Woodnutt G, Kernutt I, Mizen L
Chemotherapeutic Research Centre, Beecham Pharmaceuticals Research Division, Betchworth, Surrey, England.
Antimicrob Agents Chemother. 1987 Nov;31(11):1826-30. doi: 10.1128/AAC.31.11.1826.
The pharmacokinetics and distribution of ticarcillin and clavulanic acid were studied in rats and rabbits after intravenous coadministration of the compounds. The elimination half-lives for ticarcillin and clavulanic acid were similar in both rats (ticarcillin, 0.22 h; clavulanic acid, 0.24 h) and rabbits (ticarcillin, 0.38 h; clavulanic acid, 0.31 h). Both compounds distributed widely throughout rat tissues, and the patterns of distribution were similar to those observed for other beta-lactams. Values for penetration into rat pleural, peritoneal, and subcutaneous fluids calculated from the equation (AUCfluid/AUCserum) X 100, where AUC is the area under the concentration-time curve, were between 83 and 93% for ticarcillin and 86 and 103% for clavulanic acid. Values for penetration into tissue cages in rabbits were 139% +/- 45% for ticarcillin and 109% +/- 22% for clavulanic acid. The penetration of clavulanic acid into rabbit cerebrospinal fluid was higher (P less than 0.05) (4.0% +/- 0.61%) than that of ticarcillin (1.3% +/- 0.53%). Overall, the results show that ticarcillin and clavulanic acid distribute readily throughout body tissues and fluids and predict that the penicillin and beta-lactamase inhibitor would be present together at sites of infection.
在大鼠和兔子静脉联合给予替卡西林和克拉维酸后,对其药代动力学和分布情况进行了研究。替卡西林和克拉维酸在大鼠(替卡西林,0.22小时;克拉维酸,0.24小时)和兔子(替卡西林,0.38小时;克拉维酸,0.31小时)体内的消除半衰期相似。两种化合物在大鼠组织中广泛分布,分布模式与其他β-内酰胺类药物相似。根据公式(AUC液/AUC血清)×100计算得出的替卡西林进入大鼠胸膜、腹膜和皮下液的渗透值,其中AUC是浓度-时间曲线下的面积,替卡西林为83%至93%,克拉维酸为86%至103%。替卡西林进入兔子组织笼的渗透值为139%±45%,克拉维酸为109%±22%。克拉维酸进入兔子脑脊液的渗透率(P<0.05)(4.0%±0.61%)高于替卡西林(1.3%±0.53%)。总体而言,结果表明替卡西林和克拉维酸能迅速分布于全身组织和体液中,并预测青霉素和β-内酰胺酶抑制剂会在感染部位同时存在。