Liquid Chromatography-Electron Capture Negative Ionization- Tandem Mass Spectrometry Detection of Pesticides in a Commercial Formulation

被引:6
|
作者
Cappiello, Achille [1 ,2 ]
Termopoli, Veronica [1 ]
Palma, Pierangela [1 ,2 ]
Famiglini, Giorgio [1 ]
Saeed, Mansoor [3 ]
Perry, Simon [3 ]
Navarro, Pablo [3 ]
机构
[1] Univ Urbino, Dept Pure & Appl Sci, LC MS Lab, I-61029 Urbino, Italy
[2] Vancouver Isl Univ, Dept Chem, Nanaimo, BC V9R 5S5, Canada
[3] Jealotts Hill Int Res Ctr, Bracknell RG42 6EY, Berks, England
关键词
QUECHERS SAMPLE PREPARATION; ION CHEMICAL-IONIZATION; SOLID-PHASE EXTRACTION; GAS-CHROMATOGRAPHY; GC-MS; RESIDUE ANALYSIS; LC-MS; FRUIT; NCI; ORGANOCHLORINE;
D O I
10.1021/jasms.1c00307
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Negative chemical ionization (NCI) and electron-capture negative ionization (ECNI) are gas chromatography-mass spectrometry (GC-MS) techniques that generate negative ions in the gas phase for compounds containing electronegative atoms or functional groups. In ECNI, gas-phase thermal electrons can be transferred to electrophilic substances to produce M-center dot ions and scarce fragmentation. As a result of the electrophilicity requirements, ECNI is characterized by high-specificity and low background noise, generally lower than EI, offering lower detection limits. The aim of this work is to explore the possibility of extending typical advantages of ECNI to liquid chromatography-mass spectrometry (LC-MS). The LC is combined with the novel liquid-EI (LEI) LC-EIMS interface, the eluent is vaporized and transferred inside a CI source, where it is mixed with methane as a buffer gas. As proof of concept, dicamba and tefluthrin, agrochemicals with herbicidal and insecticidal activity, respectively, were chosen as model compounds and detected together in a commercial formulation. The pesticides have different chemical properties, but both are suitable analytes for ECNI due to the presence of electronegative atoms in the molecules. The influence of the mobile phase and other LC- and MS-operative parameters were methodically evaluated. Part-per-trillion (ppt) detection limits were obtained. Ion abundances were found to be stable with quantitative linear detection, reliable, and reproducible, with no influence from coeluting interfering compounds from the sample matrix.
引用
收藏
页码:141 / 148
页数:8
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