Bethany I. Harriss
Furosemide Cocrystals: Structures, Hydrogen Bonding, and Implications for Properties
Harriss, Bethany I.; Vella-Zarb, Liana; Wilson, Claire; Radosavljevic Evans, Ivana
Authors
Abstract
Four new crystal structures of pharmaceutical molecule furosemide with GRAS coformers are reported and correlated with the known pharmacologically relevant properties of these materials. Furosemide carboxylic acid oxygen donor−coformer aromatic nitrogen acceptor is the dominant synthon, leading to the key intermolecular interactions in the cocrystals studied.
Citation
Harriss, B. I., Vella-Zarb, L., Wilson, C., & Radosavljevic Evans, I. (2014). Furosemide Cocrystals: Structures, Hydrogen Bonding, and Implications for Properties. Crystal Growth and Design, 14(2), 783-791. https://doi.org/10.1021/cg401662d
Journal Article Type | Article |
---|---|
Publication Date | Feb 5, 2014 |
Deposit Date | Oct 21, 2014 |
Publicly Available Date | Jan 28, 2015 |
Journal | Crystal Growth and Design |
Print ISSN | 1528-7483 |
Electronic ISSN | 1528-7505 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 14 |
Issue | 2 |
Pages | 783-791 |
DOI | https://doi.org/10.1021/cg401662d |
Public URL | https://durham-repository.worktribe.com/output/1421398 |
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Copyright Statement
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Crystal growth and design, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see [insert ACS Articles on Request author-directed link to Published Work, see http://dx.doi.org/10.1021/cg401662d
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