生物污染
阳离子聚合
聚合物
模块化设计
化学
纳米技术
伤口愈合
材料科学
化学工程
抗菌活性
细胞迁移
PEG比率
细菌
抗菌剂
杀生物剂
膜
生物膜
组合化学
作者
Changsheng Wang,Cécile Berne,Hu Zhang,Karine Dufresne,Wojciech Raj,Alessia Filippini,Hui Guo,Hermine Counil,Quoc Thang Phan,Duy Anh Phạm,Nahid Hassanpour,Qiang Peng,Tzu-Hsuan Huang,Florina G. Halmac,Yves V. Brun,Xavier Banquy
标识
DOI:10.1021/acsbiomaterials.6c01161
摘要
Surface-associated and device-related bacterial infections require materials that can both eliminate pathogens and prevent microbial colonization. However, antibacterial activity in solution and antifouling performance at interfaces are governed by distinct physicochemical principles, making their integration within a single material challenging. Here, we report a modular bottlebrush polymer (BBP) platform that decouples these functions through architectural design. A library of seven BBPs with monoblock and ABA triblock architectures was synthesized to independently control side-chain charge distribution and interfacial hydration. Multivalent cationic side chains promoted efficient bacterial killing in solution, whereas hydrated PEG or zwitterionic bottlebrush layers anchored by cationic termini formed stable antifouling coatings. In diabetic mice, the BBPs showed no evidence of local irritation, systemic toxicity, or impaired wound healing. In an infected wound model, bactericidal BBPs reduced bacterial burden, while antifouling BBPs suppressed local inflammation. Their combined application improved therapeutic outcomes, demonstrating the benefit of a functionally decoupled strategy. Collectively, these findings establish a generalizable architectural framework for designing multifunctional anti-infective materials.
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