Heim-Duthoy K L, Peltier G L, Guay D R, Matzke G R
Department of Medicine, Hennepin County Medical Center, Minneapolis, Minnesota 55415.
Antimicrob Agents Chemother. 1988 Apr;32(4):485-7. doi: 10.1128/AAC.32.4.485.
The disposition of cefonicid (2 g intravenously every 24 h) was assessed in 15 patients with skin and skin structure infections. Trough and peak concentrations in serum were measured on two successive days to verify the attainment of steady state; and 1 trough and 12 postdose values of the concentration in serum were collected on the following day. Cefonicid concentrations in serum were determined by high-performance liquid chromatography. The cefonicid serum concentration versus time profile after intravenous infusion was clearly biexponential in all patients. The terminal elimination half-life determined by nonlinear regression analysis was 4.63 +/- 1.49 h (mean +/- standard deviation). The steady-state volume of distribution and total body clearance were 0.12 +/- 0.04 liter/kg and 0.369 +/- 0.110 ml/min per kg, respectively. These results are comparable to parameters derived from previous studies in noninfected normal volunteers. Thus, the disposition of cefonicid is not altered in patients with severe skin and skin structure infections.
在15例皮肤及皮肤结构感染患者中评估了头孢尼西(每24小时静脉注射2克)的处置情况。连续两天测量血清中的谷浓度和峰浓度以验证是否达到稳态;并在次日收集1次谷浓度和12次给药后血清浓度值。通过高效液相色谱法测定血清中的头孢尼西浓度。所有患者静脉输注后头孢尼西血清浓度-时间曲线均呈明显的双指数型。通过非线性回归分析确定的终末消除半衰期为4.63±1.49小时(平均值±标准差)。稳态分布容积和全身清除率分别为0.12±0.04升/千克和0.369±0.110毫升/分钟/千克。这些结果与先前在未感染正常志愿者中得出的参数相当。因此,严重皮肤及皮肤结构感染患者中头孢尼西的处置未发生改变。