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首页> 外文期刊>International Journal of Nanomedicine >Core–shell magnetic nanoparticles display synergistic antibacterial effects against Pseudomonas aeruginosa and Staphylococcus aureus when combined with cathelicidin LL-37 or selected ceragenins
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Core–shell magnetic nanoparticles display synergistic antibacterial effects against Pseudomonas aeruginosa and Staphylococcus aureus when combined with cathelicidin LL-37 or selected ceragenins

机译:核壳磁性纳米颗粒与cathelicidin LL-37或选定的陶瓷素一起使用时,对铜绿假单胞菌和金黄色葡萄球菌具有协同抗菌作用

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摘要

Core–shell magnetic nanoparticles (MNPs) are promising candidates in the development of new treatment methods against infections, including those caused by antibiotic-resistant pathogens. In this study, the bactericidal activity of human antibacterial peptide cathelicidin LL-37, synthetic ceragenins CSA-13 and CSA-131, and classical antibiotics vancomycin and colistin, against methicillin-resistant Staphylococcus aureus Xen 30 and Pseudomonas aeruginosa Xen 5, was assessed alone and in combination with core–shell MNPs. Fractional inhibitory concentration index and fractional bactericidal concentration index were determined by microdilution methods. The potential of combined therapy using nanomaterials and selected antibiotics was confirmed using chemiluminescence measurements. Additionally, the ability of tested agents to prevent bacterial biofilm formation was evaluated using crystal violet staining. In most conditions, synergistic or additive effects were observed when combinations of core–shell MNPs with ceragenins or classical antibiotics were used. Our study revealed that a mixture of membrane-active agents such as LL-37 peptide or ceragenin CSA-13 with MNPs potentialized their antibacterial properties and might be considered as a method of delaying and overcoming bacterial drug resistance.
机译:核壳磁性纳米颗粒(MNP)在开发新的抗感染方法(包括由耐药性病原体引起的感染)方面,有望成为候选者。在这项研究中,单独评估了人类抗菌肽cathelicidin LL-37,合成的ceragenins CSA-13和CSA-131以及经典抗生素万古霉素和大肠菌素对耐甲氧西林的金黄色葡萄球菌Xen 30和铜绿假单胞菌Xen 5的杀菌活性。并与核-壳MNP结合使用。微量稀释法测定了抑制分数浓度和杀菌浓度分数。使用化学发光测量结果证实了使用纳米材料和选定抗生素进行联合治疗的潜力。另外,使用结晶紫染色评估了被测试剂防止细菌生物膜形成的能力。在大多数情况下,当使用核壳型MNPs与ceragenins或经典抗生素的组合时,观察到协同或累加作用。我们的研究表明,膜活性剂(例如LL-37肽或ceragenin CSA-13)与MNP的混合物具有潜在的抗菌特性,可以被视为延迟和克服细菌耐药性的方法。

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