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Model-based optimization of the primary drying phase of oral lyophilizates

Oral lyophilizates also called orally disintegrating tablets (ODTs) are a patient friendly and convenient dosage form. They are manufactured by dosing a suspension in blister cups and subsequently freeze-drying these blisters to achieve porous tablets that disintegrate quickly (< 10 s) when place...

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Detalles Bibliográficos
Autores principales: Vanbillemont, Brecht, De Beer, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670193/
https://www.ncbi.nlm.nih.gov/pubmed/33235992
http://dx.doi.org/10.1016/j.ijpx.2020.100057
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author Vanbillemont, Brecht
De Beer, Thomas
author_facet Vanbillemont, Brecht
De Beer, Thomas
author_sort Vanbillemont, Brecht
collection PubMed
description Oral lyophilizates also called orally disintegrating tablets (ODTs) are a patient friendly and convenient dosage form. They are manufactured by dosing a suspension in blister cups and subsequently freeze-drying these blisters to achieve porous tablets that disintegrate quickly (< 10 s) when placed upon the tongue. This paper proposes a mechanistic model of the primary drying phase of these oral lyophilizates processed in cold-form blisters. A heat transfer coefficient (K(v)) and dried layer resistance (R(p)) are regressed and applied in a dynamic optimization of the primary drying phase. The optimization exercise showed the possibility of ultra-short sublimation times for polyvinyl acetate (PVA) based formulations with a primary drying time of 3.68 h for a 500 mg acetaminophen tablet.
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spelling pubmed-76701932020-11-23 Model-based optimization of the primary drying phase of oral lyophilizates Vanbillemont, Brecht De Beer, Thomas Int J Pharm X Research Paper Oral lyophilizates also called orally disintegrating tablets (ODTs) are a patient friendly and convenient dosage form. They are manufactured by dosing a suspension in blister cups and subsequently freeze-drying these blisters to achieve porous tablets that disintegrate quickly (< 10 s) when placed upon the tongue. This paper proposes a mechanistic model of the primary drying phase of these oral lyophilizates processed in cold-form blisters. A heat transfer coefficient (K(v)) and dried layer resistance (R(p)) are regressed and applied in a dynamic optimization of the primary drying phase. The optimization exercise showed the possibility of ultra-short sublimation times for polyvinyl acetate (PVA) based formulations with a primary drying time of 3.68 h for a 500 mg acetaminophen tablet. Elsevier 2020-10-31 /pmc/articles/PMC7670193/ /pubmed/33235992 http://dx.doi.org/10.1016/j.ijpx.2020.100057 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Vanbillemont, Brecht
De Beer, Thomas
Model-based optimization of the primary drying phase of oral lyophilizates
title Model-based optimization of the primary drying phase of oral lyophilizates
title_full Model-based optimization of the primary drying phase of oral lyophilizates
title_fullStr Model-based optimization of the primary drying phase of oral lyophilizates
title_full_unstemmed Model-based optimization of the primary drying phase of oral lyophilizates
title_short Model-based optimization of the primary drying phase of oral lyophilizates
title_sort model-based optimization of the primary drying phase of oral lyophilizates
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670193/
https://www.ncbi.nlm.nih.gov/pubmed/33235992
http://dx.doi.org/10.1016/j.ijpx.2020.100057
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