Abstract
A series of melt-quenched disks of amorphous celecoxib were obtained using two different cooling rates (>100 °C/min and ∼25-30 °C/min) and subjected to different compression pressures (125, 250, and 500 MPa) and dwell times (0, 30, and 60 s). The kinetics of crystallization for these differently prepared melt-quenched disks were probed using a number of methods. Low-frequency Raman spectroscopy was used to monitor isothermal crystallization kinetics, whereas dynamic differential scanning calorimetry served as a complimentary technique to identify changes in form. Although both compression parameters destabilized the amorphous celecoxib, the dwell time was found to have a more critical overall effect. Additionally, the sample history was affirmed to be a factor for limiting the magnitude of compression-induced destabilization.
Original language | English |
---|---|
Journal | Molecular Pharmaceutics |
Volume | 16 |
Issue number | 8 |
Pages (from-to) | 3678-3686 |
Number of pages | 9 |
ISSN | 1543-8384 |
DOIs | |
Publication status | Published - 2019 |
Keywords
- amorphous drugs
- celecoxib
- compression-induced destabilization
- differential scanning calorimetry
- low-frequency Raman spectroscopy