3D printing of amorphous solid dispersions: A comparison of fused deposition modeling and drop-on-powder printing.
3D printing
Additive manufacturing
Amorphous solid dispersion
Binder jetting
Drop-on-powder
Fused deposition modeling
Solubility enhancement
Journal
International journal of pharmaceutics: X
ISSN: 2590-1567
Titre abrégé: Int J Pharm X
Pays: Netherlands
ID NLM: 101753452
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
received:
28
12
2022
revised:
16
03
2023
accepted:
17
03
2023
medline:
8
4
2023
entrez:
7
4
2023
pubmed:
8
4
2023
Statut:
epublish
Résumé
Nowadays, a high number of pipeline drugs are poorly soluble and require solubility enhancement by e.g., manufacturing of amorphous solid dispersion. Pharmaceutical 3D printing has great potential in producing amorphous solid oral dosage forms. However, 3D printing techniques differ greatly in terms of processing as well as tablet properties. In this study, an amorphous formulation, which had been printed via Fused Deposition Modeling and drop-on-powder printing, also known as binder jetting, was characterized in terms of solid-state properties and physical stability. Solid state assessment was performed by differential scanning calorimetry, powder X-ray diffraction and polarized microscopy. The supersaturation performance of the amorphous solid dispersion was assessed via non-sink dissolution. We further evaluated both 3D printing techniques regarding their processability as well as tablet uniformity in terms of dimension, mass and content. Challenges and limitations of each 3D printing technique were discussed. Both techniques are feasible for the production of amorphous formulations. Results indicated that Fused Deposition Modeling is better suited for production, as the recrystallization tendency was lower. Still, filament production and printing presented a major challenge. Drop-on-powder printing can be a viable alternative for the production of amorphous tablets, when a formulation is not printable by Fused Deposition Modeling.
Identifiants
pubmed: 37025187
doi: 10.1016/j.ijpx.2023.100179
pii: S2590-1567(23)00023-3
pmc: PMC10070627
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100179Informations de copyright
© 2023 The Authors.
Déclaration de conflit d'intérêts
The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Malte Bogdahn has patent Process for the manufacture of a solid pharmaceutical administration form pending to Merck Patent GmbH. Julian Quodbach has patent Process for the manufacture of a solid pharmaceutical administration form pending to Merck Patent GmbH. Nadine Gottschalk has patent Process for the manufacture of a solid pharmaceutical administration form pending to Merck Patent GmbH.
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