Schäfer-Korting M, Korting H C, Dorn M, Mutschler E
Int J Clin Pharmacol Ther Toxicol. 1984 Jul;22(7):371-4.
To investigate ketoconazole penetration into skin, a single oral dose of 200 mg was administered to six healthy subjects. Plasma and cantharides blister fluid (CBF) levels were measured for 11 to 24 hours. In suction blister fluid (SBF) ketoconazole was determined 3, 6, and 9 hours after administration. Mean peak plasma levels of ketoconazole were found at 1 hour, they amounted to 3.03 +/- 0.55 micrograms/ml (n = 5). Apparent half-life of elimination was 1.8 hours. In cantharides blister fluid maximum ketoconazole concentrations were obtained at 6 hours being 1.05 +/- 0.32 micrograms/ml and declined rather slowly (half-life 4.2 hours; n = 3). Maximum concentrations in suction blister fluid were obtained 3 hours after administration (0.914 +/- 0.123 micrograms/ml). After 9 hours ketoconazole levels had declined to 0.216 +/- 0.044 micrograms/ml (n = 3). These concentrations exceed the ketoconazole concentrations proven to be effective in vitro up to 25 fold.
为研究酮康唑在皮肤中的渗透情况,对6名健康受试者单次口服200毫克剂量的酮康唑。在11至24小时内测量血浆和斑蝥水疱液(CBF)中的药物水平。在给药后3、6和9小时测定抽吸水疱液(SBF)中的酮康唑含量。酮康唑的平均血浆峰值水平在1小时时出现,为3.03±0.55微克/毫升(n = 5)。消除的表观半衰期为1.8小时。在斑蝥水疱液中,酮康唑的最大浓度在6小时时达到,为1.05±0.32微克/毫升,且下降相当缓慢(半衰期为4.2小时;n = 3)。抽吸水疱液中的最大浓度在给药后3小时获得(0.914±0.123微克/毫升)。9小时后,酮康唑水平降至0.216±0.044微克/毫升(n = 3)。这些浓度比体外已证实有效的酮康唑浓度高出25倍。