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In vivo time-gated fluorescence imaging with biodegradable luminescent porous silicon nanoparticles.


ABSTRACT: Fluorescence imaging is one of the most versatile and widely used visualization methods in biomedical research. However, tissue autofluorescence is a major obstacle confounding interpretation of in vivo fluorescence images. The unusually long emission lifetime (5-13 ?s) of photoluminescent porous silicon nanoparticles can allow the time-gated imaging of tissues in vivo, completely eliminating shorter-lived (<10 ns) emission signals from organic chromophores or tissue autofluorescence. Here using a conventional animal imaging system not optimized for such long-lived excited states, we demonstrate improvement of signal to background contrast ratio by >50-fold in vitro and by >20-fold in vivo when imaging porous silicon nanoparticles. Time-gated imaging of porous silicon nanoparticles accumulated in a human ovarian cancer xenograft following intravenous injection is demonstrated in a live mouse. The potential for multiplexing of images in the time domain by using separate porous silicon nanoparticles engineered with different excited state lifetimes is discussed.

SUBMITTER: Gu L 

PROVIDER: S-EPMC4154512 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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In vivo time-gated fluorescence imaging with biodegradable luminescent porous silicon nanoparticles.

Gu Luo L   Hall David J DJ   Qin Zhengtao Z   Anglin Emily E   Joo Jinmyoung J   Mooney David J DJ   Howell Stephen B SB   Sailor Michael J MJ  

Nature communications 20130101


Fluorescence imaging is one of the most versatile and widely used visualization methods in biomedical research. However, tissue autofluorescence is a major obstacle confounding interpretation of in vivo fluorescence images. The unusually long emission lifetime (5-13 μs) of photoluminescent porous silicon nanoparticles can allow the time-gated imaging of tissues in vivo, completely eliminating shorter-lived (<10 ns) emission signals from organic chromophores or tissue autofluorescence. Here using  ...[more]

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