Vat photopolymerization 3D printed microfluidic devices for organ-on-a-chip applications.


Journal

Lab on a chip
ISSN: 1473-0189
Titre abrégé: Lab Chip
Pays: England
ID NLM: 101128948

Informations de publication

Date de publication:
08 08 2023
Historique:
pmc-release: 08 08 2024
medline: 9 8 2023
pubmed: 21 7 2023
entrez: 21 7 2023
Statut: epublish

Résumé

Organs-on-a-chip, or OoCs, are microfluidic tissue culture devices with micro-scaled architectures that repeatedly achieve biomimicry of biological phenomena. They are well positioned to become the primary pre-clinical testing modality as they possess high translational value. Current methods of fabrication have facilitated the development of many custom OoCs that have generated promising results. However, the reliance on microfabrication and soft lithographic fabrication techniques has limited their prototyping turnover rate and scalability. Additive manufacturing, known commonly as 3D printing, shows promise to expedite this prototyping process, while also making fabrication easier and more reproducible. We briefly introduce common 3D printing modalities before identifying two sub-types of vat photopolymerization - stereolithography (SLA) and digital light processing (DLP) - as the most advantageous fabrication methods for the future of OoC development. We then outline the motivations for shifting to 3D printing, the requirements for 3D printed OoCs to be competitive with the current state of the art, and several considerations for achieving successful 3D printed OoC devices touching on design and fabrication techniques, including a survey of commercial and custom 3D printers and resins. In all, we aim to form a guide for the end-user to facilitate the in-house generation of 3D printed OoCs, along with the future translation of these important devices.

Identifiants

pubmed: 37476860
doi: 10.1039/d3lc00094j
pmc: PMC10448871
mid: NIHMS1920889
doi:

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3537-3560

Subventions

Organisme : NIGMS NIH HHS
ID : R15 GM123405
Pays : United States

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Auteurs

Laura A Milton (LA)

School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, Australia. yichin.toh@qut.edu.au.
Centre for Biomedical Technologies, Queensland University of Technology, Brisbane, Australia.

Matthew S Viglione (MS)

Department of Electrical and Computer Engineering, Brigham Young University, Provo, Utah, USA. nordin@byu.edu.

Louis Jun Ye Ong (LJY)

School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, Australia. yichin.toh@qut.edu.au.
Centre for Biomedical Technologies, Queensland University of Technology, Brisbane, Australia.
Max Planck Queensland Centre (MPQC) for the Materials Science of Extracellular Matrices, Queensland University of Technology, Brisbane, Australia.

Gregory P Nordin (GP)

Department of Electrical and Computer Engineering, Brigham Young University, Provo, Utah, USA. nordin@byu.edu.

Yi-Chin Toh (YC)

School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, Australia. yichin.toh@qut.edu.au.
Centre for Biomedical Technologies, Queensland University of Technology, Brisbane, Australia.
Max Planck Queensland Centre (MPQC) for the Materials Science of Extracellular Matrices, Queensland University of Technology, Brisbane, Australia.
Centre for Microbiome Research, Queensland University of Technology, Brisbane, Australia.

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Classifications MeSH