Grimalt Susana, Pozo Oscar J, Sancho Juan V, Hernández Félix
Research Institute for Pesticides and Water, University Jaume I, E-12071 Castellón, Spain.
Anal Chem. 2007 Apr 1;79(7):2833-43. doi: 10.1021/ac061233x. Epub 2007 Feb 20.
In this paper, the potential of coupling liquid chromatography with hybrid quadrupole time-of-flight mass spectrometry (LC-QTOF) for the determination of pesticides in a variety of fruit samples (orange peel and flesh, banana skin and flesh, strawberry and pear) has been explored. The quantitative application at residue levels has been proven for two insecticides (buprofezin and hexythiazox), which were satisfactorily determined at three concentration levels, 0.1, 1, and 5 mg/kg, obtaining a suitable linearity range (correlation coefficient>0.99) of more than 2 orders of magnitude. Satisfactory recoveries have been obtained for both compounds at the three levels tested in all sample matrices, with lowest calibration levels (LCL) of 0.075 and 0.01 mg/kg. The excellent potential of QTOF for identification purposes is illustrated by the high number of identification points (IPs) earned, up to 21, at the highest concentration of 5 mg/kg, or between 11 and 21 at the 0.1 and 1 mg/kg levels. The application of LC-QTOF MS to real samples revealed the presence of several positives at concentrations close to the LCL, all of which were confirmed with more than 11 IPs. The potential of QTOF for elucidation of nontarget analytes has also been demonstrated by the finding of one transformation product (TP) of buprofezin in a banana skin sample. This TP was identified by obtaining the full scan product ion spectra at different collision energies with acceptable accurate mass deviation. The work performed in this paper illustrates the suitability and excellent confirmatory potential of LC-QTOF MS for pesticides residues analysis in food samples.
本文探讨了液相色谱与混合四极杆飞行时间质谱联用(LC-QTOF)技术用于测定多种水果样品(橙皮和果肉、香蕉皮和果肉、草莓和梨)中农药的潜力。已证明该技术可用于两种杀虫剂(噻嗪酮和噻螨酮)的残留量定量分析,在0.1、1和5 mg/kg三个浓度水平下均可令人满意地测定,获得了超过2个数量级的合适线性范围(相关系数>0.99)。在所有样品基质中测试的三个水平下,两种化合物均获得了令人满意的回收率,最低校准水平(LCL)分别为0.075和0.01 mg/kg。在5 mg/kg的最高浓度下,QTOF获得了高达21个鉴定点(IP),在0.1和1 mg/kg水平下为11至21个,这表明QTOF在鉴定方面具有出色的潜力。LC-QTOF MS应用于实际样品时,发现在接近LCL的浓度下有几个阳性结果,所有这些结果均通过超过11个IP得到确认。在香蕉皮样品中发现了噻嗪酮的一种转化产物(TP),这也证明了QTOF在阐明非目标分析物方面的潜力。通过在不同碰撞能量下获得全扫描产物离子光谱,并具有可接受的精确质量偏差,对该TP进行了鉴定。本文所开展的工作表明,LC-QTOF MS适用于食品样品中农药残留分析,且具有出色的确证潜力。