Evaluation of the rheological and rupture properties of gelatin-based hydrogels blended with polymers to determine their drug diffusion behavior

In this study, the drug diffusion behavior and kinetics of gelatin hydrogels that were prepared with polymers were evaluated in terms of their rheological and rupture properties. The rheological and rupture properties of polymer-blended hydrogels prepared at pH 5.5 indicated that gelatin was homogeneously mixed with hydroxypropyl methylcellulose phthalate (HPMCP) or methacrylic acid-ethyl acrylate copolymer (Eudragit((R))) but not with hydroxypropyl methylcellulose or hydroxypropyl methylcellulose acetate succinate. We found that the release rate of nizatidine, a water-soluble drug, from the gelatin/HPMCP hydrogels might be inhibited compared with that from the gelatin/Eudragit((R)) hydrogels at pH 1.2. This was because compared to the gelatin/Eudragit((R)) hydrogels, the gelatin/HPMCP hydrogels had a higher crossover point between the strain-dependent storage and loss moduli. In addition, the gelatin/HPMCP and gelatin/Eudragit((R)) hydrogels showed an increase in rupture stress and strain when the polymer content was increased. The drug diffusion mechanism of the gelatin/HPMCP hydrogel formulations from pH 1.0 to 6.0 was identified using four kinetic models. The findings indicated that the drug diffusion behavior of the gelatin/HPMCP gels below pH 2.0 was governed by diffusion of the drug. These results demonstrate that gelatin-based hydrogels with HPMCP are potential candidates for inhibiting the release of nizatidine in a gastric pH medium.

Automated summary

This study evaluated the drug diffusion behavior and kinetics of gelatin hydrogels prepared with polymers. The results showed that gelatin was homogeneously mixed with HPMCP or Eudragit((R)) but not with other polymers. The release rate of nizatidine from gelatin/HPMCP hydrogels was inhibited compared to gelatin/Eudragit((R)) hydrogels at pH 1.2. The drug diffusion mechanism of the gelatin/HPMCP hydrogel formulations was identified using four kinetic models.