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采用固相第二抗体分离法对人血浆和尿液中的可乐定进行放射免疫测定。

Radioimmunoassay for clonidine in human plasma and urine using a solid phase second antibody separation.

作者信息

Farina P R, Homon C A, Chow C T, Keirns J J, Zavorskas P A, Esber H J

出版信息

Ther Drug Monit. 1985;7(3):344-50. doi: 10.1097/00007691-198507030-00020.

Abstract

A reliable, sensitive, and specific radioimmunoassay (RIA) procedure for the quantitation of clonidine in plasma and other biological fluids was developed. The detection limit of the assay is 2 pg based on a 200 microliters sample. Nine commonly used drugs were found not to interfere with the RIA. The utility of the assay was demonstrated in a bioavailability study of clonidine conducted with 24 healthy subjects. Clonidine was readily quantitated in plasma over 4 half-lives. This assay is suitable for pharmacokinetic and bioavailability studies as well as therapeutic drug monitoring of patients.

摘要

开发了一种可靠、灵敏且特异的放射免疫分析法(RIA),用于定量测定血浆及其他生物体液中的可乐定。基于200微升样本,该分析方法的检测限为2皮克。发现九种常用药物不干扰放射免疫分析。在对24名健康受试者进行的可乐定生物利用度研究中证明了该分析方法的实用性。在超过4个半衰期的时间内,可轻松对血浆中的可乐定进行定量。该分析方法适用于药代动力学和生物利用度研究以及患者的治疗药物监测。

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