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用于药代动力学研究的体内微透析采样。

In vivo microdialysis sampling for pharmacokinetic investigations.

作者信息

Scott D O, Sorenson L R, Steele K L, Puckett D L, Lunte C E

机构信息

Department of Chemistry, University of Kansas, Lawrence 66045.

出版信息

Pharm Res. 1991 Mar;8(3):389-92. doi: 10.1023/a:1015862003147.

Abstract

In vivo microdialysis sampling coupled to liquid chromatography was used to study acetaminophen disposition in anesthetized rats. The pharmacokinetics of acetaminophen and its sulfate and glucuronide metabolites were determined using both microdialysis sampling and collection of whole blood. For microdialysis, samples were continuously collected for over 5 hr without fluid loss using a single experimental animal. Microdialysis sampling directly assesses the free drug concentration in blood. The pharmacokinetic results obtained with microdialysis sampling were the same as those obtained from blood collection. The administration of heparin, necessary when collecting blood samples, was found to double the elimination half-life of acetaminophen. Microdialysis sampling is a powerful tool for pharmacokinetic studies, providing accurate and precise pharmacokinetic data.

摘要

采用体内微透析采样结合液相色谱法研究对乙酰氨基酚在麻醉大鼠体内的处置情况。使用微透析采样和全血采集法测定了对乙酰氨基酚及其硫酸盐和葡萄糖醛酸代谢物的药代动力学。对于微透析,使用单只实验动物连续采集样本超过5小时且无液体损失。微透析采样可直接评估血液中的游离药物浓度。微透析采样获得的药代动力学结果与采血获得的结果相同。发现采集血样时必需使用的肝素会使对乙酰氨基酚的消除半衰期延长一倍。微透析采样是药代动力学研究的有力工具,可提供准确且精确的药代动力学数据。

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