光动力疗法
活性氧
肿瘤缺氧
肿瘤微环境
化学
缺氧(环境)
癌症研究
体内
联合疗法
生物物理学
药理学
氧气
医学
肿瘤细胞
生物化学
生物
放射治疗
内科学
有机化学
生物技术
作者
Haoming Yuan,Kaixiu Chen,Jing Geng,Ziyong Wu,Chao Wang,Chao Wang,Pengfei Shi
标识
DOI:10.1002/chem.202400319
摘要
Abstract Photodynamic therapy (PDT) and chemodynamic therapy (CDT) are promising tumor treatments mediated by reactive oxygen species (ROS), which have the advantages of being minimally invasive. However, the hypoxia of tumor microenvironment and poor target ability often reduce the therapeutic effect. Here we propose a tumor targeted nanoplatform PCN‐224@Co 3 O 4 ‐HA for enhanced PDT and synergistic CDT, constructed by hyaluronate‐modified Co 3 O 4 nanoparticles decorated metal‐organic framework PCN‐224. Co 3 O 4 can catalyze the decomposition of highly expressed H 2 O 2 in tumor cells to produce oxygen and alleviate the problem of hypoxia. It can also produce hydroxyl radicals according to the Fenton‐like reaction for chemical dynamic therapy, significantly improving the therapeutic effect. The cell survival experiment showed that after in vitro treatment, 4T1 and MCF‐7 cancer cells died in a large area under the anaerobic state, while the survival ability of normal cell L02 was nearly unchanged. This result effectively indicated that PCN‐224@Co 3 O 4 ‐HA could effectively relieve tumor hypoxia and improve the effect of PDT and synergistic CDT. Cell uptake experiments showed that PCN‐224@Co 3 O 4 ‐HA had good targeting properties and could effectively aggregate in tumor cells. In vivo experiments on mice, PCN‐224@Co 3 O 4 ‐HA presented reliable biosafety performance, and can cooperate with PDT and CDT therapy to prevent the growth of tumor.
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