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Conformational Polymorphism on Imatinib Mesylate: Grinding Effects

Crystal structures of polymorphs α and β of imatinib mesylate were obtained. Thermal behavior and grinding effects were studied by X-ray powder diffraction and differential scanning calorimetry techniques. Molecules in forms α and β exhibit significant conformational differences due to dissimilar in...

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Bibliographic Details
Published in:Journal of pharmaceutical sciences 2012-02, Vol.101 (2), p.541-551
Main Authors: Grillo, Damián, Polla, Griselda, Vega, Daniel
Format: Article
Language:English
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Summary:Crystal structures of polymorphs α and β of imatinib mesylate were obtained. Thermal behavior and grinding effects were studied by X-ray powder diffraction and differential scanning calorimetry techniques. Molecules in forms α and β exhibit significant conformational differences due to dissimilar intramolecular interactions, which stabilize their molecular conformations. In spite of that, both crystal structures present a dimer-chain arrangement. Dimers are mainly determined by hydrogen bonding interactions and some weak π–π interactions. Connections between dimers are provided by mesylate ions to determine chains of dimers. Neighboring chains are linked by very weak interactions: C─H···π interactions in form α and π–π interactions in form β. At room temperature, thermal disorder was observed in the mesylate ion in form α, which could be removed at low temperatures (–123°C). Form β was found to be the more stable form at room temperature. Both polymorphs exhibit a tendency to generate amorphous material by grinding, which can be converted to a crystalline phase by either temperature or aging. When amorphous crystallization is kinetically studied at room temperature, form β is obtained after a week. Conversely, when the crystallization is activated by temperature, the final obtained crystal form depends on the starting material, proving the importance of seeding. © 2011 Wiley Periodicals, Inc. and the American Pharmacists Association.
ISSN:0022-3549
1520-6017
DOI:10.1002/jps.22772