Issue 35, 2011

In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel viaenzyme-mediated reaction for tissue regenerative medicine

Abstract

An in situ cross-linkable gelatin–poly(ethylene glycol)–tyramine (GPT) hydrogel was developed as a novel injectable material for tissue regenerative medicine. The hydrogel was formed rapidly using horseradish peroxidase (HRP) and hydrogen peroxide (H2O2). The gelation times could be controlled from five seconds to over one minute by changing the HRP concentration, and the mechanical properties could be controlled by varying the H2O2 concentration. The storage moduli of the hydrogels ranged from approximately 200 to over 8000 Pa. In addition, an in vitrocell attachment study was carried out using various cell types. The results of this study demonstrated that the GPT hydrogel, formed in situ via an enzyme-mediated reaction, was an excellent bioactive matrix for cellular behavior. Furthermore, an in vitro 3D cell study was made using the GPT hydrogels formed with different mechanical strengths, and in vivo subcutaneous injection was carried out. The in vitro and in vivo studies demonstrated that the GPT hydrogels had excellent bioactivities, and that the cellular behavior in the hydrogel matrix could be controlled. The obtained results showed that these in situ forming GPT hydrogels, with excellent bioactivities and tunable physicochemical properties, have great potential for use as injectable materials in tissue regenerative medicine and various biomedical applications.

Graphical abstract: In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel viaenzyme-mediated reaction for tissue regenerative medicine

Article information

Article type
Paper
Submitted
03 Jun 2011
Accepted
02 Jul 2011
First published
29 Jul 2011

J. Mater. Chem., 2011,21, 13180-13187

In situ cross-linkable gelatin–poly(ethylene glycol)–tyramine hydrogel viaenzyme-mediated reaction for tissue regenerative medicine

K. M. Park, K. S. Ko, Y. K. Joung, H. Shin and K. D. Park, J. Mater. Chem., 2011, 21, 13180 DOI: 10.1039/C1JM12527C

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