journal article·2015

Amorphous carbon dots with high two-photon fluorescence for cellular imaging passivated by hyperbranched poly(amino amine)

Gangsheng Tong, Jingxia Wang, Ruibin Wang, Xinqiu Guo, Lin He, Feng Qiu, Ge Wang, Bangshang Zhu, Xinyuan Zhu, Tao Liu

Publisher page

Abstract

Amorphous carbon dots (C-Dots) with high two-photon fluorescence were prepared by using citric acid (CA) as the carbon source and hyperbranched poly(amino amine) (HPAA) as the surface passivation agent through a facile hydrothermal approach. The C-Dots with an average diameter about 10 nm were readily dispersed in water. They exhibited excellent fluorescence properties and excitation-dependent fluorescence behavior with the corresponding quantum yield (QY) of 17.1% in aqueous solution. Interestingly, the C-Dots emitted bright fluorescence even in the solid state with a QY of 16.3%, which is the highest value obtained for carbon-based nanomaterials. Using the MTT assay, the C-Dots showed low cytotoxicity against L929 normal cells. Furthermore, they were easily internalized by HeLa cells and presented high quality one- and two-photon cellular imaging, suggesting significant potential for application in biological imaging.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Quantum Dots Synthesis And Properties · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Instrumental Analysis Center

Shanghai Jiao Tong University

Shanghai 200240

P. R. China

UNILAB Research Center of Chemical Reaction Engineering

State Key Laboratory of Chemical Reaction Engineering

East China University of Science and Technology

Shanghai 200237

School of Chemistry and Chemical Engineering

State Key Laboratory of Metal Matrix Composites

Funding

National Natural Science Foundation of China

References (34)

Show source-provided references
1. Xu · J. Am. Chem. Soc. · 2004 · 126 · 1273610.1021/ja040082h ↗
2. Sun · J. Am. Chem. Soc. · 2006 · 128 · 775610.1021/ja062677d ↗
3. Li · Angew. Chem., Int. Ed. · 2010 · 49 · 443010.1002/anie.200906154 ↗
4. Luo · J. Mater. Chem. B · 2013 · 1 · 211610.1039/c3tb00018d ↗
5. Wang · J. Mater. Chem. B · 2014 · 2 · 4610.1039/C3TB21370F ↗
6. Guo · Chem. Commun. · 2012 · 48 · 269210.1039/c2cc17769b ↗
7. Rahy · Carbon · 2012 · 50 · 129810.1016/j.carbon.2011.10.052 ↗
8. Hu · Chem. – Asian J. · 2013 · 8 · 103510.1002/asia.201300076 ↗
9. Liu · Angew. Chem., Int. Ed. · 2007 · 46 · 647310.1002/anie.200701271 ↗
10. Li · Carbon · 2011 · 49 · 60510.1016/j.carbon.2010.10.004 ↗
11. Tang · ACS Nano · 2012 · 6 · 510210.1021/nn300760g ↗
12. Zhu · Chem. Commun. · 2009 · 511810.1039/b907612c ↗
13. Wang · Analyst · 2012 · 137 · 539210.1039/c2an36059d ↗
14. Cao · J. Am. Chem. Soc. · 2007 · 129 · 1131810.1021/ja073527l ↗
15. Kong · Adv. Mater. · 2012 · 24 · 584410.1002/adma.201202599 ↗
16. Liu · Nano Lett. · 2013 · 13 · 243610.1021/nl400368v ↗
17. Fan · Carbon · 2014 · 71 · 8710.1016/j.carbon.2014.01.016 ↗
18. Han · Colloids Surf., B · 2012 · 100 · 20910.1016/j.colsurfb.2012.05.016 ↗
19. Zhu · Angew. Chem. · 2013 · 125 · 404510.1002/ange.201300519 ↗
20. Xie · Adv. Mater. · 2012 · 24 · 171610.1002/adma.201104962 ↗
21. Zhang · Chem. Commun. · 2012 · 48 · 1043110.1039/c2cc35966a ↗
22. Wang · Chem. Commun. · 2011 · 47 · 350210.1039/c0cc05391k ↗
23. Wang · Nanoscale · 2014 · 6 · 381810.1039/c3nr05869g ↗
24. Deng · Nanoscale · 2014 · 6 · 1038810.1039/C4NR02544J ↗
25. Zhang · ACS Nano · 2013 · 7 · 1123410.1021/nn405017q ↗
26. Wang · Biomacromolecules · 2010 · 11 · 48910.1021/bm901215s ↗
27. Kawamura · Jpn. J. Appl. Phys., Part 2 · 2004 · 43 · 772910.1143/JJAP.43.7729 ↗
28. Krysmann · J. Am. Chem. Soc. · 2012 · 134 · 74710.1021/ja204661r ↗
29. Zhu · Chem. Commun. · 2012 · 48 · 936710.1039/c2cc33844k ↗
30. H. F. Shurvell , Spectra-Structure Correlations in the Mid- and Far-Infrared, Handbook of Vibrational Spectroscopy, John Wiley & Sons Press, 2006
31. Mudunkotuwa · J. Am. Chem. Soc. · 2010 · 132 · 1498610.1021/ja106091q ↗
32. Song · RSC Adv. · 2014 · 2014 · 2718410.1039/c3ra47994c ↗
33. Resch-Genger · Nat. Methods · 2008 · 5 · 76310.1038/nmeth.1248 ↗
34. Sahu · Chem. Commun. · 2012 · 48 · 883510.1039/c2cc33796g ↗