Rapid synthesis of highly luminescent and stable Au sub(20) nanoclusters for active tumor-targeted imaging in vitroand in vivo

Rapid synthesis of protein-stabilized Au sub(20) nanoclusters (Au sub(20)NCs) with high fluorescence quantum yield (QY) up to similar to 15% is successfully achieved by manipulating the reaction kinetics. The as-obtained Au sub(20)NCs, identified by mass spectrometry, have an average size of 2.6 nm,...

Full description

Saved in:
Bibliographic Details
Published inNanoscale Vol. 6; no. 4; pp. 2261 - 2269
Main Authors Zhang, Pu, Yang, Xiao Xi, Wang, Yi, Zhao, Ning Wei, Xiong, Zu Hong, Huang, Cheng Zhi
Format Journal Article
LanguageEnglish
Published 01.01.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Rapid synthesis of protein-stabilized Au sub(20) nanoclusters (Au sub(20)NCs) with high fluorescence quantum yield (QY) up to similar to 15% is successfully achieved by manipulating the reaction kinetics. The as-obtained Au sub(20)NCs, identified by mass spectrometry, have an average size of 2.6 nm, with strong fluorescence emission at 620 nm (2.00 eV) upon excitation at either 370 nm (3.35 eV) or 470 nm (2.64 eV). The advantages of the as-obtained Au sub(20)NCs, including small sizes, high fluorescence QY, excellent photostability, non-toxicity, and good stability in biological media, make them ideal candidates as good luminescent probes for optical imaging in vitroand in vivo. Our results demonstrate that the uptake of Au sub(20)NCs by both cancer cells and tumor-bearing nude mice can be improved by receptor-mediated internalization, compared with that by passive targeting. Because of their selective accumulation at the tumor sites, the Au sub(20)NC probes can be used as potential indicators for cancer diagnosis. This work not only provides a new understanding of the rapid synthesis of highly luminescent Au sub(20)NCs but also demonstrates that the functionalized-Au sub(20)NCs are excellent probes for active tumor-targeted imaging in vitroand in vivo.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Feature-1
ISSN:2040-3364
2040-3372
DOI:10.1039/c3nr05269a