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In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures
Polymorphism denotes the existence of more than one crystal structure of a substance, and great practical and theoretical interest for the chemical and pharmaceutical industries. In many cases, it is challenging to produce a pure crystal form and establish a sensitive detection method for the identi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838872/ https://www.ncbi.nlm.nih.gov/pubmed/27097672 http://dx.doi.org/10.1038/srep24763 |
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author | Yin, Xian-Zhen Xiao, Ti-Qiao Nangia, Ashwini Yang, Shuo Lu, Xiao-Long Li, Hai-Yan Shao, Qun He, You York, Peter Zhang, Ji-Wen |
author_facet | Yin, Xian-Zhen Xiao, Ti-Qiao Nangia, Ashwini Yang, Shuo Lu, Xiao-Long Li, Hai-Yan Shao, Qun He, You York, Peter Zhang, Ji-Wen |
author_sort | Yin, Xian-Zhen |
collection | PubMed |
description | Polymorphism denotes the existence of more than one crystal structure of a substance, and great practical and theoretical interest for the chemical and pharmaceutical industries. In many cases, it is challenging to produce a pure crystal form and establish a sensitive detection method for the identification of crystal form in a mixture of polymorphs. In this study, an accurate and sensitive method based on synchrotron radiation X-ray computed microtomography (SR-μCT) was devised to identify the polymorphs of clopidogrel bisulphate (CLP). After 3D reconstruction, crystal particles were extracted and dozens of structural parameters were calculated. Whilst, the particle shapes of the two crystal forms were all irregular, the surface of CLP II was found to be rougher than CLP I. In order to classify the crystal form based on the quantitative morphological property of particles, Volume Bias Percentage based on Surface Smoothing (VBP) was defined and a new method based on VBP was successfully developed, with a total matching rate of 99.91% for 4544 particles and a lowest detectable limit of 1%. More important for the mixtures in solid pharmaceutical formulations, the interference of excipients can be avoided, a feature cannot achieved by other available analytical methods. |
format | Online Article Text |
id | pubmed-4838872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48388722016-04-27 In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures Yin, Xian-Zhen Xiao, Ti-Qiao Nangia, Ashwini Yang, Shuo Lu, Xiao-Long Li, Hai-Yan Shao, Qun He, You York, Peter Zhang, Ji-Wen Sci Rep Article Polymorphism denotes the existence of more than one crystal structure of a substance, and great practical and theoretical interest for the chemical and pharmaceutical industries. In many cases, it is challenging to produce a pure crystal form and establish a sensitive detection method for the identification of crystal form in a mixture of polymorphs. In this study, an accurate and sensitive method based on synchrotron radiation X-ray computed microtomography (SR-μCT) was devised to identify the polymorphs of clopidogrel bisulphate (CLP). After 3D reconstruction, crystal particles were extracted and dozens of structural parameters were calculated. Whilst, the particle shapes of the two crystal forms were all irregular, the surface of CLP II was found to be rougher than CLP I. In order to classify the crystal form based on the quantitative morphological property of particles, Volume Bias Percentage based on Surface Smoothing (VBP) was defined and a new method based on VBP was successfully developed, with a total matching rate of 99.91% for 4544 particles and a lowest detectable limit of 1%. More important for the mixtures in solid pharmaceutical formulations, the interference of excipients can be avoided, a feature cannot achieved by other available analytical methods. Nature Publishing Group 2016-04-21 /pmc/articles/PMC4838872/ /pubmed/27097672 http://dx.doi.org/10.1038/srep24763 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yin, Xian-Zhen Xiao, Ti-Qiao Nangia, Ashwini Yang, Shuo Lu, Xiao-Long Li, Hai-Yan Shao, Qun He, You York, Peter Zhang, Ji-Wen In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title | In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title_full | In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title_fullStr | In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title_full_unstemmed | In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title_short | In situ 3D topographic and shape analysis by synchrotron radiation X-ray microtomography for crystal form identification in polymorphic mixtures |
title_sort | in situ 3d topographic and shape analysis by synchrotron radiation x-ray microtomography for crystal form identification in polymorphic mixtures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838872/ https://www.ncbi.nlm.nih.gov/pubmed/27097672 http://dx.doi.org/10.1038/srep24763 |
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