A Radio-Pharmaceutical Fluorescent Probe for Synergistic Cancer Radiotherapy and Ratiometric Imaging of Tumor Reactive Oxygen Species

被引:60
作者
Ge, Xiaoguang [1 ,2 ]
Su, Lichao [1 ,2 ]
Chen, Zhongxiang [1 ,2 ]
Zhu, Kang [3 ]
Zhang, Xuan [1 ,2 ]
Wu, Ying [3 ]
Song, Jibin [1 ,2 ,3 ]
机构
[1] Fuzhou Univ, Coll Chem, Fujian Sci & Technol Innovat Lab Optoelect Inform, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Coll Chem, MOE Key Lab Analyt Sci Food Safety & Biol, Fuzhou 350108, Peoples R China
[3] Beijing Univ Chem Technol, Coll Chem, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Activatable Probe; Biosensor; NIR-II Fluorescence Imaging; Radiotherapy; X-Ray; RADIOSENSITIZERS;
D O I
10.1002/anie.202305744
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Radiotherapy (RT) is an effective and widely applied cancer treatment strategy in clinic. However, it usually suffers from radioresistance of tumor cells and severs side effects of excessive radiation dose. Therefore, it is highly significant to improve radiotherapeutic performance and monitor real-time tumor response, achieving precise and safe RT. Herein, an X-ray responsive radio-pharmaceutical molecule containing chemical radiosensitizers of diselenide and nitroimidazole (BBT-IR/Se-MN) is reported. BBT-IR/Se-MN exhibits enhanced radiotherapeutic effect via a multifaceted mechanisms and self-monitoring ROS levels in tumors during RT. Under X-ray irradiation, the diselenide produces high levels of ROS, leading to enhanced DNA damage of cancer cell. Afterwards, the nitroimidazole in the molecule inhibits the damaged DNA repair, offering a synergetic radiosensitization effect of cancer. Moreover, the probe shows low and high NIR-II fluorescence ratios in the absence and presence of ROS, which is suitable for precise and quantitative monitoring of ROS during sensitized RT. The integrated system is successfully applied for radiosensitization and the early prediction of in vitro and in vivo RT efficacy.
引用
收藏
页数:11
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