Redox-triggered hydrogels revealing switchable stiffness properties and shape-memory functions

Michael Fadeev, Gilad Davidson-Rozenfeld, Yonatan Biniuri, Ravit Yakobi, Rémi Cazelles, Miguel Angel Aleman-Garcia, Itamar Willner

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

The synthesis, characterization and application of redox-switchable hydrogels are described. The first system includes the crosslinking of terpyridine-functionalized acrylamide copolymer chains by redox-active metal-ion terpyridine complexes (Mn/n+1 = Ru2+/3+; Os2+/3+). The redox state of the complexes bridging the hydrogel controls the stiffness of the resulting hydrogels. The Ru2+-terpyridine polyacrylamide hydrogel reveals enhanced stiffness (G′ = 110 Pa) compared to the Ru3+-terpyridine bridged hydrogel that exhibits lower stiffness (G′ = 50 Pa). By the cyclic oxidation and reduction of the hydrogel with persulfate and dopamine, respectively, reversible switching of the hydrogel stiffness is demonstrated. Similarly, the Os3+-terpyridine-crosslinked hydrogel reveals lower stiffness (G′ = 30 Pa) compared to the Os2+-terpyridine-bridged hydrogel (G′ = 45 Pa). By the reversible oxidation and reduction of the Os2+/3+ with sodium persulfate and ascorbic acid, the switchable stiffness of the hydrogel is demonstrated. The second system involves metal-ion-crosslinked carboxymethylcellulose hydrogels (Mn+1/n = Fe3+/2+; Ru3+/2+). The reduced metal-ion-crosslinked hydrogels Fe2+-carboxymethylcellulose (formed in the presence of ascorbic acid) and the Ru2+-carboxymethylcellulose (formed in the presence of dopamine) exhibit lower stiffness values corresponding to 80 Pa and 320 Pa, respectively, while high-stiffness Fe3+- and Ru3+-carboxymethylcellulose hydrogels (formed in the presence of sodium persulfate) are observed, G′ = 210 Pa and 460 Pa, respectively. The reversible redox-stimulated switching of the stiffness of the hydrogels is demonstrated. In addition, carboxymethylcellulose chains modified with self-complementary nucleic acid tethers are crosslinked by two cooperative crosslinkers consisting of Fe3+/2+-carboxylate and DNA duplexes. The resulting Fe3+-carboxymethyl cellulose/duplex nucleic acid-bridged hydrogel exhibits high stiffness, G′ = 210 Pa, whereas the Fe2+-carboxymethylcellulose/duplex DNA reveals substantially lower stiffness, G′ = 80 Pa. The hydrogel reveals reversible shape-memory properties.

Original languageEnglish
Pages (from-to)2905-2912
Number of pages8
JournalPolymer Chemistry
Volume9
Issue number21
DOIs
StatePublished - 7 Jun 2018
Externally publishedYes

ASJC Scopus subject areas

  • Bioengineering
  • Biochemistry
  • Polymers and Plastics
  • Organic Chemistry

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