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Characterization of Mechanical Property Distributions on Tablet Surfaces
Powder densification through uniaxial compaction is governed by a number of simultaneous processes taking place on a reduced time as the result of the stress gradients within the packing, as well as the frictional and adhesive forces between the powder and the die walls. As a result of that, a densi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320771/ https://www.ncbi.nlm.nih.gov/pubmed/30322058 http://dx.doi.org/10.3390/pharmaceutics10040184 |
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author | Cabiscol, Ramon Finke, Jan Henrik Zetzener, Harald Kwade, Arno |
author_facet | Cabiscol, Ramon Finke, Jan Henrik Zetzener, Harald Kwade, Arno |
author_sort | Cabiscol, Ramon |
collection | PubMed |
description | Powder densification through uniaxial compaction is governed by a number of simultaneous processes taking place on a reduced time as the result of the stress gradients within the packing, as well as the frictional and adhesive forces between the powder and the die walls. As a result of that, a density and stiffness anisotropy is developed across the axial and radial directions. In this study, microindentation has been applied to assess and quantify the variation of the module of elasticity ([Formula: see text]) throughout the surface of cylindrical tablets. A representative set of deformation behaviors was analyzed by pharmaceutical excipients ranging from soft/plastic behavior (microcrystalline cellulose) over medium (lactose) to hard/brittle behavior (calcium phosphate) for different compaction pressures. The results of the local stiffness distribution over tablet faces depicted a linear and directly proportional tendency between a solid fraction and [Formula: see text] for the upper and lower faces, as well as remarkable stiffness anisotropy between the axial and radial directions of compaction. The highest extent of the stiffness anisotropy that was found for ductile grades of microcrystalline cellulose (MCC) in comparison with brittle powders has been attributed to the dual phenomena of overall elastic recovery and Poisson’s effect on the relaxation kinetics. As a reinforcement of this analysis, the evolution of the specific surface area elucidated the respective densification mechanism and its implementations toward anisotropy. For ductile excipients, the increase in the contact surface area as well as the reduction and closing of interstitial pores explain the reduction of surface area with increasing compaction pressure. For brittle powders, densification evolves through fragmentation and the subsequent filling of voids. |
format | Online Article Text |
id | pubmed-6320771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63207712019-01-11 Characterization of Mechanical Property Distributions on Tablet Surfaces Cabiscol, Ramon Finke, Jan Henrik Zetzener, Harald Kwade, Arno Pharmaceutics Article Powder densification through uniaxial compaction is governed by a number of simultaneous processes taking place on a reduced time as the result of the stress gradients within the packing, as well as the frictional and adhesive forces between the powder and the die walls. As a result of that, a density and stiffness anisotropy is developed across the axial and radial directions. In this study, microindentation has been applied to assess and quantify the variation of the module of elasticity ([Formula: see text]) throughout the surface of cylindrical tablets. A representative set of deformation behaviors was analyzed by pharmaceutical excipients ranging from soft/plastic behavior (microcrystalline cellulose) over medium (lactose) to hard/brittle behavior (calcium phosphate) for different compaction pressures. The results of the local stiffness distribution over tablet faces depicted a linear and directly proportional tendency between a solid fraction and [Formula: see text] for the upper and lower faces, as well as remarkable stiffness anisotropy between the axial and radial directions of compaction. The highest extent of the stiffness anisotropy that was found for ductile grades of microcrystalline cellulose (MCC) in comparison with brittle powders has been attributed to the dual phenomena of overall elastic recovery and Poisson’s effect on the relaxation kinetics. As a reinforcement of this analysis, the evolution of the specific surface area elucidated the respective densification mechanism and its implementations toward anisotropy. For ductile excipients, the increase in the contact surface area as well as the reduction and closing of interstitial pores explain the reduction of surface area with increasing compaction pressure. For brittle powders, densification evolves through fragmentation and the subsequent filling of voids. MDPI 2018-10-12 /pmc/articles/PMC6320771/ /pubmed/30322058 http://dx.doi.org/10.3390/pharmaceutics10040184 Text en © 2018 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 Cabiscol, Ramon Finke, Jan Henrik Zetzener, Harald Kwade, Arno Characterization of Mechanical Property Distributions on Tablet Surfaces |
title | Characterization of Mechanical Property Distributions on Tablet Surfaces |
title_full | Characterization of Mechanical Property Distributions on Tablet Surfaces |
title_fullStr | Characterization of Mechanical Property Distributions on Tablet Surfaces |
title_full_unstemmed | Characterization of Mechanical Property Distributions on Tablet Surfaces |
title_short | Characterization of Mechanical Property Distributions on Tablet Surfaces |
title_sort | characterization of mechanical property distributions on tablet surfaces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320771/ https://www.ncbi.nlm.nih.gov/pubmed/30322058 http://dx.doi.org/10.3390/pharmaceutics10040184 |
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