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Fabrication of Compound K-loaded Polymeric Micelle System and its Characterization in vitro and Oral Absorption Enhancement in vivo

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dc.contributor.authorHong, Sun-Mi-
dc.contributor.authorJeon, Sang-ok-
dc.contributor.authorSeo, Jo-Eun-
dc.contributor.authorChun, Kyeung-Hwa-
dc.contributor.authorOh, Dong-Ho-
dc.contributor.authorChoi, Young Wook-
dc.contributor.authorLee, Do Ik-
dc.contributor.authorJeong, Seong Hoon-
dc.contributor.authorKang, Jae Seon-
dc.contributor.authorLee, Sangkil-
dc.date.accessioned2024-08-08T05:01:07Z-
dc.date.available2024-08-08T05:01:07Z-
dc.date.issued2014-11-20-
dc.identifier.issn0253-2964-
dc.identifier.issn1229-5949-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/18301-
dc.description.abstractCompound K (CK) was formulated as polymeric micelles (PM) using Pluronic((R)) F-127 to enhance the oral absorption of CK, an intestinal bacterial metabolite of ginseng protopanaxadiol saponin. The physicochemical properties of Ck-loaded PM were characterized and an in vitro transport study using the Caco-2 cell system as well as an in vivo pharmacokinetic study using SD rats was carried out. The hydrodynamic mean particle size of CK-loaded PM (CK-PM) was 254 +/- 23.45 nm after rehydration and the drug loading efficiency was ca. 99.9%. The FT-IR. spectroscopy, X-ray diffraction, differential scanning calorimetry and scanning electron microscopy data supported the presence of a new solid phase in the PM. The P-app value of in vitro Caco-2 cell permeation of CK-PM and the oral absorption of CK was enhanced about 1.2-fold and 2.6-fold compared to CK suspension, respectively, showing that the present PM formulation enabled an enhancement of oral CK absorption.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleFabrication of Compound K-loaded Polymeric Micelle System and its Characterization in vitro and Oral Absorption Enhancement in vivo-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.5012/bkcs.2014.35.11.3188-
dc.identifier.scopusid2-s2.0-84926661541-
dc.identifier.wosid000344583300008-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.35, no.11, pp 3188 - 3194-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume35-
dc.citation.number11-
dc.citation.startPage3188-
dc.citation.endPage3194-
dc.type.docTypeArticle-
dc.identifier.kciidART001920269-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusGINSENG SAPONIN METABOLITE-
dc.subject.keywordPlusINTESTINAL BACTERIAL METABOLITE-
dc.subject.keywordPlusBLOCK-COPOLYMER MICELLES-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusBIOAVAILABILITY-
dc.subject.keywordPlusPACLITAXEL-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusASSEMBLIES-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusCARRIERS-
dc.subject.keywordAuthorAbsorption enhancement-
dc.subject.keywordAuthorCompound K-
dc.subject.keywordAuthorGinseng saponins-
dc.subject.keywordAuthorPharmacokinetics-
dc.subject.keywordAuthorPolymeric micelle-
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