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Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)

Recently, attention has been drawn to microwave-assisted freeze-drying (MFD), as it drastically reduces the typically long drying times of biopharmaceuticals in conventional freeze-drying (CFD). Nevertheless, previously described prototype machines lack important attributes such as in-chamber freezi...

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Autores principales: Härdter, Nicole, Geidobler, Raimund, Presser, Ingo, Winter, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223035/
https://www.ncbi.nlm.nih.gov/pubmed/37242584
http://dx.doi.org/10.3390/pharmaceutics15051342
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author Härdter, Nicole
Geidobler, Raimund
Presser, Ingo
Winter, Gerhard
author_facet Härdter, Nicole
Geidobler, Raimund
Presser, Ingo
Winter, Gerhard
author_sort Härdter, Nicole
collection PubMed
description Recently, attention has been drawn to microwave-assisted freeze-drying (MFD), as it drastically reduces the typically long drying times of biopharmaceuticals in conventional freeze-drying (CFD). Nevertheless, previously described prototype machines lack important attributes such as in-chamber freezing and stoppering, not allowing for the performance of representative vial freeze-drying processes. In this study, we present a new technical MFD setup, designed with GMP processes in mind. It is based on a standard lyophilizer equipped with flat semiconductor microwave modules. The idea was to enable the retrofitting of standard freeze-dryers with a microwave option, which would reduce the hurdles of implementation. We aimed to collect process data with respect to the speed, settings, and controllability of the MFD processes. Moreover, we studied the performance of six monoclonal antibody (mAb) formulations in terms of quality after drying and stability after storage for 6 months. We found drying processes to be drastically shortened and well controllable and observed no signs of plasma discharge. The characterization of the lyophilizates revealed an elegant cake appearance and remarkably good stability in the mAb after MFD. Furthermore, overall storage stability was good, even when residual moisture was increased due to high concentrations of glass-forming excipients. A direct comparison of stability data following MFD and CFD demonstrated similar stability profiles. We conclude that the new machine design is highly advantageous, enabling the fast-drying of excipient-dominated, low-concentrated mAb formulations in compliance with modern manufacturing technology.
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spelling pubmed-102230352023-05-28 Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD) Härdter, Nicole Geidobler, Raimund Presser, Ingo Winter, Gerhard Pharmaceutics Article Recently, attention has been drawn to microwave-assisted freeze-drying (MFD), as it drastically reduces the typically long drying times of biopharmaceuticals in conventional freeze-drying (CFD). Nevertheless, previously described prototype machines lack important attributes such as in-chamber freezing and stoppering, not allowing for the performance of representative vial freeze-drying processes. In this study, we present a new technical MFD setup, designed with GMP processes in mind. It is based on a standard lyophilizer equipped with flat semiconductor microwave modules. The idea was to enable the retrofitting of standard freeze-dryers with a microwave option, which would reduce the hurdles of implementation. We aimed to collect process data with respect to the speed, settings, and controllability of the MFD processes. Moreover, we studied the performance of six monoclonal antibody (mAb) formulations in terms of quality after drying and stability after storage for 6 months. We found drying processes to be drastically shortened and well controllable and observed no signs of plasma discharge. The characterization of the lyophilizates revealed an elegant cake appearance and remarkably good stability in the mAb after MFD. Furthermore, overall storage stability was good, even when residual moisture was increased due to high concentrations of glass-forming excipients. A direct comparison of stability data following MFD and CFD demonstrated similar stability profiles. We conclude that the new machine design is highly advantageous, enabling the fast-drying of excipient-dominated, low-concentrated mAb formulations in compliance with modern manufacturing technology. MDPI 2023-04-27 /pmc/articles/PMC10223035/ /pubmed/37242584 http://dx.doi.org/10.3390/pharmaceutics15051342 Text en © 2023 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
Härdter, Nicole
Geidobler, Raimund
Presser, Ingo
Winter, Gerhard
Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title_full Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title_fullStr Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title_full_unstemmed Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title_short Accelerated Production of Biopharmaceuticals via Microwave-Assisted Freeze-Drying (MFD)
title_sort accelerated production of biopharmaceuticals via microwave-assisted freeze-drying (mfd)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223035/
https://www.ncbi.nlm.nih.gov/pubmed/37242584
http://dx.doi.org/10.3390/pharmaceutics15051342
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