Bergan T, Brodwall E K, Wiik-Larsen E
Antimicrob Agents Chemother. 1979 Nov;16(5):651-4. doi: 10.1128/AAC.16.5.651.
The pharmacokinetics of intravenous bolus doses of 1.0 g of mezlocillin were studied in 13 persons with normal and reduced renal functions. In renal failure a moderate increase was observed for the terminal serum half-life(t1/2 beta). This changed from a mean of 1.1 h at a glomerular filtration rate of 100 ml/min to 1.6 h at 10 ml/min. The difference was not statistically significant. The excretion of unchanged drug in urine during 24 h was reduced from a mean of 59.4% (range, 52 to 77) in subjects with glomerular filtration rate above 50 ml/min to 10% (range, 7.9 to 12.1) in two patients with glomerular filtration rate of 10 to 20 ml/min. The volume of distribution during the beta-phase, Vd,b, was 14% of the body weight. Much of the antibiotic was metabolized, and this proportion increased upon reduction in renal function.
对13名肾功能正常和减退的受试者静脉注射1.0克美洛西林后的药代动力学进行了研究。在肾衰竭患者中,观察到终末血清半衰期(t1/2β)有适度延长。其在肾小球滤过率为100毫升/分钟时平均为1.1小时,在10毫升/分钟时变为1.6小时。差异无统计学意义。24小时内尿液中未变化药物的排泄量,在肾小球滤过率高于50毫升/分钟的受试者中平均为59.4%(范围为52%至77%),在两名肾小球滤过率为10至20毫升/分钟的患者中降至10%(范围为7.9%至12.1%)。β相分布容积(Vd,b)为体重的14%。大部分抗生素被代谢,且这一比例随肾功能减退而增加。