TY - JOUR
T1 - Enabling high-fidelity personalised pharmaceutical tablets through multimaterial inkjet 3D printing with a water-soluble excipient
AU - Rivers, Geoffrey
AU - Lion, Anna
AU - Putri, Nur Rofiqoh Eviana
AU - Rance, Graham A.
AU - Moloney, Cara
AU - Taresco, Vincenzo
AU - Crucitti, Valentina Cuzzucoli
AU - Constantin, Hannah
AU - Evangelista Barreiros, Maria Inês
AU - Cantu, Laura Ruiz
AU - Tuck, Christopher J.
AU - Rose, Felicity R.A.J.
AU - Hague, Richard J.M.
AU - Roberts, Clive J.
AU - Turyanska, Lyudmila
AU - Wildman, Ricky D.
AU - He, Yinfeng
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/6
Y1 - 2024/6
N2 - Additive manufacturing offers manufacture of personalised pharmaceutical tablets through design freedoms and material deposition control at an individual voxel level. This control goes beyond geometry and materials choices: inkjet based 3D printing enables the precise deposition (10–80 μm) of multiple materials, which permits integration of precise doses with tailored release rates; in the meanwhile, this technique has demonstrated its capability of high-volume personalised production. In this paper we demonstrate how two dissimilar materials, one water soluble and one insoluble, can be co-printed within a design envelope to dial up a range of release rates including slow (0.98 ± 0.04 mg/min), fast (4.07 ± 0.25 mg/min) and multi-stepped (2.17 ± 0.04 mg/min then 0.70 ± 0.13 mg/min) dissolution curves. To achieve this, we adopted poly-4-acryloylmorpholine (poly-ACMO) as a new photocurable water-soluble carrier and demonstrated its contemporaneous deposition with an insoluble monomer. The water soluble ACMO formulation with aspirin incorporated was successfully printed and cured under UV light and a wide variety of shapes with material distributions that control drug elution was successfully fabricated by inkjet based 3D printing technique, suggesting its viability as a future personalised solid dosage form fabrication routine.
AB - Additive manufacturing offers manufacture of personalised pharmaceutical tablets through design freedoms and material deposition control at an individual voxel level. This control goes beyond geometry and materials choices: inkjet based 3D printing enables the precise deposition (10–80 μm) of multiple materials, which permits integration of precise doses with tailored release rates; in the meanwhile, this technique has demonstrated its capability of high-volume personalised production. In this paper we demonstrate how two dissimilar materials, one water soluble and one insoluble, can be co-printed within a design envelope to dial up a range of release rates including slow (0.98 ± 0.04 mg/min), fast (4.07 ± 0.25 mg/min) and multi-stepped (2.17 ± 0.04 mg/min then 0.70 ± 0.13 mg/min) dissolution curves. To achieve this, we adopted poly-4-acryloylmorpholine (poly-ACMO) as a new photocurable water-soluble carrier and demonstrated its contemporaneous deposition with an insoluble monomer. The water soluble ACMO formulation with aspirin incorporated was successfully printed and cured under UV light and a wide variety of shapes with material distributions that control drug elution was successfully fabricated by inkjet based 3D printing technique, suggesting its viability as a future personalised solid dosage form fabrication routine.
KW - Controlled release
KW - Drug delivery
KW - Multi-material printing
KW - Polypills
KW - Water soluble
UR - http://www.scopus.com/inward/record.url?scp=85192794101&partnerID=8YFLogxK
U2 - 10.1016/j.mtadv.2024.100493
DO - 10.1016/j.mtadv.2024.100493
M3 - Article
AN - SCOPUS:85192794101
SN - 2590-0498
VL - 22
JO - Materials Today Advances
JF - Materials Today Advances
M1 - 100493
ER -