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How to Design Catechol-Containing Hydrogels for Cell Encapsulation Despite Catechol Toxicity

  • par garon@biomomentum.com

Capucine Guyot; Tommy Malaret; Francesco Touani Kameni; Marta Cerruti; Sophie Lerouge
ACS Appl. Bio Mater, Publication Date:June 20, 2023

https://doi.org/10.1021/acsabm.3c00306

15 citations · 14 en 2025–2026

Les titres, résumés et légendes des publications sont présentés en anglais.

Abstract
Catechol (cat) is a highly adhesive diphenol that can be chemically grafted to polymers such as chitosan (CH) to make them adhesive as well. However, catechol-containing materials experimentally show a large variability of toxicity, especially in vitro. While it is unclear how this toxicity emerges, most concerns are directed toward the oxidation of catechol into quinone that releases reactive oxygen species (ROS) which can, in turn, cause cell apoptosis through oxidative stress. To better understand the mechanisms at play, we examined the leaching profiles, hydrogen peroxide (H2O2) production, and in vitro cytotoxicity of several cat-chitosan (cat-CH) hydrogels that were prepared with different oxidation levels and cross-linking methods. To create cat-CH with different propensities toward oxidation, we grafted either hydrocaffeic acid (HCA, more prone to oxidation) or dihydrobenzoic acid (DHBA, less prone to oxidation) to the backbone of CH. Hydrogels were cross-linked either covalently, using sodium periodate (NaIO4) to trigger oxidative cross-linking, or physically, using sodium bicarbonate (SHC). While using NaIO4 as a cross-linker increased the oxidation levels of the hydrogels, it also significantly reduced in vitro cytotoxicity, H2O2 production, and catechol and quinone leaching in the media. For all gels tested, cytotoxicity could be directly related to the release of quinones rather than H2O2 production or catechol release, showing that oxidative stress may not be the main reason for catechol cytotoxicity, as other pathways of quinone toxicity come into play. Results also suggest that the indirect cytotoxicity of cat-CH hydrogels fabricated through carbodiimide chemistry can be reduced if (i) catechol groups are chemically bound to the polymer backbone to prevent leaching or (ii) the chosen cat-bearing molecule has a high resistance to oxidation. Coupled with the use of other cross-linking chemistries or more efficient purification methods, these strategies can be adopted to synthesize various types of cytocompatible cat-containing scaffolds.
Keywords
Catechol, chitosan, hydrogels, cytocompatibility, oxidation, ROS, quinone, carbodiimide chemistry.

Utilisation des équipements

Le résumé disponible décrit des mesures de relargage, de production de peroxyde d’hydrogène et de cytotoxicité in vitro dans des hydrogels de chitosane modifié par des catéchols, préparés avec différents niveaux d’oxydation et modes de réticulation. Il ne précise aucun essai mécanique ni rôle d’un équipement ; l’utilisation du Mach-1 Mechanical Tester ne peut donc pas être vérifiée.

Matériaux (2)

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