| Literature DB >> 30114405 |
Ke Wu1, Anu Gore2, Richard Graham2.
Abstract
This work highlights a new orthorhombic hydrate (Form 2) of cyclosporine (CsA), a widely used immunosuppressant. The uniqueness of this new form was established by powder X-ray diffractometry, solid-state nuclear magnetic resonance spectroscopy, and single crystal X-ray diffraction analysis. The crystal structure of this form was solved (P212121, a = 12.639 Å, b = 19.758 Å, c = 29.568 Å, Z = 4). In addition, the solid-state properties of Form 2 were compared with other known crystalline forms of CsA by thermal analysis, water vapor sorption analysis, Fourier-transform infrared spectroscopy, and so on. These studies suggest that Form 2 is a nonstoichiometric hydrate with distinctive hydrogen bonding modes. More importantly, Form 2 is about an order of magnitude less soluble than the commercially available tetragonal form (Form 1). An interconversion map among various CsA solid forms was built by slurry experiments. Form 2 was the most stable form in aqueous systems, whereas the previously known orthorhombic hydrate (Form 3) was the predominant form in nonaqueous vehicles. While Form 2 as a lower solubility form poses greater challenge in bioavailability enhancement, the solid-state properties of this unique hydrate may provide new drug delivery opportunities.Entities:
Keywords: Fourier-transform infrared spectroscopy (FTIR); cyclosporine (CsA); hydrate; nonstoichiometric; powder X-ray diffractometry (XRPD); single crystal X-ray diffraction (SCXRD); solid-state characterization; solid-state nuclear resonance spectroscopy (SSNMR); solubility; thermal analysis
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Year: 2018 PMID: 30114405 DOI: 10.1016/j.xphs.2018.08.002
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534