Abstract
The aim of this study was to investigate the effect of altering design variables like cross-linking and freezing temperature (at a time) on morphology of freeze-dried chitosan scaffolds and modulation of release of Diclofenac sodium (model drug). Freeze-dried chitosan scaffolds produced at − 80 °C, cross-linked with genipin, showed swelling of 163.52 ± 9.95% with sustained drug release of 26.37 ± 10.47% over 24 h (P < 0.05). In comparison, uncross-linked scaffolds produced at − 80 °C showed higher swelling of 173.58 ± 8.23% and drug release of 28.67 ± 2.40% (P < 0.05). Uncross-linked scaffolds produced using freezing temperature of − 20 °C also showed higher swelling of 228.77 ± 9.84% and release of 30.58 ± 3.25% (P < 0.05). Release kinetics followed Higuchi model with Fickian diffusion, thereby indicating a swelling-dependent release. Altering the design parameters also showed significant changes in pore size and porosity, thereby supporting the swelling and drug delivery behavior from scaffolds.
Original language | English |
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Pages (from-to) | 1759-1768 |
Number of pages | 10 |
Journal | Chemical papers |
Volume | 74 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Jun 2020 |
Externally published | Yes |
Keywords
- Chitosan scaffolds
- Freezing temperature
- Genipin
- Sustained drug release