journal article·2013-08-27

Water-Soluble Fluorinated and PEGylated Cyanostilbene Derivative: An Amphiphilic Building Block Forming Self-Assembled Organic Nanorods with Enhanced Fluorescence Emission

Seunghoon Shin, Se Hoon Gihm, Chong Rae Park, Sehoon Kim, Soo Young Park

Chemistry of Materials· Volume 25· Issue 16
Publisher page

Abstract

We report synthesis and optical/structural characterization of new fluorescent rod–coil amphiphiles based on the PEGylated α-cyanostilbene skeleton (12EO-CNMBE and 12EO-CNTFMBE) and their self-assembly behaviors in water. Distinct from the common amphiphilic behavior of nonfluorinated 12EO-CNMBE forming spherical nanostructures, fluorinated 12EO-CNTFMBE has proven to be the first example of a molecular building block that can self-assemble in water into small-dimension, small-aspect-ratio organic nanorods with aggregation-induced enhanced emission (AIEE). The robust structural integrity and hydrophobic/π-conjugated nature of the fluorinated block assembly, as well as the antifouling coating by the hydrophilic PEG block, enabled stable encapsulation of a model drug (Nile Red) within the self-assembled nanorod structure and its successful delivery through membrane filters. By virtue of these advantageous attributes along with high intracellular uptake efficiency, the 12EO-CNTFMBE nanorods manifested potential as a self-signaling fluorescent nanocarrier for the intracellular delivery of hydrophobic cargos.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Supramolecular Self-Assembly in Materials · Supramolecular Chemistry and Complexes

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

Affiliations

Center for Supramolecular Optoelectronic Materials, WCU Hybrid Materials Program, Department of Materials Science and Engineering, Seoul National University, Seoul 151-744, Korea

Center for Theragnosis, Korea Institute of Science and Technology, 39-1 Hawolgok-dong, Seongbuk-gu, Seoul 136-791, Korea

Carbon Nanomaterials Design Laboratory, Global Research Laboratory, Research Institute of Advanced Materials, and Department of Materials Science and Engineering, Seoul National University, Seoul 151-744, Korea

References (33)

Show source-provided references
1. Bae Y. · Angew. Chem., Int. Ed. · 2003 · 42 · 464010.1002/anie.200250653 ↗
2. Esfand R. · Drug. Discovery Today · 2001 · 6 · 42710.1016/S1359-6446(01)01757-3 ↗
3. Hirst A. R. · Angew. Chem., Int. Ed. · 2008 · 47 · 800210.1002/anie.200800022 ↗
4. Lim Y. B. · Chem. Soc. Rev. · 2009 · 38 · 92510.1039/b809741k ↗
5. Lee M. · Chem. Rev. · 2001 · 101 · 386910.1021/cr0001131 ↗
6. Ryu J. H. · J. Am. Chem. Soc. · 2004 · 126 · 355110.1021/ja039793q ↗
7. Ryu J. H. · Chem. Commun. · 2008 · 104310.1039/B713737K ↗
8. Parthasarathy R. V. · Chem. Mater. · 1994 · 6 · 162710.1021/cm00046a011 ↗
9. Ikkala O. · Science · 2002 · 295 · 240710.1126/science.1067794 ↗
10. Xia Y. N. · Adv. Mater. · 2003 · 15 · 35310.1002/adma.200390087 ↗
11. Murphy C. J. · Adv. Mater. · 2002 · 14 · 8010.1002/1521-4095(20020104)14:1<80::AID-ADMA80>3.0.CO;2-# ↗
12. Zhao N. N. · Angew. Chem., Int. Ed. · 2011 · 50 · 460610.1002/anie.201004915 ↗
13. Casavola M. · Nano Lett. · 2007 · 7 · 138610.1021/nl070550w ↗
14. Hong J. P. · Chem. Commun. · 2009 · 31010.1039/B816030A ↗
15. Lee S. W. · Nano Lett. · 2010 · 10 · 34710.1021/nl903722z ↗
16. Zorn M. · Macromol. Rapid Commun. · 2008 · 29 · 92210.1002/marc.200800165 ↗
17. Sanyal A. · J. Mater. Chem. · 2009 · 19 · 897410.1039/b913476j ↗
18. Geng Y. · Nat. Nanotechnol. · 2007 · 2 · 24910.1038/nnano.2007.70 ↗
19. An B. K. · J. Am. Chem. Soc. · 2004 · 126 · 1023210.1021/ja046215g ↗
20. An B. K. · J. Am. Chem. Soc. · 2002 · 124 · 1441010.1021/ja0269082 ↗
21. An B. K. · J. Am. Chem. Soc. · 2009 · 131 · 395010.1021/ja806162h ↗
22. Hirose T. · Chem. Commun. · 2009 · 583210.1039/b910531j ↗
23. Pichler K. · J. Phys.: Condens. Matter · 1993 · 5 · 7155
24. Bassler H. · Acc. Chem. Res. · 1999 · 32 · 17310.1021/ar960228k ↗
25. Kasha M. · Pure Appl. Chem. · 1965 · 11 · 37110.1351/pac196511030371 ↗
26. Kitazume T. · 1998
27. Spano F. C. · Chem. Phys. Lett. · 2000 · 331 · 710.1016/S0009-2614(00)01153-2 ↗
28. Mandal A. K. · Chem. Phys. · 2000 · 253 · 11510.1016/S0301-0104(99)00370-5 ↗
29. Spano F. C. · J. Chem. Phys. · 2010 · 132 · 09470410.1063/1.3310810 ↗
30. Lee M. · Macromolecules · 1996 · 29 · 556710.1021/ma951418y ↗
31. Würthner F. · Angew. Chem., Int. Ed. · 2011 · 50 · 337610.1002/anie.201002307 ↗
32. Qiu Y. · Adv. Drug Delivery Rev. · 2001 · 53 · 32110.1016/S0169-409X(01)00203-4 ↗
33. Haugland R. P. · 2002