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Comparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats

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dc.contributor.authorMustapha, Omer-
dc.contributor.authorKim, Kyung Soo-
dc.contributor.authorShafique, Shumaila-
dc.contributor.authorKim, Dong Shik-
dc.contributor.authorJin, Sung Giu-
dc.contributor.authorSeo, Youn Gee-
dc.contributor.authorYoun, Yu Seok-
dc.contributor.authorOh, Kyung Taek-
dc.contributor.authorYong, Chul Soon-
dc.contributor.authorKim, Jong Oh-
dc.contributor.authorChoi, Han-Gon-
dc.date.accessioned2021-06-22T14:02:45Z-
dc.date.available2021-06-22T14:02:45Z-
dc.date.issued2017-06-
dc.identifier.issn0927-7765-
dc.identifier.issn1873-4367-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/9537-
dc.description.abstractThe aim of this research was to compare three different types of cilostazol-loaded solid dispersion system including solvent-evaporated, solvent-wetted and surface-attached solid dispersion. The effect of polymers and surfactants on the aqueous solubility of cilostazol was investigated, leading to the selection of polyvinylpyrrolidone (PVP) and sodium lauryl sulphate (SLS). Employing a spray-drying technique, numerous surface-attached, solvent-evaporated and solvent-wetted solid dispersions were prepared with various amounts PVP and SLS using water, 90% ethanol and acetone, respectively. Their physicochemical properties, solubility, dissolution and oral bioavailability in rats were assessed, compared to the drug powder. Among each solid dispersion system tested, the surface-attached, solvent-evaporated and solvent-wetted solid dispersions composed of cilostazol, PVP and SLS at weight ratios of 3.0 : 0.75 :1.5, 3.0 :3.0 : 1.5 and 3.0 : 3.0 : 1.5, respectively, provided the highest drug solubility and dissolution. The solvent-evaporated solid dispersion gave homogeneous and very small spherical particles, in which the drug was changed to an amorphous state. In the solvent-wetted solid dispersion, the amorphous drug was attached to the polymer surface. Conversely, in the surface-attached solid dispersion, the carriers were adhered onto the surface of the unchanged crystalline drug. The solubility, dissolution and oral bioavailability were significantly increased in the order of solvent-evaporated > solvent-wetted > surface attached > drug powder. Thus, the type of solid dispersion considerably affected the physicochemical properties, aqueous solubility and oral bioavailability. Furthermore, the cilostazol-loaded solvent evaporated solid dispersion with the highest oral bioavailability would be actively recommended as a practical oral pharmaceutical product. (C) 2017 Elsevier B.V. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleComparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.colsurfb.2017.03.017-
dc.identifier.scopusid2-s2.0-85015360124-
dc.identifier.wosid000402348000012-
dc.identifier.bibliographicCitationCOLLOIDS AND SURFACES B-BIOINTERFACES, v.154, pp 89 - 95-
dc.citation.titleCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.citation.volume154-
dc.citation.startPage89-
dc.citation.endPage95-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusIN-VIVO EVALUATION-
dc.subject.keywordPlusORAL BIOAVAILABILITY-
dc.subject.keywordPlusGELATIN MICROCAPSULE-
dc.subject.keywordPlusENHANCED SOLUBILITY-
dc.subject.keywordPlusAQUEOUS SOLUBILITY-
dc.subject.keywordPlusFENOFIBRATE-
dc.subject.keywordPlusABSORPTION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusOPTIMIZATION-
dc.subject.keywordAuthorCilostazol-
dc.subject.keywordAuthorSolvent-evaporated solid dispersion-
dc.subject.keywordAuthorSolvent-wetted solid dispersion-
dc.subject.keywordAuthorSurface-attached solid dispersion-
dc.subject.keywordAuthorSolubility-
dc.subject.keywordAuthorCrystallinity-
dc.subject.keywordAuthorOral bioavailability-
dc.identifier.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0927776517301352-
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