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首页> 外文期刊>International journal of antimicrobial agents >Activity of moxifloxacin on biofilms produced in vitro by bacterial pathogens involved in acute exacerbations of chronic bronchitis
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Activity of moxifloxacin on biofilms produced in vitro by bacterial pathogens involved in acute exacerbations of chronic bronchitis

机译:莫西沙星对参与慢性支气管炎急性加重的细菌病原体体外产生的生物膜的活性

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摘要

The aim of this study was to assess whether moxifloxacin is able to inhibit the synthesis of and to disrupt biofilms produced in vitro by bacterial pathogens involved in acute bacterial exacerbations of chronic bronchitis. Three strains each of Haemophilus influenzae, Strepto-coccuspneumoniae, Moraxella catarrhalis, Staphylococcus aureus and Escherichia coli recently isolated from clinical respiratory specimens and capable of slime production were used. Biofilm formation on polystyrene plates was quantified spectrophotometrically by established methodologies. Moxifloxacin (0.5 mg/L) inhibited slime synthesis by >70% in S. aureus, H. influenzae and S. pneumoniae, 45-70% in E. coli and 35-70% in M. catarrhalis. Disruption of pre-formed structures was also promoted by moxifloxacin both for initial (5 h) and mature (48 h) biofilms. Drug concentrations reached during therapy (0.5-4 mg/L) resulted in a breakdown of initial biofilm of 60-80% in H. influenzae and S. pneumoniae, 48-86% in S. aureus, 37-69% in 14. catarrhalis and 51-71 % in E. coli. Mature biofilms were less susceptible to degradation. Moxifloxacin at concentrations that can be achieved in the bronchial mucosa during therapy therefore promotes a significant inhibition of biofilm synthesis and induces slime disruption, a feature that may be instrumental in reducing the exacerbations so frequently observed in this condition. (C) 2007 Published by Elsevier B.V. and the International Society of Chemotherapy.
机译:这项研究的目的是评估莫西沙星是否能够抑制与慢性支气管炎急性加重有关的细菌病原体在体外产生的生物膜的合成并破坏生物膜。最近使用了从临床呼吸道标本中分离出并能够产生粘液的三种菌株,分别为流感嗜血杆菌,链球菌,肺炎链球菌,卡他莫拉菌,金黄色葡萄球菌和大肠杆菌。聚苯乙烯板上生物膜的形成通过建立的方法进行分光光度法定量。莫西沙星(0.5 mg / L)在金黄色葡萄球菌,流感嗜血杆菌和肺炎链球菌中抑制粘液的合成> 70%,在大肠杆菌中抑制45-70%,在卡他莫拉氏菌中抑制35-70%。莫西沙星在初始(5 h)和成熟(48 h)生物膜中也促进了预形成结构的破坏。在治疗期间达到的药物浓度(0.5-4 mg / L)导致流感嗜血杆菌和肺炎链球菌的初始生物膜分解为60-80%,金黄色葡萄球菌为48-6%,14年为37-69%。粘膜炎和51-71%的大肠杆菌。成熟的生物膜不易降解。因此,在治疗期间可在支气管粘膜中达到的浓度的莫西沙星可显着抑制生物膜的合成并诱导粘液破裂,此功能可能有助于减少在这种情况下经常观察到的病情加重。 (C)2007年由Elsevier B.V.和国际化学疗法学会出版。

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