The in vitro transdermal absorption of apomorphine from microemulsions was
studied using the skin of the hairless mouse as a membrane. Two microemulsi
ons (no. 1 and 2) were prepared and thickened both containing 3.9% of apomo
rphine hydrochloride. The lipophilicity of the drug was increased by formin
g apomorphine-octanoic acid ion-pairs. The fluxes of the drug from the micr
oemulsions through hairless mouse skin were 100 mug h(-1) cm(-2) from no. 1
and 88 mug h(-1) cm(-2) from no. 2. Apomorphine in microemulsions, protect
ed from light with antioxidants, showed no degradation for up to 6 months.
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