Related Experiment Video
Updated: Jul 27, 2026

Wet Chemistry and Peptide Immobilization on Polytetrafluoroethylene for Improved Cell-adhesion
Published on: August 15, 2016
Developing and Characterizing a Biocompatible Hydrogel Obtained by Cross-Linking Gelatin with Oxidized Sodium
Chahrazed Mahmoudi1,2, Naïma Tahraoui Douma1, Hacene Mahmoudi3
1Laboratory of Water and Environment, Faculty of Technology, University Hassiba Benbouali of Chlef, Chlef 02000, Algeria.
Abstract:
The main goal of this research was to create biocompatible hydrogels using gelatin and a double cross-linking technique involving both covalent and ionic bonds to immobilize propolis. The covalent bonds were formed through Schiff base cross-links between protein-free amino groups (NH2) from the lysine residue and aldehyde groups (CHO) produced by oxidizing sodium alginate with NaIO4, while the ionic bonds were achieved using Mg2+ ions. Hydrogel films were obtained by varying the molar ratios of -CHO/-NH2 under different pH conditions (3.5 and 5.5). The presence of aldehyde groups in the oxidized sodium alginate (OSA) was confirmed using FTIR and NMR spectroscopy. The oxidation degree was monitored over 48 h, and the influence of temperature was examined. Results showed that higher -CHO/-NH2 molar ratios led to increased conversion index values of NH2 groups, and a decrease in swelling degree values was observed in mediums with pH values of 5.5 and 7.4. The encapsulation and release efficiency of propolis decreased with an increase in the hydrogel cross-linking degree. UV irradiation enhanced the antioxidant activity of both free and encapsulated propolis. These findings offer valuable insights for the biomedical and pharmaceutical fields into designing biocompatible hydrogels for propolis immobilization, with potential for controlled release.
Related Concept Videos
Dehydration Synthesis
Hydrolysis
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...
Cryo-electron Microscopy
Coagulation

