抗菌剂
两亲性
聚合物
高分子科学
化学
纳米技术
业务
材料科学
有机化学
共聚物
作者
Alain M. Bapolisi,Anne‐Catherine Lehnen,Martin Wolff,Jeffrey F. Kramer,Sergio Kogikoski,René Steinbrecher,Nicole Michler,Andreas Kiesow,Ilko Bald,Martina Obry,Sebastian Kersting,Till Stensitzki,Henrike M. Müller‐Werkmeister,Meike N. Leiske,Salvatore Chiantia,Matthias Hartlieb
标识
DOI:10.26434/chemrxiv-2025-9d5s6
摘要
Antimicrobial resistance (AMR) is a severe threat to modern health care and must be addressed to prevent millions of deaths in the coming decades. Antimicrobial polymers (APs) do not provoke resistances and are promising alternatives to conventional antibiotics. Classic APs possess an amphiphilic structure (cationic and hydrophobic). Herein we question the necessity of amphiphilicity in APs and find that hydrophobicity is not an essential quality in these polymers. Combining cationic monomers with hydrophilic subunits containing hydrogen bond donors results in excellent antibacterial activity and concurrently low unspecific toxicity. Non-amphiphilic APs have the unique ability to cluster in isolated membrane regions, creating a supramolecular multivalence that enhances their membrane activity and aggregates bacterial cells. This effect, which only unfolds in the absence of hydrophobicity opens new possibilities in the design of antimicrobial materials.
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