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Molecular Mobility and Stability Studies of Amorphous Imatinib Mesylate

Overview
Journal Pharmaceutics
Publisher MDPI
Date 2019 Jul 4
PMID 31266220
Citations 3
Authors
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Abstract

The proposed study examined the characterization and stability of solid-state amorphous imatinib mesylate (IM) after 15 months under controlled relative humidity (60 ± 5%) and temperature (25 ± 2 °C) conditions. After 2 weeks, and 1, 3, 6, and 15 months, the samples were characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray powder diffractometry (XRPD), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and scanning electron microscopy (SEM). Additionally, the amorphous form of imatinib mesylate was obtained via supercooling of the melt in a DSC apparatus, and aged at various temperatures (3, 15, 25 and 30 °C) and time periods (1-16 h). Glass transition and enthalpy relaxation were used to calculate molecular-relaxation-time parameters. The Kohlrausch-Williams-Watts (KWW) equation was applied to fit the experimental enthalpy-relaxation data. The mean molecular-relaxation-time constant () increased with decreasing ageing temperature. The results showed a high stability of amorphous imatinib mesylate adequate to enable its use in solid dosage form.

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References
1.
Craig D, Royall P, Kett V, Hopton M . The relevance of the amorphous state to pharmaceutical dosage forms: glassy drugs and freeze dried systems. Int J Pharm. 1999; 179(2):179-207. DOI: 10.1016/s0378-5173(98)00338-x. View

2.
Hancock B, Parks M . What is the true solubility advantage for amorphous pharmaceuticals?. Pharm Res. 2000; 17(4):397-404. DOI: 10.1023/a:1007516718048. View

3.
Druker B, Talpaz M, Resta D, Peng B, Buchdunger E, Ford J . Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med. 2001; 344(14):1031-7. DOI: 10.1056/NEJM200104053441401. View

4.
Yu L . Amorphous pharmaceutical solids: preparation, characterization and stabilization. Adv Drug Deliv Rev. 2001; 48(1):27-42. DOI: 10.1016/s0169-409x(01)00098-9. View

5.
Hancock B, Carlson G, Ladipo D, Langdon B, Mullarney M . Comparison of the mechanical properties of the crystalline and amorphous forms of a drug substance. Int J Pharm. 2002; 241(1):73-85. DOI: 10.1016/s0378-5173(02)00133-3. View