کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2484905 | 1114339 | 2012 | 5 صفحه PDF | دانلود رایگان |

ABSTRACTPharmaceutical hydrates have been used as clinical development candidates and in marketed products. The physical stability of hydrates can pose unique challenges to their development because of their particular sensitivity to the moisture levels in their surroundings. By conducting simple experiments early during the form selection phase of a drug candidate's development, a basic understanding of the thermodynamic and kinetic aspects of a hydrate form's stability can be attained that can facilitate the successful navigation of these challenges. Differential scanning calorimetry was used to determine the thermal and kinetic properties of a number of pharmaceutically relevant hydrates. The activation energy (Ea) of dehydration and dehydration onset temperature (Tonset) of survey compounds were compiled and analyzed. A significant number of compounds possessed both high Ea and high Tonset of dehydration, suggesting that these hydrate crystal forms were particularly stable. The results of these studies suggest that dehydration Ea and dehydration Tonset together can be used as early indicators of a crystalline hydrate's physical stability and can alert to potential challenges in developing hydrate crystal forms of drug candidates. © 2012 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:4013–4017, 2012
Journal: Journal of Pharmaceutical Sciences - Volume 101, Issue 10, October 2012, Pages 4013–4017