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Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets
The shapes of particles and their distribution in tablets, controlled by pretreatment and tableting process, determine the pharmaceutical performance of excipient like lubricant. This study aims to provide deeper insights to the relationship of the morphology and spatial distribution of stearic acid...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066036/ https://www.ncbi.nlm.nih.gov/pubmed/32175018 http://dx.doi.org/10.1016/j.ajps.2019.01.001 |
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author | Zhang, Liu Shakya, Shailendra Wu, Li Wang, Jiangtao Jin, Guanghui Sun, Huimin Yin, Xianzhen Sun, Lixin Zhang, Jiwen |
author_facet | Zhang, Liu Shakya, Shailendra Wu, Li Wang, Jiangtao Jin, Guanghui Sun, Huimin Yin, Xianzhen Sun, Lixin Zhang, Jiwen |
author_sort | Zhang, Liu |
collection | PubMed |
description | The shapes of particles and their distribution in tablets, controlled by pretreatment and tableting process, determine the pharmaceutical performance of excipient like lubricant. This study aims to provide deeper insights to the relationship of the morphology and spatial distribution of stearic acid (SA) with the lubrication efficiency, as well as the resulting tablet property. Unmodified SA particles as flat sheet-like particles were firstly reprocessed by emulsification in hot water to obtain the reprocessed SA particles with spherical morphology. The three-dimensional (3D) information of SA particles in tablets was detected by a quantitative and non-invasive 3D structure elucidation technique, namely, synchrotron radiation X-ray micro-computed tomography (SR-µCT). SA particles in glipizide tablets prepared by using unmodified SA (GUT), reprocessed SA (GRT), as well as reference listed drug (RLD) of glipizide tablets were analyzed by SR-µCT. The results showed that the reprocessed SA with better flowability contributed to similarity of breaking forces between that of GRT and RLD. SA particles in GRT were very similar to those in RLD with uniform morphology and particle size, while SA particles in GUT were not evenly distributed. These findings not only demonstrated the feasibility of SR-µCT as a new method in revealing the morphology and spatial distribution of excipient in drug delivery system, but also deepened insights of solid dosage form design into a new scale by powder engineering. |
format | Online Article Text |
id | pubmed-7066036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-70660362020-03-13 Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets Zhang, Liu Shakya, Shailendra Wu, Li Wang, Jiangtao Jin, Guanghui Sun, Huimin Yin, Xianzhen Sun, Lixin Zhang, Jiwen Asian J Pharm Sci Research article The shapes of particles and their distribution in tablets, controlled by pretreatment and tableting process, determine the pharmaceutical performance of excipient like lubricant. This study aims to provide deeper insights to the relationship of the morphology and spatial distribution of stearic acid (SA) with the lubrication efficiency, as well as the resulting tablet property. Unmodified SA particles as flat sheet-like particles were firstly reprocessed by emulsification in hot water to obtain the reprocessed SA particles with spherical morphology. The three-dimensional (3D) information of SA particles in tablets was detected by a quantitative and non-invasive 3D structure elucidation technique, namely, synchrotron radiation X-ray micro-computed tomography (SR-µCT). SA particles in glipizide tablets prepared by using unmodified SA (GUT), reprocessed SA (GRT), as well as reference listed drug (RLD) of glipizide tablets were analyzed by SR-µCT. The results showed that the reprocessed SA with better flowability contributed to similarity of breaking forces between that of GRT and RLD. SA particles in GRT were very similar to those in RLD with uniform morphology and particle size, while SA particles in GUT were not evenly distributed. These findings not only demonstrated the feasibility of SR-µCT as a new method in revealing the morphology and spatial distribution of excipient in drug delivery system, but also deepened insights of solid dosage form design into a new scale by powder engineering. Shenyang Pharmaceutical University 2020-01 2019-03-01 /pmc/articles/PMC7066036/ /pubmed/32175018 http://dx.doi.org/10.1016/j.ajps.2019.01.001 Text en © 2019 Shenyang Pharmaceutical University. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research article Zhang, Liu Shakya, Shailendra Wu, Li Wang, Jiangtao Jin, Guanghui Sun, Huimin Yin, Xianzhen Sun, Lixin Zhang, Jiwen Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title | Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title_full | Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title_fullStr | Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title_full_unstemmed | Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title_short | Multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
title_sort | multi-dimensional visualization for the morphology of lubricant stearic acid particles and their distribution in tablets |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066036/ https://www.ncbi.nlm.nih.gov/pubmed/32175018 http://dx.doi.org/10.1016/j.ajps.2019.01.001 |
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