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Identification and quantitative determination of benproperine metabolites in human plasma and urine by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法鉴定和定量测定人血浆和尿液中的苯丙氨酸代谢物

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Two novel metabolites of benproper'ine (BPP), 1-[1-methyl-2-[2-(phenylmethyl)phenoxy]ethyl]-3-piperidinol (3-OH-BPP) and 1-[1-methyl-2-[2-(phenylmethyl)phenoxy] ethyl]-4-piperidinol (4-OH-BPP), were confirmed by comparison of retention times and mass spectra with those of synthetic standards using liquid chromatography-tandem mass spectrometry. Selective and sensitive procedures were developed for the simultaneous determination of BPP, 3-OH-BPP and 4-OH-BPP in human plasma and urine. The analytes were extracted from plasma sample and enzymatically hydrolyzed urine samples by liquid-liquid extraction, separated through a Diamonsil C-18 column (150 mm x 4.6 mm i.d.) and determined by tandem mass spectrometry with an electrospray ionization interface in selected reaction monitoring mode. Dextromethorphan was used as internal standard. The mobile phase consisted of acetonitrile-water-formic acid (34:66: 1, v/v/v), and flow-rate was 0.5 ml min(-1). This method has a lower limit of quantification (LLOQ) of 60, 4.0 and 4.0 nmol l(-1) for BPP, 3-OH-BPP and 4-OH-BPP in plasma, 4.9. 4.7 and 2.4 nmol l(-1) in urine, respectively. The intra- and inter-run precision were measured to be below 9.2%, and the accuracy was within +/- 4.3% for the analytes. The method was successfully used to determine BPP, 3-OH-BPP and 4-OH-BPP in plasma and urine for pharmacokinetic investigation. The results indicated residue of 3-OH-BPP in the body at least 192 It after an oral dose of BPP. (c) 2005 Elsevier B.V. All rights reserved.
机译:苯丙氨酸(BPP)的两种新型代谢物,1- [1-甲基-2- [2-(苯甲基)苯氧基]乙基] -3-哌啶醇(3-OH-BPP)和1- [1-甲基-2通过使用液相色谱-串联质谱法比较保留时间和质谱图与合成标准品的保留时间和质谱图,确定了-[[2-(苯基甲基)苯氧基]乙基] -4-哌啶醇(4-OH-BPP)。开发了选择性和灵敏的程序,用于同时测定人血浆和尿液中的BPP,3-OH-BPP和4-OH-BPP。通过液-液萃取从血浆样品和酶水解尿液样品中提取分析物,通过Diamonsil C-18色谱柱(150 mm x 4.6 mm id)进行分离,并通过串联质谱法在选定的反应监测模式下通过电喷雾电离接口进行测定。右美沙芬用作内标。流动相由乙腈-水-甲酸(34:66:1,v / v / v)组成,流速为0.5 ml min(-1)。该方法对血浆中BPP,3-OH-BPP和4-OH-BPP的定量下限(LLOQ)为60、4.0和4.0 nmol l(-1)。分别为尿中的4.7和2.4 nmol l(-1)。测得的运行中和运行中精度低于9.2%,分析物的精度在+/- 4.3%之内。该方法已成功用于血浆和尿液中BPP,3-OH-BPP和4-OH-BPP的测定,用于药代动力学研究。结果表明,口服BPP后至少有192 It体内存在3-OH-BPP残留。 (c)2005 Elsevier B.V.保留所有权利。

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