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Forecasting cephalosporin and monobactam antibiotic half-lives in humans from data collected in laboratory animals.根据在实验动物身上收集的数据预测头孢菌素和单环β-内酰胺类抗生素在人体内的半衰期。
Antimicrob Agents Chemother. 1985 Jun;27(6):887-91. doi: 10.1128/AAC.27.6.887.
2
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3
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Dosage regimen design for pharmaceutical studies conducted in animals.在动物身上进行的药物研究的给药方案设计。
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本文引用的文献

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Pharmacokinetics of new broad-spectrum cephamycin, YM09330, parenterally administered to various experimental animals.新型广谱头孢霉素YM09330经肠胃外给药于各种实验动物后的药代动力学
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Pharmacokinetics of the cephalosporin SM-1652 in mice, rats, rabbits, dogs, and rhesus monkeys.头孢菌素SM - 1652在小鼠、大鼠、兔子、狗和恒河猴体内的药代动力学。
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The new beta-lactamase-stable cephalosporins.新型β-内酰胺酶稳定的头孢菌素。
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10
Pharmacokinetics of ceftizoxime in animals after parenteral dosing.头孢唑肟经肠胃外给药后在动物体内的药代动力学。
Antimicrob Agents Chemother. 1980 Feb;17(2):157-64. doi: 10.1128/AAC.17.2.157.

根据在实验动物身上收集的数据预测头孢菌素和单环β-内酰胺类抗生素在人体内的半衰期。

Forecasting cephalosporin and monobactam antibiotic half-lives in humans from data collected in laboratory animals.

作者信息

Mordenti J

出版信息

Antimicrob Agents Chemother. 1985 Jun;27(6):887-91. doi: 10.1128/AAC.27.6.887.

DOI:10.1128/AAC.27.6.887
PMID:3927836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC180180/
Abstract

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.

摘要

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。