Accurate low-temperature direct granule extrusion 3D printing of personalised paediatric minitablets

Medicine individualisation remains constrained by the limited availability of age-appropriate strengths and by extemporaneous practices that can compromise dose consistency. Direct extrusion 3D printing offers an alternative manufacturing method for personalised medicine, without introducing solvents, complex preparation, or post-processing that challenge the adoption in pharmacy. However, achieving uniform weight and drug content in small objects (e.g., paediatric-friendly minitablets) and lowering the preparation temperature remain challenges for direct extrusion-based 3D printing technologies. In this work, we introduce a facile low-temperature direct granules extrusion 3D printing strategy to manufacture carvedilol minitablets, starting from carvedilol powder or crushed licensed tablets as starting materials, using a high-precision pharmaceutical-grade 3D printer. Methacrylate-based polymers, polyethylene glycol, and glyceryl monostearate were used to enable extrusion at 70-75°C. When the 3D printer was challenged with minute-dimensional designs, it was possible to manufacture batches of minitablets up to 2 mm in diameter with 0.8 mm in thickness. The lowest minitablet weight variation was 1.48%, achieved with an optimal diameter of 3.6 mm and a thickness of 1.6 mm; this was also reflected in the drug content uniformity (within ± 5%). The batches also met British Pharmacopoeia requirements for dissolution (>80% in 45 min). These findings extend direct extrusion 3D printing to a viable manufacturing platform for accurate, low-dose small solid units, such as minitablets. By coupling a GMP-compliant 3D printer with a simplified preparation workflow, this work provides a realistic blueprint for integrating direct extrusion-enabled personalised minitablets into hospital pharmacy and point-of-care settings.

Authors

Institutions

Publication Details

Journal
International Journal of Pharmaceutics
Published
2026-04-13
DOI
https://doi.org/10.1016/j.ijpharm.2026.126871
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Accurate low-temperature direct granule extrusion 3D printing of personalised paediatric minitablets

Stuart Allen Jones, Paul G. Royall, Joanna Giebułtowicz, Mohamed Albed Alhnan et al.
International Journal of Pharmaceutics
3D Printing in Biomedical Research
article

Accurate low-temperature direct granule extrusion 3D printing of personalised paediatric minitablets

Stuart Allen Jones, Paul G. Royall, Joanna Giebułtowicz, Mohamed Albed Alhnan, Abdullah Isreb, Louise Bracken, Cecile Ayako Dreiss, Bambang V.E.B. Abdillah Akbar, Stephen Tomlin, Andrea Gill, Michalina Seluk, Marcelo da Silva
article en

Abstract

Medicine individualisation remains constrained by the limited availability of age-appropriate strengths and by extemporaneous practices that can compromise dose consistency. Direct extrusion 3D printing offers an alternative manufacturing method for personalised medicine, without introducing solvents, complex preparation, or post-processing that challenge the adoption in pharmacy. However, achieving uniform weight and drug content in small objects (e.g., paediatric-friendly minitablets) and lowering the preparation temperature remain challenges for direct extrusion-based 3D printing technologies. In this work, we introduce a facile low-temperature direct granules extrusion 3D printing strategy to manufacture carvedilol minitablets, starting from carvedilol powder or crushed licensed tablets as starting materials, using a high-precision pharmaceutical-grade 3D printer. Methacrylate-based polymers, polyethylene glycol, and glyceryl monostearate were used to enable extrusion at 70-75°C. When the 3D printer was challenged with minute-dimensional designs, it was possible to manufacture batches of minitablets up to 2 mm in diameter with 0.8 mm in thickness. The lowest minitablet weight variation was 1.48%, achieved with an optimal diameter of 3.6 mm and a thickness of 1.6 mm; this was also reflected in the drug content uniformity (within ± 5%). The batches also met British Pharmacopoeia requirements for dissolution (>80% in 45 min). These findings extend direct extrusion 3D printing to a viable manufacturing platform for accurate, low-dose small solid units, such as minitablets. By coupling a GMP-compliant 3D printer with a simplified preparation workflow, this work provides a realistic blueprint for integrating direct extrusion-enabled personalised minitablets into hospital pharmacy and point-of-care settings.

International Journal of PharmaceuticsVol. 697
King's College London (GB), Medical University of Warsaw (PL), Great Ormond Street Hospital for Children NHS Foundation Trust (GB), Alder Hey Children's NHS Foundation Trust (GB), Liverpool John Moores University (GB)
Openalex Percentile: Top 30%
3D Printing in Biomedical Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.