| Literature DB >> 31046176 |
Zhimei He1, Xiaolin Huang2, Chen Wang3, Xiangli Li1, Yijing Liu4, Zijian Zhou4, Sheng Wang4, Fuwu Zhang4, Zhantong Wang4, Orit Jacobson4, Jun-Jie Zhu1, Guocan Yu4, Yunlu Dai5, Xiaoyuan Chen4.
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 O2 -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.Entities:
Keywords: catalase-like activity; chemoradiation therapy; controlled drug release; radiosensitizer; tumour hypoxia
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Year: 2019 PMID: 31046176 PMCID: PMC6690394 DOI: 10.1002/anie.201902612
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336