Antibacterial biomaterials: disruption of antibiotic tolerance for resistance prevention

Ming-Kai Wang, Jian Wang, Fu-Xiao Wang, Xi Le Hu, Xiao-Peng He, Tony James, Han Liu, Jia-Can Su

Research output: Contribution to journalArticlepeer-review

Abstract

Antimicrobial resistance (AMR) remains a critical global health challenge, exacerbated by antibiotic misuse that accelerates bacterial tolerance and undermines therapeutic efficacy. The lack of new antibiotics and the high cost of drug development further intensify the urgency for the development of alternative antimicrobial strategies. Emerging evidence suggests that biomaterials can disrupt the progression from antimicrobial tolerance (AMT) to AMR, offering a promising avenue to enhance treatment outcomes and suppress the rise of resistant strains. This review outlines the transition mechanisms from bacterial tolerance to resistance and explores how biomaterials can counter these adaptations. Using properties such as electrostatic interactions, ligand coordination, and vesicular disruption, biomaterials can inhibit bacterial growth and alter the metabolism, preventing AMT-to-AMR progression. They also initiate programmed cell death pathways and generate oxidative stress through photothermal, photodynamic, and chemodynamic therapies, and can also target bacterial DNA and protein synthesis. Additionally, biomaterials enhance immune responses including neutrophil activity and macrophage polarisation. Using biofilm and intracellular infection models, we show that biomaterials effectively prevent biofilm formation and target intracellular pathogens. Finally, we summarize infection mechanisms in organoid-based models, including immune and bacteria-organoid systems. In summary, this review highlights biomaterials as versatile agents with outstanding potential for future antimicrobial strategies.
Original languageEnglish
Article number217368
JournalCoordination Chemistry Reviews
Volume550
Early online date26 Nov 2025
DOIs
Publication statusE-pub ahead of print - 26 Nov 2025

Data Availability Statement

No data was used for the research described in the article.

Funding

his work was supported in part by grants from the National Natural Science Foundation of China (Key Program: 82230071); National Natural Science Foundation of China (82202344, 92253306 and 22477030); Foundation of National Centre for Translational Medicine (Shanghai) SHU Branch (SUTIM-2023006); Jiangsu Province Natural Science Foundation Project (BK20241808); Fujian Province Natural Science Foundation Project (2024J01221); the International Cooperation Program of Shanghai Science and Technology (No. 23490711600); the National Natural Science Foundation of Shanghai Science and Technology (No. 24ZR1415400); the Shanghai Oriental Talents Youth Program (No. QNKJ2024010); the Shanghai Xuhui District Hospital Local Cooperation Project (23XHYD-20); the Open Funding Project of the State Key Laboratory of Fine Chemicals, Dalian University of Technology (KF 2402); State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, P. R. China; Ministry of Education Key Laboratory on Signaling Regulation and Targeting Therapy of Liver Cancer (Naval Medical University) (Grant. 2023-MEKLLC-MS/ZD-00*); and Shandong Laboratory Program (SYS202205) for financial support. T. D. J. wishes to thank the University of Bath and the Open Research Fund of the School of Chemistry and Chemical Engineering, Henan Normal University (2020ZD01) for support.

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