The degradation of poly(propylene fumarate-coethylene glycol) hydrogels was examined in vitro in phosphate-buffered saline at pH 7.4 and in vivo in a subcutaneous rat model. These hydrogels have potential application as biodegradable, injectable cardiovascular stents, and, as such, their mass loss,
Characterization of the in vitro macrophage response and in vivo host response to poly(ethylene glycol)-based hydrogels
β Scribed by Aaron D. Lynn; Themis R. Kyriakides; Stephanie J. Bryant
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 482 KB
- Volume
- 9999A
- Category
- Article
- ISSN
- 1549-3296
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β¦ Synopsis
Abstract
Photopolymerizable poly(ethylene glycol) (PEG)β based hydrogels have great potential as in vivo cell delivery vehicles for tissue engineering. However, their success in vivo will be dependent on the host response. The objectives for this study were to explore the in vivo host response and in vitro macrophage response to commonly used PEGβbased hydrogels, PEG and PEG containing RGD. Acellular hydrogels were implanted subcutaneously into c57bl/6 mice and the foreign body response (FBR) was compared to medical grade silicone. Our findings demonstrated PEGβRGD hydrogels resulted in a FBR similar to silicone, while PEGβonly hydrogels resulted in a robust inflammatory reaction characterized by a thick layer of macrophages at the material surface with evidence of gel degradation. In vitro, bone marrowβderived primary macrophages adhered well and similarly to PEGβbased hydrogels, silicone, and tissue culture polystyrene when cultured for 4 days. Significantly higher gene expressions of the proinflammatory cytokines, TNFβΞ± and Ilβ1Ξ², were found in macrophages seeded onto PEG compared to PEGβRGD and silicone at 1 and 2 days. PEG hydrogels were also shown to be susceptible to oxidative biodegradation. Our findings indicate that PEGβonly hydrogels are proinflammatory while RGD attenuates this negative reaction leading to a moderate FBR. Β© 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010
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