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利用液相色谱-线性离子阱质谱法对血液中的农药进行筛选。

Screening of pesticides in blood with liquid chromatography-linear ion trap mass spectrometry.

机构信息

Department of Pharmacology and Toxicology, CHU de Limoges, 87042 Limoges, France.

出版信息

Anal Bioanal Chem. 2010 Mar;396(6):2235-49. doi: 10.1007/s00216-009-3443-z. Epub 2010 Feb 9.

Abstract

In clinical or forensic toxicology, general unknown screening procedures are used to identify as many xenobiotics as possible, belonging to numerous chemical classes. We present here a general unknown screening procedure based on liquid chromatography coupled with use of a single linear ion trap mass spectrometer, and focus on the identification of pesticides and/or metabolites in whole blood. After solid-phase extraction (SPE), the compounds of interest were separated using a reversed-phase column and identified by the mass spectrometer operated first in the full-scan mass spectrometry (MS) mode, in the positive and negative polarities, followed by MS(2) and MS(3) scanning of ions selected in data-dependent acquisition. The total scan time was 2.45 s. Two mass spectral libraries (MS(2) and MS(3)), each of 450 spectra, were created for the 320 pesticides and metabolites detected after injection of pure solutions. Robustness of the spectra and matrix effects were studied and were satisfactory for the present application. Detection limits for the 320 compounds were studied by extracting 1 mL spiked blood at concentrations between 10 microg/L and 10 mg/L. If necessary, it was possible to decrease the detection limits of some compounds by 10-100-fold by scanning MS(2) in only one polarity, owing to a shorter total scan time. However, at the same time, the detection specificity decreased as no confirmation could be recorded in the following MS(3) scan and no information could be registered in the other polarity. So, in these rare cases, confirmation by another method was required.

摘要

在临床或法医毒理学中,通常使用未知物筛选程序来尽可能多地识别属于众多化学类别的外来化合物。本文介绍了一种基于液相色谱与单线性离子阱质谱联用的未知物通用筛选程序,重点关注全血中农药和/或代谢物的鉴定。固相萃取(SPE)后,使用反相柱对感兴趣的化合物进行分离,通过全扫描质谱(MS)模式在正、负极性下操作质谱仪进行鉴定,然后对数据依赖采集选择的离子进行 MS(2)和 MS(3)扫描。总扫描时间为 2.45 秒。创建了两个质谱库(MS(2)和 MS(3)),每个库包含 450 个谱图,用于在注入纯溶液后检测到的 320 种农药和代谢物。对光谱的稳健性和基质效应进行了研究,结果对于本应用是令人满意的。通过在 10 μg/L 至 10 mg/L 浓度下从 1 mL 加标血液中提取,研究了 320 种化合物的检测限。如果需要,可以通过仅在一个极性下扫描 MS(2)将某些化合物的检测限降低 10-100 倍,因为总扫描时间较短。然而,同时,由于无法在随后的 MS(3)扫描中记录确认信息,并且无法在其他极性下注册信息,因此检测特异性降低。因此,在这些罕见情况下,需要使用另一种方法进行确认。

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