肿瘤缺氧
阿霉素
化学
体内
癌症研究
放化疗
纳米技术
材料科学
化疗
医学
放射治疗
生物
内科学
生物技术
作者
Zhimei He,Xiaolin Huang,Chen Wang,Xiangli Li,Yijing Liu,Zijian Zhou,Sheng Wang,Fuwu Zhang,Zhantong Wang,Orit Jacobson,Jun‐Jie Zhu,Guocan Yu,Yunlu Dai,Xiaohong Chen
标识
DOI:10.1002/anie.201902612
摘要
Abstract Tumor hypoxia, the “Achilles’ heel” of current cancer therapies, is indispensable to drug resistance and poor therapeutic outcomes especially for radiotherapy. Here we propose an in situ catalytic oxygenation strategy in tumor using porphyrinic metal‐organic framework (MOF)‐gold nanoparticles (AuNPs) nanohybrid as a therapeutic platform to achieve O 2 ‐evolving chemoradiotherapy. The AuNPs decorated on the surface of MOF effectively stabilize the nanocomposite and serve as radiosensitizers, whereas the MOF scaffold acts as a container to encapsulate chemotherapeutic drug doxorubicin. In vitro and in vivo studies verify that the catalase‐like nanohybrid significantly enhances the radiotherapy effect, alleviating tumor hypoxia and achieving synergistic anticancer efficacy. This hybrid nanomaterial remarkably suppresses the tumor growth with minimized systemic toxicity, opening new horizons for the next generation of theranostic nanomedicines.
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