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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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Published in: | Carbohydrate polymers 2011, Vol.85 (1), p.164-172 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2011.02.010 |