Alternative reaction mechanism for the cross-linking of gelatin with glutaraldehyde

J Agric Food Chem. 2010 Jan 27;58(2):998-1003. doi: 10.1021/jf9031603.

Abstract

FT-IR, in combination with residual amino group determination using a fluorescence technique, has been used to investigate the chemical functional groups involved in the cross-linking reaction between glutaraldehyde and gelatin molecules. The results suggest that, at high pH values (i.e., close to the pK(a) of lysine), the cross-linking reaction is mainly governed by the well-known Schiff base formation, whereas at low pH (i.e., when the amino groups of lysine are protonated), the reaction may also involve the -OH groups of hydroxyproline and hydroxylysine, leading to the formation of hemiacetals.

Publication types

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

MeSH terms

  • Cross-Linking Reagents / chemistry*
  • Gelatin / chemistry*
  • Glutaral / chemistry*
  • Hydrogen-Ion Concentration
  • Kinetics

Substances

  • Cross-Linking Reagents
  • Gelatin
  • Glutaral