PEUU was processed with electrospinning to create scaffolds that incorporated collagen and that could exhibit anisotropic microstructures. The incorporation of collagen is useful as a means of increasing cell adhesion and degradation rates, with or without collagenase. At low concentrations of collagen the protein appears to lose its helical structure, although still imparting increased cell adhesion. Anisotropy is of interest in creating oriented cellular structures and to control stress translation during tissue mechanical conditioning. These scaffolds possess mechanical properties and exhibit stress-strain curves that mimic those of the native pulmonary valve.
These elastomeric matrices can provide mechanical support, but typically require long seeding and culture times to achieve high density cellular in-growth. Therefore, we have developed a micro-integrated method during which a mesh of submicron elastomeric fibers is built into the scaffold wall during the cellular placement process. Cells are electrosprayed during the electrospinning of a synthetic elastomer, which expedites the time required for scaffold construction and cell seeding. This tissue engineered construct, which is largely cellular and supported with an elastomeric fiber net, can be appropriate for soft tissue replacement including the engineering of conduit structures such as a tissue engineered blood vessel.
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