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Room‐Temperature Phosphorescence Resonance Energy Transfer for Construction of Near‐Infrared Afterglow Imaging Agents

Qianxi DangSauvage Center for Molecular Sciences Department of Chemistry Wuhan University Wuhan 430072 ChinaYuyan JiangSchool of Chemical and Biomedical Engineering Nanyang Technological University Singapore 637457 SingaporeJinfeng WangInstitute of Molecular Aggregation Science Tianjin University Tianjin 300072 ChinaJiaqiang WangInstitute of Molecular Aggregation Science Tianjin University Tianjin 300072 ChinaQunhua ZhangSauvage Center for Molecular Sciences Department of Chemistry Wuhan University Wuhan 430072 ChinaMingkang ZhangSauvage Center for Molecular Sciences Department of Chemistry Wuhan University Wuhan 430072 ChinaSimeng LuoSauvage Center for Molecular Sciences Department of Chemistry Wuhan University Wuhan 430072 ChinaYujun XieInstitute of Molecular Aggregation Science Tianjin University Tianjin 300072 ChinaKanyi PuDivision of Chemistry and Biological Chemistry School of Physical and Mathematical Sciences Nanyang Technological University Singapore 637371 SingaporeQianqian LiSauvage Center for Molecular Sciences Department of Chemistry Wuhan University Wuhan 430072 ChinaZhen LiInstitute of Molecular Aggregation Science Tianjin University Tianjin 300072 China
2020en
ABI

Annotatsiya

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.

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