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Synthesis of aligned porous poly(epsilon-caprolactone) (PCL)/hydroxyapatite (HA) composite microspheres

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dc.contributor.authorKim, Mi-Jin-
dc.contributor.authorKoh, Young-Hag-
dc.date.accessioned2021-09-06T01:41:08Z-
dc.date.available2021-09-06T01:41:08Z-
dc.date.created2021-06-18-
dc.date.issued2013-05-01-
dc.identifier.issn0928-4931-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/103256-
dc.description.abstractWe synthesized poly(epsilon-caprolactone) (PCL)/hydroxyapatite (HA) composite microspheres with an aligned porous structure and evaluated their potential applications in bone tissue engineering. A range of HA particles (0, 5, 10 and 20 wt.% in relation to the PCL polymer) were added to a PCL solution in order to improve the biocompatibility of the porous PCL/HA composite microspheres. All the synthesized microspheres showed that the HA particles were distributed well in the PCL matrix, while preserving their aligned porous structure. The average size of the PCL/HA composite microspheres increased from 62 +/- 7 to 179 +/- 95 mu m with increasing HA content from 0 to 20 wt.%. The incorporation of the HA particles to the PCL polymer led to a considerable improvement in in vitro bioactivity, which was assessed by immersing the PCL/HA composite microspheres in simulated body fluid (SBF). A number of apatite crystals could be precipitated on the surface of the aligned porous PCL/HA composite microspheres after soaking in the SBF for 7 days. (C) 2013 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectCONTROLLED DRUG-RELEASE-
dc.subjectCRYSTALLIZATION BEHAVIOR-
dc.subjectPOLYMER MICROSPHERES-
dc.subjectIN-VITRO-
dc.subjectGELATIN-
dc.subjectMICROPARTICLES-
dc.subjectSYSTEM-
dc.subjectVIVO-
dc.titleSynthesis of aligned porous poly(epsilon-caprolactone) (PCL)/hydroxyapatite (HA) composite microspheres-
dc.typeArticle-
dc.contributor.affiliatedAuthorKoh, Young-Hag-
dc.identifier.doi10.1016/j.msec.2013.01.051-
dc.identifier.scopusid2-s2.0-84875209860-
dc.identifier.wosid000317528700055-
dc.identifier.bibliographicCitationMATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, v.33, no.4, pp.2266 - 2272-
dc.relation.isPartOfMATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS-
dc.citation.titleMATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS-
dc.citation.volume33-
dc.citation.number4-
dc.citation.startPage2266-
dc.citation.endPage2272-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusCONTROLLED DRUG-RELEASE-
dc.subject.keywordPlusCRYSTALLIZATION BEHAVIOR-
dc.subject.keywordPlusPOLYMER MICROSPHERES-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusGELATIN-
dc.subject.keywordPlusMICROPARTICLES-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusVIVO-
dc.subject.keywordAuthorPolymer-
dc.subject.keywordAuthorComposite-
dc.subject.keywordAuthorHydroxyapatite-
dc.subject.keywordAuthorPore-
dc.subject.keywordAuthorIn vitro bioactivity-
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