Infection microenvironment-activated nanoparticles for NIR-II photoacoustic imaging-guided photothermal/chemodynamic synergistic anti-infective therapy.

Yang, Nan; Guo, Heng; Cao, Changyu; Wang, Xiaorui; Song, Xuejiao; Wang, Wenjun; Yang, Dongliang; Xi, Lei et al. · Biomaterials · 2021

basic_science · Level V

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Abstract

Subcutaneous abscesses caused by drug-resistant bacteria pose huge challenges to human health. The design of infection microenvironment-activated biomaterials has an advantage for the diagnosis and treatment of infective diseases due to its high specificity and efficiency. Herein, a novel theranostic platform based on Cu<sub>2</sub>O nanoparticles (NPs) is successfully constructed via a simple, fast and low-cost approach. The Cu<sub>2</sub>O NPs exhibit high sensitivity to overexpressed H<sub>2</sub>S and H<sub>2</sub>O<sub>2</sub> in the bacterial infection microenvironment. After in situ injection, the Cu<sub>2</sub>O NPs will rapidly react with the endogenous H<sub>2</sub>S to generate Cu<sub>9</sub>S<sub>8</sub> NPs, which exhibits high absorbance in the second near-infrared (NIR-II) biowindow. The Cu<sub>9</sub>S<sub>8</sub> NPs serving as NIR-II photoacoustic contrast agents can exactly distinguish between inflammatory and normal tissues. With the guidance of NIR-II photoacoustic imaging (PAI), H<sub>2</sub>S-activated photothermal antibacterial therapy (PTAT) can realize excellent antibacterial performance under 1060 nm laser irradiation. Meanwhile, the Cu<sub>2</sub>O NPs can effectively catalyze H<sub>2</sub>O<sub>2</sub> at the site of inflammation to produce hydroxyl radicals with strong antibacterial property via Fenton-like reaction, resulting in the damage of bacterial cell membrane. Furthermore, the application of Cu<sub>2</sub>O NPs can enhance epidermic migration and facilitate the re-epithelialization of the infected skin. In vivo experiment shows that 97.9% methicillin-resistant Staphylococcus aureus are eliminated by the synergistic PTAT and chemodynamic antibacterial therapy.

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