Multipurpose On‐the‐Spot Peptide‐Based Hydrogels for Skin, Cornea, and Heart Repair

Author:

Ross Alex12,Guo Xixi13,Salazar German A. Mercado12,Schejtman Sergio David Garcia1,El‐Hage Jinane1,Comtois‐Bona Maxime1,Macadam Aidan1,Guzman‐Soto Irene1,Takaya Hiroki1,Hu Kevin1,Liu Bryan1,Tu Ryan1,Siddiqi Bilal1,Anderson Erica1,Muñoz Marcelo1,Briones‐Rebolledo Patricio4,Ning Tianqin5,Griffith May6,Rotsein Benjamin2,Poblete Horacio4,Li Jianyu6,Ruel Marc1,Suuronen Erik J.13,Alarcon Emilio I.12ORCID

Affiliation:

1. Bioengineering and Therapeutic Solutions (BEaTS) program University of Ottawa Heart Institute 40 Ruskin Street Ottawa Ontario K1Y4W7 Canada

2. Department of Biochemistry Microbiology and Immunology University of Ottawa Ottawa Ontario K1H 8M5 Canada

3. Department of Cellular & Molecular Medicine University of Ottawa 451 Smyth Road Ottawa Ontario K1H8M5 Canada

4. Departamento de Bioinformática Centro de Bioinformática Simulación y Modelado (CBSM) Facultad de Ingeniería Universidad de Talca Campus Talca, 2 Norte 685 Talca 75710 Chile

5. Department of Mechanical Engineering McGill University Montreal Quebec H3A0C3 Canada

6. Department of Ophthalmology and Institute of Biomedical Engineering Université de Montréal Montreal Quebec H3C3J7 Canada

Abstract

AbstractBioinspired synthetic materials can be designed as reliable, cost‐effective, and fully controlled alternatives to natural biomaterials for treating damaged tissues and organs. However, several hurdles need to be overcome for clinical translation, particularly for biomaterials gelled in situ. These include the potential toxicity of chemical crosslinkers used in the materials' assembly or breakdown products they generate and the challenges of fine‐tuning the mechanical properties of the materials. Here, a minimalistic, adhesive soft material is developed by screening hundreds of potential formulations of self‐assembling, custom‐designed collagen‐like peptide sequences for the in situ formation of tissue‐bonding 3D hydrogels. Nine promising formulations for tissue repair are identified using a low‐volume and rapid combinatory screening approach. It is shown that simply varying the ratio of the two key components promotes adhesion and fine‐tunes the material's mechanical properties. The materials' skin and heart repair capabilities are assessed in vitro and clinically relevant animal models. The materials are also tested for corneal applications using ex vivo pig cornea models complemented by in vitro cell compatibility assays.

Funder

Canadian Institutes of Health Research

Heart and Stroke Foundation of Canada

Government of Ontario

University of Ottawa Heart Institute Foundation

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

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