Engineering the Protein Corona Structure on Gold Nanoclusters Enables Red-Shifted Emissions in the Second Near-infrared Window for Gastrointestinal Imaging.
Weili WangYifei KongJun JiangQianqian XieYang HuangGuanna LiDi WuHuizhen ZhengMeng GaoShujuan XuYanxia PanWei LiRonglin MaMei X WuXuehua LiHan ZuilhofXiaoming CaiRuibin LiPublished in: Angewandte Chemie (International ed. in English) (2020)
The application of NIR-II emitters for gastrointestinal (GI) tract imaging remains challenging due to fluorescence quenching in the digestive microenvironment. Herein, we report that red-shifting of the fluorescence emission of Au nanoclusters (AuNCs) into NIR-II region with improved quantum yields (QY) could be achieved by engineering a protein corona structure consisting of a ribonuclease-A (RNase-A) on the particle surfaces. RNase-A-encapsulated AuNCs (RNase-A@AuNCs) displayed emissions at 1050 nm with a 1.9 % QY. Compared to rare earth and silver-based NIR-II emitters, RNase-A@AuNCs had excellent biocompatibility, showing >50-fold higher sensitivity in GI tract, and migrated homogenously during gastrointestinal peristalsis to allow visualization of the detailed structures of the GI tract. RNase-A@AuNCs could successfully examine intestinal tumor mice from healthy mice, indicating a potential utility for early diagnosis of intestinal tumors.
Keyphrases
- energy transfer
- fluorescent probe
- photodynamic therapy
- high resolution
- fluorescence imaging
- sensitive detection
- drug release
- high fat diet induced
- single molecule
- protein protein
- stem cells
- quantum dots
- gold nanoparticles
- molecular dynamics
- silver nanoparticles
- label free
- amino acid
- adipose tissue
- pseudomonas aeruginosa
- cystic fibrosis
- metabolic syndrome
- small molecule
- monte carlo