光动力疗法
肿瘤缺氧
缺氧(环境)
癌症研究
体内
光敏剂
联合疗法
化学
肿瘤微环境
卟啉
葡萄糖氧化酶
生物物理学
药理学
酶
氧气
生物化学
医学
光化学
生物
内科学
肿瘤细胞
放射治疗
生物技术
有机化学
作者
Yingjie Ouyang,Peng Wang,Baoxuan Huang,Guoliang Yang,Jia Tian,Weian Zhang
标识
DOI:10.1021/acsabm.1c00174
摘要
The antitumor efficacy of photodynamic therapy (PDT) is greatly impeded by the nonspecific targeting of photosensitizers and limited oxygen supply in hypoxic tumors. Aiming to overcome the problem, a dual-locked porphyrin/enzyme-loading zeolitic imidazolate framework (ZIF) nanoplatform was constructed for starvation therapy and O2 self-sufficient PDT. The fluorescence recovery and PDT of photosensitizers could be cooperatively triggered by dual pathological parameters, the low pH and overexpressed GSH in tumor tissues, which makes the PDT process conduct precisely in a tumor microenvironment. The cascade catalysis of glucose oxidase and catalase promotes the nanoplatform dissociation, inhibits the energy supply of tumors (starvation therapy), and provides enough O2 to ameliorate the hypoxia and enhance PDT efficacy. In vitro and in vivo studies were performed to confirm the high antitumor efficacy of the porphyrin/enzyme-loading ZIF nanoplatform. Thus, this work offers a path for precise and efficient PDT-based combination therapy against a hypoxia tumor.
科研通智能强力驱动
Strongly Powered by AbleSci AI