PEG-Based Photo-Cross-Linked Networks with Adjustable Topologies and Mechanical Properties

被引:6
|
作者
Roquart, Mailie [1 ,2 ]
Kharlamova, Anna [2 ]
Celada, Lukas Marcos [2 ]
Norvez, Sophie [2 ]
Nicolaÿ, Renaud [2 ]
Corte, Laurent [1 ,2 ]
机构
[1] PSL Univ, Ctr Mat, MINES Paris, CNRS, F-91003 Evry, France
[2] PSL Univ, Mol Macromol Chem & Mat, ESPCI Paris, CNRS, F-75005 Paris, France
关键词
THIOL-ACRYLATE PHOTOPOLYMERIZATIONS; HYDROGELS; DEGRADATION; AMINE; ENE; POLY(BETA-THIOESTER)S; CHEMISTRY; CHITOSAN;
D O I
10.1021/acs.biomac.2c01265
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the synthesis of networks having adjustable topologies and mechanical properties. Our approach consists of photo polymerizing poly(ethylene glycol) diacrylates (PEG-DA) in the presence of mixtures of mono-and multifunctional thiols. We show that the introduction of monothiols as non-cross-linking transfer agents provides a simple way to tune the topology of the networks and produce soft extensible networks. In a systematic study with model short PEG-DA (Mn = 700 g center dot mol-1), we explored how the gel point and network properties, such as the swelling ratio, the soluble fraction, the viscoelastic moduli, and the ultimate stress and strain, can be adjusted by varying the ratio of thiol to acrylate functions and the average functionality of the thiol mixture. We applied this strategy to longer chains of PEG-DA (Mn = 2300 and 3200 g center dot mol-1) and varied the viscoelastic and tensile responses of these networks to optimize their adhesive performance. This simple and robust approach further enriches the toolbox of thiol- acrylate polymerization and expands the application scope of PEG-based hydrogels.
引用
收藏
页码:4454 / 4464
页数:11
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