Benoni G, Arosio E, Raimondi M G, Apolloni E, Passarella E, Lechi A, Velo G P
Antimicrob Agents Chemother. 1984 Jun;25(6):760-3. doi: 10.1128/AAC.25.6.760.
The pharmacokinetics of ceftazidime were investigated in eight normal subjects and eight patients with ascites after intravenous administration of 1 g of the drug. Samples of blood and ascitic fluid were collected for 6 h after dosage, and urine samples were collected for 24 h. Pharmacokinetic data were calculated by using a one-compartment model. The apparent volume of distribution and half-life of elimination (t1/2 beta) in patients with ascites were approximately three times those in normal subjects. In contrast, renal clearance was greater in the normal subjects. With respect to ascites, the mean area under the concentration-time curve was 95.3 +/- 38.3 micrograms X h/ml. The mean ratio of the area under the concentration-time curve for ascitic fluid to that for plasma was 69.9% (+/- 38.2). These data show that ceftazidime rapidly diffuses into the peritoneal space, in which concentrations greater than 10 micrograms/ml were present for at least 6 h.
在8名正常受试者和8名腹水患者静脉注射1g头孢他啶后,对其药代动力学进行了研究。给药后6小时采集血液和腹水样本,24小时采集尿液样本。使用单室模型计算药代动力学数据。腹水患者的表观分布容积和消除半衰期(t1/2β)约为正常受试者的三倍。相比之下,正常受试者的肾清除率更高。关于腹水,浓度-时间曲线下的平均面积为95.3±38.3微克·小时/毫升。腹水浓度-时间曲线下面积与血浆浓度-时间曲线下面积的平均比值为69.9%(±38.2)。这些数据表明,头孢他啶迅速扩散到腹膜腔,其中浓度大于10微克/毫升至少持续6小时。