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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of organophosphorus pesticides in ginseng by carbon nanotube envelope-based solvent extraction combined with ultrahigh-performance liquid chromatography mass spectrometry
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Determination of organophosphorus pesticides in ginseng by carbon nanotube envelope-based solvent extraction combined with ultrahigh-performance liquid chromatography mass spectrometry

机译:碳纳米管包膜溶剂萃取-超高效液相色谱质谱法测定人参中的有机磷农药

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摘要

A miniature extraction envelope containing multiwall carbon nanotubes, diatomite, neutral alumina, and anhydrous magnesium sulfate was developed for the solvent extraction of organophosphorus pesticides in dried ginseng. After the powder of dried ginseng sample was introduced into the envelope, the envelope was heat sealed and sonicated in acetonitrile for the extraction and clean-up of analytes. The resulting extracts were analyzed by an ultrahigh-performance liquid chromatograph with an electrospray ion source and a quadrupole orbitrap mass spectrometer (UHPLC-ESI/Q-Orbitrap MS) under target-MS2 mode, and the analytes were quantified by matrix-match calibration. Finally, the simultaneous identification and quantification of 19 pesticide residues were carried out by the present method. It is noteworthy that in this method the processes of extraction and clean-up for the analytes could be carried out and accomplished in one step. The recoveries and relative standard deviations (RSDs) of analytes were in the range of 82.6-110.8% and 1.0-10.6%, respectively. The limits of detection (LODs) and quantification (LOQs) for analytes were determined to be 0.08-0.29 mu g kg(-1) and 0.26-0.98 mu g kg(-1), respectively. Several pesticide residues investigated in this study were found in 4 real samples, with the concentrations lower than the maximum residue limit (0.050 mg kg(-1)) established by European Union. (C) 2016 Elsevier B.V. All rights reserved.
机译:开发了一种包含多壁碳纳米管,硅藻土,中性氧化铝和无水硫酸镁的微型萃取封套,用于溶剂萃取人参中的有机磷农药。将干燥的人参样品粉末引入外壳后,将外壳热封并在乙腈中超声处理,以提取和纯化分析物。在具有目标MS2模式的超高效液相色谱仪上通过电喷雾离子源和四极Orbitrap质谱仪(UHPLC-ESI / Q-Orbitrap MS)对所得提取物进行分析,并通过基质匹配校准对分析物进行定量。最后,通过本方法同时鉴定和定量了19种农药残留。值得注意的是,在这种方法中,分析物的提取和净化过程可以一步完成并完成。分析物的回收率和相对标准偏差(RSD)分别在82.6-110.8%和1.0-10.6%之间。分析物的检出限(LOD)和定量限(LOQ)分别确定为0.08-0.29μg kg(-1)和0.26-0.98μgkg(-1)。在4个实际样品中发现了本研究中调查的几种农药残留,其浓度低于欧盟规定的最大残留限量(0.050 mg kg(-1))。 (C)2016 Elsevier B.V.保留所有权利。

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