NIR-II Emissive Ru(II) Metallacycle Assisting Fluorescence Imaging and Cancer Therapy

被引:41
作者
Fan, Yifan [1 ]
Li, Chonglu [1 ]
Bai, Suya [2 ]
Ma, Xin [1 ]
Yang, Jingfang [1 ]
Guan, Xiaofang [3 ,4 ]
Sun, Yao [1 ]
机构
[1] Cent China Normal Univ, Key Lab Pesticides & Chem Biol, Minist Educ, Coll Chem, Wuhan 430079, Peoples R China
[2] Anhui Normal Univ, Key Lab Funct Mol Solids, Minist Educ, Wuhu 241000, Peoples R China
[3] Zhengzhou Cardiovasc Hosp, Zhengzhou 450016, Peoples R China
[4] 7th Peoples Hosp Zhengzhou, Zhengzhou 450016, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer theranostics; metallacycles; NIR-II; self-assembly; COMPLEXES; PHOTOSENSITIZERS; DESIGN;
D O I
10.1002/smll.202201625
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the success of emissive Ruthenium (Ru) agents in biomedicine, problems such as the visible-light excitation/emission and single chemo- or phototherapy modality still hamper their applications in deep-tissue imaging and efficient cancer therapy. Herein, an second nearinfrared window (NIR-II) emissive Ru(II) metallacycle (Ru1000, lambda(em) = 1000 nm) via coordination-driven self-assembly is reported, which holds remarkable deep-tissue imaging capability (approximate to 6 mm) and satisfactory chemo-phototherapeutic performance. In vitro results indicate Ru1000 displays promising cellular uptake, good cancer-cell selectivity, attractive anti-metastasis properties, and remarkable anticancer activity against various cancer cells, including cisplatin-resistant A549 cells (IC50 = 3.4 x 10(-6) m vs 92.8 x 10(-6) m for cisplatin). The antitumor mechanism could be attributed to Ru1000-induced lysosomal membrane damage and mitochondrial-mediated apoptotic cell death. Furthermore, Ru1000 also allows the high-performance in vivo NIR-II fluorescence imaging-guided chemo-phototherapy against A549 tumors. This work may provide a paradigm for the development of long-wavelength emissive metallacycle-based agents for future biomedicine.
引用
收藏
页数:12
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