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Development of cyclosporin A-loaded hyaluronic microsphere with enhanced oral bioavailability

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dc.contributor.authorWoo, Jong Soo-
dc.contributor.authorPiao, Ming Guan-
dc.contributor.authorLi, Dong Xun-
dc.contributor.authorRyu, Dong-Sung-
dc.contributor.authorChoi, Jun Young-
dc.contributor.authorKim, Jung-Ae-
dc.contributor.authorKim, Jeong Hoon-
dc.contributor.authorJin, Sung Giu-
dc.contributor.authorKim, Dae-Duk-
dc.contributor.authorLyoo, Won Seok-
dc.contributor.authorYong, Chul Soon-
dc.contributor.authorChoi, Han-Gon-
dc.date.accessioned2021-06-23T18:42:32Z-
dc.date.available2021-06-23T18:42:32Z-
dc.date.issued2007-12-
dc.identifier.issn0378-5173-
dc.identifier.issn1873-3476-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/43146-
dc.description.abstractTo develop a hyaluronic microsphere with the improved oral bioavailability of poorly water-soluble cyclosporin A (CsA), the microspheres were prepared with varying ratios of sodium hyaluronate (HA)/sodium lauryl sulfate (SLS)/CsA using a spray-drying technique. The effects of HA and SLS on the dissolution and solubility of CsA in microspheres were investigated. The CsA-microsphere prepared with HA/SLS/CsA at the ratio of 4/2/1 gave the highest solubility and dissolution rate of CsA among those formulae tested. As solubility and dissolution rate of CsA were increased about 17- and 2-fold compared to CsA powder, respectively, this CsA-microsphere was selected as an optimal formula for oral delivery in rats. The CsA-microsphere and Sandimmun neoral sol((R)) gave significantly higher blood levels compared with CsA powder alone. Moreover, the AUC, T-max and C-max values of CsA in CsA-microsphere were not significantly different from those in Sandimmun neoral sol((R)) in rats, indicating that CsA-microsphere was bioequivalent to the commercial product in rats. Our results demonstrated that the CsA-microsphere prepared with HA and SLS, with improved bioavailability of CsA, might have been useful to deliver a poorly water-soluble CsA. (c) 2007 Elsevier B.V. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleDevelopment of cyclosporin A-loaded hyaluronic microsphere with enhanced oral bioavailability-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijpharm.2007.08.050-
dc.identifier.scopusid2-s2.0-36048934949-
dc.identifier.wosid000251703400016-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.345, no.1-2, pp 134 - 141-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume345-
dc.citation.number1-2-
dc.citation.startPage134-
dc.citation.endPage141-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusWATER-SOLUBLE DRUGS-
dc.subject.keywordPlusDISSOLUTION RATE-
dc.subject.keywordPlusPHYSICOCHEMICAL CHARACTERIZATION-
dc.subject.keywordPlusPHARMACODYNAMIC EVALUATION-
dc.subject.keywordPlusO/W-EMULSION-
dc.subject.keywordPlusDRY ELIXIR-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusRATS-
dc.subject.keywordPlusABSORPTION-
dc.subject.keywordAuthorbioavailability-
dc.subject.keywordAuthorcyclosporin A-
dc.subject.keywordAuthorsodium hyaluronate-
dc.subject.keywordAuthorsodium lauryl sulfate-
dc.subject.keywordAuthormicrosphere-
dc.subject.keywordAuthorspray drying-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S037851730700748X?via%3Dihub-
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