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The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants

Disintegration performance was measured by analysing both water ingress and tablet swelling of pure microcrystalline cellulose (MCC) and in mixture with croscarmellose sodium using terahertz pulsed imaging (TPI). Tablets made from pure MCC with porosities of 10% and 15% showed similar swelling and t...

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Autores principales: Yassin, Samy, Goodwin, Daniel J, Anderson, Andrew, Sibik, Juraj, Wilson, D Ian, Gladden, Lynn F, Zeitler, J Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647644/
https://www.ncbi.nlm.nih.gov/pubmed/26073446
http://dx.doi.org/10.1002/jps.24544
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author Yassin, Samy
Goodwin, Daniel J
Anderson, Andrew
Sibik, Juraj
Wilson, D Ian
Gladden, Lynn F
Zeitler, J Axel
author_facet Yassin, Samy
Goodwin, Daniel J
Anderson, Andrew
Sibik, Juraj
Wilson, D Ian
Gladden, Lynn F
Zeitler, J Axel
author_sort Yassin, Samy
collection PubMed
description Disintegration performance was measured by analysing both water ingress and tablet swelling of pure microcrystalline cellulose (MCC) and in mixture with croscarmellose sodium using terahertz pulsed imaging (TPI). Tablets made from pure MCC with porosities of 10% and 15% showed similar swelling and transport kinetics: within the first 15 s, tablets had swollen by up to 33% of their original thickness and water had fully penetrated the tablet following Darcy flow kinetics. In contrast, MCC tablets with a porosity of 5% exhibited much slower transport kinetics, with swelling to only 17% of their original thickness and full water penetration reached after 100 s, dominated by case II transport kinetics. The effect of adding superdisintegrant to the formulation and varying the temperature of the dissolution medium between 20°C and 37°C on the swelling and transport process was quantified. We have demonstrated that TPI can be used to non-invasively analyse the complex disintegration kinetics of formulations that take place on timescales of seconds and is a promising tool to better understand the effect of dosage form microstructure on its performance. By relating immediate-release formulations to mathematical models used to describe controlled release formulations, it becomes possible to use this data for formulation design. © 2015 The Authors. Journal of Pharmaceutical Sciences published by Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:3440–3450, 2015
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spelling pubmed-46476442015-11-24 The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants Yassin, Samy Goodwin, Daniel J Anderson, Andrew Sibik, Juraj Wilson, D Ian Gladden, Lynn F Zeitler, J Axel J Pharm Sci Pharmaceutics, Drug Delivery and Pharmaceutical Technology Disintegration performance was measured by analysing both water ingress and tablet swelling of pure microcrystalline cellulose (MCC) and in mixture with croscarmellose sodium using terahertz pulsed imaging (TPI). Tablets made from pure MCC with porosities of 10% and 15% showed similar swelling and transport kinetics: within the first 15 s, tablets had swollen by up to 33% of their original thickness and water had fully penetrated the tablet following Darcy flow kinetics. In contrast, MCC tablets with a porosity of 5% exhibited much slower transport kinetics, with swelling to only 17% of their original thickness and full water penetration reached after 100 s, dominated by case II transport kinetics. The effect of adding superdisintegrant to the formulation and varying the temperature of the dissolution medium between 20°C and 37°C on the swelling and transport process was quantified. We have demonstrated that TPI can be used to non-invasively analyse the complex disintegration kinetics of formulations that take place on timescales of seconds and is a promising tool to better understand the effect of dosage form microstructure on its performance. By relating immediate-release formulations to mathematical models used to describe controlled release formulations, it becomes possible to use this data for formulation design. © 2015 The Authors. Journal of Pharmaceutical Sciences published by Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:3440–3450, 2015 Blackwell Publishing Ltd 2015-10 2015-06-12 /pmc/articles/PMC4647644/ /pubmed/26073446 http://dx.doi.org/10.1002/jps.24544 Text en © 2015 The Authors. Journal of Pharmaceutical Sciences published by Wiley Periodicals, Inc. and the American Pharmacists Association http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmaceutics, Drug Delivery and Pharmaceutical Technology
Yassin, Samy
Goodwin, Daniel J
Anderson, Andrew
Sibik, Juraj
Wilson, D Ian
Gladden, Lynn F
Zeitler, J Axel
The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title_full The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title_fullStr The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title_full_unstemmed The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title_short The Disintegration Process in Microcrystalline Cellulose Based Tablets, Part 1: Influence of Temperature, Porosity and Superdisintegrants
title_sort disintegration process in microcrystalline cellulose based tablets, part 1: influence of temperature, porosity and superdisintegrants
topic Pharmaceutics, Drug Delivery and Pharmaceutical Technology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647644/
https://www.ncbi.nlm.nih.gov/pubmed/26073446
http://dx.doi.org/10.1002/jps.24544
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