Rapid synthesis of highly luminescent and stable Au20 nanoclusters for active tumor-targeted imaging in vitro and in vivoElectronic supplementary information (ESI) available: Additional figures and tables. See DOI: 10.1039/c3nr05269a

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

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Main Authors Zhang, Pu, Yang, Xiao Xi, Wang, Yi, Zhao, Ning Wei, Xiong, Zu Hong, Huang, Cheng Zhi
Format Journal Article
LanguageEnglish
Published 30.01.2014
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Abstract Rapid synthesis of protein-stabilized Au 20 nanoclusters (Au 20 NCs) with high fluorescence quantum yield (QY) up to ∼15% is successfully achieved by manipulating the reaction kinetics. The as-obtained Au 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 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 vitro and in vivo . Our results demonstrate that the uptake of Au 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 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 20 NCs but also demonstrates that the functionalized-Au 20 NCs are excellent probes for active tumor-targeted imaging in vitro and in vivo . Receptor-mediated uptake of nanoprobes for tumor-targeting in vitro and in vivo is systematically studied using newly prepared luminescent Au 20 nanoclusters.
AbstractList Rapid synthesis of protein-stabilized Au 20 nanoclusters (Au 20 NCs) with high fluorescence quantum yield (QY) up to ∼15% is successfully achieved by manipulating the reaction kinetics. The as-obtained Au 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 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 vitro and in vivo . Our results demonstrate that the uptake of Au 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 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 20 NCs but also demonstrates that the functionalized-Au 20 NCs are excellent probes for active tumor-targeted imaging in vitro and in vivo . Receptor-mediated uptake of nanoprobes for tumor-targeting in vitro and in vivo is systematically studied using newly prepared luminescent Au 20 nanoclusters.
Author Wang, Yi
Huang, Cheng Zhi
Xiong, Zu Hong
Zhao, Ning Wei
Zhang, Pu
Yang, Xiao Xi
AuthorAffiliation Education Ministry Key Laboratory on Luminescence and Real-Time Analysis
School of Physical Science and Technology
Southwest University
Shimadzu (China) Co
Life Science & Clinical Medicine Department
College of Pharmaceutical Sciences
School of Chemistry and Chemical Engineering
AuthorAffiliation_xml – name: Shimadzu (China) Co
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– name: School of Chemistry and Chemical Engineering
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– name: Life Science & Clinical Medicine Department
– name: Southwest University
– name: Education Ministry Key Laboratory on Luminescence and Real-Time Analysis
Author_xml – sequence: 1
  givenname: Pu
  surname: Zhang
  fullname: Zhang, Pu
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  givenname: Xiao Xi
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  givenname: Yi
  surname: Wang
  fullname: Wang, Yi
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  givenname: Ning Wei
  surname: Zhao
  fullname: Zhao, Ning Wei
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  givenname: Zu Hong
  surname: Xiong
  fullname: Xiong, Zu Hong
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  givenname: Cheng Zhi
  surname: Huang
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Electronic supplementary information (ESI) available: Additional figures and tables. See DOI
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