Ultrabright red AIEgens for two-photon vascular imaging with high resolution and deep penetration.

Chem Sci

Department of Chemistry , Hong Kong Branch of Chinese National Engineering Research Centre for Tissue Restoration and Reconstruction , Institute for Advanced Study , Division of Biomedical Engineering , State Key Laboratory of Molecular Neuroscience and Division of Life Science , Hong Kong University of Science and Technology, Clear Water Bay , Kowloon , Hong Kong . Email:

Published: March 2018

Reported here is a successful strategy for the design of ultrabright red luminogens with aggregation-induced emission (AIE) features, donor-acceptor structures, and intense charge transfer effects. These luminogens show no aggregation caused emission quenching in the solid state and have high quantum efficiency. They can be fabricated into AIE dots by a simple nanoprecipitation procedure. The AIE dots exhibit high brightness, a large Stokes shift, good biocompatibility, satisfactory photostability, and a high two-photon absorption cross section. The AIE dots can be utilized as highly efficient fluorescent probes for deep-tissue imaging by a two-photon technique, which outperforms the one-photon technique under the same experimental conditions, in terms of penetration depth and image contrast. This is the first report of using highly emissive AIE dots for the accurate measurement of capillary diameters in mouse ears. Such a strategy sheds light on the development of efficient solid state red/NIR emitters for biological applications.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914133PMC
http://dx.doi.org/10.1039/c7sc04820cDOI Listing

Publication Analysis

Top Keywords

aie dots
16
ultrabright red
8
solid state
8
aie
5
red aiegens
4
aiegens two-photon
4
two-photon vascular
4
vascular imaging
4
high
4
imaging high
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!