Fabrication of 3D printed mutable drug delivery devices: a comparative study of volumetric and digital light processing printing

Mutable devices and dosage forms have the capacity to dynamically transform dimensionally, morphologically and mechanically upon exposure to non-mechanical external triggers. By leveraging these controllable transformations, these systems can be used as minimally invasive alternatives to implants and residence devices, foregoing the need for complex surgeries or endoscopies. 4D printing, the fabrication of 3D-printed structures that evolve their shape, properties, or functionality in response to stimuli over time, allows the production of such devices. This study explores the potential of volumetric printing, a novel vat photopolymerisation technology capable of ultra-rapid printing speeds, by comparing its performance against established digital light processing (DLP) printing in fabricating hydrogel-based drug-eluting devices. Six hydrogel formulations consisting of 2-(acryloyloxy)ethyl]trimethylammonium chloride solution, lithium phenyl-2,4,6-trimethylbenzoylphosphinate, varying molecular weights of the crosslinking monomer, poly(ethylene glycol) diacrylate, and paracetamol as a model drug were prepared for both vat photopolymerisation technologies. Comprehensive studies were conducted to investigate the swelling and water sorption profiles, drug release kinetics, and physicochemical properties of each formulation. Expandable drug-eluting 4D devices were successfully fabricated within 7.5 s using volumetric printing and were shown to display equivalent drug release kinetics to prints created using DLP printing, demonstrating drug release, swelling, and water sorption properties equivalent to or better than those of DLP-printed devices. The reported findings shed light on the advantages and limitations of each technology for creating these dynamic drug delivery systems and provides a direct comparison between the two technologies, while highlighting the promising potential of volumetric printing and further expanding the growing repertoire of pharmaceutical printing.

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Publication Details

Journal
Drug Delivery and Translational Research
Published
2024-08-23
DOI
https://doi.org/10.1007/s13346-024-01697-5
Citations
12
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
2.21
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article

Fabrication of 3D printed mutable drug delivery devices: a comparative study of volumetric and digital light processing printing

Abdul W. Basit, Álvaro Goyanes, Jun Jie Ong, Haya A. Alfassam et al.
12 citations
Drug Delivery and Translational Research
3D Printing in Biomedical Research
2.21
article

Fabrication of 3D printed mutable drug delivery devices: a comparative study of volumetric and digital light processing printing

Abdul W. Basit, Álvaro Goyanes, Jun Jie Ong, Haya A. Alfassam, Eduardo Díaz-Torres, Gareth R. Williams, Ye Chan Oh
article en
12 citations

Abstract

Mutable devices and dosage forms have the capacity to dynamically transform dimensionally, morphologically and mechanically upon exposure to non-mechanical external triggers. By leveraging these controllable transformations, these systems can be used as minimally invasive alternatives to implants and residence devices, foregoing the need for complex surgeries or endoscopies. 4D printing, the fabrication of 3D-printed structures that evolve their shape, properties, or functionality in response to stimuli over time, allows the production of such devices. This study explores the potential of volumetric printing, a novel vat photopolymerisation technology capable of ultra-rapid printing speeds, by comparing its performance against established digital light processing (DLP) printing in fabricating hydrogel-based drug-eluting devices. Six hydrogel formulations consisting of 2-(acryloyloxy)ethyl]trimethylammonium chloride solution, lithium phenyl-2,4,6-trimethylbenzoylphosphinate, varying molecular weights of the crosslinking monomer, poly(ethylene glycol) diacrylate, and paracetamol as a model drug were prepared for both vat photopolymerisation technologies. Comprehensive studies were conducted to investigate the swelling and water sorption profiles, drug release kinetics, and physicochemical properties of each formulation. Expandable drug-eluting 4D devices were successfully fabricated within 7.5 s using volumetric printing and were shown to display equivalent drug release kinetics to prints created using DLP printing, demonstrating drug release, swelling, and water sorption properties equivalent to or better than those of DLP-printed devices. The reported findings shed light on the advantages and limitations of each technology for creating these dynamic drug delivery systems and provides a direct comparison between the two technologies, while highlighting the promising potential of volumetric printing and further expanding the growing repertoire of pharmaceutical printing.

Drug Delivery and Translational ResearchVol. 15(5)
King Abdulaziz City for Science and Technology (SA), Universidad de La Laguna (ES), Medway School of Pharmacy (GB), Universidade de Santiago de Compostela (ES), Parkwood Hospital (GB), University College London (GB)
Good health and well-being
Openalex Percentile: Top 12%
3D Printing in Biomedical Research
2.21
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