Synergetic Antibacterial Nanoparticles with Broad‐Spectrum for Wound Healing and Lung Infection Therapy

The problem of antimicrobial resistance (AMR) caused by the abuse of antibiotics is becoming serious. The development of antibacterial materials with synergistic efficiency and treatment of deep tissue/organ infections is imminent. Herein, synergistic antibacterial nanoparticles (MPH NPs) are prepar...

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Veröffentlicht in:Advanced functional materials 2024-09, Vol.34 (39), p.n/a
Hauptverfasser: Guo, Lei, Tang, Yixin, Wang, Lu, Zhou, Rui, Wang, Siyuan, Xu, Huiqing, Yang, Xi, Zhang, Jizhou, Chen, Jie, Xu, Caina, Li, Yanhui, Tian, Huayu
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Sprache:eng
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Zusammenfassung:The problem of antimicrobial resistance (AMR) caused by the abuse of antibiotics is becoming serious. The development of antibacterial materials with synergistic efficiency and treatment of deep tissue/organ infections is imminent. Herein, synergistic antibacterial nanoparticles (MPH NPs) are prepared by loading antibacterial peptide polymyxin B (PMB) on Fe‐based MOF (MIL‐100) with hyaluronic acid (HA) modification. MPH NPs exerts antibacterial effects by chemodynamic therapy (CDT) and the release of PMB. MPH NPs have broad‐spectrum antibacterial properties on Gram‐negative bacteria (E. coli, 100%), Gram‐positive bacteria (S. aureus, 98.5 %), and MRSA (98.4%). Importantly, MPH NPs not only promote the healing of infected wounds but also target lungs to accomplish organ infection therapy. Therefore, this study provides a new strategy for designing a synergetic anti‐AMR bacteria system and the function for deep tissue/organ infection therapy in the future. A synergistic antibacterial nanoparticles (MPH NPs) are prepared by loading antibacterial peptide polymyxin B (PMB) on Fe‐MOF (MIL‐100) with hyaluronic acid (HA) modification. MPH NPs have synergistic broad‐spectrum antibacterial properties on E. coli, S. aureus, and MRSA by chemodynamic therapy (CDT) and release of PMB. MPH NPs can be used for wound healing and lung infection therapy.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202403188