首页> 外文期刊>Photochemistry and Photobiology: An International Journal >In Vitro Photodynamic Inactivation Effects of Ru(II) Complexes on Clinical Methicillin-resistant Staphylococcus aureus Planktonic and Biofilm Cultures
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In Vitro Photodynamic Inactivation Effects of Ru(II) Complexes on Clinical Methicillin-resistant Staphylococcus aureus Planktonic and Biofilm Cultures

机译:Ru(II)配合物对耐甲氧西林金黄色葡萄球菌浮游生物和生物膜培养的体外光动力灭活作用。

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摘要

Photosensitizers (PSs) combined with light are able to generate antimicrobial effects. Ru(II) complexes have been recognized as a novel class of PSs. In this study, we investigated the effectiveness of photodynamic inactivation (PDI) mediated by three Ru(II) polypyridine complexes, 1-3, against four isolates of clinical methicillin-resistant Staphylococcus aureus (MRSA-1, MRSA-2, MRSA-3 and MRSA-4). In PDI of a planktonic culture of MRSA-1, compound 3 showed the highest efficacy, likely owing to its advantageous light absorption, O-1(2) quantum yield and bacterial cellular binding. The PDI efficacy of 3 was further evaluated against all other strains and MRSA-1 biofilms. At appropriate PS concentrations, viability reduction of 100% or 96.83% was observed in planktonic or biofilm forms of MRSA, respectively. The mechanisms of action were investigated using negative staining transmission electron microscopy (TEM), confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). It was demonstrated that PDI of planktonic bacteria was achieved primarily through damage to the cell envelope. Biofilms were eliminated through both the destruction of their structure and inactivation of the individual bacterial cells. In conclusion, Ru(II) complexes, especially 3, are potential candidates for the effective photodynamic control of MRSA infections.
机译:光敏剂(PSs)与光结合能够产生抗菌作用。 Ru(II)配合物已被认为是一类新颖的PS。在这项研究中,我们研究了由三种Ru(II)聚吡啶复合物1-3介导的光动力学灭活(PDI)对临床耐甲氧西林金黄色葡萄球菌(MRSA-1,MRSA-2,MRSA-3和MRSA-4)。在MRSA-1浮游文化的PDI中,化合物3显示出最高的功效,这可能是由于其有利的光吸收,O-1(2)量子产率和细菌细胞结合。进一步评估了PDI对其他所有菌株和MRSA-1生物膜的功效3。在适当的PS浓度下,分别在浮游生物或生物膜形式的MRSA中观察到活力降低100%或96.83%。使用负染色透射电子显微镜(TEM),共聚焦激光扫描显微镜(CLSM)和扫描电子显微镜(SEM)研究了作用机理。结果表明,浮游细菌的PDI主要是通过破坏细胞膜来实现的。生物膜通过破坏其结构和使单个细菌细胞失活而被消除。总之,Ru(II)配合物,特别是3种,是有效控制MRSA感染的光动力的潜在候选者。

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