Maksymiuk A W, Levine H B, Bodey G P
Antimicrob Agents Chemother. 1982 Jul;22(1):43-6. doi: 10.1128/AAC.22.1.43.
Twenty-seven patients with advanced malignancies were given 200 mg of ketoconazole orally every 6 or 12 h. Blood samples were collected during these intervals and after the last dose to determine plasma concentrations and half-lives. The mean plasma concentrations measured after the initial dose were 1.7 +/- 1.1 microgram/ml at 2 h, 0.9 +/- 0.2 microgram/ml at 6 h, and 0.7 +/- 0.4 microgram/ml at 8 h. Plasma concentrations rose significantly in patients on the every-6-h schedule. Concentrations were more variable in patients on the every-12-h schedule, and changes in mean plasma concentrations after 7 and 14 days were not significant. Half-lives ranged from 1.3 to 11.6 h in individual patients. The mean half-life for all patients studied was 3.7 +/- 0.6 h on day 1. The calculated area under the curve was 12.0 +/- 4.7 micrograms-h/ml on day 1; it increased after 7 and 14 days of administration (every-6-h schedule), suggesting plasma binding or wide drug distribution or both. Saturation of storage compartments is also suggested. Less than 1% of the administered dose was recoverable as active drug from the urine over 6 h.
27例晚期恶性肿瘤患者每6或12小时口服200毫克酮康唑。在这些间隔期间以及最后一剂后采集血样,以测定血浆浓度和半衰期。初始剂量后2小时测得的平均血浆浓度为1.7±1.1微克/毫升,6小时为0.9±0.2微克/毫升,8小时为0.7±0.4微克/毫升。每6小时给药一次的患者血浆浓度显著升高。每12小时给药一次的患者浓度变化更大,7天和14天后平均血浆浓度变化不显著。个体患者的半衰期为1.3至11.6小时。研究的所有患者第1天的平均半衰期为3.7±0.6小时。第1天计算的曲线下面积为12.0±4.7微克-小时/毫升;给药7天和14天后(每6小时给药一次方案)增加,提示血浆结合或药物广泛分布或两者兼有。也提示储存室饱和。在6小时内,从尿液中回收的给药剂量中活性药物不到1%。