Comparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats
DC Field | Value | Language |
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dc.contributor.author | Mustapha, Omer | - |
dc.contributor.author | Kim, Kyung Soo | - |
dc.contributor.author | Shafique, Shumaila | - |
dc.contributor.author | Kim, Dong Shik | - |
dc.contributor.author | Jin, Sung Giu | - |
dc.contributor.author | Seo, Youn Gee | - |
dc.contributor.author | Youn, Yu Seok | - |
dc.contributor.author | Oh, Kyung Taek | - |
dc.contributor.author | Yong, Chul Soon | - |
dc.contributor.author | Kim, Jong Oh | - |
dc.contributor.author | Choi, Han-Gon | - |
dc.date.accessioned | 2021-06-22T14:02:45Z | - |
dc.date.available | 2021-06-22T14:02:45Z | - |
dc.date.issued | 2017-06 | - |
dc.identifier.issn | 0927-7765 | - |
dc.identifier.issn | 1873-4367 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/9537 | - |
dc.description.abstract | The 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.extent | 7 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER | - |
dc.title | Comparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats | - |
dc.type | Article | - |
dc.publisher.location | 네델란드 | - |
dc.identifier.doi | 10.1016/j.colsurfb.2017.03.017 | - |
dc.identifier.scopusid | 2-s2.0-85015360124 | - |
dc.identifier.wosid | 000402348000012 | - |
dc.identifier.bibliographicCitation | COLLOIDS AND SURFACES B-BIOINTERFACES, v.154, pp 89 - 95 | - |
dc.citation.title | COLLOIDS AND SURFACES B-BIOINTERFACES | - |
dc.citation.volume | 154 | - |
dc.citation.startPage | 89 | - |
dc.citation.endPage | 95 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biophysics | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.relation.journalWebOfScienceCategory | Biophysics | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.subject.keywordPlus | IN-VIVO EVALUATION | - |
dc.subject.keywordPlus | ORAL BIOAVAILABILITY | - |
dc.subject.keywordPlus | GELATIN MICROCAPSULE | - |
dc.subject.keywordPlus | ENHANCED SOLUBILITY | - |
dc.subject.keywordPlus | AQUEOUS SOLUBILITY | - |
dc.subject.keywordPlus | FENOFIBRATE | - |
dc.subject.keywordPlus | ABSORPTION | - |
dc.subject.keywordPlus | STABILITY | - |
dc.subject.keywordPlus | NANOPARTICLES | - |
dc.subject.keywordPlus | OPTIMIZATION | - |
dc.subject.keywordAuthor | Cilostazol | - |
dc.subject.keywordAuthor | Solvent-evaporated solid dispersion | - |
dc.subject.keywordAuthor | Solvent-wetted solid dispersion | - |
dc.subject.keywordAuthor | Surface-attached solid dispersion | - |
dc.subject.keywordAuthor | Solubility | - |
dc.subject.keywordAuthor | Crystallinity | - |
dc.subject.keywordAuthor | Oral bioavailability | - |
dc.identifier.url | https://linkinghub.elsevier.com/retrieve/pii/S0927776517301352 | - |
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