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Al +3 ion cross-linked and acetalated gellan hydrogel network beads for prolonged release of glipizide

Considering relatively fast drug release rate of Ca +2/gellan beads in phosphate buffer solution, a novel glipizide-loaded bead system was developed through ionotropic gelation of gellan with trivalent Al +3 ions and covalent cross-linking with glutaraldehyde (GA). Following GA-treatment, spherical...

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Bibliographic Details
Published in:Carbohydrate polymers 2011, Vol.85 (1), p.164-172
Main Authors: Maiti, Sabyasachi, Ranjit, Somdipta, Mondol, Ranjit, Ray, Somasree, Sa, Biswanath
Format: Article
Language:English
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Summary:Considering relatively fast drug release rate of Ca +2/gellan beads in phosphate buffer solution, a novel glipizide-loaded bead system was developed through ionotropic gelation of gellan with trivalent Al +3 ions and covalent cross-linking with glutaraldehyde (GA). Following GA-treatment, spherical Al +3/gellan beads contracted leaving wrinkles on bead surface. A maximum of 97.67% drug entrapment efficiency was achieved; however GA-treatment reduced the same by 11.89%. All the beads released only 10% drug in acidic medium in 2 h; however it was found 38–47% for Al +3/gellan beads and only 15% for GA-treated beads in weakly alkaline medium. The drug release did correlate well with their swelling behaviors. The anomalous drug transport mechanism shifted to super case II transport for GA-treated beads, where the polymer relaxation phenomenon was dominant. The drug was relatively stable, amorphous in the beads. Thus both GA-treated and -untreated Al +3/gellan beads could be useful carriers for the controlled oral delivery of glipizide.
ISSN:0144-8617
1879-1344
DOI:10.1016/j.carbpol.2011.02.010