Furfuryl- and Maleimido Polysaccharides: Synthetic Strategies Toward Functional Biomaterials

Macromol Biosci. 2018 Nov;18(11):e1800258. doi: 10.1002/mabi.201800258. Epub 2018 Oct 1.

Abstract

In context with facile and efficient syntheses of functional polymeric materials, the combination of polysaccharides and functional moieties based on renewable resources is a sustainable and valuable approach. This review presents alternatives to prominent click reactions utilizing biopolymer derivatives with furfuryl and maleimide groups. On the one hand, the cross-linking by Diels-Alder reaction of these polymers enables the synthesis of novel materials in the fields of self-healing polymers, tissue engineering, and drug delivery. On the other hand, thiol-ene click reactions allow their conjugation to complex (bio)molecules. Different synthetic strategies are reviewed and the applicability of functional materials is evaluated.

Keywords: biomaterials; furoates; maleimides; polysaccharides; syntheses.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biocompatible Materials* / chemical synthesis
  • Biocompatible Materials* / chemistry
  • Biocompatible Materials* / pharmacology
  • Cycloaddition Reaction / methods
  • Drug Delivery Systems / methods*
  • Furans / chemistry
  • Maleimides / chemistry
  • Polysaccharides* / chemical synthesis
  • Polysaccharides* / chemistry
  • Polysaccharides* / pharmacology
  • Tissue Engineering / methods
  • Zebrafish / embryology*

Substances

  • Biocompatible Materials
  • Furans
  • Maleimides
  • Polysaccharides
  • maleimide