León Nuria, Pastor Agustín, Yusà Vicent
Public Health Laboratory of Valencia, Avenida Catalunya 21, 46020 Valencia, Spain; Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, FISABIO - Public Health, Avenida Catalunya 21, 46020 Valencia, Spain.
Analytical Chemistry Department, Universidad de Valencia, Edifici Jeroni Muñoz, 50, Dr. Moliner, Burjassot, 46100 Valencia, Spain.
Talanta. 2016;149:43-52. doi: 10.1016/j.talanta.2015.11.032. Epub 2015 Nov 14.
A comprehensive strategy combining a quantitative method for 77 banned veterinary drugs, mycotoxins, ergot alkaloids and plant toxins, and a post-target screening for 425 substances including pesticides and environmental contaminants in feed were developed using a QuEChERS-based extraction and an ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS). The quantitative method was validated after previous statistical optimisation of the main parameters governing ionisation, and presented recoveries ranging, in general, from 80 to 120%, with a precision in terms of Relative Standard Deviation (RSD) lower than 20%. The full-scan accurate mass data were acquired with a resolving power of 50000 FWHM and a mass accuracy lower than 5ppm. The method LOQ was lower than 12.5µgkg(-1) for the majority of the veterinary drugs and plant toxins and 20µgkg(-1) for ergot alkaloids. For post-target screening a customised theoretical database including the exact mass, the polarity of acquisition and the expected adducts was built and used for post-run retrospective screening. The analytical strategy was applied to 32 feed samples collected from farms of the Valencia Region (Spain). Florfenicol, zearalenone and atropine were identified and quantified at concentrations around 10µgkg(-1). In the post-target screening of the real samples, Sulfadiazine, Thrimetoprin and Pirimiphosmethyl were tentatively identified.
采用基于QuEChERS的萃取方法和超高效液相色谱-高分辨率质谱联用技术(UHPLC-HRMS),开发了一种综合策略,该策略结合了对77种禁用兽药、霉菌毒素、麦角生物碱和植物毒素的定量方法,以及对饲料中包括农药和环境污染物在内的425种物质的靶向筛查方法。在对控制电离的主要参数进行统计优化后,对定量方法进行了验证,其回收率一般在80%至120%之间,相对标准偏差(RSD)精度低于20%。以50000 FWHM的分辨率和低于5ppm的质量精度采集全扫描精确质量数据。大多数兽药和植物毒素的方法定量限低于12.5µgkg(-1),麦角生物碱的定量限为20µgkg(-1)。对于靶向筛查,建立了一个定制的理论数据库,包括精确质量、采集极性和预期加合物,并用于运行后回顾性筛查。该分析策略应用于从西班牙巴伦西亚地区农场采集的32份饲料样本。氟苯尼考、玉米赤霉烯酮和阿托品的浓度约为10µgkg(-1),已被识别和定量。在实际样品的靶向筛查中,磺胺嘧啶、甲氧苄啶和甲基嘧啶磷被初步识别。