首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development and validation of a multi-residue method for the determination of pesticides in honeybees using acetonitrile-based extraction and gas chromatography-tandem quadrupole mass spectrometry
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Development and validation of a multi-residue method for the determination of pesticides in honeybees using acetonitrile-based extraction and gas chromatography-tandem quadrupole mass spectrometry

机译:乙腈萃取-气相色谱-串联四极杆质谱法测定蜜蜂中农药残留的多残留方法的建立与验证

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An optimized analytical method employing gas chromatography-tandem quadrupole mass spectrometry (GC-MS/MS) has been developed for the simultaneous screening of roughly 150 pesticides in honeybees suspected of poisoning by pesticides during field spraying. In this work, a sample preparation approach based on acetonitrile extraction followed by dispersive solid-phase extraction (d-SPE) cleanup was implemented and validated for pesticides in honeybees for the first time. The procedure involved homogenization of a 2 g sample (23 insects on average) with acetonitrile-water mixture followed by salting out with citrate buffer, magnesium sulphate and sodium chloride. An amount of matrix constituents with limited solubility in acetonitrile was reduced in the extract by precipitation at low-temperature (freezing-out cleanup). Hereafter, d-SPE cleanup was carried out using primary secondary amine (PSA), octadecyl (08) and graphitized carbon black (GCB). This combination of cleanup steps ensured efficient extract purification. Linearity of the calibration curves was studied using matrix-matched standards in the concentration range between 4 and 500 ng mL(-1) (equivalent to 10 and 1250 ng g(-1)), and coefficients of determination (R-2) were >= 0.99 for approximately 90% of the targeted compounds. The recovery data were obtained by spiking honeybees samples free of pesticides at three concentration levels of 10, 50, and 500 ng g(-1) (approximately 0.9, 4.3, 43.5 ng per bee). At these spiking levels 47, 77 and 92% of the targeted compounds were recovered, respectively. Generally the recoveries were in the range between 70 and 120% with precision values, expressed as relative standard deviation (RSD) <= 20%. The expanded uncertainty was estimated following a "top down" empirical model as being 28% on average (coverage factor k = 2. confidence level 95%). Preliminary results from practical application to analysis of real samples are presented. A total of 25 samples of honeybees from suspected pesticides poisoning incidents were analyzed, in which 10 different pesticides were determined.
机译:已开发出一种采用气相色谱-串联四极杆质谱(GC-MS / MS)的优化分析方法,用于在田间喷涂过程中同时筛查涉嫌被农药中毒的蜜蜂中的大约150种农药。在这项工作中,首次实施了基于乙腈萃取然后进行分散固相萃取(d-SPE)净化的样品制备方法,并首次对蜜蜂中的农药进行了验证。该过程包括用乙腈-水混合物将2 g样品(平均23种昆虫)均质化,然后用柠檬酸盐缓冲液,硫酸镁和氯化钠盐析。通过在低温下沉淀(冷冻清除),减少了提取物中乙腈溶解度有限的基质成分的数量。此后,使用伯仲胺(PSA),十八烷基(08)和石墨化炭黑(GCB)进行d-SPE净化。净化步骤的这种组合确保了有效的提取物净化。使用浓度为4到500 ng mL(-1)(相当于10到1250 ng g(-1))的基质匹配标准液研究校准曲线的线性度,测定系数(R-2)为对于大约90%的目标化合物,≥0.99。通过以10、50和500 ng g(-1)的三种浓度水平(每只蜜蜂大约0.9、4.3、43.5 ng)加标不含农药的蜜蜂样品来获得回收率数据。在这些加标水平下,分别回收了47%,77%和92%的目标化合物。通常,回收率在70%至120%范围内,精度值表示为相对标准偏差(RSD)<= 20%。根据“自上而下”的经验模型,扩展后的不确定性估计为平均28%(覆盖率k =2。置信度95%)。给出了从实际应用到实际样品分析的初步结果。总共分析了25例涉嫌农药中毒事件的蜜蜂样品,其中确定了10种不同的农药。

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