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Antibacterial Activity of Non-Cytotoxic Amino Acid-Modified Polycationic Dendrimers against Pseudomonas aeruginosa and Other Non-Fermenting Gram-Negative Bacteria

机译:非细胞毒性氨基酸改性的聚静脉树枝状大分子对铜绿假单胞菌和其他非发酵革兰氏阴性细菌的抗菌活性

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摘要

Due to the rapid increase of antimicrobial resistance with ensuring therapeutic failures, the purpose of this study was to identify novel synthetic molecules as alternatives to conventional available, but presently ineffective antibiotics. Variously structured cationic dendrimers previously reported have provided promising outcomes. However, the problem of their cytotoxicity towards eukaryotic cells has not been completely overcome. We have now investigated the antibacterial activities of three not cytotoxic cationic dendrimers (G5Ds: G5H, G5K, and G5HK) against several multidrug-resistant (MDR) clinical strains. All G5Ds displayed remarkable activity against MDR non-fermenting Gram-negative species such as , , and (MICs = 0.5–33.2 µM). In particular, very low MIC values (0.5–2.1 µM) were observed for G5K, which proved to be more active than the potent colistin (2.1 versus 3.19 µM) against . Concerning its mechanism of action, in time-killing and turbidimetric studies, G5K displayed a rapid non-lytic bactericidal activity. Considering the absence of cytotoxicity of these new compounds and their potency, comparable or even higher than that provided by the dendrimers previously reported, G5Ds may be proposed as promising novel antibacterial agents capable of overcoming the alarming resistance rates of several nosocomial non-fermenting Gram-negative pathogens.
机译:由于确保治疗失败的抗微生物抗性的快速增加,本研究的目的是将新的合成分子识别为常规可用的替代品,但目前无效的抗生素。以前报道的各种结构化阳离子树枝状体提供了有希望的结果。然而,它们对真核细胞的细胞毒性问题尚未完全克服。我们现在研究了三个不是细胞毒性阳离子树枝状大分子(G5DS:G5H,G5K和G5HK)的抗菌活性,针对几种多药(MDR)临床菌株。所有G5D都针对MDR非发酵革兰氏阴性物种(如MICS =0.5-33.2μm)显示出显着的活动。特别地,对于G5K观察到非常低的MIC值(0.5-2.1μm),其被证明比强效菌氨酸(2.1与3.19μm)更活跃。关于其作用机制,在杀死时间杀死和浊度研究中,G5K显示出快速的非裂谷杀菌活性。考虑到这些新化合物的细胞毒性及其效力,可比或甚至高于先前报道的树枝状过敏仪提供的,可以提出G5DS作为能够克服几种医院非发酵革兰克的令人震惊的抗菌剂的有前途的新抗菌剂 - 阴性病原体。

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