Polyurethane (PU) scaffolds prepared by solvent casting/particulate leaching (SCPL) combined with centrifugation

This article reports an enhanced solvent casting/particulate (salt) leaching (SCPL) method developed for preparing three-dimensional porous polyurethane (PU) scaffolds for cardiac tissue engineering. The solvent for the preparation of the PU scaffolds was a mixture of dimethylformamide (DFM) and tetrahydrofuran (THF). The enhanced method involved the combination of a conventional SCPL method and a step of centrifugation, with the centrifugation being employed to improve the pore uniformity and the pore interconnectivity of scaffolds. Highly porous three-dimensional scaffolds with a well interconnected porous structure could be achieved at the polymer solution concentration of up to 20% by air or vacuum drying to remove the solvent. When the salt particle sizes of 212-295, 295-425, or 425-531 µm and a 15% w/v polymer solution concentration were used, the porosity of the scaffolds was between 83-92% and the compression moduli of the scaffolds were between 13 kPa and 28 kPa. Type I collagen acidic solution was introduced into the pores of a PU scaffold to coat the collagen onto the pore walls throughout the whole PU scaffold. The human aortic endothelial cells (HAECs) cultured in the collagen-coated PU scaffold for 2 weeks were observed by scanning electron microscopy (SEM). It was shown that the enhanced SCPL method and the collagen coating resulted in a spatially uniform distribution of cells throughout the collagen-coated PU scaffold.

[1]  N. Kotov,et al.  Three-dimensional cell culture matrices: state of the art. , 2008, Tissue engineering. Part B, Reviews.

[2]  K. Woodhouse,et al.  Polyurethane films seeded with embryonic stem cell-derived cardiomyocytes for use in cardiac tissue engineering applications. , 2005, Biomaterials.

[3]  Jan Feijen,et al.  Preparation of interconnected highly porous polymeric structures by a replication and freeze-drying process. , 2003, Journal of biomedical materials research. Part B, Applied biomaterials.

[4]  N. Hasırcı,et al.  Polyurethanes in biomedical applications. , 2004, Advances in experimental medicine and biology.

[5]  Anthony P. Hollander,et al.  Biopolymer methods in tissue engineering , 2003 .

[6]  R. Misra,et al.  Biomaterials , 2008 .

[7]  S. Gogolewski,et al.  Biodegradable porous polyurethane scaffolds for tissue repair and regeneration. , 2006, Journal of biomedical materials research. Part A.

[8]  P. E. McHugh,et al.  Bioreactors for Cardiovascular Cell and Tissue Growth: A Review , 2003, Annals of Biomedical Engineering.

[9]  Peter X Ma,et al.  Biomimetic materials for tissue engineering. , 2008, Advanced drug delivery reviews.

[10]  P. Zammaretti,et al.  Cardiac tissue engineering: regeneration of the wounded heart. , 2004, Current opinion in biotechnology.

[11]  Jia-cong Shen,et al.  Cartilage tissue engineering PLLA scaffold with surface immobilized collagen and basic fibroblast growth factor. , 2005, Biomaterials.

[12]  M. Sefton,et al.  Tissue engineering. , 1998, Journal of cutaneous medicine and surgery.

[13]  Jan Feijen,et al.  Porous polymeric structures for tissue engineering prepared by a coagulation, compression moulding and salt leaching technique. , 2003, Biomaterials.

[14]  David J Mooney,et al.  Salt fusion: an approach to improve pore interconnectivity within tissue engineering scaffolds. , 2002, Tissue engineering.

[15]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[16]  Junzo Tanaka,et al.  Culturing of skin fibroblasts in a thin PLGA-collagen hybrid mesh. , 2005, Biomaterials.

[17]  D. Hutmacher,et al.  Scaffolds in tissue engineering bone and cartilage. , 2000, Biomaterials.

[18]  A. Mak,et al.  Transfer of collagen coating from porogen to scaffold: Collagen coating within poly(dl-lactic-co-glycolic acid) scaffold , 2007 .

[19]  A. Pennings,et al.  Preparation of a polyurethane scaffold for tissue engineering made by a combination of salt leaching and freeze-drying of dioxane , 2006 .