A cancer cell and lysosome dual-targeted photosensitizer for fluorescence imaging and photodynamic therapy

被引:3
作者
Su, Chaorui [1 ]
Xing, Peipei [1 ,2 ]
Zhang, Jinghui [1 ]
Ma, Xiaolin [1 ]
Wu, Xinyue [3 ]
Zhu, Mengliang [1 ,3 ]
Zhang, Xiaoshuang [4 ]
Du, Hongwu [4 ,5 ]
Bian, Yongzhong [1 ,5 ]
Jiang, Jianzhuang [1 ,5 ]
机构
[1] Univ Sci & Technol Beijing, Beijing Key Lab Sci & Applicat, Funct Mol & Crystalline Mat, Dept Chem, Beijing 100083, Peoples R China
[2] Beijing Vocat Coll Agr, Beijing 102442, Peoples R China
[3] Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[4] Univ Sci & Technol Beijing, Dept Biol, Beijing 100083, Peoples R China
[5] Univ Sci & Technol Beijing, Beijing Adv Innovat Ctr Mat Genome Engn, Daxing Res Inst, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Porphyrin; Cancer cell; Lysosome; Cell imaging; Photodynamic therapy; OXYGEN; GENERATION; PROBES; CHALLENGES; STRATEGIES; ORGANELLE; BODIPY; DESIGN; AGENTS;
D O I
10.1016/j.dyepig.2023.111861
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel cancer cell and lysosome dual-targeted photosensitizer (PS) termed by BMP was developed for fluo-rescence imaging and photodynamic therapy (PDT). BMP consists of a porphyrin(Zn) core with appropriate singlet-triplet state distribution enables it to function as an imaging agent as well as a PS, a biotin moiety that can target cancer cells, and a morpholine group specific to lysosomes. Intracellular experiments demonstrated that the dual-targeted photosensitizer BMP could preferably accumulate in cancer cells and subsequently locate within lysosome organelles. Upon irradiation, BMP could generate red fluorescence emission (phi em = 6.3%) and singlet oxygen (1O2, phi Delta = 55%) for the dual functionality of cell imaging and PDT, respectively. Notably, BMP exhibited much higher photocytotoxicity toward cancer cells (A549 cells) compared to normal cells (BEAS-2B cells). Importantly, 1O2 produced by BMP induced oxidative damage of lysosomes, and subsequently triggered cell death of A549 cells, as evidenced by the loss of morphological integrity and cell rupture.
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页数:11
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