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Application of QuEChERS-based purification coupled with isotope dilution gas chromatography-mass spectrometry method for the determination of N-nitrosamines in soy sauce

机译:基于QuEChERS的纯化结合同位素稀释气相色谱-质谱法测定酱油中的亚硝胺

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摘要

A sensitive and rapid method involving an improved approach called the quick, easy, cheap, effective, rugged, and safe (QuEChERS) purification method and isotope dilution gas chromatography-mass spectrometry (GC-MS) was established to determine six N-nitrosamines (NAs) in soy sauce. Samples were firstly extracted by ethyl acetate. Then the extraction solution was concentrated by slow nitrogen gas blowing and subsequently purified using the QuEChERS-based purification method. Separation of six target NAs was performed on an INNOWAX polar capillary chromatographic column. All of the samples were detected by selected ion monitoring (SIM) mode of GC-MS and N-nitrosodimethylamine-d(6) (NDMA-d(6)) and N-nitrosodipropylamine-d(14) (NDPA-d(14)) were used as internal standards. The developed method was validated in terms of the linearity, limit of detection (LOD), matrix effects, specificity, accuracy and precision. Results indicated that this method is of good specificity with almost negligible matrix effects. Linear relations of six NAs were favourable in the range of 2.0-200 mu g L-1 and the correlation coefficients were greater than 0.9994. The LODs were lower than 1 mu g kg(-1) (0.4-0.9 mu g kg(-1)) and the limits of quantitation (LOQs) of the method were within the range of 1.2-3.0 mu g kg(-1). The mean recoveries for negative light and dark soy sauce samples at three spiked concentration levels were in the range of 80.2-112% with overall relative standard deviation (RSD) values (n = 6) of 2.5-6.8%. The validated method was simple and rapid, with good repeatability, and was successfully applied to determine the concentrations of NAs in soy sauce.
机译:建立了灵敏快速的方法,涉及一种称为快速,简便,廉价,有效,坚固耐用且安全的改进方法(QuEChERS)纯化方法和同位素稀释气相色谱-质谱法(GC-MS),以确定六种N-亚硝胺( NAs)在酱油中。样品首先用乙酸乙酯萃取。然后,通过缓慢吹入氮气浓缩萃取液,然后使用基于QuEChERS的纯化方法进行纯化。在INNOWAX极性毛细管色谱柱上进行六个目标NA的分离。通过选择的GC-MS离子监测(SIM)模式和N-亚硝基二甲胺-d(6)(NDMA-d(6))和N-亚硝基二丙胺-d(14)(NDPA-d(14) ))用作内部标准。所开发的方法在线性,检测限(LOD),基质效应,特异性,准确性和精密度方面得到了验证。结果表明,该方法具有良好的特异性,几乎没有基质效应。六个NA的线性关系在2.0-200μgL-1的范围内是有利的,并且相关系数大于0.9994。 LOD低于1μg kg(-1)(0.4-0.9μg kg(-1)),该方法的定量限(LOQs)在1.2-3.0μg kg(-1)范围内)。三种加标浓度的淡味和深色酱油样品的平均回收率在80.2-112%的范围内,总相对标准偏差(RSD)值(n = 6)为2.5-6.8%。经过验证的方法简便,快速,重复性好,已成功用于测定酱油中NAs的浓度。

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