光动力疗法
肿瘤缺氧
过氧化氢酶
缺氧(环境)
转移
化学
癌症研究
过氧化氢
医学
药理学
体内
病理
抗氧化剂
放射治疗
癌症
生物化学
内科学
生物
氧气
有机化学
生物技术
作者
Junjing Yin,Haiqiang Cao,Hong Wang,Kaoxiang Sun,Yaping Li,Zhiwen Zhang
标识
DOI:10.1016/j.apsb.2020.06.004
摘要
Hypoxia is a serious impediment to current treatments of many malignant tumors. Catalase, an antioxidant enzyme, is capable of decomposing endogenous hydrogen peroxide (H2O2) into oxygen for tumor reoxygenation, but suffered from in vivo instability and limited delivery to deep interior hypoxic regions in tumor. Herein, a deep-penetrated nanocatalase-loading DiIC18 (5, DiD) and soravtansine ([email protected]) were provided by coating catalase nanoparticles with PEGylated phospholipids membrane, stimulating the structure and function of erythrocytes to relieve tumor hypoxia for enhanced chemo-photodynamic therapy. After intravenous administration, [email protected] preferentially accumulated at tumor sites, flexibly penetrated into the interior regions of tumor mass and remarkably relieved the hypoxic status in tumor. Notably, the [email protected] + laser treatment produced striking inhibition of tumor growth and resulted in a 97.2% suppression of lung metastasis. Thus, the phospholipids membrane-coated nanocatalase system represents an encouraging nanoplatform to relieve tumor hypoxia and synergize the chemo-photodynamic cancer therapy.
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