Controlled protein release from electrospun biodegradable fiber mesh composed of poly(epsilon-caprolactone) and poly(ethylene oxide)

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dc.contributor.authorKim, Taek Gyoungko
dc.contributor.authorLee, Doo Sungko
dc.contributor.authorPark, Tae Gwanko
dc.date.accessioned2009-11-10T08:06:56Z-
dc.date.available2009-11-10T08:06:56Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2007-06-
dc.identifier.citationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.338, no.1-2, pp.276 - 283-
dc.identifier.issn0378-5173-
dc.identifier.urihttp://hdl.handle.net/10203/12370-
dc.description.abstractA blend mixture of poly(epsilon-caprolactone) (PCL) and poly(ethylene oxide) (PEO) was electrospun to produce fibrous meshes that could release a protein drug in a controlled manner. Various biodegradable polymers, such as poly(L-lactic acid) (PLLA), poly(epsilon-caprolactone) (PCL), and poly(D,L-lactic-co-glycolic acid) (PLGA) were dissolved, along with PEO and lysozyme, in a mixture of chloroform and dimethylsulfoxide (DMSO). The mixture was electrospun to produce lysozyme loaded fibrous meshes. Among the polymers, the PCL/PEO blend meshes showed good morphological stability upon incubation in the buffer solution, resulting in controlled release of lysozyme over an extended period with reduced initial bursts. With varying the PCL/PEO blending ratio, the release rate of lysozyme from the corresponding meshes could be readily modulated. The lysozyme release was facilitated by increasing the amount of PEO, indicating that entrapped lysozyme was mainly released out by controlled dissolution of PEO from the blend meshes. Lysozyme released from the electrospun fibers retained sufficient catalytic activity. (c) 2007 Elsevier B.V. All rights reserved.-
dc.description.sponsorshipNational Research Laboratory grant from the Ministry of Science and Technology, and the grant (KRF-2004-005-D00070) from the Korea Research Foundation and the Polymer Technology Institute, Sungkyunkwan University, Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherElsevier Science Bv-
dc.subjectPOLY(D,L-LACTIC-CO-GLYCOLIC ACID) MICROSPHERES-
dc.subjectEXTRACELLULAR-MATRIX-
dc.subjectPOLY(L-LACTIC ACID)-
dc.subjectSUSTAINED-RELEASE-
dc.subjectBLOCK-COPOLYMERS-
dc.subjectDELIVERY-SYSTEM-
dc.subjectNANOFIBER-
dc.subjectMORPHOLOGY-
dc.subjectBLENDS-
dc.subjectDEGRADATION-
dc.titleControlled protein release from electrospun biodegradable fiber mesh composed of poly(epsilon-caprolactone) and poly(ethylene oxide)-
dc.typeArticle-
dc.identifier.wosid000247494600037-
dc.identifier.scopusid2-s2.0-34248639861-
dc.type.rimsART-
dc.citation.volume338-
dc.citation.issue1-2-
dc.citation.beginningpage276-
dc.citation.endingpage283-
dc.citation.publicationnameINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.identifier.doi10.1016/j.ijpharm.2007.01.040-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorKim, Taek Gyoung-
dc.contributor.nonIdAuthorLee, Doo Sung-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorelectro-spinning-
dc.subject.keywordAuthorbiodegradable-
dc.subject.keywordAuthornanofibers-
dc.subject.keywordAuthorprotein release-
dc.subject.keywordAuthorlysozyme-
dc.subject.keywordPlusPOLY(D,L-LACTIC-CO-GLYCOLIC ACID) MICROSPHERES-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusPOLY(L-LACTIC ACID)-
dc.subject.keywordPlusSUSTAINED-RELEASE-
dc.subject.keywordPlusBLOCK-COPOLYMERS-
dc.subject.keywordPlusDELIVERY-SYSTEM-
dc.subject.keywordPlusNANOFIBER-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusBLENDS-
dc.subject.keywordPlusDEGRADATION-
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