Novel polyurethanes with interconnected porous structure induce in vivo tissue remodeling and accompanied vascularization

• Published in: Journal of biomedical materials research. Part A 2010-10, Vol.95A (1), p.198-208
• Main Authors: Jovanovic, D., Engels, G. E., Plantinga, J. A., Bruinsma, M., van Oeveren, W., Schouten, A. J., van Luyn, M. J. A., Harmsen, M. C.
• Format: Article
• Language: English
• Subjects: Animals; biocompatibility; Biological and medical sciences; Cell Death - drug effects; Crystallization; degradation; Endotoxins - metabolism; Male; Materials Testing; Medical sciences; Microscopy, Electron, Scanning; Neovascularization, Physiologic - drug effects; polyurethanes; Polyurethanes - chemical synthesis; Polyurethanes - chemistry; Polyurethanes - pharmacology; Porosity - drug effects; Prosthesis Implantation; Rats; Rats, Wistar; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases; Sus scrofa; Technology. Biomaterials. Equipments; Tissue Engineering - methods; tissue remodeling; γ-butyrolactone
• ISSN: 1549-3296; 1552-4965; 1552-4965
• DOI: 10.1002/jbm.a.32817

Tissue engineering and regenerative medicine have furnished a vast range of modalities to treat either damaged tissue or loss of soft tissue or its function. In most approaches, a temporary porous scaffold is required to support tissue regeneration. The scaffold should be designed such that the turnover synchronizes with tissue remodeling and regeneration at the implant site. Segmented polyester urethanes (PUs) used in this study were based on ε‐caprolactone (CL) and co‐monomers D,L‐lactide (D,L‐L) and γ‐butyrolactone (BL), and 1,4‐butanediisocyanate (BDI). In vitro, the PUs were nontoxic and haemocompatible. To test in vivo biocompatibility, the PUs were further processed into porous structures and subcutaneously implanted in rats for a period up to 21 days. Tissue remodeling and scaffold turnover was associated with a mild tissue response. The tissue response was characterized by extensive vascularization through the interconnected pores, with low numbers of macrophages on the edges and stroma formation inside the pores of the implants. The tissue ingrowth appeared to be related to the extent of microphase separation of the PUs and foam morphology. By day 21, all of the PU implants were highly vascularized, confirming the pores were interconnected. Degradation of P(CL/D,L‐L)‐PU was observed at this time, whereas the other two PU types remained intact. The robust method reported here of manufacturing and processing, good mechanical properties, and in vivo tissue response of the porous P(CL/D,L‐L)‐PU and PBCL‐PU makes them excellent candidates as biomaterials with an application for soft tissue remodeling, for example, for cardiovascular regeneration. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.