首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of seven neonicotinoid insecticides in beeswax by liquid chromatography coupled to electros,mpray-mass spectrometry using a fused-core column
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Determination of seven neonicotinoid insecticides in beeswax by liquid chromatography coupled to electros,mpray-mass spectrometry using a fused-core column

机译:液相色谱-电喷雾质谱联用液相色谱法测定蜂蜡中七种新烟碱类杀虫剂

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摘要

A new method has been developed to measure seven neonicotinoid insecticides (acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam) in beeswax using liquid chromatography (LC) coupled to electrospray ionization mass spectrometry (ESI-MS) detection. Beeswax was melted and diluted in an n-hexane/isopropanol (8:2, v/v) mixture. After this, liquid extraction with water was performed followed by a clean-up on diatomaceous material based cartridges. The compounds were eluted with acetone, and the resulting solution was evaporated until dry and reconstituted with a mixture of water and acetonitrile 50:50 (v/v). The separation of all compounds was achieved in less than 15min using a C_(18) reverse-phase fused-core column (Kinetex? C_(18), 150mm×4.6mm i.d.) and a mobile phase composed of a mixture of 0.1% formic acid in water and acetonitrile in gradient elution mode at 0.5mL/min. This method was fully validated in terms of selectivity, linearity, precision and recovery. Low limits of detection and quantification could be achieved for all analytes ranging from 0.4 to 2.3μg/kg, and from 1.5 to 7.0μg/kg, respectively. Finally, the proposed method was applied to an analysis of neonicotinoid residues in beeswax samples from apiaries located close to fruit orchards.
机译:已开发出一种新方法来测量液相色谱(LC)与电喷雾电离质谱(ESI-MS)结合检测蜂蜡中的七种新烟碱类杀虫剂(扑热息痛,可比丁,双呋喃,吡虫啉,尼替吡喃,噻虫啉和噻虫嗪)。将蜂蜡熔化并在正己烷/异丙醇(8:2,v / v)混合物中稀释。此后,用水萃取液体,然后在基于硅藻土材料的药筒上进行清洁。用丙酮洗脱化合物,并将所得溶液蒸发直至干燥,并用水和乙腈以50:50(v / v)的混合物复溶。使用C_(18)反相熔核色谱柱(Kinetex?C_(18),150mm×4.6mm内径)和由0.1%甲酸混合物组成的流动相,可以在不到15分钟的时间内完成所有化合物的分离。以0.5mL / min的梯度洗脱模式将水和乙腈中的乙酸该方法在选择性,线性,精密度和回收率方面得到了充分验证。所有分析物的检出限和定量限均低,分别为0.4至2.3μg/ kg和1.5至7.0μg/ kg。最后,将所提出的方法用于分析果园附近蜂房蜂蜡样品中的新烟碱残留。

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