Literature DB >> 21437791

Microemulsion microstructure influences the skin delivery of an hydrophilic drug.

Wafa Naoui1, Marie-Alexandrine Bolzinger, Bernard Fenet, Jocelyne Pelletier, Jean-Pierre Valour, Rafik Kalfat, Yves Chevalier.   

Abstract

PURPOSE: We aimed to investigate the influence of microemulsion nanoscale organization as either oil-in-water droplets, water-in-oil droplets, or bicontinuous structures on skin delivery of drugs assisted by microemulsions.
METHODS: Three microemulsions of different microstructure, o/w, w/o, and bicontinuous at the skin temperature (32°C), having the same oil and water contents and containing the same ingredients were selected using the Kahlweit fish phase diagrams method. The microemulsions are quaternary mixtures of the Polysorbate 21 (Tween®21) and Sorbitan monolaurate (Span®20) surfactants, isononyl isononanoate oil and water. The microemulsion nanostructure was characterized by electrical conductivity, Pulsed Field Gradient Spin-Echo NMR and Small-Angle Neutron Scattering measurements. The Franz cell method was used to monitor skin absorption of caffeine loaded in microemulsions over 24 h exposure to excised pig skin.
RESULTS: Three microemulsions with the three structures were selected, keeping the same composition but the Tween®21/Span®20 ratio. The transdermal flux of caffeine was in the order aqueous solution ≈ w/o < bicontinuous < o/w microemulsion. The o/w microemulsion allows the permeation of 50% of the applied dose within 24 h.
CONCLUSIONS: The structure of microemulsions is of relevance for skin absorption. The water-continuous structures allow faster transport of hydrophilic drugs.

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Year:  2011        PMID: 21437791     DOI: 10.1007/s11095-011-0404-y

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  22 in total

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3.  Microemulsions as topical drug delivery vehicles: in-vitro transdermal studies of a model hydrophilic drug.

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5.  Percutaneous release of caffeine from microemulsion, emulsion and gel dosage forms.

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6.  Pickering w/o emulsions: drug release and topical delivery.

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7.  Comparative enhancer effects of Span20 with Tween20 and Azone on the in vitro percutaneous penetration of compounds with different lipophilicities.

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