Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2487407 | Journal of Pharmaceutical Sciences | 2008 | 11 Pages |
Abstract
In the present work, authors produced tablets of anhydrous sodium naproxen by wet granulation using a highâshear mixerâgranulator. Drug hydrated to the tetrahydrated form, as observed by Xâray powder diffractometry. After wet granulation, authors then performed two different drying procedures, obtaining granules of different water content and crystallographic characteristics. The first procedure dried granules in the highâshear mixerâgranulator by applying vacuum at room temperature (batch A), while the second employed the same apparatus and time, under vacuum at 40°C (batch B). Xâray powder diffractometry revealed that the sodium naproxen (SN) contained in batch A granules was a mixture of dihydrated and tetrahydrated forms (as demonstrated by the coexistence of peaks typical of both hydrated forms), while that of batch B granules was a mixture of monohydrated and tetrahydrated forms. This means that differences in drying procedures could lead to products of different crystallographic properties. The behavior under compression was evaluated, revealing that batch A offered the best tabletability and compressibility. These results make it possible to conclude that differences in the crystallographic properties and water content of SN are such that different hydration/drying processes can alter the drug crystal form and thus the tabletability of the resulting granules. © 2008 WileyâLiss, Inc. and the American Pharmacists Association J Pharm Sci 97:5263-5273, 2008
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Authors
Piera Di Martino, Ledjan Malaj, Roberta Censi, Sante Martelli,