| Literature DB >> 28043131 |
Frank Theil1, Sankaran Anantharaman1, Samuel O Kyeremateng1, Holger van Lishaut1, Sebastian H Dreis-Kühne1, Jörg Rosenberg1, Markus Mägerlein1, Gerd H Woehrle1.
Abstract
Kinetically stabilized amorphous solid dispersions are inherently metastable systems. Therefore, such systems are generally considered prone to recrystallization. In some cases, the formation of crystals will impact the bioavailability of the active pharmaceutical ingredient in these formulations. Recrystallization therefore may present a significant risk for patients as it potentially lowers the effective dose of the pharmaceutical formulation. This study indicates that such metastable formulations may indeed remain fully amorphous even after more than two decades of storage under ambient conditions. Different formulations of nifedipine stored for 25 years were compared with freshly prepared samples. A thorough physicochemical characterization including polarized light microscopy, differential scanning calorimetry, X-ray powder diffraction, and transmission Raman spectroscopy was undertaken. This in-depth characterization indicates no signs of recrystallization in the stored samples. The observations presented here prove that long-term stability of amorphous solid dispersions much beyond the typical shelf life for pharmaceutical formulations is indeed possible by kinetic stabilization alone. These findings implicate a reevaluation of the propensity to recrystallize for kinetically stabilized amorphous solid dispersions.Entities:
Keywords: amorphous solid dispersion; crystallinity; long-term stability; nifedipine; physicochemical characterization; recrystallization
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Year: 2016 PMID: 28043131 DOI: 10.1021/acs.molpharmaceut.6b00783
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939