Abstract
In vitro and in vivo skin permeability studies were conducted to investigate properties of several candidate transdermal chemical collection devices (TCDs). The TCD consists of a binding reservoir of activated charcoal suspended in a gel medium which is occlusively placed in direct contact with the skin. Binding of three model compounds (theophylline, methotrexate, and parathion) was studied in hydrophilic (agarose or PVA/PVP) and lipophilic (silicone) gel/carbon compositions. The effects of gel composition, compound hydrophilicity/lipophilicity, and hydration of skin on quantity of transdermally collected chemical and 'apparent' permeability were investigated using a 'fuzzy' rat animal model. In vitro and in vivo apparent permeability coefficients (Kp; cm/h) for amphophilic theophylline (6.95 x 10(-4) and 8.34 x 10(-4), respectively) and hydrophilic methotrexate (3.5 x 10(-3) and 3.2 x 10(-4), respectively) using an agarose aquagel TCD were greater than the corresponding Kp values obtained when silicone lipogel TCDs were employed (0.3 x 10(-4) and 3.2 x 10(-4), respectively, for theophylline; no measurable methotrexate was collected). Occlusive hydration of skin profoundly increased permeability of the hydrophyilic model compound, methotrexate. In vivo Kp values for lipophilic parathion were greater with a silicone TCD (6.7 x 10(-4) than with an agarose TCD (3.8 x 10(-4). We conclude that it is possible to influence transdermal chemical collection through modifications in the gel composition and by hydration of the skin.
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