Food Science and Nutrition Department, XaRTA (Catalonian Reference Network on Food Technology), University of Barcelona, Food and Nutrition Torribera Campus, Av. Prat de la Riba, 171, 08921 S.ta Coloma de Gramenet, Spain.
J Chromatogr A. 2013 Nov 29;1318:180-8. doi: 10.1016/j.chroma.2013.10.015. Epub 2013 Oct 10.
A simple, reliable, selective and sensitive method for the determination of volatile thiols at trace levels in lipid matrices was developed. The method consisted of a single-step derivatization/extraction procedure followed by electrospray ionization-high performance liquid chromatography-high resolution mass spectrometry (ESI-HPLC-HRMS) analysis using ebselen as a derivatization agent. The analytical conditions were optimized in a lipid model system (triolein) and virgin olive oil (VOO), both spiked with seven representative volatile thiols. The method was validated and the sensitivity, precision, accuracy and selectivity were evaluated. The experimental limit of quantification (LOQ) of the tested thiols in the VOO matrix ranged from 0.05 to 0.5ng/kg. Moreover, the intra-day relative standard deviation (RSD) was in general lower than 10%, except for esters, which reached RSD values of around 13%. The inter-day RDS ranged between 9.6% and 36.6%. The recovery in VOO ranged from 79% to 20% for derivatives with the highest and lowest polarity, respectively. The methodology was applied to the analysis of some VOO samples. Within this first probe sample, some of the VOO analyzed presented concentrations of 4-methoxy-2-methyl-2-butanethiol above the LOQ, ranging between 0.2 and 1.9ng/kg. The advantage of using full-scan acquisition mode when working with HRMS is that it allows the use of a non-target approach based on the fragmentation of thiol derivatives yielding a main product ion at m/z 275.9922 C13H10ONSe and that corresponded to the ebselen moiety of the derivatives. Any positive finding satisfied the identification and confirmation criteria established during the validation: retention time drift <3-fold the standard deviation of the method, mass accuracy <2ppm with real resolution ≥20,000 (full width at half maximum) at the mass range of interest, and the presence of isotope ions containing (80)Se and (78)Se, respectively.
开发了一种简单、可靠、选择性和灵敏的方法,用于测定脂质基质中痕量挥发性硫醇。该方法包括单步衍生/提取程序,然后使用依布硒啉作为衍生化剂,通过电喷雾电离-高效液相色谱-高分辨率质谱(ESI-HPLC-HRMS)分析。在脂质模型系统(三油酸甘油酯)和初榨橄榄油(VOO)中优化了分析条件,两者均加入了七种代表性挥发性硫醇。对方法进行了验证,评估了灵敏度、精密度、准确度和选择性。在 VOO 基质中测试的硫醇的实验定量限(LOQ)范围为 0.05 至 0.5ng/kg。此外,日内相对标准偏差(RSD)通常低于 10%,除酯外,其 RSD 值约为 13%。日间 RSD 范围在 9.6%至 36.6%之间。在 VOO 中的回收率范围为最高和最低极性衍生物的 79%至 20%。该方法应用于一些 VOO 样品的分析。在这个初步探针样品中,一些分析的 VOO 中 4-甲氧基-2-甲基-2-丁硫醇的浓度高于 LOQ,范围在 0.2 至 1.9ng/kg 之间。在使用 HRMS 时,采用全扫描采集模式的优点是它允许使用基于硫醇衍生物断裂的非靶向方法,产生主要产物离子 m/z 275.9922 C13H10ONSe,对应于衍生物的依布硒啉部分。任何阳性发现都满足验证过程中建立的鉴定和确认标准:保留时间漂移<方法标准偏差的 3 倍、质量精度<2ppm,真实分辨率≥20,000(半峰全宽)在感兴趣的质量范围内,以及存在分别含有(80)Se 和(78)Se 的同位素离子。