AbstractIn order to modify the xanthan gum (XG) polysaccharide and to develop the hydrogels meant for the drug delivery, we have prepared XG-g-poly [HEMA-co-AA] superporous hydrogel (SPH) through chemical cross-linking by graft copolymerization of 2-hydroxyethyl methacrylate (HEMA) and acrylic acid (AA) on to XG via redox initiator system of ammonium persulfate (APS) and N, N, N', N'-tetramethylethylenediamine (TMED), in the presence of N, N'-methylenebisacrylamide (MBA) crosslinking agent, sodium bicarbonate foaming agent, a triblock copolymer of polyoxyethylene/ polyoxypropylene/ polyoxyethylene as a foam stabilizer. Characterization of SPH was done by FT-IR, TGA, SEM, HPLC and GCMS. The prepared SPH were successfully loaded with Doxofylline (DF) drug and formulation H 10 showed higher % drug content (98±2.3) and % drug entrapment efficiency (83±2.0). From the in Vitro drug release study in pH progressive media, formulation H 10 showed comparatively higher release extending upto 24h.The mechanism of DF release from the SPH matrix was found to be of diffusion type.
CITATION STYLE
Gils, P. S., Ray, D., & Sahoo, P. K. (2010). Controlled Release of Doxofylline from Biopolymer Based Hydrogels. American Journal of Biomedical Sciences, 373–383. https://doi.org/10.5099/aj100400373
Mendeley helps you to discover research relevant for your work.