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Preparation and Properties of Alginate/Polyaspartate Composite Hydrogels
This study examined the swelling behavior and in vitro release of a model drug, tetracycline-HCl, from alginate and alginate-polyaspartate (Alg-PASP) composite gel beads. The alginate and Alg-PASP composite beads were prepared using an ionic crosslinking method with aqueous Ca 2+ . Their microporous...
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Published in: | Macromolecular research 2008, 16(1), , pp.45-50 |
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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: | This study examined the swelling behavior and
in vitro
release of a model drug, tetracycline-HCl, from alginate and alginate-polyaspartate (Alg-PASP) composite gel beads. The alginate and Alg-PASP composite beads were prepared using an ionic crosslinking method with aqueous Ca
2+
. Their microporous morphology was observed by scanning electron microscopy. The swelling ratio of the beads in different media varied according to their composition, cross-linking density (Ca
2+
concentration), and pH of the aqueous medium. The
in vitro
release experiment of the tetracycline-HCl encapsulated beads in different media suggests that the release of the drug is governed mainly by the swelling properties of the polymer network. The presence of PASP was found to significantly influence the swelling properties and drug release profile. |
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ISSN: | 1598-5032 2092-7673 |
DOI: | 10.1007/BF03218959 |