NIR-Responsive Nanoplatform Based on CuO2 with Self-Supplied H2O2/O2 for Synergistic Photodynamic-Chemodynamic-Photothermal Therapy of Skin Abscesses

光热治疗 材料科学 单线态氧 过氧化氢 光动力疗法 吲哚青绿 纳米技术 激进的 光热效应 过氧化苯甲酰 癌症治疗 抗菌剂 巨噬细胞极化 氧气 活性氧 热疗 生物医学工程 癌症治疗 芬顿反应 生物相容性材料 伤口愈合 光化学 过氧化物 肿瘤微环境
作者
Yingnan Zhu,Jiahang Si,Tiantian Xu,Lan Zheng,Xinyu Xiao,Xiaohan Sun,Ding He,Yuze Dong
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:17 (38): 53131-53144 被引量:2
标识
DOI:10.1021/acsami.5c11434
摘要

Chemodynamic therapy (CDT) and photodynamic therapy (PDT) have emerged as promising strategies for treating skin abscesses. However, their therapeutic efficacy is fundamentally constrained by the hypoxic and hydrogen peroxide-deficient microenvironment characteristic of abscesses. Herein, we developed a near-infrared (NIR) light-responsive nanoplatform (ICG/CuO2@PCM) by encapsulating copper peroxide (CuO2) and indocyanine green (ICG) within a phase-change material (PCM), which enables control over self-supplied H2O2/O2 release via an NIR-triggered cascade. Upon irradiation, ICG-mediated photothermal conversion elevates the temperature beyond the PCM melting threshold, triggering a burst release of CuO2 and ICG. CuO2 generates hydroxyl radicals (•OH) through a Fenton-like reaction in the acidic wound microenvironment. Additionally, CuO2 can thermally decompose under photothermal conditions to produce a sustained oxygen supply, which ICG immediately converts into singlet oxygen (1O2), thereby enhancing PDT efficiency. Furthermore, photothermal therapy not only enhances the efficiency of CDT but also provides additional antibacterial support. Remarkably, ICG/CuO2@PCM (NPs), coupled with irradiation, accelerate abscess wound recovery by dispersing biofilm, killing bacteria, and promoting macrophage polarization toward an anti-inflammatory phenotype. Overall, this NIR-responsive nanoplatform highlights the promise in controlled modulation of microenvironment-adaptive antimicrobial strategies to overcome current limitations of hypoxic infections.
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