The recent availability of tazarotene, the first receptor-selective retinoi
d, provides a much-needed addition to the therapeutic armamentarium for mil
d-to-moderate plaque psoriasis. Tazarotene gel offers a welcome combination
of good efficacy and cosmetic acceptability, with minimal risk of systemic
adverse effects. The selectivity of tazarotene for the beta and gamma subt
ypes of retinoic acid receptors suggests a targeted action on psoriatic ker
atinocytes, which may help to minimize the risk of adverse effects. The pot
ential for adverse effects is further minimized by the limited transcutaneo
us absorption of tazarotene, its rapid metabolism into hydrophilic metaboli
tes. and its rapid elimination from the body. These pharmacokinetic feature
s ensure that plasma levels of tazarotene and its main metabolite, tazarote
nic acid, are minimized - thus limiting systemic exposure. The hydrophilici
ty of the metabolites also limits systemic exposure by ensuring that accumu
lation does not occur in lipophilic tissues.