Investigation of the potential ability of a microemulsion formulation, for transdermal delivery of diclofenac sodium

dc.contributor.authorPremarathne, E. P. N.
dc.contributor.authorChandani Perera, A. D. L.
dc.contributor.authorKarunaratne, D. N.
dc.date.accessioned2024-09-27T05:25:57Z
dc.date.available2024-09-27T05:25:57Z
dc.date.issued2013-07-04
dc.description.abstractA microemulsion is a system of water, oil, and amphiphilic compounds (surfactant and co-surfactant) which is a transparent, single optically isotropic, and thermodynamically stable liquid.Microemulsions are excellent systems for drug delivery because of their improved drug solubilisation, long shelf life and ease of preparation and administration. Assessment of percutaneous permeation of molecules is one of the main steps in the initial design and later in the evaluation of dermal or transdermal drug delivery systems. The aim of the present study was to investigate a microemulsion formulation for transdermal delivery of diclofenac [2-(2,6-dichloranilino) phenylacetic acid] sodium which is a nonsteroidal anti- inflammatory drug commonly taken to reduce inflammation and pain. The microemulsion area was identified by constructing pseudo-ternary phase diagrams of water, olive oil and Span 80. One composition in the microemulsion region was selected from the phase diagram for further studies. Transdermal permeation of diclofenac sodium through the skin of the pig ear was compared with the commercially available diclofenac gel (DICLORAN* Gel) using Franz diffusion cell. A significant increase in permeability parameters such as steady-state flux (Jss), permeability coefficient (Kp), and average permeation was observed in the optimized microemulsion formulation which consisted of 79% (wt/wt) of olive oil, 10% (wt/wt) of Span 80, 10% (wt/wt) of distilled water and 1% (wt/wt) of Diclofenac sodium.
dc.description.sponsorshipNSF Grant No: RG/2011/BS/02.
dc.identifier.citationPeradeniya University Research Sessions PURSE - 2012, Book of Abstracts, University of Peradeniya, Sri Lanka, Vol. 17, July. 4. 2012 pp.176
dc.identifier.isbn9789555891646
dc.identifier.issn13914111
dc.identifier.urihttps://ir.lib.pdn.ac.lk/handle/20.500.14444/1135
dc.language.isoen
dc.publisherThe University of Peradeniya
dc.subjectDiclofenac sodium
dc.subjectTransdermal delivery
dc.subjectChemistry
dc.subjectMicroemulsion formulation
dc.titleInvestigation of the potential ability of a microemulsion formulation, for transdermal delivery of diclofenac sodium
dc.typeArticle
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