4.6 Article

Indomethacin: Effect of Diffusionless Crystal Growth on Thermal Stability during Long-Term Storage

Journal

MOLECULES
Volume 28, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28041568

Keywords

amorphous indomethacin; crystallization; kinetic prediction; particle size; storage

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Differential scanning calorimetry and Raman spectroscopy were used to investigate the crystallization behavior of amorphous indomethacin powders. The research found that the formation of the alpha-form was accelerated under conditions of increased mobility, increased mechanical defects, and prolonged free-surface nucleation. Additionally, two separate crystal growth modes were identified, originating from either mechanical defects or the free surface. A rating of 7 out of 10 is given for the importance of this study.
Differential scanning calorimetry and Raman spectroscopy were used to study the non-isothermal and isothermal crystallization behavior of amorphous indomethacin powders (with particle sizes ranging from 50 to 1000 mu m) and their dependence on long-term storage conditions, either 0-100 days stored freely at laboratory ambient temperatures and humidity or placed in a desiccator at 10 degrees C. Whereas the gamma-form polymorph always dominated, the accelerated formation of the alpha-form was observed in situations of heightened mobility (higher temperature and heating rate), increased amounts of mechanically induced defects, and prolonged free-surface nucleation. A complex crystallization behavior with two separated crystal growth modes (originating from either the mechanical defects or the free surface) was identified both isothermally and nonisothermally. The diffusionless glass-crystal (GC) crystal growth was found to proceed during the long-term storage at 10 degrees C and zero humidity, at the rate of similar to 100 mu m of the gamma-form surface crystalline layer being formed in 100 days. Storage at the laboratory temperature (still below the glass transition temperature) and humidity led only to a negligible/nondetectable GC growth for the fine indomethacin powders (particle size below similar to 150 mu m), indicating a marked suppression of GC growth by the high density of mechanical defects under these conditions. The freely stored bulk material with no mechanical damage and a smooth surface exhibited zero traces of GC growth (as confirmed by microscopy) after >150 days of storage. The accuracy of the kinetic predictions of the indomethacin crystallization behavior was rather poor due to the combined influences of the mechanical defects, competing nucleation, and crystal growth processes of the two polymorphic phases as well as the GC growth complex dependence on the storage conditions within the vicinity of the glass transition temperature. Performing paired isothermal and nonisothermal kinetic measurements is thus highly recommended in macroscopic crystallization studies of drugs with similarly complicated crystal growth behaviors.

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