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dc.contributor.authorOtto, Daniel P.
dc.contributor.authorDe Villiers, Melgardt M.
dc.date.accessioned2015-02-09T10:50:51Z
dc.date.available2015-02-09T10:50:51Z
dc.date.issued2013
dc.identifier.citationOtto, D.P. & De Villiers, M.M. 2013. The experimental evaluation and molecular dynamics simulation of a heat-enhanced transdermal delivery system. AAPS PharmSciTech, 14(1):111-120. [https://doi.org/10.1208/s12249-012-9900-6]en_US
dc.identifier.issn1530-8832
dc.identifier.urihttp://hdl.handle.net/10394/13327
dc.identifier.urihttps://doi.org/10.1208/s12249-012-9900-6
dc.identifier.urihttps://link.springer.com/article/10.1208%2Fs12249-012-9900-6
dc.description.abstractTransdermal delivery systems are useful in cases where preferred routes such as the oral route are not available. However, low overall extent of delivery is seen due to the permeation barrier posed by the skin. Chemical penetration enhancers and invasive methods that disturb the structural barrier function of the skin can be used to improve transdermal drug delivery. However, for suitable drugs, a fast-releasing transdermal delivery system can be produced by incorporating a heating source into a transdermal patch. In this study, a molecular dynamics simulation showed that heat increased the diffusivity of the drug molecules, resulting in faster release from gels containing ketoprofen, diclofenac sodium, and lidocaine HCl. Simulations were confirmed by in vitro drug release studies through lipophilic membranes. These correlations could expand the application of heated transdermal delivery systems for use as fast-release-dosage forms.en_US
dc.language.isoenen_US
dc.publisherSpringer
dc.subjectDiffusionen_US
dc.subjectheateden_US
dc.subjectpatchen_US
dc.subjectketoprofenen_US
dc.subjectmolecularen_US
dc.subjectdynamicsen_US
dc.subjecttransdermalen_US
dc.titleThe experimental evaluation and molecular dynamics simulation of a heat-enhanced transdermal delivery systemen_US
dc.typeArticleen_US
dc.contributor.researchID11333561 - Otto, Daniel Petrus


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