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Combining SLA 3D printing and soft lithography for fast, versatile, and accessible high-resolution fabrication of customised multiscale cell culture devices with complex designs

View ORCID ProfileCathleen Hagemann, Matthew C. D. Bailey, Valentina Maria Lionello, Noreen Khokhar, Pacharaporn Suklai, View ORCID ProfileCarmen Moreno-Gonzalez, Kelly O’Toole, George Konstantinou, Eleonora Giagnorio, View ORCID ProfileMads Bergholt, View ORCID ProfileAlbane Imbert, View ORCID ProfileFrancesco Saverio Tedesco, View ORCID ProfileAndrea Serio
doi: https://doi.org/10.1101/2022.02.22.481424
Cathleen Hagemann
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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  • ORCID record for Cathleen Hagemann
Matthew C. D. Bailey
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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Valentina Maria Lionello
2The Francis Crick Institute, London NW1 1AT, UK
3Department of Cell and Developmental Biology, University College London, London WC1E6DE, UK
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Noreen Khokhar
2The Francis Crick Institute, London NW1 1AT, UK
3Department of Cell and Developmental Biology, University College London, London WC1E6DE, UK
6Randall Centre for Cell and Molecular Biophysics, King’s College London, London SE1 1UL, UK
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Pacharaporn Suklai
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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Carmen Moreno-Gonzalez
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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Kelly O’Toole
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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George Konstantinou
2The Francis Crick Institute, London NW1 1AT, UK
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Eleonora Giagnorio
2The Francis Crick Institute, London NW1 1AT, UK
3Department of Cell and Developmental Biology, University College London, London WC1E6DE, UK
5Neurology IV - Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan 20133, Italy.
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Mads Bergholt
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
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Albane Imbert
2The Francis Crick Institute, London NW1 1AT, UK
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Francesco Saverio Tedesco
2The Francis Crick Institute, London NW1 1AT, UK
3Department of Cell and Developmental Biology, University College London, London WC1E6DE, UK
4Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health & Great Ormond Street Hospital for Children, London, UK
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Andrea Serio
1Centre for Craniofacial & Regenerative Biology, King’s College London, London SE1 9RT, UK
2The Francis Crick Institute, London NW1 1AT, UK
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  • For correspondence: andrea.serio@kcl.ac.uk
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Abstract

Commercially available cell culture devices are designed to increase the complexity of simple cell culture models to provide better experimental platforms for biological systems. From microtopography, microwells, plating devices and microfluidic systems to larger constructs for specific applications like live imaging chamber slides, a wide variety of culture devices with different geometries have become indispensable in biology labs. However, the techniques used for their fabrication can be out of reach for most wet labs due to cost and availability of specialised equipment or the need for engineering expertise. Moreover, these techniques also have technical limitations to the volumes, shapes and dimensions they can generate. For these reasons, creating customisable devices tailored to lab-specific biological questions remains difficult to apply.

Taking advantage of low-cost, high-resolution desktop resin 3D printers combined with PDMS soft-lithography we have developed an optimised microfabrication pipeline capable of generating a wide variety of customisable devices for cell culture and tissue engineering in an easy, fast reproducible way for a fraction of the cost of conventional microfabrication or commercial alternatives. This technique enables the manufacture of complex devices across scales bridging the gap between microfabrication and fused deposition moulding (FDM) printing. The method we describe allows for the efficient treatment of resin-based 3D printed constructs for PDMS curing, using a combination of curing steps, washes and surface treatments. Together with the extensive characterisation of the fabrication pipeline, we provide several proof-of-principle applications ranging from simple 2D culture devices to large tissue engineering constructs and organoid formation systems.

We believe this methodology will be applicable in any wet lab, irrespective of prior expertise or resource availability and will therefore enable a wide adoption of tailored microfabricated devices across many fields of biology.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Incorrect axis labelling in figure 5

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted February 24, 2022.
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Combining SLA 3D printing and soft lithography for fast, versatile, and accessible high-resolution fabrication of customised multiscale cell culture devices with complex designs
Cathleen Hagemann, Matthew C. D. Bailey, Valentina Maria Lionello, Noreen Khokhar, Pacharaporn Suklai, Carmen Moreno-Gonzalez, Kelly O’Toole, George Konstantinou, Eleonora Giagnorio, Mads Bergholt, Albane Imbert, Francesco Saverio Tedesco, Andrea Serio
bioRxiv 2022.02.22.481424; doi: https://doi.org/10.1101/2022.02.22.481424
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Combining SLA 3D printing and soft lithography for fast, versatile, and accessible high-resolution fabrication of customised multiscale cell culture devices with complex designs
Cathleen Hagemann, Matthew C. D. Bailey, Valentina Maria Lionello, Noreen Khokhar, Pacharaporn Suklai, Carmen Moreno-Gonzalez, Kelly O’Toole, George Konstantinou, Eleonora Giagnorio, Mads Bergholt, Albane Imbert, Francesco Saverio Tedesco, Andrea Serio
bioRxiv 2022.02.22.481424; doi: https://doi.org/10.1101/2022.02.22.481424

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