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EGF-Loaded Hyaluronic Acid Based Microparticles as Effective Carriers in a Wound Model

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dc.contributor.authorKang, Sun-Woong-
dc.contributor.authorChoi, Jong-Jin-
dc.contributor.authorKim, Ha-Na-
dc.contributor.authorSeo, Joseph-
dc.contributor.authorPark, Soon-Jung-
dc.contributor.authorKim, Eun-Young-
dc.contributor.authorPark, Se-Pil-
dc.contributor.authorHuh, Kang Moo-
dc.contributor.authorChung, Hyung-Min-
dc.contributor.authorChung, Ho Yun-
dc.contributor.authorMoon, Sung-Hwan-
dc.date.accessioned2024-01-09T03:31:33Z-
dc.date.available2024-01-09T03:31:33Z-
dc.date.issued2017-05-
dc.identifier.issn0934-0866-
dc.identifier.issn1521-4117-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/69823-
dc.description.abstractEpidermal growth factor (EGF) is widely recognized to be involved in the regenerative process, but only a few studies document its effect on acute wounds when EGF release is sustained over a period of time by encapsulation in an emulsion-based hydrogel. Among hydrogels, hyaluronic acid (HA) is a promising carrier because it is biodegradable and known to bind to the components of the Extracellular Matrix (ECM) which undergoes remodeling during regeneration. Coupled with EGF in microparticulates, it may serve to directly deliver the cytokine to the impaired ECM to stimulate cells for ECM remodeling. In this study, a very simple and effective way is demonstrated to produce EGF-conjugated HA microspheres for the purpose of targeted and sustained EGF delivery to damaged ECM in acute wounds. This approach is advantageous due to its simplicity which may serve to accelerate research in wound regeneration and relevant drug discovery.-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleEGF-Loaded Hyaluronic Acid Based Microparticles as Effective Carriers in a Wound Model-
dc.typeArticle-
dc.identifier.doi10.1002/ppsc.201600320-
dc.identifier.bibliographicCitationPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, v.34, no.5-
dc.description.isOpenAccessN-
dc.identifier.wosid000403919000002-
dc.identifier.scopusid2-s2.0-85017357754-
dc.citation.number5-
dc.citation.titlePARTICLE & PARTICLE SYSTEMS CHARACTERIZATION-
dc.citation.volume34-
dc.type.docTypeArticle-
dc.publisher.location독일-
dc.subject.keywordAuthordelivery systems-
dc.subject.keywordAuthorepidermal growth factor-
dc.subject.keywordAuthorhyaluronic acid-
dc.subject.keywordAuthormicroparticles-
dc.subject.keywordAuthorwound healing-
dc.subject.keywordPlusEPIDERMAL-GROWTH-FACTOR-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusREPAIR-
dc.subject.keywordPlusMICROSPHERES-
dc.subject.keywordPlusVIVO-
dc.subject.keywordPlusRATS-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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