首页> 外文期刊>Archives of pharmacal research >Simultaneous determination of methamphetamine, 3,4-methylenedioxy-N-methylamphetamine, 3,4-methylenedioxy-N-ethylamphetamine, N,N-dimethylamphetamine, and their metabolites in urine by liquid chromatography-electrospray ionization-tandem mass spectro
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Simultaneous determination of methamphetamine, 3,4-methylenedioxy-N-methylamphetamine, 3,4-methylenedioxy-N-ethylamphetamine, N,N-dimethylamphetamine, and their metabolites in urine by liquid chromatography-electrospray ionization-tandem mass spectro

机译:液相色谱-电喷雾电离串联质谱法同时测定尿液中的甲基苯丙胺,3,4-亚甲二氧基-N-甲基苯丙胺,3,4-亚甲二氧基-N-乙基苯丙胺,N,N-二甲基苯丙胺及其代谢物

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A liquid chromatography-electrospray ionization-tandem mass spectrometric (LC-ESI-MS/MS) method was developed and validated for the simultaneous detection and quantification of seven amphetamine derivatives (amphetamine (AP), methamphetamine (MA), 3,4-methylenedioxy-N-amphetamine (MDA), 3,4-methylenedioxy-N-methamphetamine (MDMA), 3,4-methylenedioxy-N-ethylamphetamine (MDEA), N,N-dimethylamphetamine (DMA), and N,N-dimethylamphetamine-N-oxide (DMANO)) in human urine. Seven deuterium-labeled compounds were prepared for use as internal standards to quantify the analytes. One milliliter of urine was combined with 1 mL of 0.2 M sodium carbonate buffer solution (pH 9.0) before solid phase extraction (SPE). An Oasis HLB SPE column followed by chromatographic separation on a Capcell Pak C18 MG-II column (150 x 2.0 mm I.D., 5 microm) and electrospray mass spectrometry with multiple reaction monitoring were used for selective and sensitive detection. The use of ammonium formate (5 mM, pH adjusted to 4.0 with formic acid, Solvent A) and acetonitrile (Solvent B) as the mobile phase at a flow rate of 230 microL/min was found to be the most effective for the separation. The linear ranges were 5.0-1000 ng/mL for AP, MDA, MDMA, MDEA, DMA, and DMANO and 10.0-1000 ng/mL for MA, with good correlation coefficients (r2 > 0.996). The intra-day, inter-day, and interperson precisions were within 14.6%, 12.1% and 15.5%, respectively. The intra-day, inter-day, and interperson accuracies were between -11.6 and 9.0%, -7.9 and 2.3%, and -13.2 and 4.3%, respectively. The limits of detection (LODs) for each analytical compound were lower than 1.95 ng/mL. The recovery ranged from 72.3 to 103.3%. The applicability of the developed method was examined by analyzing several urine samples from confirmed drug abusers.
机译:建立了液相色谱-电喷雾电离串联质谱(LC-ESI-MS / MS)方法并验证了该方法可同时检测和定量7种苯丙胺衍生物(苯丙胺(AP),甲基苯丙胺(MA),3,4-亚甲基二氧基) -N-苯丙胺(MDA),3,4-亚甲二氧基-N-甲基苯丙胺(MDMA),3,4-亚甲二氧基-N-乙基苯丙胺(MDEA),N,N-二甲基苯丙胺(DMA)和N,N-二甲基苯丙胺人尿中的N-氧化物(DMANO))。制备了七个氘标记的化合物用作内标,以定量分析物。在固相萃取(SPE)之前,将1毫升尿液与1 mL 0.2 M碳酸钠缓冲溶液(pH 9.0)合并。使用Oasis HLB SPE色谱柱,然后在Capcell Pak C18 MG-II色谱柱(150 x 2.0 mm内径,5微米)上进行色谱分离,并采用具有多个反应监测功能的电喷雾质谱进行选择性和灵敏检测。发现使用甲酸铵(5 mM,用甲酸将pH调节至4.0,溶剂A)和乙腈(溶剂B)作为流动相以230 microL / min的流速进行分离最有效。 AP,MDA,MDMA,MDEA,DMA和DMANO的线性范围为5.0-1000 ng / mL,MA的线性范围为10.0-1000 ng / mL,具有良好的相关系数(r2> 0.996)。日内,日间和人际精度分别在14.6%,12.1%和15.5%之内。日内,日间和人际间的准确度分别在-11.6和9.0%之间,-7.9和2.3%之间以及-13.2和4.3%之间。每种分析化合物的检出限(LOD)均低于1.95 ng / mL。回收率从72.3%到103.3%。通过分析已确认吸毒者的几个尿液样品,检查了所开发方法的适用性。

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