Biodegradable hydrogels in which drug release was controlled by sol-gel tra
nsition were prepared. Gelatin was used as a component because it exhibits
sol-gel transition in response to temperature changes. Glycidyl methacrylat
ed (GMA) dextran was crosslinked by low dose gamma-irradiation in the prese
nce of gelatin and the model drugs, beta-galactosidase (beta-GA), bovine se
rum albumin (BSA) or 5-fluorouracil (5-FU). The enzyme activity of beta-GA
remained greater than 95% after irradiation. Temperature-responsive release
of beta-GA and BSA resulted from the sol-gel transition of gelatin. Sol-ge
l transition was confirmed by the temperature dependence of the spin-spin r
elaxation time of the gel polymer protons. The protein release rate was aff
ected by both the degree of GMA substitution and the gelatin concentration.
Desired release rate could be achieved by adjusting these factors. The rel
ease rate of 5-FU was not affected by the sol-gel transition of gelatin. (C
) 1999 Elsevier Science Ltd. All rights reserved.