Männistö P T, Mäntylä R, Nykänen S, Lamminsivu U, Ottoila P
Antimicrob Agents Chemother. 1982 May;21(5):730-3. doi: 10.1128/AAC.21.5.730.
Single oral doses of ketoconazole (200 mg) or miconazole (250 mg) were given in a randomized cross-over study to 10 healthy volunteers. Ketoconazole with administered (i) after fasting (both brand 1 [Orion Pharmaceutical Co.] and brand 2 [Janssen Pharmaceutica] were tested), (ii) after a standardized meal (660 kilocalories; 2,772 kJ) (brand 1), and (iii) with 300 ml of orange juice (pH 3.8) (brand 1). Miconazole was administered after fasting. Venous blood samples for high-performance liquid chromatography determinations of ketoconazole and gas chromatographic analyses of miconazole were drawn periodically up to 24 h. The concentrations of ketoconazole in sera attained with the two brands were not statistically different. The peak concentrations of ketoconazole attained with brand 1 were 4.1 +/- 0.3 micrograms/ml (mean +/- standard error of the mean) after fasting, 2.3 +/- 0.3 micrograms/ml after the standardized meal (P less than 0.01), and 3.6 +/- 0.2 micrograms/ml with orange juice. The peak concentrations were reached in 1.4, 2.3 (P less than 0.05), and 1.8 h, respectively, whereas the areas under the serum concentration-time curves were 14.4 +/- 2.21, 8.6 +/- 1.33 (P less than 0.05), and 13.4 +/- 1.30 micrograms.h/ml, respectively. The half-lives (1.7 to 2 h) did not vary significantly among the different regimens. Compared with ketoconazole, oral absorption of miconazole was poor (peak concentration, 0.47 +/- 0.7 micrograms/ml; time to reach the peak concentration, 2.6 h; area under the serum concentration-time curve, 1.10 +/- 0.20 micrograms.h/ml).
在一项随机交叉研究中,给10名健康志愿者单次口服酮康唑(200毫克)或咪康唑(250毫克)。酮康唑的给药方式为:(i)空腹后给药(对品牌1[奥立安制药公司]和品牌2[杨森制药公司]均进行了测试),(ii)标准化餐后给药(660千卡;2772千焦)(品牌1),以及(iii)与300毫升橙汁(pH值3.8)一起给药(品牌1)。咪康唑在空腹后给药。定期采集静脉血样,用于通过高效液相色谱法测定酮康唑以及通过气相色谱法分析咪康唑,持续时间长达24小时。两个品牌的酮康唑血清浓度无统计学差异。品牌1在空腹后酮康唑的峰值浓度为4.1±0.3微克/毫升(平均值±平均标准误差),标准化餐后为2.3±0.3微克/毫升(P<0.01),与橙汁一起给药时为3.6±0.2微克/毫升。达到峰值浓度的时间分别为1.4、2.3(P<0.05)和1.8小时,而血清浓度-时间曲线下面积分别为14.4±2.21、8.6±1.33(P<0.05)和13.4±1.30微克·小时/毫升。不同给药方案的半衰期(1.7至2小时)无显著差异。与酮康唑相比,咪康唑的口服吸收较差(峰值浓度,0.47±0.7微克/毫升;达到峰值浓度的时间,2.6小时;血清浓度-时间曲线下面积,1.10±0.20微克·小时/毫升)。