Table 1 |
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| Bone tissue engineering applications of polyurethanes | |||
| Animal models | Polyurethane scaffolds | Major conclusions | Reference |
| Iliac crest (sheep) | Porous scaffolds synthesized from HMDI, PEO-PPO-PEO, and PCL at various ratios. Pore size, 300 to 2,000 μm; porosity, 85% | At 18 and 25 months, all the defects in the ilium implanted with polyurethane bone substitutes had healed with new bone. | Gogolewski and Gorna ([2007]), Gogolewski et al. ([2006]) |
| The extent of bone healing depended on the chemical composition of the polymer from which the implant was made. | |||
| The implants from polymers with the incorporated calcium-complexing additive were the most effective promoters of bone healing, followed by those with vitamin D and polysaccharide-containing polymer. | |||
| There was no bone healing in the control defects. | |||
| Bone marrow stromal cells | BDI with PCL films | Bone marrow stromal cells were cultured on rigid polymer films under osteogenic conditions for up to 21 days. This study demonstrated the suitability of this family of PEUUs for bone tissue engineering applications. | Kavlock et al. ([2007]) |
| Femoral condyle | LTI with PCL-co-PGA-co-PDLLA | Extensive cellular infiltration deep to the implant and new bone formation at 6 weeks | Dumas et al. ([2010]) |
| Chondrocytes | Porous scaffolds synthesized from HMDI with PCL and ISO | Although the covalent incorporation of the isoprenoid molecule into the polyurethane chain modified the surface chemistry of the polymer, it did not affect the viability of attached chondrocytes. | Eglin et al. ([2010]) |
| The change of surface characteristics and the more open pore structure of the scaffolds produced from the isoprenoid-modified polyurethane are beneficial for the seeding efficiency and the homogeneity of the tissue-engineered constructs. | |||
Chen et al. Progress in Biomaterials 2012 1:2 doi:10.1186/2194-0517-1-2