Events2nd Canadian Peptide and Protein Community Virtual Meeting
Published
This submission belongs to the session Posters. Poster Session of the event 2nd Canadian Peptide and Protein Community Virtual Meeting
Published date
16 Nov, 2024
Academic Editor
author-avatarWilliam D. Lubell
Citation
Marcelo Munoz, Aidan MacAdam, Jinane El Hage, Alex Ross, May Griffith, Isabelle Brunette, Emilio Alarcon, Low Energy Blue pulsed Light-activated Peptide Injectable Materials for Restoring Thinning Corneas, in Proceedings of 2nd Canadian Peptide and Protein Community Virtual Meeting, 16 December 2024, MDPI: Basel, Switzerland
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Low Energy Blue pulsed Light-activated Peptide Injectable Materials for Restoring Thinning Corneas

Aidan MacAdam 1
Jinane El Hage 1
Alex Ross 1
Isabelle Brunette 3
Emilio Alarcon 4
1. Bioengineering and Therapeutic Solutions (BEaTS) program, University of Ottawa Heart Institute, 40 Ruskin Street, Ottawa, Ontario, K1Y4W7, Canada, Canada
2. Department of Ophthalmology, Université de Montréal, Montreal, QC, H3C 3J7, Canada, Canada
3. Centre Universitaire d’Ophtalmologie de l’Université de Montréal à l'Hôpital Maisonneuve-Rosemont, Montreal, QC, H1T 2M4, Canada, Canada
4. Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario, K1H 8M5, Canada, Canada
Abstract

Many alternatives to human donor corneas are being developed to meet the global shortage of donated tissues. However, corneal transplantation remains the gold standard for diseases resulting in thinning corneas. In this work, transparent low-energy photoactivated extracellular matrix peptide-mimicking materials are developed for intrastromal injection to restore stromal thickness. The injectable biomaterials are comprised of short peptides and glycosaminoglycans (chondroitin, hyaluronic acid) that assemble into a hydrogel when pulsed with low-energy blue light. The dosage of pulsed-blue light needed for material activation is minimal at 8.5 mW cm-2, thus circumventing any blue light cytotoxicity. Intrastromal injection of these light-activated biomaterials in rat corneas show that two iterations of the formulations remain stable in situ without stimulating significant inflammation or neovascularization. The use of low light intensities and the ability of the developed materials to stably rebuild and change the curvature of the cornea tissue make these formulations attractive for clinical translation.

Keywords
Cornea repair
peptides
light-activated
injectable materials
keratoconus
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