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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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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). |
format | Online Article Text |
id | pubmed-3857085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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