Bright red aggregation-induced emission nanoparticles for multifunctional applications in cancer therapy

被引:43
作者
Zhang, Liping [1 ]
Che, Weilong [1 ]
Yang, Zhiyu [2 ]
Liu, Xingman [1 ]
Liu, Shi [2 ]
Xie, Zhigang [2 ]
Zhu, Dongxia [1 ]
Su, Zhongmin [1 ]
Tang, Ben Zhong [3 ]
Bryce, Martin R. [4 ]
机构
[1] Northeast Normal Univ, Key Lab Nanobiosensing & Nanobioanal, Univ Jilin Prov, Dept Chem, 5268 Renmin St, Changchun 130024, Jilin, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[3] Hong Kong Univ Sci & Technol, State Key Lab Mol Neurosci, Inst Adv Study, Inst Mol Funct Mat,Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[4] Univ Durham, Dept Chem, Durham DH1 3LE, England
基金
英国工程与自然科学研究理事会;
关键词
HIGHLY EFFICIENT; PHOTODYNAMIC THERAPY; DELAYED FLUORESCENCE; AIEGEN; DOTS; DESIGN;
D O I
10.1039/c9sc06310b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing multifunctional photosensitizers (PSs) is needed to effectively simplify cancer treatment, but it remains a big challenge. Here, two red-emitting AIE-active, donor-acceptor (D-A) PSs with small Delta E-ST and their AIE nanoparticles, are rationally designed and synthesized. The PS1 NPs exhibit bright red-emission with high quantum yield, appropriate O-1(2) generation ability and good biocompatibility. More importantly, PS1 NPs can strongly light up the cytoplasm by gently shaking the cells for only 5 s at room temperature, indicating ultrafast staining and mild incubation conditions. In vitro and in vivo cell tracing demonstrate that PS1 NPs can track cells over 14 days, and effectively inhibit tumor growth upon irradiation. To the best of our knowledge, this work is the first example of a PS that integrates image-guided PDT, ultrafast staining and long-term tracing functions, demonstrating the "all-in-one" concept which offers great advantages for potential clinical applications.
引用
收藏
页码:2369 / 2374
页数:6
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