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Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders
The relevance of the polymorphic form, particle size, and processing of mannitol for the mechanical properties of solid oral dosage forms was examined. Thus, particle and powder properties of spray granulated β D-mannitol, β D-mannitol, and δ D-mannitol were assessed in this study with regards to th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611586/ https://www.ncbi.nlm.nih.gov/pubmed/36297563 http://dx.doi.org/10.3390/pharmaceutics14102128 |
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author | Mareczek, Lena Riehl, Carolin Harms, Meike Reichl, Stephan |
author_facet | Mareczek, Lena Riehl, Carolin Harms, Meike Reichl, Stephan |
author_sort | Mareczek, Lena |
collection | PubMed |
description | The relevance of the polymorphic form, particle size, and processing of mannitol for the mechanical properties of solid oral dosage forms was examined. Thus, particle and powder properties of spray granulated β D-mannitol, β D-mannitol, and δ D-mannitol were assessed in this study with regards to their manufacturability. D-mannitol is a commonly used excipient in pharmaceutical formulations, especially in oral solid dosage forms, and can be crystallized as three polymorphic forms, of which β is the thermodynamically most stable form and δ is a kinetically stabilized polymorph. A systematic analysis of the powders as starting materials and their respective roller compacted granules is presented to elucidate the multidimensional effects of powder and granules characteristics such as polymorphic form, particle size, and preprocessing on the resulting tablets’ mechanical properties. In direct compression and after roller compaction, δ polymorph displayed superior tableting properties over β mannitol, but was outperformed by spray granulated β mannitol. This could be primarily correlated to the higher specific surface area, leading to higher bonding area and more interparticle bonds within the tablet. Hence, it was shown that surface characteristics and preprocessing can prevail over the impact of polymorphism on manufacturability for oral solid dosage forms. |
format | Online Article Text |
id | pubmed-9611586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96115862022-10-28 Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders Mareczek, Lena Riehl, Carolin Harms, Meike Reichl, Stephan Pharmaceutics Article The relevance of the polymorphic form, particle size, and processing of mannitol for the mechanical properties of solid oral dosage forms was examined. Thus, particle and powder properties of spray granulated β D-mannitol, β D-mannitol, and δ D-mannitol were assessed in this study with regards to their manufacturability. D-mannitol is a commonly used excipient in pharmaceutical formulations, especially in oral solid dosage forms, and can be crystallized as three polymorphic forms, of which β is the thermodynamically most stable form and δ is a kinetically stabilized polymorph. A systematic analysis of the powders as starting materials and their respective roller compacted granules is presented to elucidate the multidimensional effects of powder and granules characteristics such as polymorphic form, particle size, and preprocessing on the resulting tablets’ mechanical properties. In direct compression and after roller compaction, δ polymorph displayed superior tableting properties over β mannitol, but was outperformed by spray granulated β mannitol. This could be primarily correlated to the higher specific surface area, leading to higher bonding area and more interparticle bonds within the tablet. Hence, it was shown that surface characteristics and preprocessing can prevail over the impact of polymorphism on manufacturability for oral solid dosage forms. MDPI 2022-10-07 /pmc/articles/PMC9611586/ /pubmed/36297563 http://dx.doi.org/10.3390/pharmaceutics14102128 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mareczek, Lena Riehl, Carolin Harms, Meike Reichl, Stephan Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title | Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title_full | Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title_fullStr | Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title_full_unstemmed | Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title_short | Understanding the Multidimensional Effects of Polymorphism, Particle Size and Processing for D-Mannitol Powders |
title_sort | understanding the multidimensional effects of polymorphism, particle size and processing for d-mannitol powders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611586/ https://www.ncbi.nlm.nih.gov/pubmed/36297563 http://dx.doi.org/10.3390/pharmaceutics14102128 |
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