光动力疗法
光热治疗
吲哚青绿
肿瘤缺氧
材料科学
活性氧
放射治疗
过氧化氢酶
纳米壳
肿瘤微环境
癌症研究
体内
激进的
荧光
生物物理学
纳米技术
化学
纳米颗粒
酶
肿瘤细胞
医学
生物化学
病理
有机化学
生物
生物技术
内科学
量子力学
物理
作者
Xiaoyu Chen,Chunhua Zhao,Dingxin Liu,Kunpeng Lin,Jingnan Lu,Shuang Zhao,Yang Jiang,Huan-Xin Lin
标识
DOI:10.1021/acsami.3c00056
摘要
Reactive oxygen species-mediated therapeutic strategies, including chemodynamic therapy (CDT) and photodynamic therapy (PDT), have exhibited translational promise for effective cancer management. However, monotherapy often ends up with the incomplete elimination of the entire tumor due to inherent limitations. Herein, we report a core-shell-structured Pd1.7Bi@CeO2-ICG (PBCI) nanoplatform constructed by a facile and effective strategy for synergistic CDT, PDT, and photothermal therapy. In the system, both Pd1.7Bi and CeO2 constituents exhibit peroxidase- and catalase-like characteristics, which not only generate cytotoxic hydroxyl radicals (•OH) for CDT but also produce O2 in situ and relieve tumor hypoxia for enhanced PDT. Furthermore, upon 808 nm laser irradiation, Pd1.7Bi@CeO2 and indocyanine green (ICG) coordinately prompt favorable photothermia, resulting in thermodynamically amplified catalytic activities. Meanwhile, PBCI is a contrast agent for near-infrared fluorescence imaging to determine the optimal laser therapeutic window in vivo. Consequently, effective tumor elimination was realized through the above-combined functions. The as-synthesized unitary PBCI theranostic nanoplatform represents a potential one-size-fits-all approach in multimodal synergistic therapy of hypoxic tumors.
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