声动力疗法
活性氧
化学
渗透(战争)
小泡
谷胱甘肽
纳米颗粒
生物物理学
纳米技术
材料科学
生物化学
膜
运筹学
生物
工程类
酶
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
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 Mn2+ 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 T1 -MR imaging due to the released Mn2+ , and inhibited orthotopic liver tumor growth via synergistic SDT/CDT.
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