Visualization of Protease Activity In Vivo Using an Activatable Photo-Acoustic Imaging Probe Based on CuS Nanoparticles

被引:142
作者
Yang, Kai [1 ,2 ]
Zhu, Lei [2 ,3 ]
Nie, Liming [2 ]
Sun, Xiaolian [2 ]
Cheng, Liang [1 ]
Wu, Chenxi [2 ]
Niu, Gang [2 ]
Chen, Xiaoyuan [2 ]
Liu, Zhuang [1 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[2] NIBIB, LOMIN, NIH, Bethesda, MD 20892 USA
[3] Xiamen Univ, Sch Publ Hlth, Ctr Mol Imaging & Translat Med, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Peptide; Photoacoustic imaging; Enzyme cleavage; Copper sulfide; MMPs detection; PHOTOTHERMAL ABLATION; MATRIX METALLOPROTEINASES; CARBON NANOTUBES; AGENTS; SENSITIVITY; GRAPHENE;
D O I
10.7150/thno.7217
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Herein, we for the first time report a novel activatable photoacoustic (PA) imaging nano-probe for in vivo detection of cancer-related matrix metalloproteinases (MMPs). A black hole quencher 3 (BHQ3) which absorbs red light is conjugated to near-infrared (NIR)-absorbing copper sulfide (CuS) nanoparticles via a MMP-cleavable peptide linker. The obtained CuS-peptide-BHQ3 (CPQ) nano-probe exhibits two distinctive absorption peaks at 630 nm and 930 nm. Inside the tumor microenviorment where MMPs present, the MMP-sensitive peptide would be cleaved, releasing BHQ3 from the CuS nanoparticles, the former of which as a small molecule is then rapidly cleared out from the tumor, whereas the latter of which as large nanoparticles would retain inside the tumor for a much longer period of time. As the result, the PA signal at 680 nm which is contributed by BHQ3 would be quickly diminished while that at 930 nm would be largely retained. The PA signal ratio of 680 nm /930 nm could thus serve as an in vivo indicator of MMPs activity inside the tumor. Our work presents a novel strategy of in vivo sensing of MMPs based on PA imaging, which should offer remarkably improved detection depth compared with traditional optical imaging techniques.
引用
收藏
页码:134 / 141
页数:8
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