Rodriguez-Barbero J, Mariño E L, Dominguez-Gil A
Antimicrob Agents Chemother. 1985 Oct;28(4):544-7. doi: 10.1128/AAC.28.4.544.
The pharmacokinetics of cefmetazole, a new parenteral cephalosporin, administered intravenously and intramuscularly at a dose of 30 mg/kg to two groups of seven healthy volunteers were studied. Concentrations in serum were monitored over 8 h by a high-pressure liquid chromatography technique. The plasma concentration-time data were statistically fitted to a biexponential equation for both administration routes, and the data were analyzed by a two- and one-compartment kinetic model, respectively. For the dose range and the administration routes used, the pharmacokinetics of cefmetazole proved to be essentially linear, with clearances from plasma ranging between 3.8 and 12.5 liters/h. The mean maximum concentration in plasma after intramuscular administration of the drug was 90.1 micrograms/ml at 0.7 h. The elimination half-life, about 1.3 h, did not show statistically significant differences for the two routes of administration studied.
对两组各7名健康志愿者进行研究,静脉注射和肌肉注射剂量为30mg/kg的新型胃肠外头孢菌素头孢美唑的药代动力学。采用高压液相色谱技术在8小时内监测血清浓度。两种给药途径的血浆浓度-时间数据均经统计学拟合为双指数方程,并分别用二室和一室动力学模型进行分析。在所使用的剂量范围和给药途径下,头孢美唑的药代动力学基本呈线性,血浆清除率在3.8至12.5升/小时之间。肌肉注射该药后,血浆中平均最大浓度在0.7小时时为90.1微克/毫升。消除半衰期约为1.3小时,在所研究的两种给药途径中未显示出统计学上的显著差异。