| Literature DB >> 24216278 |
Rudy Bonfilio1, Jockastta S Leal, Olímpia M M Santos, Gislaine R Pereira, Antônio C Doriguetto, Magali B de Araújo.
Abstract
Chlorthalidone (CTD) is an antihypertensive drug and exhibits four crystalline forms: I, II, III and IV. In this paper, the incidence of CTD polymorphs in raw materials and in tablets as well as the solubility and dissolution properties of forms I and II have been studied. Raw materials were named as A, B, C, D, and E and tablets as Reference, G1, G2 and S. Using powder X-ray diffraction and infrared spectroscopy analyses we found that A, B, E, Reference and G1 contain CTD form I; C, D and S contain predominantly form II; and G2 contain a mixture of both forms. Solubility experiments showed that form II is up to 49% more soluble than form I and dissolution studies showed a significantly effect of the polymorphism on the dissolution of CTD from tablets. Based on these results, it was concluded that only the CTD form I is acceptable for preparation of tablet form. Moreover, we proposed the polymorphic quality control of CTD raw materials and tablets.Entities:
Keywords: Attenued total reflection infrared spectroscopy; Chlorthalidone; Dissolution studies; Polymorphs; Powder X-ray diffraction
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Year: 2013 PMID: 24216278 DOI: 10.1016/j.jpba.2013.10.020
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935