声动力疗法
活性氧
化学
渗透(战争)
小泡
谷胱甘肽
杰纳斯
纳米颗粒
肿瘤微环境
生物物理学
纳米技术
癌症研究
材料科学
生物化学
医学
膜
肿瘤细胞
酶
工程类
生物
运筹学
作者
Xiahui Lin,Shuya Liu,Xuan Zhang,Rong Zhu,Shan Chen,Xiaohong Chen,Jibin Song,Huanghao Yang
标识
DOI:10.1002/anie.201912768
摘要
Abstract Sonodynamic therapy (SDT) has the advantages of high penetration, non‐invasiveness, and controllability, and it is suitable for deep‐seated tumors. However, there is still a lack of effective sonosensitizers with high sensitivity, safety, and penetration. Now, ultrasound (US) and glutathione (GSH) dual responsive vesicles of Janus Au‐MnO nanoparticles (JNPs) were coated with PEG and a ROS‐sensitive polymer. Upon US irradiation, the vesicles were disassembled into small Janus Au‐MnO nanoparticles (NPs) with promoted penetration ability. Subsequently, GSH‐triggered MnO degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn 2+ for chemodynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation. This also allowed dual‐modality photoacoustic imaging in the second near‐infrared (NIR) window and T 1 ‐MR imaging due to the released Mn 2+ , and inhibited orthotopic liver tumor growth via synergistic SDT/CDT.
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