Hypoxia-triggered photothermal/drug combination therapy of tumors using a perylene diimide molecular capsule

被引:1
作者
Yang, Fei [1 ,2 ]
Wang, Guo [2 ]
Huang, Kecheng [1 ]
Xu, Yanqing [1 ]
Feng, Xiao [1 ]
Wang, Weizhi [1 ]
Wei, Wei [2 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Key Lab Med Mol Sci & Pharmaceut Engn, Minist Ind & Informat Technol, Beijing 100081, Peoples R China
[2] Capital Normal Univ, Dept Chem, Beijing Key Lab Opt Mat & Photon Devices, Beijing 100048, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金; 北京市自然科学基金;
关键词
hypoxia-responsive photothermal agent; cyclophanes; host-guest system; near-infrared; combination therapy; RADICAL-ANIONS; AGGREGATION; LIPOSOMES;
D O I
10.1007/s11426-024-2231-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hypoxia is a common characteristic of tumors and associated with poor outcome in most cancer types, thus hypoxia-triggered combined therapeutic systems with well-defined structure hold significant promise for achieving specific and effective tumor destruction. Herein, a water-soluble perylene diimide (PDI) cyclophane "Gemini Box" (GBox-14+) is demonstrated as both a hypoxia-responsive photothermal agent and a drug capsule for tumor-specific combination therapy. First, owing to the covalent enclosure of PDI chromophore by double-sided molecular straps, GBox-14+ can significantly stabilize labile PDI radical anions generated through bioreduction at the lesion site of hypoxic tumors, leading to high-efficiency near-infrared photothermal ablation of tumors. Meanwhile, GBox-14+ can act as a molecular capsule to bind water-insoluble antitumor drugs camptothecin and hydroxycamptothecin in 1:1 host-guest stoichiometry with high affinities, greatly enhancing the water solubility of drugs. Eventually, such drug-loading cyclophane system as a hypoxia-activated photothermal/drug combined therapeutic platform exhibits more effective inhibition of tumor growth than the single treatment under identical conditions. This study significantly extends the application range of host-guest cyclophane systems and opens a promising avenue to structurally uniform combined therapeutic agents against hypoxic tumors with improved specificity.
引用
收藏
页码:1009 / 1017
页数:9
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