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Co-Crystal Screening of Diclofenac

In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological activity. In order to identify new solid forms of...

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Detalles Bibliográficos
Autores principales: Aakeröy, Christer B., Grommet, Angela B., Desper, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857085/
https://www.ncbi.nlm.nih.gov/pubmed/24310599
http://dx.doi.org/10.3390/pharmaceutics3030601
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author Aakeröy, Christer B.
Grommet, Angela B.
Desper, John
author_facet Aakeröy, Christer B.
Grommet, Angela B.
Desper, John
author_sort Aakeröy, Christer B.
collection PubMed
description In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological activity. In order to identify new solid forms of diclofenac—an analgesic with extremely poor aqueous solubility for which few co-crystal structures have been determined—a range of pyrazoles, pyridines, and pyrimidines were screened for co-crystal formation using solvent assisted grinding and infrared spectroscopy with an overall success rate of 50%. The crystal structures of three new diclofenac co-crystals are reported herein: (diclofenac)·(2-aminopyrimidine), (diclofenac)·(2-amino-4,6-dimethylpyrimidine), and (diclofenac)·(2-amino-4-chloro-6-methylpyrimidine).
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spelling pubmed-38570852013-12-16 Co-Crystal Screening of Diclofenac Aakeröy, Christer B. Grommet, Angela B. Desper, John Pharmaceutics Article In the pharmaceutical industry, co-crystals are becoming increasingly valuable as crystalline solids that can offer altered/improved physical properties of an active pharmaceutical ingredient (API) without changing its chemical identity or biological activity. In order to identify new solid forms of diclofenac—an analgesic with extremely poor aqueous solubility for which few co-crystal structures have been determined—a range of pyrazoles, pyridines, and pyrimidines were screened for co-crystal formation using solvent assisted grinding and infrared spectroscopy with an overall success rate of 50%. The crystal structures of three new diclofenac co-crystals are reported herein: (diclofenac)·(2-aminopyrimidine), (diclofenac)·(2-amino-4,6-dimethylpyrimidine), and (diclofenac)·(2-amino-4-chloro-6-methylpyrimidine). MDPI 2011-08-31 /pmc/articles/PMC3857085/ /pubmed/24310599 http://dx.doi.org/10.3390/pharmaceutics3030601 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Aakeröy, Christer B.
Grommet, Angela B.
Desper, John
Co-Crystal Screening of Diclofenac
title Co-Crystal Screening of Diclofenac
title_full Co-Crystal Screening of Diclofenac
title_fullStr Co-Crystal Screening of Diclofenac
title_full_unstemmed Co-Crystal Screening of Diclofenac
title_short Co-Crystal Screening of Diclofenac
title_sort co-crystal screening of diclofenac
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857085/
https://www.ncbi.nlm.nih.gov/pubmed/24310599
http://dx.doi.org/10.3390/pharmaceutics3030601
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