Recent investigations both in vitro and in human subjects proved the benefi
t/risk ratio of prednicarbate (PC) to exceed those of halogenated topical g
lucocorticoids about 2-fold. To obtain a further highly desired increase by
drug targeting to viable epidermis. PC was incorporated into solid lipid n
anoparticles (SLN). Keratinocyte and fibroblast monolayer cultures, reconst
ructed epidermis and excised human skin served to evaluate SLN toxicity and
PC absorption. Well-tolerated preparations (e.g. cellular viability 94.5%,
following 18 h incubation of reconstructed epidermis) were obtained. PC pe
netration into human skin increased by 30% as compared to PC cream, permeat
ion of reconstructed epidermis increased even 3-fold. The present study sho
ws the great potential of SLN to improve drug absorption by the skin. (C) 2
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