期刊
NANO LETTERS
卷 19, 期 5, 页码 2985-2992出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.9b00140
关键词
NIR-II imaging; NIR-IIa imaging; bone imaging; rare earth doped nanoparticles; thrombus
类别
资金
- Department of Radiology, Stanford University
- National Key R&D Program of China [2018YFC0910602]
- National Natural Science Foundation of China [61525503, 61620106016, 61835009, 81727804, 61775145]
- Guangdong Natural Science Foundation Innovation Team [2014A030312008]
- China Postdoctoral Science Foundation [2017M622762, 2018T110889]
As a newly noninvasive emerging modality, NIR-II fluorescence imaging (1000-1700 nm) has many advantages over conventional visible and NIR-I imaging (700-900 nm). Unfortunately, only a few NIR-II fluorophores are suitable for bone imaging. Here, we report an NIR-II fluorophore based on DSPE-mPEG encapsulated rare earth doped nanoparticles (RENPs@DSPE-mPEG), which shows inherent affinity to bone without linking any targeting ligands, and thus, it provides an alternative noninvasive and nonradiation strategy for skeletal system mapping and bone disease diagnoses. Interestingly, within the NIR-II window, imaging at a longer wavelength (1345 nm) provides a higher resolution and signal-to-noise ratio than imaging at 1064 nm, even though the quantum yield at 1064 nm is 2-fold higher than that at 1345 nm. Besides bone imaging, RENP5@DSPE-mPEG show an imaging application in blood vessels and lymph nodes. Importantly, RENPs@DSPE-mPEG can be internalized by circulating white blood increase efficient nanoparticle delivery in the fields such as immunotherapy and improve the diagnostic and therapeutic efficacy of cancer-targeted nanoparticles in clinical applications.
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