Protein polymer hydrogels: Effects of endotoxin on biocompatibility

Author:

Beenken-Rothkopf Liese N1,Karfeld-Sulzer Lindsay S1,Zhang Xiaomin2,Kissler Hermann2,Michie Sara A3,Kaufman Dixon B42,Fontaine Magali J35,Barron Annelise E146

Affiliation:

1. Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA

2. Institute of BioNanotechnology in Medicine, Northwestern University, Chicago, IL, USA

3. Department of Surgery, Division of Organ Transplantation, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA

4. Department of Pathology, Stanford School of Medicine, Stanford University, Stanford, CA, USA

5. Stanford Blood Center, Stanford School of Medicine, Stanford University, Palo Alto, CA, USA

6. Department of Bioengineering, Stanford University, Stanford, CA, USA

Abstract

Protein polymer-based hydrogels have shown potential for tissue engineering applications, but require biocompatibility testing for in vivo use. Enzymatically crosslinked protein polymer-based hydrogels were tested in vitro and in vivo to evaluate their biocompatibility. Endotoxins present in the hydrogel were removed by Trition X-114 phase separation. The reduction of endotoxins decreased TNF-α production by a macrophage cell line in vitro; however, significant inflammatory response was still present compared to collagen control gels. A branched PEG molecule and dexamethasone were added to the hydrogel to reduce the response. In vitro testing showed a decrease in the TNF-α levels with the addition of dexamethasone. In vivo implantations into the epididymal fat pad of C57/BL6 mice, however, indicated a decreased inflammatory mediated immune response with a hydrogel treated with both PEGylation and endotoxin reduction. This study demonstrates the importance of endotoxin testing and removal in determining the biocompatibility of biomaterials.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials

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