3D Printing of Customized Drug Delivery Systems with Controlled Architecture via Reversible Addition‐Fragmentation Chain Transfer Polymerization

Title
3D Printing of Customized Drug Delivery Systems with Controlled Architecture via Reversible Addition‐Fragmentation Chain Transfer Polymerization
Publication Date
2023-05
Author(s)
Bagheri, Ali
( author )
OrcID: https://orcid.org/0000-0003-3484-5856
Email: abagheri@une.edu.au
UNE Id une-id:abagheri
Asadi-Eydivand, Mitra
Rosser, Adam A
( author )
OrcID: https://orcid.org/0000-0002-4123-7704
Email: arosser3@une.edu.au
UNE Id une-id:arosser3
Fellows, Christopher M
( author )
OrcID: https://orcid.org/0000-0002-8976-8651
Email: cfellows@une.edu.au
UNE Id une-id:cfellows
Brown, Trevor C
( author )
OrcID: https://orcid.org/0000-0002-8277-2498
Email: tbrown3@une.edu.au
UNE Id une-id:tbrown3
Type of document
Journal Article
Language
en
Entity Type
Publication
Publisher
Wiley-VCH Verlag GmbH & Co KGaA
Place of publication
Germany
DOI
10.1002/adem.202201785
UNE publication id
une:1959.11/55215
Abstract
3D printing via reversible addition-fragmentation chain transfer (RAFT) polymerization has been recently developed to expand the scope of 3D printing technologies. A potentially high-impact but relatively unexplored opportunity that can be provided by RAFT-mediated 3D printing is a pathway toward personalized medicine through manufacturing bespoke drug delivery systems (DDSs). Herein, 3D printing of drug-eluting systems with precise geometry, size, drug dosage, and release duration/profiles is reported. This is achieved through engineering a range of 3D models with precise interconnected channel-pore structure and geometric proportions in architectural patterns. Notably, the application of the RAFT process is crucial in manufacturing materials with highly resolved macroscale features by confining curing to exposure precincts. This approach also allows spatiotemporal control of the drug loading and compositions within different layers of the scaffolds. The ratio between the polyethylene glycol units and the acrylate units in the crosslinkers is found to be a critical factor, with a higher ratio increasing swelling capacity, and thus enhancing the drug release profile, from the drug-eluting systems. This proof-of-concept research demonstrates that RAFT-mediated 3D printing enables the production of personalized drug delivery materials, providing a pathway to replace the “one-size-fits-all” approach in traditional health care.
Link
Citation
Advanced Engineering Materials, 25(10), p. 1-9
ISSN
1527-2648
1438-1656
Start page
1
End page
9
Rights
Attribution 4.0 International

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