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Modelling the Compaction Step of a Platform Direct Compression Process
The ability to predict formulation behaviour at production scale during formulation design can reduce the time to market and decrease product development costs. However, it is challenging to extrapolate compaction settings for direct compression formulations between tablet press models during scale-...
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/PMC9027228/ https://www.ncbi.nlm.nih.gov/pubmed/35456529 http://dx.doi.org/10.3390/pharmaceutics14040695 |
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author | Peddapatla, Raghu V. G. Slevin, Conor Sheridan, Gerard Beirne, Caoimhe Swaminathan, Shrikant Browning, Ivan O’Reilly, Clare Worku, Zelalem A. Egan, David Sheehan, Stephen Crean, Abina M. |
author_facet | Peddapatla, Raghu V. G. Slevin, Conor Sheridan, Gerard Beirne, Caoimhe Swaminathan, Shrikant Browning, Ivan O’Reilly, Clare Worku, Zelalem A. Egan, David Sheehan, Stephen Crean, Abina M. |
author_sort | Peddapatla, Raghu V. G. |
collection | PubMed |
description | The ability to predict formulation behaviour at production scale during formulation design can reduce the time to market and decrease product development costs. However, it is challenging to extrapolate compaction settings for direct compression formulations between tablet press models during scale-up and transfer from R&D to commercial production. The aim of this study was to develop statistical process models to predict tablet tensile strength, porosity and disintegration time from compaction parameters (pre-compression and main compression force, and press speed), for three formulations, with differing deformation characteristics (plastic, brittle and elastic), on three tablet press models (one pilot-scale tablet press (KG RoTab) and two production-scale presses (Fette 1200i and GEA Modul P)). The deformation characteristics of yield pressure and elastic recovery were determined for the model placebo formulations investigated. To facilitate comparison of dwell time settings between tablet press models, the design of experiments (DoE) approach was 9 individual 16-run response surface DoEs (3 formulation × 3 press models), whose results were combined to create a polynomial regression model for each tablet property. These models predicted tablet tensile strength, porosity and disintegration time and enabled the construction of design spaces to produce tablets with specified target properties, for each formulation on each press. The models were successfully validated. This modelling approach provides an understanding of the compaction behaviour of formulations with varying deformation behaviour on development and commercial tablet press models. This understanding can be applied to inform achievable production rates at a commercial scale, during the formulation development. |
format | Online Article Text |
id | pubmed-9027228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90272282022-04-23 Modelling the Compaction Step of a Platform Direct Compression Process Peddapatla, Raghu V. G. Slevin, Conor Sheridan, Gerard Beirne, Caoimhe Swaminathan, Shrikant Browning, Ivan O’Reilly, Clare Worku, Zelalem A. Egan, David Sheehan, Stephen Crean, Abina M. Pharmaceutics Article The ability to predict formulation behaviour at production scale during formulation design can reduce the time to market and decrease product development costs. However, it is challenging to extrapolate compaction settings for direct compression formulations between tablet press models during scale-up and transfer from R&D to commercial production. The aim of this study was to develop statistical process models to predict tablet tensile strength, porosity and disintegration time from compaction parameters (pre-compression and main compression force, and press speed), for three formulations, with differing deformation characteristics (plastic, brittle and elastic), on three tablet press models (one pilot-scale tablet press (KG RoTab) and two production-scale presses (Fette 1200i and GEA Modul P)). The deformation characteristics of yield pressure and elastic recovery were determined for the model placebo formulations investigated. To facilitate comparison of dwell time settings between tablet press models, the design of experiments (DoE) approach was 9 individual 16-run response surface DoEs (3 formulation × 3 press models), whose results were combined to create a polynomial regression model for each tablet property. These models predicted tablet tensile strength, porosity and disintegration time and enabled the construction of design spaces to produce tablets with specified target properties, for each formulation on each press. The models were successfully validated. This modelling approach provides an understanding of the compaction behaviour of formulations with varying deformation behaviour on development and commercial tablet press models. This understanding can be applied to inform achievable production rates at a commercial scale, during the formulation development. MDPI 2022-03-23 /pmc/articles/PMC9027228/ /pubmed/35456529 http://dx.doi.org/10.3390/pharmaceutics14040695 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 Peddapatla, Raghu V. G. Slevin, Conor Sheridan, Gerard Beirne, Caoimhe Swaminathan, Shrikant Browning, Ivan O’Reilly, Clare Worku, Zelalem A. Egan, David Sheehan, Stephen Crean, Abina M. Modelling the Compaction Step of a Platform Direct Compression Process |
title | Modelling the Compaction Step of a Platform Direct Compression Process |
title_full | Modelling the Compaction Step of a Platform Direct Compression Process |
title_fullStr | Modelling the Compaction Step of a Platform Direct Compression Process |
title_full_unstemmed | Modelling the Compaction Step of a Platform Direct Compression Process |
title_short | Modelling the Compaction Step of a Platform Direct Compression Process |
title_sort | modelling the compaction step of a platform direct compression process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027228/ https://www.ncbi.nlm.nih.gov/pubmed/35456529 http://dx.doi.org/10.3390/pharmaceutics14040695 |
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