## Abstract Peptide activated poly(ethylene glycol) (PEG)‐based hydrogels have received wide attention as material for tissue engineering application. However, the close structure of these materials may pose severe barriers to tissue invasion and nutrient transport. The aim of this work was to synt
Biodegradable poly(ethylene glycol) hydrogels crosslinked with genipin for tissue engineering applications
✍ Scribed by Moffat, Kristen L. ;Marra, Kacey G.
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 324 KB
- Volume
- 71B
- Category
- Article
- ISSN
- 0021-9304
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✦ Synopsis
Abstract
In this study amino‐terminated poly(ethylene glycol) (PEG‐diamine) hydrogels were crosslinked with genipin, a chemical naturally derived from the gardenia fruit. Dissolution, swelling, and PEG–genipin release properties were determined. The dissolution studies indicated that the hydrogels are water soluble, and that the dissolution rate was concentration, mass, and temperature dependent. The dissolution rates are easily tailored from 3 min to >100 days. The PEG–genipin release study indicated that the greatest release occurs within the first 24 h of immersion in water, and that incubation at 37 °C elicits a greater initial release than samples incubated at room temperature for all genipin concentrations. Through scanning electron microscopy it was observed that the hydrogels are porous, and surface morphology changes before and after swelling. Furthermore, smooth muscle cell (SMC) adhesion studies indicated that the PEG–genipin hydrogel is a suitable substrate for SMC seeding. Overall, the results of these studies indicate that PEG–genipin hydrogels may provide potential scaffolding for a variety of tissue engineering applications. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 71B: 181–187, 2004
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