Investigation of the Diels–Alder reaction as a cross-linking mechanism for degradable poly(ethylene glycol) based hydrogels

2013 ◽  
Vol 1 (37) ◽  
pp. 4855 ◽  
Author(s):  
Susanne Kirchhof ◽  
Ferdinand P. Brandl ◽  
Nadine Hammer ◽  
Achim M. Goepferich
2019 ◽  
Vol 123 (7) ◽  
pp. 4125-4132 ◽  
Author(s):  
Madeline Vauthier ◽  
Loïc Jierry ◽  
Miguel L. Martinez Mendez ◽  
Yann-Matthieu Durst ◽  
Julien Kelber ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (78) ◽  
pp. 74757-74764 ◽  
Author(s):  
Ismail Altinbasak ◽  
Rana Sanyal ◽  
Amitav Sanyal

Poly(ethylene glycol)-based redox-responsive hydrogels have been preparedviathe Diels–Alder reaction between a furan-containing hydrophilic copolymer and a disulfide-containing bis-maleimide based crosslinker.


2013 ◽  
Vol 013 (7) ◽  
pp. 903-908
Author(s):  
Jin Yu-cun ◽  
Lu Yi ◽  
Yu Lin ◽  
Cao Mo-yuan ◽  
Xiong Han ◽  
...  

2012 ◽  
Vol 562-564 ◽  
pp. 405-408 ◽  
Author(s):  
Hong Liang Wei ◽  
Ya Li Feng ◽  
Hui Juan Chu ◽  
Kai Yao

A novel kind of supramolecular structrued hydrogels were fabricated by Diels-Alder click reaction between furan-functionalized polypseudorotaxanes and polymeric dienophiles. Firstly, polypseudorotaxanes were prepared by supramolecular self-assembly of furan-terminated poly(ethylene glycol)(PEG) and α-cyclodextrins (CDs) in water. And polymeric dienophiles were synthesized by a coupling reaction between copolymer of hydroxyethyl methacrylate and N,N-dimethyl acrylamide and N-maleoyl alanine (AMI). The supramolecular structured hydrogels were prepared by Diels-Alder reaction in water.


2015 ◽  
Vol 90 ◽  
pp. 21-24 ◽  
Author(s):  
Pamela de Cuadro ◽  
Tiina Belt ◽  
Katri S. Kontturi ◽  
Mehedi Reza ◽  
Eero Kontturi ◽  
...  

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