A generic approach towards afterglow luminescent nanoparticles for ultrasensitive in vivo imaging

Afterglow imaging with long-lasting luminescence after cessation of light excitation provides opportunities for ultrasensitive molecular imaging; however, the lack of biologically compatible afterglow agents has impeded exploitation in clinical settings. This study presents a generic approach to tra...

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Veröffentlicht in:Nature communications 2019-05, Vol.10 (1), p.2064-10, Article 2064
Hauptverfasser: Jiang, Yuyan, Huang, Jiaguo, Zhen, Xu, Zeng, Ziling, Li, Jingchao, Xie, Chen, Miao, Qingqing, Chen, Jie, Chen, Peng, Pu, Kanyi
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Sprache:eng
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Zusammenfassung:Afterglow imaging with long-lasting luminescence after cessation of light excitation provides opportunities for ultrasensitive molecular imaging; however, the lack of biologically compatible afterglow agents has impeded exploitation in clinical settings. This study presents a generic approach to transforming ordinary optical agents (including fluorescent polymers, dyes, and inorganic semiconductors) into afterglow luminescent nanoparticles (ALNPs). This approach integrates a cascade photoreaction into a single-particle entity, enabling ALNPs to chemically store photoenergy and spontaneously decay it in an energy-relay process. Not only can the afterglow profiles of ALNPs be finetuned to afford emission from visible to near-infrared (NIR) region, but also their intensities can be predicted by a mathematical model. The representative NIR ALNPs permit rapid detection of tumors in living mice with a signal-to-background ratio that is more than three orders of magnitude higher than that of NIR fluorescence. The biodegradability of the ALNPs further heightens their potential for ultrasensitive in vivo imaging. Afterglow luminescence is used to reduce background noise and increase sensitivity; however, biocompatible afterglow materials are limited. Here, the authors report on an approach to turn standard optical agents into afterglow nanoparticles and demonstrate the application in tumour imagining in vivo.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-10119-x