Lanina Svetlana A, Toledo Patricia, Sampels Sabine, Kamal-Eldin Afaf, Jastrebova Jelena A
Department of Food Science, Division of Food Chemistry, Swedish University of Agricultural Sciences, SE-750 07 Uppsala, Sweden.
J Chromatogr A. 2007 Jul 20;1157(1-2):159-70. doi: 10.1016/j.chroma.2007.04.058. Epub 2007 May 1.
ESI and APCI ionization techniques in both negative and positive ion modes were evaluated for simultaneous LC-MS analysis of the four tocopherol homologues (alpha, beta, gamma and delta). The ESI and APCI ionization of tocopherols in positive ion mode was not efficient and proceeded via two competitive mechanisms, with the formation of protonated pseudo-molecular ions and molecular ions, which adversely influenced the repeatability of MS signal. Ionization in negative ion mode in both ESI and APCI was more efficient as it only produced target deprotonated pseudo-molecular ions. The APCI in negative ion mode showed larger linearity range, lower detection limits and was less sensitive to the differences in chemical structure of analytes and nature of applied solvents than negative ion ESI. Negative ion APCI was, therefore, chosen for the development of LC-MS method for simultaneous determination of the four tocopherols in foods. A baseline separation of the tocopherols was achieved on novel pentafluorophenyl silica-based column Fluophase PFP. The use of methanol-water (95:5, v/v) as a mobile phase was preferable to the use of acetonitrile-water due to considerable gain in MS signal. The limits of quantifications were 9 ng/mL for alpha-tocopherol, 8 ng/mL for beta- and gamma- and 7.5 ng/mL for delta-tocopherol when 2 microL was injected. This method was successfully applied to determination of tocopherols in sunflower oil and milk.
评估了电喷雾电离(ESI)和大气压化学电离(APCI)技术在正离子和负离子模式下对四种生育酚同系物(α、β、γ和δ)进行同时液相色谱-质谱(LC-MS)分析的情况。生育酚在正离子模式下的ESI和APCI电离效率不高,通过两种竞争机制进行,会形成质子化的准分子离子和分子离子,这对质谱信号的重复性产生了不利影响。ESI和APCI在负离子模式下的电离效率更高,因为它只产生目标去质子化准分子离子。负离子模式下的APCI显示出更大的线性范围、更低的检测限,并且与负离子ESI相比,对分析物化学结构差异和所用溶剂性质的敏感性更低。因此,选择负离子APCI来开发用于同时测定食品中四种生育酚的LC-MS方法。在新型的基于五氟苯基硅胶的Fluophase PFP柱上实现了生育酚的基线分离。由于质谱信号有显著提高,使用甲醇-水(95:5,v/v)作为流动相比使用乙腈-水更可取。当进样2微升时,α-生育酚的定量限为9纳克/毫升,β-和γ-生育酚为8纳克/毫升,δ-生育酚为7.5纳克/毫升。该方法成功应用于葵花籽油和牛奶中生育酚的测定。