Drop-on-powder 3D printing of amorphous high dose oral dosage forms: Process development, opportunities and printing limitations.

3D Printing 3D, three-dimensional 3DP, three-dimensional printing AM, additive manufacturing API, active pharmaceutical ingredient ASD, amorphous solid dispersion Additive manufacturing Amorphous solid dispersion BCS, Biopharmaceutics Classification System Binder jetting DSC, differential scanning calorimetry DoP, drop-on-powder Drop-on-powder printing FDA, U.S. Food and Drug Administration FDM, fused deposition modeling HME, hot-melt extrusion KTZ, ketoconazole Process development SODF, solid oral dosage form Solubility enhancement dpmm, dots per millimeter

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
Historique:
received: 27 09 2022
revised: 21 12 2022
accepted: 22 12 2022
entrez: 23 1 2023
pubmed: 24 1 2023
medline: 24 1 2023
Statut: epublish

Résumé

Drop-on-powder 3D printing is able to produce highly drug loaded solid oral dosage forms. However, this technique is mainly limited to well soluble drugs. The majority of pipeline compounds is poorly soluble, though, and requires solubility enhancement, e.g., via formation of amorphous solid dispersions. This study presents a detailed and systematic development approach for the production of tablets containing high amounts of a poorly soluble, amorphized drug via drop-on-powder 3D printing (also known as binder jetting). Amorphization of the compound was achieved via hot-melt extrusion using the exemplary system of the model compound ketoconazole and copovidone as matrix polymer at drug loadings of 20% and 40%. The milled extrudate was used as powder for printing and the influence of inks and different ink-to-powder ratios on recrystallization of ketoconazole was investigated in a material-saving small-scale screening. Crystallinity assessment was performed using differential scanning calorimetry and polarized light microscopy to identify even small traces of crystallinity. Printing of tablets showed that the performed small-scale screening was capable to identify printing parameters for the development of amorphous and mechanically stable tablets via drop-on-powder printing. A stability study demonstrated physically stable tablets over twelve weeks at accelerated storage conditions.

Identifiants

pubmed: 36687376
doi: 10.1016/j.ijpx.2022.100151
pii: S2590-1567(22)00042-1
pmc: PMC9850179
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100151

Informations de copyright

© 2022 Published by Elsevier B.V.

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. Nadine Gottschalk 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.

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Auteurs

Nadine Gottschalk (N)

Institute of Pharmaceutics and Biopharmaceutics, Heinrich Heine University, Düsseldorf, Germany.
Merck KGaA, Darmstadt, Germany.

Alicia Burkard (A)

Merck KGaA, Darmstadt, Germany.

Julian Quodbach (J)

Institute of Pharmaceutics and Biopharmaceutics, Heinrich Heine University, Düsseldorf, Germany.
Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Netherlands.

Malte Bogdahn (M)

Merck KGaA, Darmstadt, Germany.

Classifications MeSH