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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10223035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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