Photodynamic therapy has been developed as a prospective cancer treatment in recent years. Nevertheless, conventional photosensitizers suffer from lacking recognition and specificity to tumors, which causing severe side effects to normal tissues, while the enzyme-activated photosensitizers are capable of solving these conundrums due to high selectivity towards tumors. APN (Aminopeptidase N, APN/CD13), a tumor marker, has become a crucial targeting substance owing to its highly expressed on the cell membrane surface in various tumors, which has become a key point in the research of anti-tumor drug and fluorescence probe. Based on it, herein an APN-activated near-infrared (NIR) photosensitizer (APN-CyI) for tumor imaging and photodynamic therapy has been firstly developed and successfully applied in vitro and in vivo. Studies showed that APN-CyI could be activated by APN in tumor cells, hydrolyzed to fluorescent CyI-OH, which specifically located in mitochondria in cancer cells and exhibited a high singlet oxygen yield under NIR irradiation, and efficiently induced cancer cell apoptosis. Dramatically, the in vivo assays on Balb/c mice showed that APN-CyI could achieve NIR fluorescence imaging (λ(em) = 717 nm) for endogenous APN in tumors and possessed an efficient tumor suppression effect under NIR irradiation.
An APN-activated NIR photosensitizer for cancer photodynamic therapy and fluorescence imaging.
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作者:Zhou Xiao, Li Haidong, Shi Chao, Xu Feng, Zhang Zhen, Yao Qichao, Ma He, Sun Wen, Shao Kun, Du Jianjun, Long Saran, Fan Jiangli, Wang Jingyun, Peng Xiaojun
| 期刊: | Biomaterials | 影响因子: | 12.900 |
| 时间: | 2020 | 起止号: | 2020 Sep;253:120089 |
| doi: | 10.1016/j.biomaterials.2020.120089 | ||
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