Disappearing polymorphs and the role of reaction by-products: the case of sulphathiazole

Blagden, N. and Davey, R. J. and Rowe, R. and Roberts, R. (1998) Disappearing polymorphs and the role of reaction by-products: the case of sulphathiazole. International Journal of Pharmaceutics, 172 (1-2). pp. 169-177. ISSN 0378-5173

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Item Type:Article
Item Status:Live Archive

Abstract

A combined modelling and experimental strategy has been applied to the problem of reaction by-product influence on the appearance of sulphathaizole polymorphs from aqueous solution. From pure aqueous solution after 24 h the most stable phase, form IV was isolated. This work shows for the first time that a reaction by-product, ethamidosulphathiazole, from the final hydrolysis stage at concentrations as low as 1 mol. stabilises the metastable modification, form I. In the presence of 1.0-0.5 mol. forms II and III are stabilised. Only at concentration below 0.5 mol. does the transformation proceed to form IV as in the pure solution. The role of the impurity was accounted for from an analysis of the respective hydrogen bond networks and crystal morphologies of each phase. Copyright (C) 1998 Elsevier Science B.V.

Keywords:sulfathiazole, aqueous solution, article, crystal structure, drug impurity, hydrogen bond, hydrolysis, molecular stability, phase transition, priority journal
Subjects:B Subjects allied to Medicine > B200 Pharmacology, Toxicology and Pharmacy
Divisions:College of Science > School of Pharmacy
ID Code:8781
Deposited On:09 May 2013 12:52

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