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Mixed Reversible Covalent Crosslink Kinetics Enable Precise, Hierarchical Mechanical Tuning of Hydrogel Networks
Author(s) -
Yesilyurt Volkan,
Ayoob Andrew M.,
Appel Eric A.,
Borenstein Jeffrey T.,
Langer Robert,
Anderson Daniel G.
Publication year - 2017
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201605947
Subject(s) - phenylboronic acid , covalent bond , kinetics , self healing hydrogels , materials science , relaxation (psychology) , dynamic covalent chemistry , peg ratio , dynamic mechanical analysis , stress relaxation , molecular dynamics , nanotechnology , chemical engineering , polymer chemistry , molecule , chemistry , polymer , computational chemistry , supramolecular chemistry , organic chemistry , composite material , catalysis , psychology , social psychology , physics , finance , creep , quantum mechanics , engineering , economics
Hydrogels play a central role in a number of medical applications and new research aims to engineer their mechanical properties to improve their capacity to mimic the functional dynamics of native tissues. This study shows hierarchical mechanical tuning of hydrogel networks by utilizing mixtures of kinetically distinct reversible covalent crosslinks. A methodology is described to precisely tune stress relaxation in PEG networks formed from mixtures of two different phenylboronic acid derivatives with unique diol complexation rates, 4‐carboxyphenylboronic acid, and o ‐aminomethylphenylboronic acid. Gel relaxation time and the mechanical response to dynamic shear are exquisitely controlled by the relative concentrations of the phenylboronic acid derivatives. The differences observed in the crossover frequencies corresponding to p K a differences in the phenylboronic acid derivatives directly connect the molecular kinetics of the reversible crosslinks to the macroscopic dynamic mechanical behavior. Mechanical tuning by mixing reversible covalent crosslinking kinetics is found to be independent of other attributes of network architecture, such as molecular weight between crosslinks.