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Original Research

Microwave-aided skin drug penetration and retention of 5-fluorouracil-loaded ethosomes

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Pages 1209-1219 | Received 22 Mar 2016, Accepted 18 May 2016, Published online: 16 Jun 2016
 

ABSTRACT

Objectives: Skin drug retention is required in local treatment of skin cancer. This study investigated the interplay effects of ethosomes and microwave in transdermal drug delivery. Skin pre-treatment by microwave and applied with liquified medicine is deemed to ‘cement’ the skin thereby raising skin drug deposition.

Methods: 5-fluorouracil-loaded ethosomes were prepared and subjected to size, zeta potential, morphology, drug content, drug release and skin permeation tests. The molecular characteristics of untreated, microwave and/or ethosome-treated skins were examined by Fourier transform infrared and raman spectroscopy, thermal and electron microscopy techniques.

Results: The skin drug retention was promoted using larger ethosomes with negative zeta potentials that repelled anionic lipids of skin and hindered vesicle permeation into deep layers. These ethosomes had low ethanol content. They were less able to fluidize the lipid and defluidize the protein domains at epidermis to enlarge aqueous pores for drug permeation. Pre-treatment of skin by 2450 MHz microwave for 2.5 min further increased skin drug penetration and retention of low ethanol ethosomes and provided lower drug permeation than cases treated for 1.15 min and 5 min. A 2.5 min treatment might be accompanied by specific dermal protein fluidization via C=O moiety which translated to macromolecular swelling, narrowing of intercellular spaces at lower skin layers, increased drug retention and reduced drug permeation.

Conclusion: Ethosomes and microwave synergized to promote skin drug retention.

Declaration of interest

The authors wish to express their heart-felt thanks to MOSTI, MOHE, IRMI, UiTM (Universiti Teknologi MARA [0141903]), Malaysia and Gomal University, Pakistan for fund and facility support. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

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