June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
Fabrication of a microfluidic chip using 3D printing for evaluating ocular cytotoxicity
Author Affiliations & Notes
  • Chau-Minh Phan
    School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada
    Centre for Eye and Vision Research Limited, Hong Kong, Hong Kong
  • Megala Ramasamy
    School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada
  • Brandon Ho
    School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada
    Centre for Eye and Vision Research Limited, Hong Kong, Hong Kong
  • Alex Hui
    School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada
  • Lyndon William Jones
    School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada
    Centre for Eye and Vision Research Limited, Hong Kong, Hong Kong
  • Footnotes
    Commercial Relationships   Chau-Minh Phan None; Megala Ramasamy None; Brandon Ho None; Alex Hui None; Lyndon Jones Alcon, Code F (Financial Support), CooperVision, Code F (Financial Support), Johnson & Johnson, Code F (Financial Support), Bausch & Lomb, Code F (Financial Support), Allergan, Code F (Financial Support), i-MED Pharma, Code F (Financial Support), Novartis, Code F (Financial Support), Menicon, Code F (Financial Support)
  • Footnotes
    Support  This project was supported and funded by the Canadian Optometric Education Fund (COETF), Centre for Bioengineering and Biotechnology (CBB), Mitacs through Mitacs through the Mitacs Accelerate program, and the Hong Kong Special Administrative Region Government and InnoHK
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 3586. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Chau-Minh Phan, Megala Ramasamy, Brandon Ho, Alex Hui, Lyndon William Jones; Fabrication of a microfluidic chip using 3D printing for evaluating ocular cytotoxicity. Invest. Ophthalmol. Vis. Sci. 2023;64(8):3586.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose : To develop a PDMS (polydimethyl siloxane) microfluidic chip to evaluate ocular cytotoxicity with ophthalmic formulations and materials.

Methods : The microfluidic chip was designed using CAD software (FreeCAD), and the moulds of the chips were printed using (1) a stereolithography (SLA) and (2) digital light processing (DLP) 3D printer. The printed moulds were washed with isopropyl alcohol (IPA), UV-cured for 1-hour at 60oC, followed by heating in an oven at 120oC for 2 hours to remove any unreacted polymers. The surface of the chips was smoothed with sandpaper with increasing grit, followed by an application of nail polish. The moulds were then cast with PDMS, a gas-permeable and clear polymer commonly used for the fabrication of microfluidic chips. The moulds and chips were imaged using SEM (scanning electron microscopy). The light transmittance of the chips was also measured. The PDMS top half of the chip was adhered to a microscope slide using medical-grade double-sided tape. For a pilot study, the PDMS chips were sterilized via autoclaving, coated with 0.1% polydopamine to improve their surface wettability, and then seeded with immortalized human corneal epithelial cells (HCEC). After 2 days of incubation in a nutrient media broth (no flow), cell adhesion and growth were evaluated using light microscopy.

Results : Both 3D printers were able to print moulds with high resolution, with channel dimensions as low as 100 µm, and with faster print times for the DLP printer. SEM images revealed that moulds that were both sanded and had a nail coating were significantly smoother than the original 3D-printed moulds. The chips cast from the polished moulds were transparent, with >85% transmittance from 450-700 nm, and could be used to image cells through a microscope. The microfluidic chips were able to handle flow rates up to 1 mL/min for 24 hours without any signs of leakage. HCEC cells were able to adhere and grow on the coated PDMS microfluidic chip after 2 days.

Conclusions : This study showed that SLA and DLP printers could be used to fabricate PDMS microfluidic chips as a low-cost rapid prototyping approach. The fabricated chips were clear and could be used to incorporate HCEC cells. Future work will examine the viability of cells under different flow rates and shear stress conditions on these chips.

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

 

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×