首页> 外文期刊>Journal of Environmental Science and Health, Part B: Pesticides, Food Contaminants, and Agricultural Wastes >Multiresidue analysis of organochlorine and pyrethroid pesticides in ground beef meat by gas chromatography-mass spectrometry
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Multiresidue analysis of organochlorine and pyrethroid pesticides in ground beef meat by gas chromatography-mass spectrometry

机译:气相色谱-质谱法分析牛肉末中有机氯和拟除虫菊酯类农药的残留

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摘要

A multiresidue method was developed and optimized for the identification/quantification of organochlorine pesticides (OCPs) and pyrethroids (PYRs) in beef meat samples. Samples extraction was performed by an automated solvent extractor and the extracts were cleaned-up by a tandem-cartridge system consisting of an Extrelut NT3 combined with a Sep-Pack C18 cartridge and a florisil minicartridge. Analysis was finally carried out by gas chromatography coupled with quadrupole mass spectrometry (GC/MS). The performance of the method was investigated in terms of linearity, accuracy, precision, detection limit (LOD) and quantification limit (LOQ). Good linearity was obtained, with correlation coefficients (r2) higher than 0.98. Mean recoveries were found in the ranges 70-110 % and 84-99 % for the investigated OCPs and PYRs, respectively, with the exception of extremely volatile hexachlorobenzene (HCB). RSD% turned out to range from 2 to 15 %. LOQ values were in the range 0.005-0.1 mg/kg for either class of compounds. The method developed was successfully tested on 50 commercial beef meat samples from the market area of Rome (Italy), proving to be a useful tool in routine multiresidue analysis of OCPs and PYRs for monitoring purposes. None of the compounds of interest were observed above their respective LOQ.
机译:开发并优化了一种多残留方法,用于牛肉肉样品中有机氯农药(OCP)和拟除虫菊酯(PYR)的鉴定/定量。通过自动溶剂萃取器进行样品萃取,并通过串联式药筒系统对萃取物进行净化,该系统由Extrelut NT3结合Sep-Pack C18药筒和弗洛里西尔微型药筒组成。最后,通过气相色谱与四极杆质谱联用(GC / MS)进行分析。从线性,准确性,精密度,检测限(LOD)和定量限(LOQ)方面研究了该方法的性能。获得了良好的线性,相关系数(r 2 )高于0.98。除极易挥发的六氯苯(HCB)外,所研究的OCP和PYR的平均回收率分别在70-110%和84-99%的范围内。 RSD%的范围为2%至15%。任一类化合物的LOQ值都在0.005-0.1 mg / kg的范围内。所开发的方法已在罗马(意大利)市场上的50种商业牛肉样品上成功进行了测试,被证明是用于监测OCP和PYR的常规多残留分析的有用工具。在各自的LOQ以上均未观察到目标化合物。

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