Jaresko G S, Barriere S L, Johnson B L
Department of Pharmaceutical Services, University of California, Los Angeles 90024.
Antimicrob Agents Chemother. 1992 Oct;36(10):2233-8. doi: 10.1128/AAC.36.10.2233.
Ampicillin-sulbactam, ticarcillin-clavulanate, cefoxitin, cefotetan, and ceftizoxime are promoted for the treatment of mixed aerobic-anaerobic bacterial infections. Their activities have been compared in vitro but not in vivo. In order to assess the in vivo activities of these agents in serum and interstitial fluid, we administered single, intravenous doses of these antimicrobial agents to healthy subjects. Concentrations of the antimicrobial agents in serum and suction-induced blister fluid and bactericidal activity were measured by high-pressure liquid chromatography and the standard methodology of the National Committee for Clinical Laboratory Standards, respectively. The organisms used for bactericidal activity tests were one isolate each of Staphylococcus aureus, Klebsiella pneumoniae, and Bacteroides fragilis. Pharmacokinetic parameters in serum and blister fluid were similar to those derived in other investigations. Of note were the high and prolonged concentrations of ticarcillin and cefotetan in blister fluid, despite high-level serum protein binding. The bactericidal activities in serum and blister fluid reflected the relative in vitro activities and kinetic dispositions of the various antimicrobial agents except for the bactericidal activity of cefotetan, which was substantially lower in blister fluid than serum, despite a blister fluid:serum area under the concentration-time curve ratio of 1.5. Similarly, the activity of ticarcillin-clavulanate in blister fluid was also substantially less than would have been predicted by the blister fluid:serum ratio of the area under the concentration-time curve of 1.1, possibly because of the low concentrations of clavulanate in blister fluid. The rankings of the in vivo bactericidal activities of the five drugs were as follows: for S. aureus, ampicillin-sulbactam > ticarcillin-clavulanate > ceftizoxime > cefoxitin > cefotetan; for K. pneumoniae, ceftizoxime > cefotetan > ampicillin-sulbactam = ticarcillin-clavulanate > cefoxitin; and for B.fragilis, ticarcillin-clavulanate > cefotetan > ceftizoxime > ampicillin-sulbactam = cefoxitin.
氨苄西林 - 舒巴坦、替卡西林 - 克拉维酸、头孢西丁、头孢替坦和头孢唑肟被推荐用于治疗需氧菌与厌氧菌混合感染。它们的活性已在体外进行了比较,但尚未进行体内比较。为了评估这些药物在血清和组织间液中的体内活性,我们给健康受试者静脉注射了单剂量的这些抗菌药物。分别通过高压液相色谱法和美国国家临床实验室标准委员会的标准方法测定血清和抽吸诱导水疱液中抗菌药物的浓度及杀菌活性。用于杀菌活性测试的菌株分别为金黄色葡萄球菌、肺炎克雷伯菌和脆弱拟杆菌各一株。血清和水疱液中的药代动力学参数与其他研究得出的参数相似。值得注意的是,尽管替卡西林和头孢替坦与血清蛋白结合率高,但它们在水疱液中的浓度高且持续时间长。血清和水疱液中的杀菌活性反映了各种抗菌药物的相对体外活性和动力学特性,但头孢替坦除外,尽管其水疱液与血清的浓度 - 时间曲线下面积比为1.5,但其在水疱液中的杀菌活性明显低于血清。同样,替卡西林 - 克拉维酸在水疱液中的活性也明显低于根据其水疱液与血清浓度 - 时间曲线下面积比1.1所预测的活性,这可能是因为水疱液中克拉维酸的浓度较低。这五种药物的体内杀菌活性排名如下:对于金黄色葡萄球菌,氨苄西林 - 舒巴坦>替卡西林 - 克拉维酸>头孢唑肟>头孢西丁>头孢替坦;对于肺炎克雷伯菌,头孢唑肟>头孢替坦>氨苄西林 - 舒巴坦 = 替卡西林 - 克拉维酸>头孢西丁;对于脆弱拟杆菌,替卡西林 - 克拉维酸>头孢替坦>头孢唑肟>氨苄西林 - 舒巴坦 = 头孢西丁。