Abstract

The possibility of using fish skin as model membrane tostudy drug permeation and penetration enhancement by cyclodextrins was investigated.The permeability of the skin from four species of fish, Anarhichas lupus (catfish),Pleuronectes platessa (Plaice), Hippoglossus hippoglossus (Halibut)and Anarhichas minor (Spotted catfish), was compared in a Franz diffusion cell set-up using 1% hydrocortisone aqueous solution as a donor phase. The drug fluxthrough fish skin was more than 100 times faster than the flux through hairless mouse skin and more than 10 000 times faster than through snake skin. Catfishskin was most easily accessible and was therefore used for further study. The octanol-water partition coefficient did not affect the transmembrane flux of small molecules whereas the aqueous diffusion coefficient could be correlated with the flux.The hydrocortisone flux of from aqueous hydroxypropyl-β-cyclodextrin solutions, which were saturated with the drug, increased with increasing cyclodextrinconcentration. From these and other observations it was concluded that small moleculesare transported through fish skin in aqueous channels. The properties of thesechannels resemble the properties of the aqueous diffusion layer present in human andanimal skin and other types of biological membranes. Previous studies have shown thatcyclodextrins will enhance drug delivery by increasing aqueous diffusion rate. Catfish skin can therefore be a good model membrane to study penetration enhancementby cyclodextrins.

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