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Sustained and controlled release of daunomycin from cross-linked poly(aldehyde guluronate) hydrogels

✍ Scribed by Kamal H. Bouhadir; Geneveive M. Kruger; Kuen Yong Lee; David J. Mooney


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
250 KB
Volume
89
Category
Article
ISSN
0022-3549

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✦ Synopsis


We have incorporated daunomycin, an antineoplastic agent, into a biodegradable hydrogel through a labile covalent bond. In brief, sodium alginate was chemically broken down to low molecular weight and followed by oxidation to prepare poly-(aldehyde guluronate). Adipic dihydrazide was used to incorporate the drug into the polymer backbone and cross-link the polymer to form hydrogels. Daunomycin can be released from the hydrogel after the hydrolysis of the covalent linkage between the drug and the polymer. A wide range of release profiles of daunomycin (e.g., from 2 days to 6 weeks) has been achieved using these materials, and the biological activity of the released daunomycin was maintained.


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