Coscollà Clara, León Nuria, Pastor Agustín, Yusà Vicent
Public Health Laboratory of Valencia-FISABIO, 21, Avenida Catalunya, 46020 Valencia, Spain.
Analytical Chemistry Department, Universit of Valencia, Edifici Jeroni Muñoz, Dr. Moliner 50, 46100 Burjassot, Spain.
J Chromatogr A. 2014 Nov 14;1368:132-42. doi: 10.1016/j.chroma.2014.09.067. Epub 2014 Oct 2.
A comprehensive strategy for the analysis of current airborne pesticides has been developed using liquid chromatography coupled to high resolution mass spectrometry. The methodology includes both quantitative target analysis and post-run target screening analysis. The quantitative method was validated after a previous statistical optimisation of the main factors governing the ion source ionization and a study of the single-stage Orbitrap fragmentation through the HCD cell. The quantitative method presented recoveries ranging from 73 to 116%, with precision (RSD) lower than 20%, for the 35 substances in the scope of the target method. The full-scan accurate mass data were acquired with a resolving power of 50000 FWHM (scan speed, 2 Hz), and alternating two acquisition events, ESI+ without fragmentation and ESI+ with fragmentation. The method-LOQ was 6.5 pg m(-3) for most of the target pesticides. For post-target screening a customized theoretical database, that included pesticides, metabolites and other substances such as emerging flame retardants was built up. For identification, accurate exact mass with less than 5 ppm, and some diagnostic ions including isotopes and/or fragments were used. The strategy was applied to ten samples collected in a rural area of Valencia (Spain). Four pesticides, namely carbendazim, metalaxyl, myclobutanil and terbuthylazine, were detected in concentrations from 16 pg m(-3) to 174 pg m(-3). Some pesticides and metabolites (endothal, fenfuram, terbuthylazine-2-OH), in addition to two flame retardants were tentatively identified in the post-run target screening analysis.
已开发出一种使用液相色谱与高分辨率质谱联用分析当前空气中农药的综合策略。该方法包括定量目标分析和运行后目标筛查分析。在对控制离子源电离的主要因素进行先前的统计优化以及通过HCD池对单级轨道阱碎片化进行研究之后,对定量方法进行了验证。对于目标方法范围内的35种物质,定量方法的回收率在73%至116%之间,精密度(相对标准偏差)低于20%。全扫描精确质量数据以50000 FWHM的分辨率(扫描速度为2 Hz)采集,并交替进行两个采集事件,即不进行碎片化的ESI+和进行碎片化的ESI+。大多数目标农药的方法定量下限为6.5 pg m(-3)。对于运行后筛查,建立了一个定制的理论数据库,其中包括农药、代谢物和其他物质,如新型阻燃剂。为了进行鉴定,使用了精确质量误差小于5 ppm的精确质量以及一些诊断离子,包括同位素和/或碎片。该策略应用于在西班牙巴伦西亚农村地区采集的10个样品。检测到四种农药,即多菌灵、甲霜灵、腈菌唑和特丁津,浓度范围为16 pg m(-3)至174 pg m(-3)。在运行后目标筛查分析中,除了两种阻燃剂外,还初步鉴定出了一些农药和代谢物(棉隆、呋菌胺、特丁津-2-OH)。