Pieke Eelco N, Granby Kit, Trier Xenia, Smedsgaard Jørn
Research Group for Analytical Food Chemistry, National Food Institute, Technical University of Denmark, Kemitorvet Building 202, Kgs. Lyngby, DK-2800, Denmark.
Anal Chim Acta. 2017 Jul 4;975:30-41. doi: 10.1016/j.aca.2017.03.054. Epub 2017 Apr 10.
Risk assessment of exposure to chemicals from food and other sources rely on quantitative information of the occurrence of these chemicals. As screening analysis is increasingly used, a strategy to semi-quantify unknown or untargeted analytes is required. A proof of concept strategy to semi-quantifying unknown substances in LC-MS was investigated by studying the responses of a chemically diverse marker set of 17 analytes using an experimental design study. Optimal conditions were established using two optimization parameters related to weak-responding compounds and to the overall response. All the 17 selected analytes were semi-quantified using a different analyte to assess the quantification performance under various conditions. It was found that source conditions had strong effects on the responses, with the range of low-response signals varying from -80% to over +300% compared to centerpoints. Positive electrospray (ESI+) was found to have more complex source interactions than negative electrospray (ESI-). Choice of quantification marker resulted in better quantification if the retention time difference was minimized (12 out of 12 cases error factor < 4.0) rather than if the accurate mass difference was minimized (7 out of 12 cases error factor < 4.0). Using optimal conditions and retention time selection, semi-quantification in ESI+ (70% quantified, average prediction error factor 2.08) and ESI- (100% quantified, average prediction error factor 1.74) yielded acceptable results for untargeted screening. The method was successfully applied to an extract of food contact material containing over 300 unknown substances. Without identification and authentic standards, the method was able to estimate the concentration of a virtually unlimited number of compounds thereby providing valuable data to prioritize compounds in risk assessment studies.
食品及其他来源化学物质暴露的风险评估依赖于这些化学物质存在情况的定量信息。随着筛查分析的使用日益增多,需要一种对半定量未知或非靶向分析物的策略。通过使用实验设计研究,研究了一组包含17种化学性质各异的标志物的分析物的响应,以此来探究液相色谱 - 质谱联用(LC - MS)中未知物质半定量的概念验证策略。利用与弱响应化合物及整体响应相关的两个优化参数建立了最佳条件。使用不同的分析物对所有17种选定的分析物进行半定量,以评估各种条件下的定量性能。结果发现,源条件对响应有强烈影响,与中心点相比,低响应信号范围从 - 80% 到超过 + 300% 不等。发现正电喷雾(ESI +)比负电喷雾(ESI -)具有更复杂的源相互作用。如果保留时间差异最小化(12个案例中有12个误差因子 < 4.0),而不是精确质量差异最小化(12个案例中有7个误差因子 < 4.0),则选择定量标志物会带来更好的定量效果。使用最佳条件和保留时间选择,ESI +(70% 可定量,平均预测误差因子2.08)和ESI -(100% 可定量,平均预测误差因子1.74)的半定量对于非靶向筛查产生了可接受的结果。该方法已成功应用于含有300多种未知物质的食品接触材料提取物。在没有鉴定和真实标准品的情况下,该方法能够估计几乎无限数量化合物的浓度,从而为风险评估研究中的化合物优先级排序提供有价值的数据。