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dc.contributor.authorNajib, Omaima N.
dc.contributor.authorKirton, Stewart B.
dc.contributor.authorMartin, Gary P.
dc.contributor.authorBotha, Michelle J.
dc.contributor.authorSallam, Al Sayed
dc.contributor.authorMurnane, Darragh
dc.date.accessioned2021-03-12T11:00:02Z
dc.date.available2021-03-12T11:00:02Z
dc.date.issued2020-10-31
dc.identifier.citationNajib , O N , Kirton , S B , Martin , G P , Botha , M J , Sallam , A S & Murnane , D 2020 , ' Multivariate analytical approaches to identify key molecular properties of vehicles, permeants and membranes that affect permeation through membranes ' , Pharmaceutics , vol. 12 , no. 10 , 958 . https://doi.org/10.3390/pharmaceutics12100958
dc.identifier.issn1999-4923
dc.identifier.urihttp://hdl.handle.net/2299/24085
dc.description© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
dc.description.abstractThere has been considerable recent interest in employing computer models to investigate the relationship between the structure of a molecule and its dermal penetration. Molecular permeation across the epidermis has previously been demonstrated to be determined by a number of physicochemical properties, for example, the lipophilicity, molecular weight and hydrogen bonding ability of the permeant. However little attention has been paid to modeling the combined effects of permeant properties in tandem with the properties of vehicles used to deliver those permeants or to whether data obtained using synthetic membranes can be correlated with those obtained using human epidermis. This work uses Principal Components Analysis (PCA) to demonstrate that, for studies of the diffusion of three model permeants (caffeine, methyl paraben and butyl paraben) through synthetic membranes, it is the properties of the oily vehicle in which they are applied that dominated the rates of permeation and flux. Simple robust and predictive descriptor-based quantitative structure–permeability relationship (QSPR) models have been developed to support these findings by utilizing physicochemical descriptors of the oily vehicles to quantify the differences in flux and permeation of the model compounds. Interestingly, PCA showed that, for the flux of co-applied model permeants through human epidermis, the permeation of the model permeants was better described by a balance between the physicochemical properties of the vehicle and the permeant rather than being dominated solely by the vehicle properties as in the case of synthetic model membranes. The important influence of permeant solubility in the vehicle along with the solvent uptake on overall permeant diffusion into the membrane was substantiated. These results confirm that care must be taken in interpreting permeation data when synthetic membranes are employed as surrogates for human epidermis; they also demonstrate the importance of considering not only the permeant properties but also those of both vehicle and membrane when arriving at any conclusions relating to permeation data.en
dc.format.extent18
dc.format.extent1080503
dc.language.isoeng
dc.relation.ispartofPharmaceutics
dc.subjectEnhancer of drug penetration
dc.subjectMembrane interaction
dc.subjectOily vehicle
dc.subjectPCA
dc.subjectPermeability
dc.subjectQSPR
dc.subjectPharmaceutical Science
dc.titleMultivariate analytical approaches to identify key molecular properties of vehicles, permeants and membranes that affect permeation through membranesen
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionNatural Product Chemistry and Drug Design
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionAirway Group
dc.contributor.institutionPharmaceutical Analysis and Product Characterisation
dc.contributor.institutionPharmaceutics
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85092458257&partnerID=8YFLogxK
rioxxterms.versionofrecord10.3390/pharmaceutics12100958
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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