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Surface Induced Phenytoin Polymorph. 1. Full Structure Solution by Combining Grazing Incidence X-ray Diffraction and Crystal Structure Prediction
[Image: see text] Understanding the behavior and properties of molecules assembled in thin layers requires knowledge of their crystalline packing. The drug phenytoin (5,5-diphenylhydantoin) is one of the compounds that can be grown as a surface induced polymorph. By using grazing incidence X-ray dif...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839513/ https://www.ncbi.nlm.nih.gov/pubmed/31728132 http://dx.doi.org/10.1021/acs.cgd.9b00857 |
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author | Braun, Doris E. Rivalta, Arianna Giunchi, Andrea Bedoya-Martinez, Natalia Schrode, Benedikt Venuti, Elisabetta Della Valle, Raffaele Guido Werzer, Oliver |
author_facet | Braun, Doris E. Rivalta, Arianna Giunchi, Andrea Bedoya-Martinez, Natalia Schrode, Benedikt Venuti, Elisabetta Della Valle, Raffaele Guido Werzer, Oliver |
author_sort | Braun, Doris E. |
collection | PubMed |
description | [Image: see text] Understanding the behavior and properties of molecules assembled in thin layers requires knowledge of their crystalline packing. The drug phenytoin (5,5-diphenylhydantoin) is one of the compounds that can be grown as a surface induced polymorph. By using grazing incidence X-ray diffraction, the monoclinic unit cell of the new form II can be determined, but, due to crystal size and the low amount of data, a full solution using conventional structure solving strategies fails. In this work, the full solution has been obtained by combining computational structure generation and experimental results. The comparison between the bulk and the new surface induced phase reveals significant packing differences of the hydrogen-bonding network, which might be the reason for the faster dissolution of form II with respect to form I. The results are very satisfactory, and the method might be adapted for other systems, where, due to the limited amount of experimental data, one must rely on additional approaches to gain access to more detailed information to understand the solid-state behavior. |
format | Online Article Text |
id | pubmed-6839513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68395132019-11-12 Surface Induced Phenytoin Polymorph. 1. Full Structure Solution by Combining Grazing Incidence X-ray Diffraction and Crystal Structure Prediction Braun, Doris E. Rivalta, Arianna Giunchi, Andrea Bedoya-Martinez, Natalia Schrode, Benedikt Venuti, Elisabetta Della Valle, Raffaele Guido Werzer, Oliver Cryst Growth Des [Image: see text] Understanding the behavior and properties of molecules assembled in thin layers requires knowledge of their crystalline packing. The drug phenytoin (5,5-diphenylhydantoin) is one of the compounds that can be grown as a surface induced polymorph. By using grazing incidence X-ray diffraction, the monoclinic unit cell of the new form II can be determined, but, due to crystal size and the low amount of data, a full solution using conventional structure solving strategies fails. In this work, the full solution has been obtained by combining computational structure generation and experimental results. The comparison between the bulk and the new surface induced phase reveals significant packing differences of the hydrogen-bonding network, which might be the reason for the faster dissolution of form II with respect to form I. The results are very satisfactory, and the method might be adapted for other systems, where, due to the limited amount of experimental data, one must rely on additional approaches to gain access to more detailed information to understand the solid-state behavior. American Chemical Society 2019-09-17 2019-11-06 /pmc/articles/PMC6839513/ /pubmed/31728132 http://dx.doi.org/10.1021/acs.cgd.9b00857 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Braun, Doris E. Rivalta, Arianna Giunchi, Andrea Bedoya-Martinez, Natalia Schrode, Benedikt Venuti, Elisabetta Della Valle, Raffaele Guido Werzer, Oliver Surface Induced Phenytoin Polymorph. 1. Full Structure Solution by Combining Grazing Incidence X-ray Diffraction and Crystal Structure Prediction |
title | Surface Induced Phenytoin Polymorph. 1. Full Structure
Solution by Combining Grazing Incidence X-ray Diffraction and
Crystal Structure Prediction |
title_full | Surface Induced Phenytoin Polymorph. 1. Full Structure
Solution by Combining Grazing Incidence X-ray Diffraction and
Crystal Structure Prediction |
title_fullStr | Surface Induced Phenytoin Polymorph. 1. Full Structure
Solution by Combining Grazing Incidence X-ray Diffraction and
Crystal Structure Prediction |
title_full_unstemmed | Surface Induced Phenytoin Polymorph. 1. Full Structure
Solution by Combining Grazing Incidence X-ray Diffraction and
Crystal Structure Prediction |
title_short | Surface Induced Phenytoin Polymorph. 1. Full Structure
Solution by Combining Grazing Incidence X-ray Diffraction and
Crystal Structure Prediction |
title_sort | surface induced phenytoin polymorph. 1. full structure
solution by combining grazing incidence x-ray diffraction and
crystal structure prediction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839513/ https://www.ncbi.nlm.nih.gov/pubmed/31728132 http://dx.doi.org/10.1021/acs.cgd.9b00857 |
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