Enhanced transdermal delivery of AZT (Zidovudine) using iontophoresis and penetration enhancer

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dc.contributor.authorOh, SYko
dc.contributor.authorJeong, SYko
dc.contributor.authorPark, Tae Gwanko
dc.contributor.authorLee, JHko
dc.date.accessioned2009-10-16T02:17:13Z-
dc.date.available2009-10-16T02:17:13Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1998-02-
dc.identifier.citationJOURNAL OF CONTROLLED RELEASE, v.51, no.2-3, pp.161 - 168-
dc.identifier.issn0168-3659-
dc.identifier.urihttp://hdl.handle.net/10203/11827-
dc.description.abstractThe effect of current, its magnitude and penetration enhancers (propylene glycol/oleic acid) on the transdermal flux of AZT (Zidovudine) across hairless mouse skin was studied and the results were compared. The in vitro iontophoretic flux from AZT solution increased to about 5-40 fold that obtained by passive diffusion, depending on the magnitude of current density. When the donor side was karaya gum matrix, instead of solution, the flux enhancement effect by iontophoresis was much smaller. Incorporation of penetration enhancers into the matrix increased the passive flux 2-50 fold, depending on the amount of penetration enhancers in the matrix. These enhancers worked synergistically with iontophoresis in the transdermal transport: a much larger flux than that expected from a simple additive effect was observed. Electrical resistance data from our previous work is utilized to further discuss this synergistic effect. (C) 1998 Elsevier Science B.V.-
dc.description.sponsorship1994 Special Fund for University Research Institute, Korea Research Foundationen
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherELSEVIER SCIENCE BV-
dc.titleEnhanced transdermal delivery of AZT (Zidovudine) using iontophoresis and penetration enhancer-
dc.typeArticle-
dc.identifier.wosid000072419400007-
dc.type.rimsART-
dc.citation.volume51-
dc.citation.issue2-3-
dc.citation.beginningpage161-
dc.citation.endingpage168-
dc.citation.publicationnameJOURNAL OF CONTROLLED RELEASE-
dc.identifier.doi10.1016/S0168-3659(97)00162-4-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorOh, SY-
dc.contributor.nonIdAuthorJeong, SY-
dc.contributor.nonIdAuthorLee, JH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthoriontophoresis-
dc.subject.keywordAuthorAZT-
dc.subject.keywordAuthorpropylene glycol-
dc.subject.keywordAuthoroleic acid-
dc.subject.keywordAuthorresistance-
dc.subject.keywordAuthorsynergistic effect-
dc.subject.keywordPlusOLEIC-ACID-
dc.subject.keywordPlusSKIN PERMEABILITY-
dc.subject.keywordPlusSTRATUM-CORNEUM-
dc.subject.keywordPlusDRUG DELIVERY-
dc.subject.keywordPlusMOUSE SKIN-
dc.subject.keywordPlusINVITRO-
dc.subject.keywordPlusPOLYPEPTIDES-
dc.subject.keywordPlusPERMEATION-
dc.subject.keywordPlusESTRADIOL-
dc.subject.keywordPlusPEPTIDES-
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