Controlled drug release via minimization of burst release in pH-response kappa-carrageenan/polyvinyl alcohol hydrogels

Kappa-carrageenan/polyvinyl alcohol cross-linked hydrogels was formulated using genipin as a natural and non-toxic cross-linker to achieve a controlled drug release. β-Carotene was immobilized and the release study was evaluated under in vitro conditions. Monitoring β-carotene release was carried out by structure modification using cross-linker and minimization of burst release. It was found that using genipin can stop burst release in the hydrogels and control active material better than native films as a result of structural modification. This suggests that the burst release is depended highly on the degree of cross-linking and the mesh space available for drug diffusion. Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) are carried out to study the characteristics changes of native and cross-linked hydrogels. Also, field emission scanning electron microscope (FESEM) was performed to study microstructure of hydrogels. The transport mechanism seems to be determined by the strength of the gel network due to genipin concentration changes. Finally, diffusion coefficient is determined for native and cross-linked hydrogel.

Figure optionsDownload high-quality image (347 K)Download as PowerPoint slideHighlight
► We synthesized new hydrogel using genipin as a natural cross-linker.
► We studied the characterization of modified and non-modified gel.
► Monitoring β-carotene release was carried out by structure modification using genipin.
► We showed that cross-linking has caused significant elimination of burst release.
► Diffusion coefficient is determined for native and cross-linked hydrogel.