Chitosan-g-hematin: enzyme-mimicking polymeric catalyst for adhesive hydrogels

Acta Biomater. 2014 Jan;10(1):224-33. doi: 10.1016/j.actbio.2013.09.014. Epub 2013 Sep 24.

Abstract

Phenol derivative-containing adhesive hydrogels has been widely recognized as having potential for biomedical applications, but their conventional production methods, utilizing a moderate/strong base, alkaline buffers, the addition of oxidizing agents or the use of enzymes, require alternative approaches to improve their biocompatibility. In this study, we report a polymeric, enzyme-mimetic biocatalyst, hematin-grafted chitosan (chitosan-g-hem), which results in effective gelation without the use of alkaline buffers or enzymes. Furthermore, gelation occurs under mild physiological conditions. Chitosan-g-hem biocatalyst (0.01%, w/v) has excellent catalytic properties, forming chitosan-catechol hydrogels rapidly (within 5 min). In vivo adhesive force measurement demonstrated that the hydrogel formed by the chitosan-g-hem activity showed an increase in adhesion force (33.6 ± 5.9 kPa) compared with the same hydrogel formed by pH-induced catechol oxidation (20.6 ± 5.5 kPa) in mouse subcutaneous tissue. Using the chitosan-g-hem biocatalyst, other catechol-functionalized polymers (hyaluronic acid-catechol and poly(vinyl alcohol)-catechol) also formed hydrogels, indicating that chitosan-g-hem can be used as a general polymeric catalyst for preparing catechol-containing hydrogels.

Keywords: Catechol; Chitosan; Hematin; Horseradish peroxidase; Hydrogel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesives / pharmacology*
  • Animals
  • Catalysis / drug effects
  • Cell Survival / drug effects
  • Chitosan / analogs & derivatives*
  • Chitosan / chemical synthesis
  • Chitosan / chemistry
  • Chitosan / pharmacology*
  • Cross-Linking Reagents / chemistry
  • Enzymes / metabolism*
  • Hemin / analogs & derivatives*
  • Hemin / chemical synthesis
  • Hemin / chemistry
  • Hemin / pharmacology
  • Hydrogels / pharmacology*
  • Hydrogen-Ion Concentration / drug effects
  • Mice
  • NIH 3T3 Cells
  • Polymers / pharmacology*
  • Solubility / drug effects

Substances

  • Adhesives
  • Cross-Linking Reagents
  • Enzymes
  • Hydrogels
  • Polymers
  • Hemin
  • Chitosan