journal article·2012-04-24

In Situ Supramolecular Assembly and Modular Modification of Hyaluronic Acid Hydrogels for 3D Cellular Engineering

Kyeng Min Park, Jeong-A Yang, Hyuntae Jung, Junseok Yeom, Ji Sun Park, Keun-Hong Park, Allan S. Hoffman, Sei Kwang Hahn, Kimoon Kim

ACS Nano· Volume 6· Issue 4
Publisher page

Abstract

A facile in situ supramolecular assembly and modular modification of biocompatible hydrogels were demonstrated using cucurbit[6]uril-conjugated hyaluronic acid (CB[6]-HA), diaminohexane-conjugated HA (DAH-HA), and tags-CB[6] for cellular engineering applications. The strong and selective host-guest interaction between CB[6] and DAH made possible the supramolecular assembly of CB[6]/DAH-HA hydrogels in the presence of cells. Then, the 3D environment of CB[6]/DAH-HA hydrogels was modularly modified by the simple treatment with various multifunctional tags-CB[6]. Furthermore, we could confirm in situ formation of CB[6]/DAH-HA hydrogels under the skin of nude mice by sequential subcutaneous injections of CB[6]-HA and DAH-HA solutions. The fluorescence of modularly modified fluorescein isothiocyanate (FITC)-CB[6] in the hydrogels was maintained for up to 11 days, reflecting the feasibility to deliver the proper cues for cellular proliferation and differentiation in the body. Taken together, CB[6]/DAH-HA hydrogels might be successfully exploited as a 3D artificial extracellular matrix for various tissue engineering applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Hydrogels: synthesis, properties, applications · Advanced Materials and Mechanics

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

Affiliations

Department of Biomedical Science, College of Life Science, CHA University, 606-16, Yeoksam 1-dong, Kangnam-gu, Seoul, 135-081, Korea

Department of Bioengineering, University of Washington, Box 351720, Seattle, Washington 98195, United States

References (31)

Show source-provided references
1. Friedl P. · Cell. Mol. Life Sci. · 2000 · 57 · 4110.1007/s000180050498 ↗
2. Hoffman A. S. · Adv. Drug Delivery Rev. · 2002 · 54 · 310.1016/S0169-409X(01)00239-3 ↗
3. Lutolf M. P. · Nat. Biotechnol. · 2005 · 23 · 4710.1038/nbt1055 ↗
4. Kiyonaka S. · Nat. Mater. · 2004 · 3 · 5810.1038/nmat1034 ↗
5. DeForest C. A. · Nat. Mater. · 2009 · 8 · 65910.1038/nmat2473 ↗
6. Ruel-Gariepy E · Eur. J. Pharm. Biopharm. · 2004 · 58 · 40910.1016/j.ejpb.2004.03.019 ↗
7. Chiu Y. L. · Biomaterials · 2009 · 30 · 487710.1016/j.biomaterials.2009.05.052 ↗
8. Obara K. · Biomaterials · 2003 · 24 · 343710.1016/S0142-9612(03)00220-5 ↗
9. Wu D. Q. · Langmuir · 2008 · 24 · 1030610.1021/la8006876 ↗
10. Pek Y. S. · Nat. Nanotechnol. · 2008 · 3 · 67110.1038/nnano.2008.270 ↗
11. Appel E. A. · J. Am. Chem. Soc. · 2010 · 132 · 1425110.1021/ja106362w ↗
12. Salem A. K. · Adv. Mater. · 2003 · 15 · 21010.1002/adma.200390047 ↗
13. Ehrbar M. · Nat. Mater. · 2008 · 7 · 80010.1038/nmat2250 ↗
14. Kretschmann O. · Angew. Chem., Int. Ed. · 2006 · 45 · 436110.1002/anie.200504539 ↗
15. Okumura Y. · Adv. Mater. · 2001 · 13 · 48510.1002/1521-4095(200104)13:7<485::AID-ADMA485>3.0.CO;2-T ↗
16. Huh K. M. · Macromolecules · 2001 · 34 · 865710.1021/ma0106649 ↗
17. Koopmans C. · Macromolecules · 2008 · 41 · 741810.1021/ma801202f ↗
18. Mock W. L. · Top. Curr. Chem. · 1995 · 175 · 110.1007/3-540-58800-0_16 ↗
19. Kim K. · Chem. Soc. Rev. · 2002 · 31 · 9610.1039/a900939f ↗
20. Kim Y. · Chem.—Eur. J. · 2009 · 15 · 614310.1002/chem.200900305 ↗
21. Park K. M. · Chem. Commun. · 2009 · 1 · 7110.1039/B815009E ↗
22. Park K. M. · Small · 2010 · 6 · 143010.1002/smll.201000293 ↗
23. Kim D. · Angew. Chem., Int. Ed. · 2007 · 46 · 347110.1002/anie.200604526 ↗
24. Lapcik L. · Chem. Rev. · 1998 · 98 · 266310.1021/cr941199z ↗
25. Killops K. L. · J. Am. Chem. Soc. · 2008 · 130 · 506210.1021/ja8006325 ↗
26. Oh E. J. · J. Controlled Release · 2010 · 141 · 210.1016/j.jconrel.2009.09.010 ↗
27. Kim K. · Chem. Soc. Rev. · 2007 · 36 · 26710.1039/B603088M ↗
28. Jung H. · Biomaterials · 2011 · 32 · 768710.1016/j.biomaterials.2011.06.060 ↗
29. Lutolf M. P. · Proc. Natl. Acad. Sci. U.S.A. · 2003 · 100 · 541310.1073/pnas.0737381100 ↗
30. Csoka A. B. · Matrix Biol. · 2001 · 20 · 49910.1016/S0945-053X(01)00172-X ↗
31. Pierschbacher M. D. · J. Biol. Chem. · 1987 · 262 · 1729410.1016/S0021-9258(18)45376-8 ↗