| Literature DB >> 33175432 |
Qianxi Dang1, Yuyan Jiang2, Jinfeng Wang1, Jiaqiang Wang3, Qunhua Zhang1, Mingkang Zhang1, Simeng Luo1, Yujun Xie3, Kanyi Pu2,4, Qianqian Li1, Zhen Li1,3.
Abstract
Afterglow imaging that detects photons after cessation of optical excitation avoids tissue autofluorescence and thus possesses higher sensitivity than traditional fluorescence imaging. Purely organic molecules with room-temperature phosphorescence (RTP) have emerged as a new library of benign afterglow agents. However, most RTP luminogens only emit visible light with shallow tissue penetration, constraining their in vivo applications. This study presents an organic RTP nanoprobe (mTPA-N) with emission in the NIR range for in vivo afterglow imaging. Such a probe is composed of RTP molecule (mTPA) as the phosphorescent generator and an NIR-fluorescent dye as the energy acceptor to enable room-temperature phosphorescence resonance energy transfer (RT-PRET), ultimately resulting in redshifted phosphorescent emission at 780 nm. Because of the elimination of background noise and redshifted afterglow luminescence in a biologically transparent window, mTPA-N permits imaging of lymph nodes in living mice with a high signal-to-noise ratio. This study thus opens up a universal approach to develop organic RTP luminogens into NIR afterglow imaging agents via construction of RT-PRET.Entities:
Keywords: in vivo imaging; near-infrared afterglow; phosphorescence resonance energy transfer; room-temperature phosphorescence
Year: 2020 PMID: 33175432 DOI: 10.1002/adma.202006752
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849