Controlling macromolecular structures towards effective antimicrobial polymers

被引:198
作者
Ganewatta, Mitra S. [1 ]
Tang, Chuanbing [1 ]
机构
[1] Univ S Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
基金
美国国家科学基金会;
关键词
Macromolecular architecture; Bacterial resistance; Antimicrobial polymer; HOST-DEFENSE PEPTIDES; POLY(PROPYLENE IMINE) DENDRIMERS; BIOLOGICALLY-ACTIVE POLYMERS; QUATERNARY AMMONIUM; ANTIBACTERIAL ACTIVITY; HEMOLYTIC ACTIVITIES; CHEMICAL-STRUCTURE; PHOSPHONIUM SALTS; POLY(ETHYLENE IMINE)S; TRIBLOCK COPOLYMERS;
D O I
10.1016/j.polymer.2015.03.007
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Drug resistance of pathogenic bacteria is a major global problem leading humanity towards a pre-antibiotic era. Decline in the discovery of novel antibiotics and the lack of a resilient platform to develop novel antimicrobial agents worsens the situation. Amphiphilic antimicrobial polymers, which have roots coming from antimicrobial peptides, show promise as potent antimicrobials having low susceptibility for developing resistance, unlike small molecular antibiotics. This feature article highlights recent advances in the fabrication of membrane-active antimicrobial polymers. The design of various types of macromolecular architectures with control of structural parameters such as hydrophobicity/ hydrophilicity balance, molecular weight, and ionic groups will be emphasized in order to achieve strong antimicrobial activities while minimizing toxicity to mammalian cells. Advanced polymeric assemblies with well-defined nanostructures including core/shell shaped nano-objects and polymeric vesicles are also discussed. Lastly, current challenges and future directions in the field of antimicrobial polymers for ensuing practical biomedical applications are presented. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:A1 / A29
页数:29
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