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Analytical Study of Trichlorfon Residues in Kaki Fruit and Cauliflower Samples by Liquid Chromatography-Electrospray Tandem Mass Spectrometry

机译:液相色谱-电喷雾串联质谱法分析柿果和花椰菜样品中敌百虫的残留量

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A detailed analytical study on trichlorfon residues in selected vegetables samples has been carried out,focused on the reliable quantification and confirmation of this compound,and on stability of residues under storage.As a consequence,a rapid and sensitive LC-ESI-MS/MS method has been developed for the determination of residues of this insecticide in kaki fruit (flesh and peel) and cauliflower samples.Extraction was performed with acetonitrile using a high-speed blender.After 4-fold dilution of the extract with water,20 muL.was directly injected in the LC-ESI-MS/MS system (triple quadrupole),using matrix-matched standards calibration for quantification.Under optimized MS/MS conditions,limit of detections between 0.006 and 0.013 mg/kg were reached,and a limit of quantification of 0.05 mg/kg was established,with a runtime of only 15 min.Recoveries from spiked blank samples at 0.05 and 0.5 mg/kg were in the range 83-101% with relative standard deviations lower than 10%.The method was applied to treated and untreated samples collected from field residues trials,using quality control samples analysis for the evaluation of the method.Despite the acquisition of two MS/MS transitions in selected reaction monitoring mode,the analysis of treated samples revealed the presence of a chromatographic peak close to the analyte that corresponded to a trichlorfon isobaric compound that shared the same MS/MS transitions.This unusual situation in LC-MS/MS-based procedures required the application of an efficient chromatographic separation to avoid this interference.All experiments have been made in compliance with the principles of Good Laboratory Practices (GLP) and following the European SANCO guidelines for pesticides residue analysis (PRA).
机译:已对选定蔬菜样品中的敌百虫残留物进行了详细的分析研究,重点是对该化合物的可靠定量和确认以及残留物的稳定性。因此,快速而灵敏的LC-ESI-MS / MS建立了测定柿果(果肉和果皮)和花椰菜样品中这种杀虫剂残留量的方法,使用高速搅拌器用乙腈进行萃取,用水将提取物稀释4倍,然后稀释至20μL。将其直接注入LC-ESI-MS / MS系统(三重四极杆)中,使用与基质匹配的标准品进行定量。在优化的MS / MS条件下,检出限达到0.006至0.013 mg / kg之间建立了0.05 mg / kg的定量方法,运行时间仅为15分钟.0.05和0.5 mg / kg的加标空白样品的回收率在83-101%范围内,相对标准偏差低于10%。 ap对通过田间残留试验收集的处理和未处理样品进行分析,使用质量控制样品分析进行方法评估。尽管在选定的反应监测模式下获得了两个MS / MS转换,但对处理样品的分析表明存在色谱图接近于与具有相同MS / MS跃迁的敌百虫等压化合物相对应的分析物的峰。基于LC-MS / MS的程序中的这种不寻常情况要求应用有效的色谱分离来避免这种干扰。遵循良好实验室规范(GLP)的原则,并遵循欧洲SANCO农药残留分析(PRA)指南。

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