Özet
This article describes the preparation and characterization of BSA and bFGF-loaded PLGA microspheres and assesses the effect of entrapment procedure and in vitro release conditions. In the experiments, changing the PVA concentration from 3 to 5% (w/v) in the pre-emulsion inner phase led to a change in particle size and encapsulation efficiency of BSA-loaded and bFGF-loaded PLGA microspheres from 1 to 0.7 μm and from 73 to 65%, respectively. The in vitro release of the bFGF from PLGA microspheres was much lower than BSA-loaded PLGA microspheres. For all of the formulations, BSA and bFGF retained integrity after the microencapsulation process as evaluated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Besides, the cell proliferation-stimulating activity of bFGF was evaluated by using BALB/c 3T3 cells and it was shown that the bioactivity of bFGF was increased by adding heparin to the release medium.
| Orijinal dil | İngilizce |
|---|---|
| Sayfa (başlangıç-bitiş) | 371-375 |
| Sayfa sayısı | 5 |
| Dergi | Journal of Drug Delivery Science and Technology |
| Hacim | 15 |
| Basın numarası | 5 |
| DOI'lar | |
| Yayın durumu | Yayınlandı - 2005 |
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