Schneider W, Keller B, Degen P H
Research and Development Department, Pharmaceuticals Division, Basle, Switzerland.
J Chromatogr. 1989 Mar 17;488(1):275-82. doi: 10.1016/s0378-4347(00)82952-7.
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.
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。