Fagerquist C K, Hellerstein M K, Faubert D, Bertrand M J
Department of Nutritional Sciences and Toxicology, University of California, Berkeley, USA.
J Am Soc Mass Spectrom. 2001 Jun;12(6):754-61. doi: 10.1016/S1044-0305(01)00227-6.
An important problem in mass isotopomer abundance mass spectrometry (MIAMS) is the dependence of measured mass isotopomer abundances on sample concentration. We have evaluated the role of ionization energy on mass isotopomer abundance ratios of methyl palmitate as a function of sample concentration. Ionization energy was varied using electron impact ionization (EI) and metastable atom bombardment (MAB). The latter generates a beam of metastable species capable of ionizing analyte molecules by Penning ionization. We observed that ionization of methyl palmitate by EI (70 eV) showed the greatest molecular ion fragmentation and also showed the greatest dependence of relative isotopomer abundance ratios on sample concentration. Ionization using the 3P2 and 3P0 states of metastable krypton (9.92 and 10.56 eV, respectively) resulted in almost no molecular ion fragmentation, and the isotopomer abundances quantified were essentially independent of sample concentration. Ionization using the 3P2 and 3P0 states of metastable argon (11.55 and 11.72 eV, respectively) showed molecular ion fragmentation intermediate between that of EI and MAB(Kr) and showed an isotopomer concentration dependence which was less severe than that observed with EI but more severe than that observed with MAB(Kr). The observed decrease in the dependence of isotopomer abundance on sample concentration with a decrease in molecular ion fragmentation is consistent with the hypothesis that proton transfer from a fragment cation to a neutral molecule is the gas phase reaction mechanism responsible for the concentration dependence. Alternative explanations, e.g., hydrogen abstraction from a neutral molecule to a molecular cation, is not supported by these results. Moreover, the MAB ionization technique shows potential for eliminating one source of error in MIAMS measurements of methyl palmitate, in particular, and of fatty acids methyl esters, in general.
在质量同位素异构体丰度质谱分析(MIAMS)中,一个重要问题是所测质量同位素异构体丰度对样品浓度的依赖性。我们评估了电离能对棕榈酸甲酯质量同位素异构体丰度比的影响,该影响是作为样品浓度的函数。通过电子轰击电离(EI)和亚稳原子轰击(MAB)来改变电离能。后者会产生一束亚稳物种,能够通过潘宁电离使分析物分子电离。我们观察到,EI(70电子伏特)对棕榈酸甲酯的电离显示出最大程度的分子离子碎片化,并且相对同位素异构体丰度比也对样品浓度表现出最大的依赖性。使用亚稳氪的3P2和3P0态(分别为9.92和10.56电子伏特)进行电离,几乎不会产生分子离子碎片化,并且所定量的同位素异构体丰度基本与样品浓度无关。使用亚稳氩的3P2和3P0态(分别为11.55和11.72电子伏特)进行电离,显示出的分子离子碎片化程度介于EI和MAB(Kr)之间,并且显示出的同位素异构体浓度依赖性比EI所观察到的要弱,但比MAB(Kr)所观察到的要强。随着分子离子碎片化程度降低,观察到的同位素异构体丰度对样品浓度的依赖性减弱,这与以下假设一致:从碎片阳离子到中性分子的质子转移是导致浓度依赖性的气相反应机制。这些结果不支持其他解释,例如从中性分子到分子阳离子的氢提取。此外,MAB电离技术尤其在消除棕榈酸甲酯以及一般脂肪酸甲酯的MIAMS测量中的一个误差来源方面显示出潜力。