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Well‐Defined Poly(ethylene glycol) Hydrogels with Enhanced Mechanical Performance Prepared by Thermally Induced Copper‐Catalyzed Azide–Alkyne Cycloaddition
Author(s) -
Li Ke Wen,
Cen Lian,
Zhou Chao,
Zhang Ao Kai,
Yao Fang,
Tan Lin Hua,
Xu Li Qun,
Fu Guo Dong
Publication year - 2016
Publication title -
macromolecular materials and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.913
H-Index - 96
eISSN - 1439-2054
pISSN - 1438-7492
DOI - 10.1002/mame.201600222
Subject(s) - ethylene glycol , biocompatibility , self healing hydrogels , materials science , peg ratio , click chemistry , azide , cycloaddition , polymer chemistry , alkyne , chemical engineering , catalysis , organic chemistry , chemistry , metallurgy , finance , economics , engineering
Poly(ethylene glycol) (PEG)‐based hydrogels have attracted increasing attention in recent years due to their good biocompatibility and low cost. However, the PEG‐based hydrogels prepared by traditional methods exhibit a poor machinability due to their disordered network structure. Herein, the preparation of well‐defined PEG‐based hydrogel via a facile thermally induced copper‐catalyzed azide–alkyne cycloaddition (CuAAC) reaction is demonstrated. To accomplish this, thermochemically reduced Cu(I) catalyst is adopted to trigger “click” cross‐linking, resulting in a well‐defined PEG network. The as‐synthesized PEG‐based hydrogel exhibits good mechanical performance with a tensile strength of 2.51 MPa, which is higher than the traditional PEG‐based hydrogels prepared from CuSO 4 /NaSac‐mediated or CuBr/ligand‐catalyzed CuAAC. Moreover, in vitro cytotoxicity and in vivo porcine subcutaneous implantation tests demonstrate that the as‐synthesized PEG‐based hydrogel has a good biocompatibility and low toxicity, making it a promising candidate for the applications in biomedical devices and tissue engineering.