Lode H, Warns H, Kemmerich B, Knothe H, Koeppe P
Eur J Clin Microbiol. 1983 Apr;2(2):116-21. doi: 10.1007/BF02001576.
The pharmacokinetics of ceftizoxime, a new beta-lactam antibiotic, were studied in eight normal volunteers after single and multiple i.v. doses of 2 X 2 g daily for eight days. The mean maximum serum concentration after the first 20 min of infusion on the first day was 176.9 +/- 32.9 micrograms/ml decreasing to 11.0 +/- 4.1 micrograms/ml after 4 h and to 0.67 +/- 0.2 micrograms/ml after 12 h. Mean 12 h urine recovery was 78.8 +/- 9.0%. The half-life of ceftizoxime was 136 +/- 36 min. Volume of distribution was 22.9 +/- 8.1 1/100 kg body weight, AUCtot 208 +/- 33 micrograms/ml x h, total body clearance 151 +/- 33 ml/min, and renal clearance 110 +/- 23 ml/min. No ceftizoxime accumulation was registered during the administration period. Computed multiple-dose values were in good agreement with the measured values, and the pharmacokinetic parameters on the first, fourth and eighth days showed no significant differences. During the study period, the fecal flora displayed a reduction of sensitive gram-negative aerobic bacteria, a slight increase in the amount of enterococci (10(6) to 10(8)/g feces), and no change in the number of Bacteroides fragilis. Some resistant gram-negative strains increased during the administration period, but most of them could no longer be detected two weeks after administration. Tolerance of ceftizoxime was good in four volunteers. Four other volunteers had gastro-intestinal symptoms and mild fever reactions. One female volunteer was assumed to have an allergic drug reaction. Biochemical, hematological, virological and serological data showed no abnormalities in seven volunteers.
对8名正常志愿者单次及多次静脉注射新的β-内酰胺类抗生素头孢唑肟(每日2×2g,共8天)后的药代动力学进行了研究。第一天输注开始后20分钟的平均血清最高浓度为176.9±32.9μg/ml,4小时后降至11.0±4.1μg/ml,12小时后降至0.67±0.2μg/ml。12小时尿液回收率平均为78.8±9.0%。头孢唑肟的半衰期为136±36分钟。分布容积为22.9±8.1 l/100kg体重,AUCtot为208±33μg/ml·h,总体清除率为151±33ml/分钟,肾清除率为110±23ml/分钟。给药期间未发现头孢唑肟蓄积。计算的多剂量值与实测值吻合良好,第一天、第四天和第八天的药代动力学参数无显著差异。在研究期间,粪便菌群中敏感的需氧革兰阴性菌数量减少,肠球菌数量略有增加(从10⁶/g粪便增至10⁸/g粪便),脆弱拟杆菌数量无变化。给药期间一些耐药革兰阴性菌株数量增加,但给药两周后大多数已无法检测到。4名志愿者对头孢唑肟耐受性良好。另外4名志愿者出现胃肠道症状和轻度发热反应。一名女性志愿者被认为发生了药物过敏反应。7名志愿者的生化、血液学、病毒学和血清学数据均无异常。