIC. Morphological changes including filamentous forms of E. coli and cluster formation and swelling of S. aureus were also observed, mainly from 1/2 MIC to 1/8 and 1/16 MIC. These findings are discussed in terms of dose-effect relationships and the interpolation of this pharmacodynamic data with the pharmacokinetics curve of gemifloxacin.
本研究旨在调查新开发的氟喹诺酮类抗生素吉米沙星的亚抑菌浓度干扰细菌黏附机制的能力。将人颊上皮细胞与金黄色葡萄球菌和大肠杆菌一起孵育,并在吉米沙星从1/2 MIC至1/128 MIC的系列稀释液存在下培养。从1/2 MIC至1/32 MIC观察到金黄色葡萄球菌和大肠杆菌的黏附均显著减少。还观察到形态学变化,包括大肠杆菌的丝状形态以及金黄色葡萄球菌的聚集形成和肿胀,主要出现在1/2 MIC至1/8和1/16 MIC。根据剂量效应关系以及将该药效学数据与吉米沙星的药代动力学曲线进行内插来讨论这些发现。