Influence of a microemulsion vehicle on cutaneous bioequivalence of a lipophilic model drug assessed by microdialysis and pharmacodynamics

Purpose. The aim of the study was to investigate the cutaneous bioequivalen ce of a lipophilic model drug (lidocaine) applied in a novel topical microe mulsion vehicle, compared to a conventional oil-in-water (O/W) emulsion, as sessed by a pharmacokinetics microdialysis model and a pharmacodynamic meth od. Methods. Dermal delivery of lidocaine was estimated by microdialysis in 8 v olunteers. Absorption coefficients and lag times were determined by pharmac okinetic modelling of the microdialysis data. Subsequently, the anaesthetic effect of the treatments was assessed by mechanical stimuli using von Frey hairs in 12 volunteers. Results The microemulsion formulation increased the cutaneous absorption co efficient of lidocaine 2.9 times (95% confidence interval: 1.9/4.6) compare d with the O/W emulsion-based cream. Also, lag time decreased from 110 +/- 43 min to 87 +/- 32 min (P = 0.02). The compartmental pharmacokinetic model provided an excellent fit of the concentration-time curves with reliable e stimation of absorption coefficient and lag time. A significant anaesthetic effect was found for both active treatments compared to placebo (P < 0.02) , but the effect did not diverge significantly between the two formulations . Conclusions. The microemulsion vehicle can be applied to increase dermal dr ug delivery of lipophilic drugs in humans. The microdialysis technique comb ined with an appropriate pharmacokinetic model provides a high sensitivity in bioequivalence studies of topically applied substances.