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dc.contributor.author이승진*
dc.date.accessioned2016-08-28T12:08:28Z-
dc.date.available2016-08-28T12:08:28Z-
dc.date.issued2006*
dc.identifier.issn1598-5032*
dc.identifier.otherOAK-3534*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219753-
dc.description.abstractTwo types of injectable system using thermosensitive chitosan (chitosan-g-NIPAAm), hydrogel and microparticles (MPs)-embedded hydrogel were developed as drug carriers for controlled release and their pharmaceutical potentials were investigated. 5-Fluorouracil (5-FU)-loaded, biodegradable PLGA MPs were prepared by a double emulsion method and then simply mixed with an aqueous solution of thermosensitive chitosan at room temperature. All 5-FU release rates from the hydrogel matrix were faster than bovine serum albumin (BSA), possibly due to the difference in the molecular weight of the drugs. The 5-FU release profile from MPs-embedded hydrogel was shown to reduce the burst effect and exhibit nearly zero-order release behavior from the beginning of each initial stage. Thus, these MPs-embedded hydrogels, as well as thermosensitive chitosan hydrogel, have promising potential as an injectable drug carrier for pharmaceutical applications.*
dc.languageEnglish*
dc.titleThermosensitive chitosan as an injectable carrier for local drug delivery*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume14*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage461*
dc.relation.lastpage465*
dc.relation.journaltitleMacromolecular Research*
dc.identifier.wosidWOS:000240423300011*
dc.identifier.scopusid2-s2.0-33748792019*
dc.author.googleBae J.W.*
dc.author.googleGo D.H.*
dc.author.googlePark K.D.*
dc.author.googleLee S.J.*
dc.contributor.scopusid이승진(57196249292)*
dc.date.modifydate20260611125815*
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약학대학 > 약학과 > Journal papers
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