KMID : 0043319950180010018
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Archives of Pharmacal Research 1995 Volume.18 No. 1 p.18 ~ p.21
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Drug Release from Bioerodible Hydrogels Composed of Poly-¥å-caprolactone/poly(ethylene glycol) Macromer Semiinterpenhetrating Polymer Networks
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Kim Sung-Ho
Ha Jeong-Hun Jung Yong-Jae Cho Chong-Su
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Abstract
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Poly(ethylene glycol)(PEG) macrocers teminated with acrylate groups and semi-interpenetrating polymer networks (IPNs) composed of poly-.epsilon.-capolactone(PCL) and PEG macromer were syntheswized with the aim of obtaining a bioerodible hydrogel that could be used to release drugs for implantable delivery system. Polymerization of PEG macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Non-crosslinked PCL chains were interpenetrated into the cross-linked three-dimensions networks of PEG. The IPNs, largw drug loading lower concentration of PEG macromer in the IPNs concentration and the higher molecular weight of PEG macromer. Also, 5-FU was more fast released than hydrocortisone to the increased water solubility.
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KEYWORD
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PEG macromer, IPNs, PCL, Bioerodible, Hydrogel
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