Korea Polymer Journal, Vol.2, No.2, 91-95, October, 1994
Bioerodible Hydrogel Based on Interpenetrating Polymer Networks Composed of Poly(D,L-lactic acid) and Poly(ethylene glycol) Macromer
Poly(ethylene glycol) (PEG) macromers terminated with acrylate groups and semi-interpenetrating polymer networks (IPNs) composed of poly(D,L-lactic acid)(PLA) and PEG macromer were synthesized and characterized with the aim of obtaining a bioerokeble hydrogel that could be used to release drugs. Polymerization of PEG macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Glass transition temperature (Tg) and melting temperature (Tm) of PEG network and PLA in the IPNs were shifted, indicating an interpenetration of PLA and PEG chains. It was found that water content decreased with increasing PLA weight fraction due to the hydrophobicity of PLA. These IPNs gels degrade upon hydrolysis and their degradation rates can be controled by cross-linking density and the nature of PEG and the mole fraction of PEG in the IPNs.
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