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基于中性粒细胞细胞外陷阱的铋基多肽纳米网用于协同治疗细菌感染。

Neutrophil Extracellular Traps-Inspired Bismuth-Based Polypeptide Nanonets for Synergetic Treatment of Bacterial Infections.

机构信息

State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, China.

Mathematics and Physics Department, North China electronic Power University, Baoding, 210096, China.

出版信息

Adv Healthc Mater. 2024 Nov;13(28):e2401993. doi: 10.1002/adhm.202401993. Epub 2024 Jul 27.

DOI:10.1002/adhm.202401993
PMID:39072961
Abstract

Excessive use of antibiotics and the formation of bacterial biofilms can lead to persistent infections caused by drug-resistant bacteria, rendering ineffective immune responses and even life-threatening. There is an urgent need to explore synergistic antibacterial therapies across all stages of infection. Drawing inspiration from the antibacterial properties of neutrophil extracellular traps (NETs) and integrating the bacterial biofilm dispersal mechanism involving boronic acid-catechol interaction, the multifunctional bismuth-based polypeptide nanonets (PLBA-Bi-Fe-TA) are developed. These nanonets are designed to capture bacteria through a coordination complex involving cationic polypeptides (PLBA) with boronic acid-functionalized side chains, alongside metal ions (bismuth (Bi) and iron (Fe)), and tannic acid (TA). Leveraging the nanoconfinement-enhanced high-contact network-driven multiple efficiency, PLBA-Bi-Fe-TA demonstrates the excellent ability to swiftly capture bacteria and their extracellular polysaccharides. This interaction culminates in the formation of a highly hydrophilic complex, effectively enabling the rapid inhibition and dispersion of antibiotic-resistant bacterial biofilms, while Fe-TA shows mild photothermal ability to further assist fluffy mature biofilm. In addition, Bi is beneficial to regulate the polarization of macrophages to pro-inflammatory phenotype to further kill escaping biofilm bacteria. In summary, this novel approach offers a promising bionic optimization strategy for treating bacterial-associated infections at all stages through synergetic treatment.

摘要

过度使用抗生素和细菌生物膜的形成会导致耐药菌引起的持续性感染,使免疫反应失效,甚至危及生命。迫切需要探索贯穿感染各个阶段的协同抗菌治疗方法。受中性粒细胞细胞外陷阱 (NETs) 的抗菌特性启发,并整合涉及硼酸-儿茶酚相互作用的细菌生物膜分散机制,开发了多功能基于铋的多肽纳米网(PLBA-Bi-Fe-TA)。这些纳米网旨在通过涉及带硼酸功能侧链的阳离子多肽(PLBA)与金属离子(铋(Bi)和铁(Fe))以及单宁酸(TA)的配位复合物捕获细菌。利用纳米限域增强的高接触网络驱动的多种效率,PLBA-Bi-Fe-TA 表现出迅速捕获细菌及其细胞外多糖的优异能力。这种相互作用最终形成了一种高亲水性的复合物,有效地实现了对抗生素耐药性细菌生物膜的快速抑制和分散,而 Fe-TA 则显示出温和的光热能力,以进一步帮助蓬松成熟的生物膜。此外,Bi 有利于调节巨噬细胞向促炎表型的极化,以进一步杀死逃逸的生物膜细菌。总之,这种新方法通过协同治疗为治疗各个阶段的细菌相关感染提供了一种有前途的仿生优化策略。

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