Analytical Chemistry Research Group, Department of Physical and Analytical Chemistry, University of Jaén, Campus Las Lagunillas, Edificio B-3, 23071 Jaén, Spain.
J Chromatogr A. 2010 Jun 11;1217(24):3736-47. doi: 10.1016/j.chroma.2010.04.025. Epub 2010 Apr 18.
In this study, a comprehensive evaluation of two simple sample treatment methodologies has been carried out for the development of large-scale multi-residue methods for pesticide testing in olive oil. The proposed methodologies are based on (a) liquid-liquid partitioning with acetonitrile followed by dispersive solid-phase extraction clean-up using graphitized carbon black, primary-secondary amine and C(18) sorbents; (b) liquid partitioning with acetonitrile saturated with petroleum ether followed by matrix solid-phase dispersion (MSPD) using aminopropyl as sorbent material and a Florisil cartridge for final clean-up in the elution step. To evaluate the proposed sample treatment methodologies, 105 representative multi-class pesticides were studied using fast liquid chromatography-electrospray time-of-flight mass spectrometry (LC-TOFMS). For validation purposes, recoveries studies were carried out at 10 and 100microgkg(-1) levels, yielding recovery rates in the range 70-130% for 72% of analytes using liquid-liquid procedure and for 57% analytes using MSPD procedure. The LC-MS method provided good linearity, precision and accuracy. The limits of detection obtained were lower than 10microgkg(-1) for more than 85% analytes using both sample treatment methodologies. In addition, minor matrix effects (i.e. signal suppression or enhancement < or =20%) were observed in ca. 70% of the studied compounds. Data obtained shows that both sample treatment methodologies proposed can be successfully applied for large-scale pesticide testing in olive oil samples, showing the ability to quickly detect trace amount of over one hundred target species with different physicochemical properties, without requiring expensive instrumentation for sample treatment step and involving relatively low amounts of solvent consumption and waste generation.
本研究对两种简单的样品处理方法进行了全面评估,以开发橄榄油中农药多残留检测的大规模方法。所提出的方法基于(a)用乙腈进行液-液分配,然后用石墨化炭黑、伯仲胺和 C(18)吸附剂进行分散固相萃取净化;(b)用乙腈与石油醚饱和进行液-液分配,然后用氨基丙基作为吸附材料进行基质固相分散(MSPD),最后在洗脱步骤中用 Florisil 小柱进行最终净化。为了评估所提出的样品处理方法,使用快速液相色谱-电喷雾飞行时间质谱(LC-TOFMS)对 105 种代表性多类农药进行了研究。为了验证目的,在 10 和 100μgkg(-1)水平进行了回收率研究,使用液-液程序,72%的分析物回收率在 70-130%范围内,使用 MSPD 程序,57%的分析物回收率在 70-130%范围内。LC-MS 方法具有良好的线性、精密度和准确性。使用两种样品处理方法,超过 85%的分析物的检测限低于 10μgkg(-1)。此外,约 70%的研究化合物观察到较小的基质效应(即信号抑制或增强 <或=20%)。所获得的数据表明,所提出的两种样品处理方法都可以成功地应用于橄榄油样品中的大规模农药检测,能够快速检测到具有不同物理化学性质的一百多种目标化合物的痕量,而不需要昂贵的仪器进行样品处理步骤,并且涉及相对较少的溶剂消耗和废物产生。