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人体内氯去甲安定的血浆水平。

Plasma levels of chlorodesmethyldiazepam in humans.

作者信息

Dal Bo L, Marcucci F, Mussini E, Perbellini D, Castellani A, Fresia P

出版信息

Biopharm Drug Dispos. 1980 Jan-Mar;1(3):123-6. doi: 10.1002/bdd.2510010306.

DOI:10.1002/bdd.2510010306
PMID:6778522
Abstract

Chlorodesmethyldiazepam (I) concentrations were followed for 72 h in the plasma of four volunteers given 2 mg of the drug orally. The drug appears to be well absorbed, reaching peak plasma levels of 20--30 ng ml-1 1--2 h after administration; 72 h after administration, plasma concentrations are still measurable (5 ng ml-1). The analytical method involved a single extraction of I from the plasma into benzene followed by centrifugation, evaporation, and gas-chromatographic analysis of the samples.

摘要

对四名口服2毫克氯去甲安定(I)的志愿者的血浆进行了72小时的跟踪监测。该药物似乎吸收良好,给药后1-2小时血浆浓度达到峰值20-30纳克/毫升;给药72小时后,血浆浓度仍可测量(5纳克/毫升)。分析方法包括将血浆中的I单次萃取到苯中,然后离心、蒸发,对样品进行气相色谱分析。

相似文献

1
Plasma levels of chlorodesmethyldiazepam in humans.人体内氯去甲安定的血浆水平。
Biopharm Drug Dispos. 1980 Jan-Mar;1(3):123-6. doi: 10.1002/bdd.2510010306.
2
Analysis of chlorodesmethyldiazepam and its metabolites in plasma and urine.
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引用本文的文献

1
Pharmacokinetics of chlordesmethyldiazepam after single-dose oral administration in humans.去甲氯氮卓单次口服给药在人体内的药代动力学。
Eur J Drug Metab Pharmacokinet. 1986 Jul-Sep;11(3):171-4. doi: 10.1007/BF03189844.
2
Pharmacokinetics and bioavailability of intravenous and oral chlordesmethyldiazepam in humans.氯地西泮静脉注射和口服给药在人体中的药代动力学及生物利用度
Eur J Clin Pharmacol. 1988;34(1):109-12. doi: 10.1007/BF01061430.