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Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation

High-pressure crystallisation has been successfully used as an alternative technique to prepare Form II of a non-steroidal anti-inflammatory drug, mefenamic acid (MA). A single crystal of Form II, denoted as high-pressure Form II, was grown at 0.3 GPa from an ethanolic solution by using a diamond an...

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Autores principales: Abbas, Nasir, Oswald, Iain D. H., Pulham, Colin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489933/
https://www.ncbi.nlm.nih.gov/pubmed/28509850
http://dx.doi.org/10.3390/pharmaceutics9020016
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author Abbas, Nasir
Oswald, Iain D. H.
Pulham, Colin R.
author_facet Abbas, Nasir
Oswald, Iain D. H.
Pulham, Colin R.
author_sort Abbas, Nasir
collection PubMed
description High-pressure crystallisation has been successfully used as an alternative technique to prepare Form II of a non-steroidal anti-inflammatory drug, mefenamic acid (MA). A single crystal of Form II, denoted as high-pressure Form II, was grown at 0.3 GPa from an ethanolic solution by using a diamond anvil cell. A comparison of the crystal structures shows that the efficient packing of molecules in Form II was enabled by the structural flexibility of MA molecules. Compression studies performed on a single crystal of Form I resulted in a 14% decrease of unit cell volume up to 2.5 GPa. No phase transition was observed up to this pressure. A reconstructive phase transition is required to induce conformational changes in the structure, which was confirmed by the results of crystallisation at high pressure.
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spelling pubmed-54899332017-06-30 Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation Abbas, Nasir Oswald, Iain D. H. Pulham, Colin R. Pharmaceutics Article High-pressure crystallisation has been successfully used as an alternative technique to prepare Form II of a non-steroidal anti-inflammatory drug, mefenamic acid (MA). A single crystal of Form II, denoted as high-pressure Form II, was grown at 0.3 GPa from an ethanolic solution by using a diamond anvil cell. A comparison of the crystal structures shows that the efficient packing of molecules in Form II was enabled by the structural flexibility of MA molecules. Compression studies performed on a single crystal of Form I resulted in a 14% decrease of unit cell volume up to 2.5 GPa. No phase transition was observed up to this pressure. A reconstructive phase transition is required to induce conformational changes in the structure, which was confirmed by the results of crystallisation at high pressure. MDPI 2017-05-16 /pmc/articles/PMC5489933/ /pubmed/28509850 http://dx.doi.org/10.3390/pharmaceutics9020016 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abbas, Nasir
Oswald, Iain D. H.
Pulham, Colin R.
Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title_full Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title_fullStr Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title_full_unstemmed Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title_short Accessing Mefenamic Acid Form II through High-Pressure Recrystallisation
title_sort accessing mefenamic acid form ii through high-pressure recrystallisation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489933/
https://www.ncbi.nlm.nih.gov/pubmed/28509850
http://dx.doi.org/10.3390/pharmaceutics9020016
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