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Blue-Emissive Upconversion Nanoparticles for Low-Power-Excited Bioimaging in Vivo

Liu, Qian, Yang, Tianshe, Feng, Wei, Li, Fuyou·2012·Journal of the American Chemical Society

Abstract

Water-soluble upconversion luminescent (UCL) nanoparticles based on triplet-triplet annihilation (TTA) were successfully prepared by coloading sensitizer (octaethylporphyrin Pd complex) and annihilator (9,10-diphenylanthracene) into silica nanoparticles. The upconversion luminescence quantum yield of the nanoparticles can be as high as 4.5% in aqueous solution. As determined by continuous kinetic scan, the nanoparticles have excellent photostability. Such TTA-based upconversion nanoparticles show low cytotoxicity and were successfully used to label living cells with very high signal-to-noise ratio. UCL imaging with the nanoparticles as probe is capable of completely eliminating background fluorescence from either endogenous fluorophores of biological sample or the colabeled fluorescent probe. In particular, such blue-emissive upconversion nanoparticles were successfully applied in lymph node imaging in vivo of living mouse with excellent signal-to-noise ratio (>25), upon low-power density excitation of continuous-wave 532 laser (8.5 mW cm(-2)). Such high-contrast and low-power excited bioimaging in vivo with a blue-emissive upconversion nanoparticle as probe may extend the arsenal of currently available luminescent bioimaging in vitro and in vivo.

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Metadata

Authors
Liu, Q., Yang, T., Feng, W., & Li, F.
Venue
Journal of the American Chemical Society
Published
2012-03-09
Volume
134
Issue
11
Pages
5390-5397
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2317180730
Cited by
437
References
0
FWCI
22.88
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Blue-Emissive Upconversion Nanoparticles for Low-Power-Excited Bioimaging in Vivo. https://app.cochat.ai/papers/10.1021/ja3003638
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Liu, Q., Yang, T., Feng, W., & Li, F. (2012). Blue-Emissive Upconversion Nanoparticles for Low-Power-Excited Bioimaging in Vivo. Journal of the American Chemical Society. https://doi.org/10.1021/ja3003638

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