Wu A H, Onigbinde T A, Wong S S, Johnson K G
Department of Pathology and Laboratory Medicine, University of Texas Medical School, Houston 77030.
J Anal Toxicol. 1992 Mar-Apr;16(2):137-41. doi: 10.1093/jat/16.2.137.
An underivatized methane chemical ionization (CI) assay for measuring amphetamines in urine was evaluated against derivatized electron impact (EI) assays using a gas chromatograph-ion trap mass spectrometer. The full-scan CI mass spectra of methamphetamine, ephedrine/pseudoephedrine, and phentermine were compared with the full scan and three-ion EI mass spectra of heptafluorobutyric anhydride (HFBA) and 4-carbethoxyhexafluorobutyryl chloride (CB) derivatives. The fragmentation patterns for these compounds were nearly identical for the three major high molecular weight ions (m/z 254, 210, and 169 for EI-HFBA derivatives, and m/z 308, 262, and 280 for EI-CB derivatives). The CI mass spectra of the underivatized drugs contained more discernible differences at the higher molecular weights, including m/z 119, 148, and 150 for methamphetamine, 148, 166, and 176 for ephedrine/pseudoephedrine, and 91, 133, and 150 for phentermine. The within-run precision ranged from 7-9% for CI versus 5-6% for EI with HFBA derivatization (mean 500 ng/mL, n = 5). The limits of detection (LOD) for amphetamine and methamphetamine were 2.4 and 8.6 ng/mL, respectively, for CI versus 0.7 and 1.4 ng/mL for EI. The limits of quantitation (LOQ) were 4.5 and 19.1 ng/mL for CI versus 1.4 and 5.7 ng/mL for EI. The use of full-scan mass spectral analysis with either electron impact or chemical ionization provides additional qualitative data that may be helpful for measuring methamphetamine in the presence of other sympathomimetic amines.
使用气相色谱 - 离子阱质谱仪,对一种用于测量尿液中苯丙胺类药物的未衍生化甲烷化学电离(CI)分析方法与衍生化电子轰击(EI)分析方法进行了评估。将甲基苯丙胺、麻黄碱/伪麻黄碱和苯丁胺的全扫描CI质谱图与七氟丁酸酐(HFBA)和4 - 乙氧羰基六氟丁酰氯(CB)衍生物的全扫描和三离子EI质谱图进行了比较。对于这三种主要的高分子量离子(EI - HFBA衍生物的m/z 254、210和169,以及EI - CB衍生物的m/z 308、262和280),这些化合物的碎裂模式几乎相同。未衍生化药物的CI质谱图在较高分子量处包含更多可辨别的差异,包括甲基苯丙胺的m/z 119、148和150,麻黄碱/伪麻黄碱的m/z 148、166和176,以及苯丁胺的m/z 91、133和150。CI方法的批内精密度范围为7 - 9%,而EI与HFBA衍生化方法的批内精密度为5 - 6%(均值500 ng/mL,n = 5)。苯丙胺和甲基苯丙胺的CI检测限(LOD)分别为2.4和8.6 ng/mL,而EI的检测限分别为0.7和1.4 ng/mL。CI的定量限(LOQ)为4.5和19.1 ng/mL,而EI的定量限为1.4和5.7 ng/mL。使用电子轰击或化学电离的全扫描质谱分析可提供额外的定性数据,这可能有助于在存在其他拟交感神经胺的情况下测量甲基苯丙胺。