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Biodegradable dextran-polylactide hydrogel network and its controlled release of albumin.

Authors :
Zhang Y
Chu CC
Source :
Journal of biomedical materials research [J Biomed Mater Res] 2001 Jan; Vol. 54 (1), pp. 1-11.
Publication Year :
2001

Abstract

The objective of this paper was to study the release of bovine serum albumin (BSA) from a series of biodegradable hydrogels having a wide range of hydrophilicity to hydrophobicity, swelling, and biodegradation properties. BSA was incorporated into a series of biodegradable hydrogels made from a dextran derivative of allyl isocyanate (dex-AI, as the hydrophilic constituent) and poly(DL-lactic acid) diacrylate macromer (PDLLAM, as the hydrophobic constituent). The release kinetics of BSA from these dex-AI/PDLLAM hydrogels was studied. Laser confocal scanning microscopy was used to investigate the morphological change of the hydrogels, as well as BSA distribution in the hydrogels, as a function of dex-AI to PDLLAM composition ratio and incubation time. We found that the incorporation of PDLLAM into dex-AI reduced the initial burst release of BSA due to its more homogeneous distribution in the hydrogels. As the PDLLAM component increased, the rate of formation of a loose three-dimensional (3D) network structure increased; consequently, the sustained rate and extent of BSA release increased. Both release index and diffusion coefficient (from release kinetics data) increased as the PDLLAM component increased in the hydrogels. The data suggest that the release of BSA was controlled by both diffusion of BSA through swelling of the hydrophilic phase during an early stage, and degradation of the hydrophobic phase during a late stage, and also that the magnitude of diffusion versus degradation controlled release is dependent on composition ratio and immersion time.<br /> (Copyright 2000 John Wiley & Sons, Inc.)

Details

Language :
English
ISSN :
0021-9304
Volume :
54
Issue :
1
Database :
MEDLINE
Journal :
Journal of biomedical materials research
Publication Type :
Academic Journal
Accession number :
11077397
Full Text :
https://doi.org/10.1002/1097-4636(200101)54:1<1::aid-jbm1>3.0.co;2-m