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Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting
The deformation behavior of particles under pressure dominates the mechanical properties of solid dosage forms. In this study, the in situ 3D deformation of two polymorphs (I and II) of clopidogrel bisulfate (CLP) was determined to illustrate pressure distribution profiles within the tablet by the d...
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/PMC4766417/ https://www.ncbi.nlm.nih.gov/pubmed/26911359 http://dx.doi.org/10.1038/srep21770 |
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author | Yin, Xian-Zhen Wu, Li Li, Ying Guo, Tao Li, Hai-Yan Xiao, Ti-Qiao York, Peter Nangia, Ashwini Gui, Shuang-Ying Zhang, Ji-Wen |
author_facet | Yin, Xian-Zhen Wu, Li Li, Ying Guo, Tao Li, Hai-Yan Xiao, Ti-Qiao York, Peter Nangia, Ashwini Gui, Shuang-Ying Zhang, Ji-Wen |
author_sort | Yin, Xian-Zhen |
collection | PubMed |
description | The deformation behavior of particles under pressure dominates the mechanical properties of solid dosage forms. In this study, the in situ 3D deformation of two polymorphs (I and II) of clopidogrel bisulfate (CLP) was determined to illustrate pressure distribution profiles within the tablet by the deformation of the crystalline particles for the first time. Synchrotron radiation X-ray computed microtomography (SR-μCT) was utilized to visualize and quantify the morphology of thousands crystalline particles of CLP I and CLP II before and after compression. As a result, the deformation was examined across scale dimensions from microns to the size of the final dosage form. Three dimensional parameters such as volume, sphericity, oblate and prolate of individual particle and distributions were computed and analyzed for quantitative comparison to CLP I and CLP II. The different degrees of deformation under the same compression conditions of CLP I and CLP II were observed and characterized quantitatively. The map of deformation degrees within the tablet illustrated the heterogeneous pressure distribution in various regions of the compacted tablet. In conclusion, the polymorph deformation behaviors demonstrated by SR-μCT quantitative structure analysis deepen understanding of tableting across dimensions from microns to millimeters for the macrostrcuture of tablet. |
format | Online Article Text |
id | pubmed-4766417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47664172016-03-02 Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting Yin, Xian-Zhen Wu, Li Li, Ying Guo, Tao Li, Hai-Yan Xiao, Ti-Qiao York, Peter Nangia, Ashwini Gui, Shuang-Ying Zhang, Ji-Wen Sci Rep Article The deformation behavior of particles under pressure dominates the mechanical properties of solid dosage forms. In this study, the in situ 3D deformation of two polymorphs (I and II) of clopidogrel bisulfate (CLP) was determined to illustrate pressure distribution profiles within the tablet by the deformation of the crystalline particles for the first time. Synchrotron radiation X-ray computed microtomography (SR-μCT) was utilized to visualize and quantify the morphology of thousands crystalline particles of CLP I and CLP II before and after compression. As a result, the deformation was examined across scale dimensions from microns to the size of the final dosage form. Three dimensional parameters such as volume, sphericity, oblate and prolate of individual particle and distributions were computed and analyzed for quantitative comparison to CLP I and CLP II. The different degrees of deformation under the same compression conditions of CLP I and CLP II were observed and characterized quantitatively. The map of deformation degrees within the tablet illustrated the heterogeneous pressure distribution in various regions of the compacted tablet. In conclusion, the polymorph deformation behaviors demonstrated by SR-μCT quantitative structure analysis deepen understanding of tableting across dimensions from microns to millimeters for the macrostrcuture of tablet. Nature Publishing Group 2016-02-25 /pmc/articles/PMC4766417/ /pubmed/26911359 http://dx.doi.org/10.1038/srep21770 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 Wu, Li Li, Ying Guo, Tao Li, Hai-Yan Xiao, Ti-Qiao York, Peter Nangia, Ashwini Gui, Shuang-Ying Zhang, Ji-Wen Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title | Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title_full | Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title_fullStr | Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title_full_unstemmed | Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title_short | Visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
title_sort | visualization and quantification of deformation behavior of clopidogrel bisulfate polymorphs during tableting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766417/ https://www.ncbi.nlm.nih.gov/pubmed/26911359 http://dx.doi.org/10.1038/srep21770 |
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