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采用带电子捕获检测的气相色谱法测定生物材料中的新型单胺氧化酶抑制剂溴法罗明及其主要代谢物。

Determination of the new monoamine oxidase inhibitor brofaromine and its major metabolite in biological material by gas chromatography with electron-capture detection.

作者信息

Schneider W, Keller B, Degen P H

机构信息

Research and Development Department, Pharmaceuticals Division, Basle, Switzerland.

出版信息

J Chromatogr. 1989 Mar 17;488(1):275-82. doi: 10.1016/s0378-4347(00)82952-7.

DOI:10.1016/s0378-4347(00)82952-7
PMID:2715286
Abstract

A sensitive gas chromatographic assay for the simultaneous determination of brofaromine [4-(7-bromo-5-methoxy-2-benzofuranyl)piperidine hydrochloride], a new monoamine oxidase-A inhibitor, and its major metabolite was developed and validated. After addition of 4-(5-bromo-2-benzofuranyl)piperidine as internal standard, the compounds were isolated from biological fluids by liquid-liquid extraction at basic pH. After derivatization with heptafluorobutyric anhydride the compounds were chromatographed using a packed column (OV-17) and an electron-capture detector. The limit of quantitation was ca. 0.03 nmol per sample (10 ng) for both compounds. analysis of spiked samples demonstrated the good accuracy and precision of the method, which is suitable for use in pharmacokinetic and bioavailability studies. The method was applied to samples from an experiment in a healthy volunteer treated with a single oral dose of 75 mg of brofaromine hydrochloride. Plasma profiles before and after enzymic hydrolysis showed that about one-third of the total brofaromine in plasma and practically all of the major metabolite (O-desmethylbrofaromine) were present in the conjugated form.

摘要

建立并验证了一种灵敏的气相色谱分析法,用于同时测定新型单胺氧化酶-A抑制剂溴法罗明[4-(7-溴-5-甲氧基-2-苯并呋喃基)哌啶盐酸盐]及其主要代谢物。加入4-(5-溴-2-苯并呋喃基)哌啶作为内标后,通过在碱性pH下进行液-液萃取从生物流体中分离出这些化合物。用七氟丁酸酐衍生化后,使用填充柱(OV-17)和电子捕获检测器对化合物进行色谱分析。两种化合物的定量限约为每个样品0.03 nmol(10 ng)。加标样品分析表明该方法具有良好的准确性和精密度,适用于药代动力学和生物利用度研究。该方法应用于一名健康志愿者单次口服75 mg盐酸溴法罗明实验的样品。酶水解前后的血浆图谱显示,血浆中总溴法罗明的约三分之一以及几乎所有主要代谢物(O-去甲基溴法罗明)均以结合形式存在。

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Determination of the new monoamine oxidase inhibitor brofaromine and its major metabolite in biological material by gas chromatography with electron-capture detection.采用带电子捕获检测的气相色谱法测定生物材料中的新型单胺氧化酶抑制剂溴法罗明及其主要代谢物。
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引用本文的文献

1
Influence of age, frailty and liver function on the pharmacokinetics of brofaromine.年龄、虚弱状态及肝功能对溴法罗明药代动力学的影响。
Eur J Clin Pharmacol. 1996;49(5):387-91. doi: 10.1007/BF00203783.
2
Role of cytochrome P4502D6 in the metabolism of brofaromine. A new selective MAO-A inhibitor.细胞色素P4502D6在溴法罗明(一种新型选择性单胺氧化酶-A抑制剂)代谢中的作用。
Eur J Clin Pharmacol. 1993;45(3):265-9. doi: 10.1007/BF00315394.
3
Correlations of plasma and urinary phenylacetic acid and phenylethylamine concentrations with eating behavior and mood rating scores in brofaromine-treated women with bulimia nervosa.
在接受溴法罗明治疗的神经性贪食症女性中,血浆和尿液中苯乙酸及苯乙胺浓度与进食行为和情绪评分的相关性。
J Psychiatry Neurosci. 1994 Jul;19(4):282-8.
4
Biochemistry and pharmacology of reversible inhibitors of MAO-A agents: focus on moclobemide.单胺氧化酶A(MAO-A)可逆性抑制剂的生物化学与药理学:聚焦吗氯贝胺
J Psychiatry Neurosci. 1993 Nov;18(5):214-25.