Bioresponsive nano-antibacterials for H(2)S-sensitized hyperthermia and immunomodulation against refractory implant-related infections

用于H₂S敏化热疗和免疫调节治疗难治性植入物相关感染的生物响应性纳米抗菌剂

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Abstract

There is an increasingly growing demand for nonantibiotic strategies to overcome drug resistance in bacterial biofilm infections. Here, a novel "gas-sensitized hyperthermia" strategy is proposed for appreciable bacteria killing by the smart design of a metal-organic framework (MOF)-sealed Prussian blue-based nanocarrier (MSDG). Once the biofilm microenvironment (BME) is reached, the acidity-activated MOF degradation allows the release of diallyl trisulfide and subsequent glutathione-responsive generation of hydrogen sulfide (H(2)S) gas. Upon near-infrared irradiation, H(2)S-sensitized hyperthermia arising from MSDG can efficiently eliminate biofilms through H(2)S-induced extracellular DNA damage and heat-induced bacterial death. The generated H(2)S in the biofilm can stimulate the polarization of macrophages toward M2 phenotype for reshaping immune microenvironment. Subsequently, the secretion of abundant regeneration-related cytokines from M2 macrophages accelerates tissue regeneration by reversing the infection-induced pro-inflammatory environment in an implant-related infection model. Collectively, such BME-responsive nano-antibacterials can achieve biofilm-specific H(2)S-sensitized thermal eradiation and immunomodulatory tissue remodeling, thus realizing the renaissance of precision treatment of refractory implant-related infections.

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