Monomer-Induced Customization of UV-Cured Atelocollagen Hydrogel Networks


Liang, He ORCID: 0000-0002-7361-4690, Wood, David, Russell, Stephen and Tronci, Giuseppe (2018) Monomer-Induced Customization of UV-Cured Atelocollagen Hydrogel Networks. Frontiers in Chemistry, 6 (DEC). p. 626.

Access the full-text of this item by clicking on the Open Access link.
[img] Text
Monomer-Induced Customization of UV-Cured Atelocollagen Hydrogel Networks.pdf - Published version
Download (1MB)

Abstract

The covalent functionalization of type I atelocollagen with either 4-vinylbenzyl or methacrylamide residues is presented as a simple synthetic strategy to achieve customizable, cell-friendly UV-cured hydrogel networks with widespread clinical applicability. Molecular parameters, i.e., the type of monomer, degree of atelocollagen functionalization and UV-curing solution, have been systematically varied and their effect on gelation kinetics, swelling behavior, elastic properties, and enzymatic degradability investigated. UV-cured hydrogel networks deriving from atelocollagen precursors functionalized with equivalent molar content of 4-vinylbenzyl (<i>F</i> <sub>4<i>VBC</i></sub> = 18 ± 1 mol.%) and methacrylamide (<i>F</i> <sub><i>MA</i></sub> = 19 ± 2 mol.%) adducts proved to display remarkably-different swelling ratio (<i>SR</i> = 1963 ± 58-5202 ± 401 wt.%), storage modulus (<i>G</i>' = 17 ± 3-390 ± 99 Pa) and collagenase resistance (μ <sub><i>rel</i></sub> = 18 ± 5-56 ± 5 wt.%), similarly to the case of UV-cured hydrogel networks obtained with the same type of methacrylamide adduct, but varied degree of functionalization (<i>F</i> <sub><i>MA</i></sub> = 19 ± 2 - 88 ± 1 mol.%). UV-induced network formation of 4VBC-functionalized atelocollagen molecules yielded hydrogels with increased stiffness and enzymatic stability, attributed to the molecular rigidity of resulting aromatized crosslinking segment, whilst no toxic response was observed with osteosarcoma G292 cells. Although to a lesser extent, the pH of the UV-curing solution also proved to affect macroscopic hydrogel properties, likely due to the altered organization of atelocollagen molecules during network formation. By leveraging the knowledge gained with classic synthetic networks, this study highlights how the type of monomer can be conveniently exploited to realize customizable atelocollagen hydrogels for personalized medicine, whereby the structure-property relationships can be controlled to meet the requirements of unmet clinical applications.

Item Type: Article
Uncontrolled Keywords: type 1 atelocollagen, covalent network, UV-curing, monomer, 4-vinylbenzyl chloride, methacrylic anhydride
Depositing User: Symplectic Admin
Date Deposited: 15 Mar 2019 16:17
Last Modified: 19 Jan 2023 00:56
DOI: 10.3389/fchem.2018.00626
Open Access URL: https://doi.org/10.3389/fchem.2018.00626
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3034356
Dimensions
Altmetric
CORE (COnnecting REpositories)