| Literature DB >> 28412482 |
Jun-Hui Deng1, Tong-Bu Lu2, Changquan Calvin Sun3, Jia-Mei Chen4.
Abstract
Dapagliflozin (DAP) is a potent and selective sodium-glucose contransporter-2 inhibitor, for treating type 2 diabetes. DAP propanediol monohydrate (DAP-PDO-H2O, 1:1:1) is the solid form used in the current tablet product to address the severe hygroscopicity problem of DAP free form. DAP-PDO-H2O, however, suffers the problem of instability when exposed to high temperature, which renders it amorphous. In this work, we report on the preparation and evaluation of a new 1:1 cocrystal between DAP and citric acid (DAP-CA). The DAP-CA cocrystal exhibits superior stability against high temperature and high relative humidity without compromising dissolution and tableting performance. Thus, DAP-CA is a promising solid form for developing the next generation DAP tablet products with improved performance.Entities:
Keywords: Acetonitrile (PubChem CID: 6342); Citric acid (PubChem CID: 311); Dapagliflozin (PubChem CID: 9887712); Dapagliflozin propanediol (PubChem CID: 24906252); Isopropyl acetate (PubChem CID: 7915)
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Year: 2017 PMID: 28412482 DOI: 10.1016/j.ejps.2017.04.008
Source DB: PubMed Journal: Eur J Pharm Sci ISSN: 0928-0987 Impact factor: 4.384