4.8 Article

Space-Selective Chemodynamic Therapy of CuFe5O8 Nanocubes for Implant-Related Infections

Journal

ACS NANO
Volume 14, Issue 10, Pages 13391-13405

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c05255

Keywords

CuFe5O8 nanocubes; biofilm microenvironment; chemodynamic therapy; immunomodulation; implant-related infections; extracellular DNA

Funding

  1. National Natural Science Foundation of China [81974324, 81772309, 81802181, 51872094]
  2. National Funds for Distinguished Young Scientists [51725202]
  3. Shanghai Sailing Program [18YF1418800]
  4. Key Project of Shanghai Science and Technology Commission [19JC1412000]

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Implant-related infections (IRIs) are a serious complication after orthopedic surgery, especially when a biofilm develops and establishes physical and chemical barriers protecting bacteria from antibiotics and the hosts local immune system. Effectively eliminating biofilms is essential but difficult, as it requires not only breaking the physical barrier but also changing the chemical barrier that induces an immunosuppressive microenvironment. Herein, tailored to a biofilm microenvironment (BME), we proposed a space-selective chemodynamic therapy (CDT) strategy to combat IRIs using metastable CuFe5O8 nanocubes (NCs) as smart Fenton-like reaction catalysts whose activity can be regulated by pH and H2O2 concentration. In the biofilm, extracellular DNA (eDNA) was cleaved by high levels of hydroxyl radicals ((OH)-O-center dot) catalyzed by CuFe5O8 NCs, thereby disrupting the rigid biofilm. Outside the biofilm with relatively higher pH and lower H2O2 concentration, lower levels of generated (OH)-O-center dot effectively reversed the immunosuppressive microenvironment by inducing pro-inflammatory macrophage polarization. Biofilm fragments and exposed bacteria were then persistently eliminated through the collaboration of pro-inflammatory immunity and (OH)-O-center dot. The spatially selective activation of CDT and synergistic immunomodulation exerted excellent effects on the treatment of IRIs in vitro and in vivo. The anti-infection strategy is expected to provide a method to conquer IRIs.

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