| Literature DB >> 33406659 |
Ryoma Tanaka1, Supisara Osotprasit2, Jomjai Peerapattana2, Kazuhide Ashizawa3, Yusuke Hattori1,3, Makoto Otsuka1,3.
Abstract
The manufacturing of solid pharmaceutical dosage forms composed of cocrystals requires numerous processes during which there is risk of dissociation into parent molecules. Resonant acoustic wet granulation (RAG) was devised in an effort to complete theophylline-citric acid (THPCIT) cocrystal formation during the granulation process, thereby reducing the number of operations. In addition, the influence of granulation liquid was investigated. A mixture of anhydrous THP (drug), anhydrous CIT (coformer), and hydroxypropyl cellulose (granulating agent) was processed by RAG with water or ethanol as a granulation liquid. The purposes were to (i) form granules using RAG as a breakthrough method; (ii) accomplish the cocrystallization during the integrated unit operation; and (iii) characterize the final solid product (i.e., tablet). The RAG procedure achieved complete cocrystal formation (>99%) and adequately sized granules (d50: >250 μm). The granulation using water (GW) facilitated formation of cocrystal hydrate which were then transformed into anhydrous cocrystal after drying, while the granulation using ethanol (GE) resulted in the formation of anhydrous cocrystal before and after drying. The dissolution of the highly dense GW tablet, which was compressed from granules including fine powder due to the dehydration, was slower than that of the GE tablet.Entities:
Keywords: cocrystal; crystallization; dehydration; formulation; granulation; hydrate; physical characterization; polymorphism; resonant acoustic mixer; solvate
Year: 2021 PMID: 33406659 PMCID: PMC7823328 DOI: 10.3390/pharmaceutics13010056
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321