Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Chemistry for Energy Materials, Fudan University, Shanghai, 200433, P. R. China.
Adv Mater. 2018 Feb;30(7). doi: 10.1002/adma.201704833. Epub 2018 Jan 8.
Tumor hypoxia is typically presented in the central region of solid tumors, which is mainly caused by an inadequate blood flow and oxygen supply. In the conventional treatment of hypoxic human tumors, not only the oxygen-dependent photodynamic therapy (PDT), but also antitumor drug-based chemotherapy, is considerably limited. The use of direct oxygen delivering approach with oxygen-dependent PDT or chemotherapy may potentiate the reactive oxygen species (ROS)-mediated cytotoxicity of the drug toward normal tissues. Herein, a synergetic one-for-all mesoporous cerium oxide upconversion biophotocatalyst is developed to achieve intratumorally endogenous H O -responsive self-sufficiency of O and near-infrared light controlled PDT simultaneously for overcoming hypoxia cancer. Furthermore, the sufficient O plays an important role in overcoming the chemotherapeutic drug-resistant cancer caused by hypoxia, therefore inducing tumor cell apoptosis significantly.
肿瘤缺氧通常存在于实体瘤的中央区域,主要是由于血流和氧气供应不足所致。在缺氧人类肿瘤的常规治疗中,不仅依赖于氧的光动力疗法(PDT),而且基于抗肿瘤药物的化学疗法也受到相当大的限制。使用具有依赖于氧的 PDT 或化疗的直接供氧方法可能会增强药物对正常组织的 ROS 介导的细胞毒性。在此,开发了协同的多用途介孔氧化铈上转换生物光催化剂,以实现在肿瘤内内源 H2O2 响应性自供氧和近红外光控制 PDT 以克服缺氧癌症。此外,充足的 O2 对于克服由缺氧引起的化疗药物耐药性癌症起着重要作用,因此可以显著诱导肿瘤细胞凋亡。