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dc.contributor.authorDrakulić, B.J.
dc.contributor.authorJuranić, I.O.
dc.contributor.authorErić, S.
dc.contributor.authorZloh, Mire
dc.date.accessioned2013-03-21T13:59:43Z
dc.date.available2013-03-21T13:59:43Z
dc.date.issued2008-11-03
dc.identifier.citationDrakulić , B J , Juranić , I O , Erić , S & Zloh , M 2008 , ' Role of complexes formation between drugs and penetration enhancers in transdermal delivery ' , International Journal of Pharmaceutics , vol. 363 , no. 1-2 , pp. 40-49 . https://doi.org/10.1016/j.ijpharm.2008.06.032
dc.identifier.issn0378-5173
dc.identifier.otherPURE: 1447744
dc.identifier.otherPURE UUID: 77ae129c-6c4a-41c5-a7a5-47d4e273bdeb
dc.identifier.otherScopus: 51749091289
dc.identifier.urihttp://hdl.handle.net/2299/10255
dc.descriptionMEDLINE® is the source for the MeSH terms of this document.
dc.description.abstractThe use of chemical penetration enhancers (CPE) is growing due to their ability to improve drug delivery through the skin. A possible mechanism of penetration enhancement could involve the complex formation between drug and components in the pharmaceutical formulation, thus altering the physicochemical properties of the active substance. Here, modelling studies indicate that hydrocarbon and oxygen-containing terpenes (penetration enhancers) could form complexes with drugs. Satisfactory correlations have been obtained between the predicted molecular properties of enhancers and their enhancement effectsen
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofInternational Journal of Pharmaceutics
dc.titleRole of complexes formation between drugs and penetration enhancers in transdermal deliveryen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionMedicinal and Analytical Chemistry
dc.description.statusPeer reviewed
dc.relation.schoolSchool of Life and Medical Sciences
dcterms.dateAccepted2008-11-03
rioxxterms.versionofrecordhttps://doi.org/10.1016/j.ijpharm.2008.06.032
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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