Mordenti J
Antimicrob Agents Chemother. 1985 Jun;27(6):887-91. doi: 10.1128/AAC.27.6.887.
The postdistribution half-lives of 10 cephalosporin and 2 monobactam antibiotics in humans were predicted from data obtained in other mammals. This forecasting was accomplished with the allometric equation t1/2 = aWb, where a is the y intercept and b is the slope obtained from the log-log plot of antibiotic half-life (t1/2) versus body weight (W). Dimensionless similarity criteria were used to produce a biological clock for ceftizoxime elimination. The creation of the biological clock, which measured physiologic time (heartbeats) rather than chronologic time (minutes), demonstrated that ceftizoxime half-life was identical in five mammals. This methodology will contribute to infectious disease research through a greater understanding of pharmacokinetic scaling in mammals.
根据在其他哺乳动物身上获得的数据,预测了10种头孢菌素和2种单环β-内酰胺类抗生素在人体内的分布后半衰期。这种预测是通过异速生长方程t1/2 = aWb完成的,其中a是y轴截距,b是从抗生素半衰期(t1/2)与体重(W)的对数-对数图中获得的斜率。使用无量纲相似准则来生成头孢唑肟消除的生物钟。该生物钟测量的是生理时间(心跳次数)而非时间顺序(分钟),结果表明头孢唑肟在五种哺乳动物中的半衰期是相同的。这种方法将通过更深入地了解哺乳动物的药代动力学标度,为传染病研究做出贡献。