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Determination of pesticides in milk-based infant formulas by pressurized liquid extraction followed by gas chromatography tandem mass spectrometry

机译:加压液相萃取-气相色谱串联质谱法测定乳基婴儿配方食品中的农药

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摘要

An efficient and selective automated analytical method for the determination and quantification of a selected group of 12 organochlorine and organophosphorous pesticides in milk-based infant formulas has been developed. The samples were extracted by pressurized liquid extraction (PLE) and analysed using GC-MS/MS. The use of alumina as the fat retainer in the PLE extraction cell, together with the application of an injector temperature program during the GC injection process, avoided typical matrix interferences without the application of additional cleanup steps. Mean recoveries of between 70 and 110% were achieved for most of the compounds, except for chlorpyrifos methyl (50%), vinclozoline (48%), fenitrothion (56%) and procymidone (53%), with relative standard deviations ranging from 9 to 17%. Low limits of quantification were obtained for the studied compounds, from 0.01 to 2.6 μg kg?1, thus guaranteeing their accurate determination within the rigorous requirements established for baby food. The validated method was applied to a pilot monitoring study in Spain. Twenty five samples of different brands of powdered infant formulas were obtained from supermarkets. Positive findings of endosulfan I, endosulfan II, fenitrothion, chlorpyrifos ethyl and bifenthrin were detected at concentrations ranging from 0.03 to 5.03 μg kg?1.
机译:已经开发出一种高效,选择性的自动分析方法,用于确定和定量乳基婴儿配方食品中的一组选定的12种有机氯和有机磷农药。通过加压液体萃取(PLE)萃取样品,并使用GC-MS / MS分析。在PLE萃取池中使用氧化铝作为脂肪滞留剂,以及在GC进样过程中使用进样器温度程序,避免了典型的基质干扰,而无需执行额外的净化步骤。除甲基毒死rif(50%),长春唑啉(48%),杀nitro硫酮(56%)和吡虫酮(53%)外,大多数化合物的平均回收率在70%至110%之间。相对标准偏差为9至17%。所研究化合物的定量限很低,为0.01至2.6μgkg?1 ,从而保证了其对婴儿食品的严格要求下的准确测定。经验证的方法已应用于西班牙的试点监测研究。从超市获得了二十五个不同品牌的婴儿配方粉的样品。在浓度范围为0.03至5.03μgkg?1 下,检测到硫丹I,硫丹II,杀,硫磷,毒死rif乙基和联苯菊酯的阳性结果。

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