The purpose of this study was to compare the effect of polymer foam morphology and density prior to compaction on the kinetics of isoniazid (INH) release from the final highdensity extruded matrices. The feasibility of preparing low density foams of several biopolymers, including poly(Llactide) (PLL
In vitro release kinetics of proteins from bioactive foams
β Scribed by Lenza, R. F. S. ;Jones, J. R. ;Vasconcelos, W. L. ;Hench, L. L.
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 187 KB
- Volume
- 67A
- Category
- Article
- ISSN
- 0021-9304
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β¦ Synopsis
Abstract
This study describes an approach to obtaining 3βD scaffolds for tissue engineering that allows the incorporation and release of biologically active proteins to stimulate cell function. Laminin was adsorbed on the textured surfaces of binary 70S30C (70 mol % SiO~2~, 30 mol % CaO) and ternary 58S (60 mol % SiO~2~, 36 mol % CaO, 4 mol % P~2~O~5~) foams. The covalent bonds between the binding sites of the proteins and the ligands on the scaffolds' surfaces did not denaturate the proteins. In vitro studies show that the foams modified with chemical groups and coated with laminin were bioactive, as demonstrated by the formation of a crystalline hydroxy carbonate apatite (HCA) layer formed on the surfaces of the foams upon exposure to simulated body fluid (SBF). The release of proteins from the foams also was investigated. Sustained and controlled release from the scaffolds over a 30βday period was achieved. Laminin release from the bioactive foams followed the dissolution rate of the material network. These results suggest that bioactive foams have the potential to act as scaffolds for softβtissue engineering with a controlled release of proteins that can induce tissue formation or regeneration. Β© 2003 Wiley Periodicals, Inc. J Biomed Mater Res 67A: 121β129, 2003
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