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首页> 外文期刊>Forensic science international >The use of a sulfonated capillary on chiral capillary electrophoresis/mass spectrometry of amphetamine-type stimulants for methamphetamine impurity profiling
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The use of a sulfonated capillary on chiral capillary electrophoresis/mass spectrometry of amphetamine-type stimulants for methamphetamine impurity profiling

机译:磺化毛细管在苯丙胺类兴奋剂用于甲基苯丙胺杂质分析的手性毛细管电泳/质谱中的应用

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摘要

Chiral capillary electrophoresis/tandem mass spectrometry (CE/MS/MS) using a chemically modified capillary containing sulfonated groups was developed for the following 8 amphetamine-type stimulants (ATS): amphetamine, methamphetamine (MA), norephedrine, norpseudoephedrine, ephedrine (EP), pseudoephedrine (pEP), dimethylamphetamine and methylephedrine. The running buffer was 10 mM formic acid containing 20 mM highly sulfated gamma-cyclodextrin (pH 2.5) as the chiral selector. All 16 enantiomers were well resolved within 60 min, and precisely identified due to their characteristic mass spectra. Further, the RSDs of the migration times of the analytes were no more than 0.3% without any standardization. (1R,2S)-(-)-EP and (1S,2S)-(+)-pEP, which are important ATS impurities originating in the precursors, were added to a highly concentrated MA solution (1 mg/mL) and analyzed as mock samples for MA impurity analysis. Acceptable repeatability of the migration times of ()-EP and (+)-pEP (ca. 0.3% RSDs) was still observed without interference from the large amount of MA. The limits of detection (LOD) of (-)-EP and (+)-pEP were approximately 2 mu g/mL, therefore, their LOD as the impurity concentrations were calculated at about 0.2%. Seized MA samples were dissolved in water at a high concentration (1 mg/mL) and analyzed by this method. (-)-EP and (+)-pEP were clearly detected as impurities. Although these compounds had similar migration times and mass spectral patterns, the fine repeatability allowed easy identification of the impurities by a simple comparison of the absolute migration times of the specimens and those of authentic standards. This study is the first to report the use of a chemically modified capillary for the impurity profiling on CE/MS/MS. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:针对以下8种苯丙胺类兴奋剂(ATS)开发了使用含有磺化基团的化学修饰毛细管的手性毛细管电泳/串联质谱(CE / MS / MS):苯丙胺,甲基苯丙胺(MA),去氧麻黄碱,去甲伪麻黄碱,麻黄碱(EP ),伪麻黄碱(pEP),二甲基苯丙胺和甲基麻黄碱。运行缓冲液是10 mM甲酸,其中含有20 mM高度硫酸化的γ-环糊精(pH 2.5)作为手性选择剂。所有16种对映异构体均在60分钟内得到良好分离,并由于其特征质谱而得到了精确鉴定。此外,在没有任何标准化的情况下,分析物迁移时间的RSD不超过0.3%。将(1R,2S)-(-)-EP和(1S,2S)-(+)-pEP(它们是源自前体的重要ATS杂质)添加到高浓度MA溶液(1 mg / mL)中并进行分析作为MA杂质分析的模拟样品。仍然观察到()-EP和(+)-pEP迁移时间的可重复性(约0.3%RSD),而不受大量MA的干扰。 (-)-EP和(+)-pEP的检出限(LOD)约为2μg / mL,因此,它们的LOD(杂质浓度)约为0.2%。将缉获的MA样品以高浓度(1 mg / mL)溶于水中,并通过此方法进行分析。清楚地检测到(-)-EP和(+)-pEP为杂质。尽管这些化合物具有相似的迁移时间和质谱图,但通过简单比较样品和真实标准品的绝对迁移时间,可以实现良好的重复性,从而易于鉴定杂质。这项研究是第一个报告使用化学修饰的毛细管在CE / MS / MS上进行杂质分析的研究。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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