G-CSF loaded biodegradable PLGA nanoparticles prepared by a single oil-in-water emulsion method

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dc.contributor.authorChoi, SHko
dc.contributor.authorPark, Tae Gwanko
dc.date.accessioned2009-11-10T04:56:21Z-
dc.date.available2009-11-10T04:56:21Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-03-
dc.identifier.citationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.311, no.1-2, pp.223 - 228-
dc.identifier.issn0378-5173-
dc.identifier.urihttp://hdl.handle.net/10203/12339-
dc.description.abstractA new formulation method was developed for preparing poly(D,L-lactic-co-glycolic acid) (PLGA) nanoparticles loaded with recombinant human granulocyte colony-stimulating factor (rhG-CSF). Lyophilized rhG-CSF powder and PLGA polymer were directly co-dissolved in a single organic phase, and the resulting solution was dispersed into an aqueous Solution. PLGA nanoparticles encapsulating rhG-CSF were produced by a spontaneous emulsion/solvent diffusion method. In this manner, rhG-CSF was molecularly dissolved in the polymer phase. Release profile of rhG-CSF from PLGA nanoparticles was compared with those from two kinds of PLGA microparticles which were separately prepared by either single oil-in-water (O/W) or double water-in-oil-in-water (W/O/W) emulsion technique. The sizes of rhG-CSF loaded nanoparticles, O/W microparticles, and W/O/W microparticles were about 257 nm, 4.7 mu m, and 4.3 mu m, respectively. For rhG-CSF nanoparticles,about 90% of encapsulated rhG-CSF was released out in a sustained manner from PLGA nanoparticles over a 1 week period, but for rhG-CSF microparticles, only about 20% of rhG-CSF Could be released out during the same period. Reversed phase and size exclusion chromatograms revealed that the structural integrity of released rhG-CSF from nanoparticles was nearly intact, compared to that of native rhG-CSF. (c) 2005 Elsevier B.V. All rights reserved.-
dc.description.sponsorshipthe Ministry of Health and Welfare, Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherELSEVIER SCIENCE BV-
dc.subjectPOLY(D,L-LACTIC-CO-GLYCOLIC ACID) MICROSPHERES-
dc.subjectCOLONY-STIMULATING FACTOR-
dc.subjectHUMAN GROWTH-HORMONE-
dc.subjectCONTROLLED DELIVERY-
dc.subjectRELEASE MECHANISM-
dc.subjectORGANIC-SOLVENTS-
dc.subjectPROTEIN RELEASE-
dc.subjectSTABILITY-
dc.subjectMICROPARTICLES-
dc.subjectMICROENCAPSULATION-
dc.titleG-CSF loaded biodegradable PLGA nanoparticles prepared by a single oil-in-water emulsion method-
dc.typeArticle-
dc.identifier.wosid000236526600030-
dc.identifier.scopusid2-s2.0-33644625226-
dc.type.rimsART-
dc.citation.volume311-
dc.citation.issue1-2-
dc.citation.beginningpage223-
dc.citation.endingpage228-
dc.citation.publicationnameINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.identifier.doi10.1016/j.ijpharm.2005.12.023-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorChoi, SH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorrhG-CSF-
dc.subject.keywordAuthorbiodegradable-
dc.subject.keywordAuthorPLGA-
dc.subject.keywordAuthornanoparticles-
dc.subject.keywordAuthorsustained release-
dc.subject.keywordPlusPOLY(D,L-LACTIC-CO-GLYCOLIC ACID) MICROSPHERES-
dc.subject.keywordPlusCOLONY-STIMULATING FACTOR-
dc.subject.keywordPlusHUMAN GROWTH-HORMONE-
dc.subject.keywordPlusCONTROLLED DELIVERY-
dc.subject.keywordPlusRELEASE MECHANISM-
dc.subject.keywordPlusORGANIC-SOLVENTS-
dc.subject.keywordPlusPROTEIN RELEASE-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusMICROPARTICLES-
dc.subject.keywordPlusMICROENCAPSULATION-
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