Dipartimento di Scienze Pure ed Applicate, Università degli Studi di Urbino Carlo Bo, 61029, Urbino, Italy.
Dipartimento di Scienze Pure ed Applicate, Università degli Studi di Urbino Carlo Bo, 61029, Urbino, Italy.
J Chromatogr A. 2020 Sep 13;1627:461421. doi: 10.1016/j.chroma.2020.461421. Epub 2020 Jul 19.
Herein we present an efficient, column-switching method that relies on a custom-made T-union passive diffusion micromixer to assist water dilution and promote trap solute focusing of a high sample volume dissolved in pure organic solvent using a 0.075 mm i.d. nano-LC column. This method allows injecting 20 μL (or higher) of sample volume, speeding up the analysis time, with a 400-fold increase of the limits of quantitation for selected compounds. Five pesticides in different media were used as model compounds, and the analyses were carried out with a triple quadrupole mass spectrometer equipped with a Liquid Electron Ionization (LEI) LC-MS interface working in multiple reaction monitoring (MRM) mode. The system microfluidics were investigated using COMSOL modeling software. Robustness of the entire system was evaluated using a post-extraction addition soil extracts with limits of detection values spanning from 0.10 to 0.45 µg/L. Reproducible results in terms of peak area, peak shape, and retention times were achieved in soil matrix. Repeatability test on peak area variations were lower than 10%.
本文提出了一种高效的柱切换方法,该方法依赖于定制的 T 型三通无源扩散微混合器,以辅助水稀释并促进溶解在纯有机溶剂中的高样品体积的阱溶质聚焦,使用 0.075 毫米内径的纳流 LC 柱。该方法允许进样 20 μL(或更高)的样品量,从而缩短分析时间,并将选定化合物的定量限提高了 400 倍。以五种不同介质中的农药作为模型化合物,使用配备有液体电子电离(LEI)LC-MS 接口的三重四极杆质谱仪,以多重反应监测(MRM)模式进行分析。使用 COMSOL 建模软件研究了系统微流控。通过对添加了提取后的土壤提取物进行后萃取,评估了整个系统的稳健性,检测限范围从 0.10 到 0.45 µg/L。在土壤基质中实现了峰面积、峰形和保留时间的可重现结果。峰面积变化的重复性测试低于 10%。