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首页> 外文期刊>RSC Advances >Rapid bactericidal activity of an amphiphilic polyacrylate terpolymer system comprised of same-centered comonomers with 2-carbon and 6-carbon spacer arms and an uncharged repeat unit
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Rapid bactericidal activity of an amphiphilic polyacrylate terpolymer system comprised of same-centered comonomers with 2-carbon and 6-carbon spacer arms and an uncharged repeat unit

机译:两亲聚丙烯酸酯三元共聚物体系的快速杀菌活性,该体系由具有2-碳和6-碳间隔臂和不带电荷的重复单元的同心共聚单体组成

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The global health threat of antimicrobial resistance has created a pressing need to develop practical alternatives to conventional antibiotic agents. Peptide mimetic synthetic amphiphilic polymers are known to non-specifically disrupt the bacterial cell surface thus leading to highly hindered bacterial resistance development. We investigated the antibacterial activities of a terpolymer macromolecular architecture with a combination of 6-carbon and 2-carbon spacer arms (distance from polymer backbone to pendent cationic center) interspersed with counits with hydrophobic side groups. A random copolymer with a combination of 6-carbon spacer arm repeat units (60 mol%) and 2-carbon spacer arm (40 mol%) units is moderately active against bacteria and shows very low hemolytic activity. Incorporation of comonomer units with alkyl side groups, by replacing different levels of 2-carbon spacer arm counit, led to substantial increments in antibacterial activities without detrimental effects on hemolytic activities leading to highly selective (bacteria over red blood cells) antibacterial activity. Time-kill studies revealed rapid bactericidal activity of the terpolymer against both Staphylococcus aureus and Escherichia coli with 100% killing efficiency achieved within 1?h of polymer treatment, corresponding to a 5-log reduction of bacterial colony forming units. These results indicate the high potential of this amphiphilic terpolymer architecture in the development of alternatives to antibiotics.
机译:抗菌素耐药性对全球健康的威胁迫切需要开发出常规抗生素替代品。已知肽模拟合成两亲聚合物可非特异性破坏细菌细胞表面,从而导致高度阻碍细菌耐药性的发展。我们研究了具有6个碳原子和2个碳原子的间隔臂(从聚合物主链到下垂的阳离子中心的距离)与疏水侧基共存的散布的三元共聚物高分子结构的抗菌活性。具有6-碳间隔臂重复单元(60mol%)和2-碳间隔臂重复单元(40mol%)单元的组合的无规共聚物对细菌具有中等活性,并且显示出非常低的溶血活性。通过取代不同水平的2碳间隔臂共基单元将共聚单体单元与烷基侧基结合,可导致抗菌活性显着增加,而对溶血活性无不利影响,从而导致高度选择性(红细胞细菌)的抗菌活性。时间杀灭研究表明,三元共聚物对金黄色葡萄球菌和大肠杆菌均具有快速杀菌活性,在聚合物处理后的1小时内达到100%的杀灭效率,相当于5细菌菌落形成单位的对数减少。这些结果表明,这种两亲三元共聚物结构在开发抗生素替代品方面具​​有很高的潜力。

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