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Structure and Physicochemical Characterization of a Naproxen-Picolinamide Cocrystal

Kerr, H.E.; Softley, L.K.; Suresh, K.; Hodgkinson, P.; Evans, I.R.

Structure and Physicochemical Characterization of a Naproxen-Picolinamide Cocrystal Thumbnail


Authors

H.E. Kerr

L.K. Softley

K. Suresh

I.R. Evans



Abstract

Naproxen (NPX) is a nonsteroidal anti-inflammatory drug with pain- and fever-relieving properties, currently marketed in the sodium salt form to overcome solubility problems; however, alternative solutions for improving its solubility across all pH values are desirable. NPX is suitable for cocrystal formation, with hydrogen-bonding possibilities via the COOH group. The crystal structure is presented of a 1:1 cocrystal of NPX with picolinamide as a coformer [systematic name: (S)-2-(6-meth­oxy­naphthalen-2-yl)propanoic acid-pyridine-2-carbox­amide (1/1), C14H14O3·C6H6N2O]. The pharmaceutically relevant physical properties were investigated and the intrinsic dissolution rate was found to be essentially the same as that of commercial naproxen. An NMR crystallography approach was used to investigate the H-atom positions in the two crystallographically unique COOH-CONH hydrogen-bonded dimers. 1H solid-state NMR distinguished the two carboxyl protons, despite the very similar crystallographic environments. The nature of the hydrogen bonding was confirmed by solid-state NMR and density functional theory calculations.

Citation

Kerr, H., Softley, L., Suresh, K., Hodgkinson, P., & Evans, I. (2017). Structure and Physicochemical Characterization of a Naproxen-Picolinamide Cocrystal. Acta Crystallographica Section C: Structural Chemistry, C73(3), https://doi.org/10.1107/s2053229616011980

Journal Article Type Article
Acceptance Date Jul 22, 2016
Online Publication Date Feb 6, 2017
Publication Date Mar 1, 2017
Deposit Date Jun 23, 2016
Publicly Available Date Feb 8, 2017
Journal Acta Crystallographica Section C: Structural Chemistry
Publisher International Union of Crystallography
Peer Reviewed Peer Reviewed
Volume C73
Issue 3
DOI https://doi.org/10.1107/s2053229616011980

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http://creativecommons.org/licenses/by/4.0/

Copyright Statement
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.





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