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Tytuł pozycji:

Part I: Significant reduction of lyophilization process times by using novel matrix based scaffolds.

Tytuł:
Part I: Significant reduction of lyophilization process times by using novel matrix based scaffolds.
Autorzy:
Kullmann D; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland. Electronic address: .
Martinez CL; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland.
Lümkemann J; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland.
Huwyler J; Division of Pharmaceutical Technology, Department of Pharmaceutical Sciences, University of Basel, 4056 Basel, Switzerland.
Źródło:
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V [Eur J Pharm Biopharm] 2023 Mar; Vol. 184, pp. 248-261. Date of Electronic Publication: 2022 Dec 15.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: Amsterdam : Elsevier Science
Original Publication: Stuttgart : Wissenschaftliche Verlagsgesellschaft, c1991-
MeSH Terms:
Chemistry, Pharmaceutical*/methods
Desiccation*
Humans ; Freeze Drying/methods ; Pharmaceutical Preparations ; Antibodies, Monoclonal/chemistry
Contributed Indexing:
Keywords: 3D-printing; Intermediate process container; Lyophilization; Monoclonal antibody; Porous structure
Substance Nomenclature:
0 (Pharmaceutical Preparations)
0 (Antibodies, Monoclonal)
Entry Date(s):
Date Created: 20221218 Date Completed: 20230228 Latest Revision: 20230228
Update Code:
20240105
DOI:
10.1016/j.ejpb.2022.12.008
PMID:
36529257
Czasopismo naukowe
To improve the long-term stability of drugs with limited stability (e.g., biologicals such as monoclonal antibodies, antibody drug conjugates or peptides), some pharmaceuticals endure a lengthy and cost-intensive process called lyophilization. While the shelf life of lyophilized drugs may be prolonged compared to their liquid form, the drawbacks come in the form of intensified manufacturing, preparation, and dosing efforts. The use of glass vials as the primary container unit for lyophilized products hinders their complication-free, fast and flexible use, as they require a skilled healthcare professional and an aseptic environment in which to prepare them. The feasibility of substituting glass vials with novel container designs offering the complete transfer of the lyophilizate cake into modern administration devices, while reducing the economic footprint of the lyophilization process, was investigated. The lyophilization process of a monoclonal antibody solution was studied by assessing primary drying conditions, homogeneity of the drying process, and critical quality attributes after successful lyophilization. The creation of novel container designs utilized vacuum-forming to generate confined containers with removable bottoms and rapid prototyping, including subtractive and additive manufacturing methods, to generate porous 3D structures for drug housing. The novel container designs generated lyophilizates twice as fast and achieved a threefold faster reconstitution compared to their vial counterparts, without adaptation of the processing conditions. We conclude that the use of intermediate process containers offers significant relief for healthcare professionals in terms of reduced probability of handling errors, while drug manufacturers benefit from the accelerated processing times, increased batch homogeneity, and sustainability.
Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2022. Published by Elsevier B.V.)

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