Issue 38, 2024

Customized A–D–A type molecule to construct a nitric oxide nanogenerator with enhanced antibacterial activity for infected wound healing

Abstract

Bacterial infections pose an increasingly serious threat to global health due to the development of drug-resistant strains. Developing a method to efficiently kill bacteria and promote tissue repair is imperative to decrease the damage from bacterial infection, especially infected wounds. Herein, a biofriendly and light-controlled nitric oxide (NO) generator HFB with simultaneous bacterial killing and wound repair properties is reported based on a tailored light-responsive molecule F(EIBC)2. HFB demonstrates an appropriate photothermal conversion efficiency of 33.4% and type I reactive oxygen species (˙OH and H2O2) generation capability to simultaneously trigger NO generation and potently kill bacteria. Furthermore, HFB can effectively eradicate mature bacterial biofilms with the aid of favorable permeability of NO. Additionally, HFB effectively eradicates Staphylococcus aureus in infected wounds of living mice and accelerates healing via NO-induced angiogenesis and collagen deposition. Owing to the encapsulated human serum albumin (HSA), heavy metal-free feature, and synergistic killing mechanism, HFB exhibits good biosafety to surrounding tissue and major organs. This work provides a novel dual-functional photo-responsive molecule and a potential light-controlled release platform for the treatment of bacterial infections.

Graphical abstract: Customized A–D–A type molecule to construct a nitric oxide nanogenerator with enhanced antibacterial activity for infected wound healing

Supplementary files

Article information

Article type
Paper
Submitted
03 Jun 2024
Accepted
14 Aug 2024
First published
14 Aug 2024

J. Mater. Chem. B, 2024,12, 9675-9685

Customized A–D–A type molecule to construct a nitric oxide nanogenerator with enhanced antibacterial activity for infected wound healing

Y. Wang, X. Wang, C. Zhang, R. Li, J. Li, H. Shi, C. Zhang and L. Feng, J. Mater. Chem. B, 2024, 12, 9675 DOI: 10.1039/D4TB01201A

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