Synthesis and characterization of chitosan hydrogels cross-linked with dicarboxylic acids

Chitosan hydrogels cross-linked with dicarboxylic acids were prepared. Succinic, glutaric and adipic acid were used as cross-linking agents, the goal being to compare the effect of the length of the chain on the behavior of the material obtained. The swelling properties were studied at different pHs...

Full description

Autores:
Valderruten Posso, Nora Elena
Zuluaga, Héctor Fabio
Ruiz Durantez, Eduardo
Valverde, Jonathan D.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2014
Institución:
Universidad ICESI
Repositorio:
Repositorio ICESI
Idioma:
eng
OAI Identifier:
oai:repository.icesi.edu.co:10906/79907
Acceso en línea:
http://www.sciencedirect.com/science/article/pii/S1381514814001746
http://hdl.handle.net/10906/79907
http://dx.doi.org/10.1016/j.reactfunctpolym.2014.08.006
Palabra clave:
Hydrogels
Dicarboxylic acids
Drug release
Viscoelasticity
Biochemistry research
Métodos de investigación en bioquímica
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:Chitosan hydrogels cross-linked with dicarboxylic acids were prepared. Succinic, glutaric and adipic acid were used as cross-linking agents, the goal being to compare the effect of the length of the chain on the behavior of the material obtained. The swelling properties were studied at different pHs and temperatures, and it was discovered that these properties depend particularly on the pH of the environment. Creep-recovery and stress-relaxation studies were performed to determine mechanical properties and the chitosan/succinic acid hydrogels exhibited a completely viscous behavior. Thermal studies were carried out using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). DSC results revealed that the materials obtained are completely amorphous. Acetaminophen was used as a positive control for the release kinetics studies. Upon fitting the results to a specific mathematical model, it was determined that the release process is controlled by diffusion and relaxation of the polymer network.