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Phase behavior of itraconazole-phenol mixtures and its pharmaceutical applications

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dc.contributor.authorPark, Chun-Woong-
dc.contributor.authorMansour, Heidi M.-
dc.contributor.authorOh, Tack-Oon-
dc.contributor.authorKim, Ju-Young-
dc.contributor.authorHa, Jung-Myung-
dc.contributor.authorLee, Beom-Jin-
dc.contributor.authorChi, Sang-Cheol-
dc.contributor.authorRhee, Yun-Seok-
dc.contributor.authorPark, Eun-Seok-
dc.date.accessioned2022-12-27T01:36:12Z-
dc.date.available2022-12-27T01:36:12Z-
dc.date.issued2012-10-15-
dc.identifier.issn0378-5173-
dc.identifier.issn1873-3476-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/21951-
dc.description.abstractThe aims of this study were to examine the phase behavior of itraconazole-phenol mixtures and assess the feasibility of topical formulations of itraconazole using eutectic mixture systems. Itraconazole-phenol eutectic mixtures were characterized using differential scanning calorimetry, Fourier transform infrared spectroscopy, H-1-nuclear magnetic resonance, and powder X-ray diffractometry. The skin permeation rates of itraconazole-phenol eutectic formulations were determined using Franz diffusion cells fitted with excised hairless mouse skins. Itraconazole can form eutectic compounds with phenol, and the hydrogen-bonding interactions between the carbonyl group in the itraconazole and hydroxyl group in phenol play a major role in itraconazole-phenol eutectic formation. Despite its high molecular weight and hydrophobicity, the drug (i.e., itraconazole) can be permeated through excised hairless mouse skins from itraconazole-phenol eutectic formulations. The findings of this study emphasize the capabilities of the topical application of itraconazole via external preparations. (c) 2012 Elsevier B.V. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titlePhase behavior of itraconazole-phenol mixtures and its pharmaceutical applications-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijpharm.2012.07.054-
dc.identifier.scopusid2-s2.0-84865304491-
dc.identifier.wosid000308597600073-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.436, no.1-2, pp 652 - 658-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume436-
dc.citation.number1-2-
dc.citation.startPage652-
dc.citation.endPage658-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusSOLID DISPERSION-
dc.subject.keywordPlusBETA-CYCLODEXTRIN-
dc.subject.keywordPlusDOSE PHARMACOKINETICS-
dc.subject.keywordPlusPOLYETHYLENE-GLYCOL-
dc.subject.keywordPlusMOLECULAR MOBILITY-
dc.subject.keywordPlusT-G-
dc.subject.keywordPlusFORMULATION-
dc.subject.keywordPlusBIOAVAILABILITY-
dc.subject.keywordPlusSOLUBILITY-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordAuthorItraconazole-
dc.subject.keywordAuthorPhenol-
dc.subject.keywordAuthorEutectic mixture-
dc.subject.keywordAuthorTopical-
dc.subject.keywordAuthorSkin permeation-
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