首页> 外文期刊>Journal of Agricultural and Food Chemistry >Simultaneous Quantitative Determination of Melamine and Cyanuric Acid in Cow's Milk and Milk-Based Infant Formula by Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry
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Simultaneous Quantitative Determination of Melamine and Cyanuric Acid in Cow's Milk and Milk-Based Infant Formula by Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry

机译:通过液相色谱 - 电喷雾电离串联质谱法同时定量测定牛奶和牛奶基婴儿配方的三聚氰胺和氰尿酸的测定

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An isotope dilution liquid chromatography-electrospray ionization tandem mass spectrometry method for the simultaneous determination of melamine and cyanuric acid in cow's milk (range of 0-6.3 mg/kg) and milk-based infant formulas (ranges of 0-0.3 and 0-2.0 mg/kg) is described. This quantitative method entails simple sample preparation, limited to a protein precipitation in acetoni-trile/water followed by a centrifugation and direct injection of the supernatant. Selected reaction monitoring of two diagnostic transition reactions for each analyte and each corresponding (~(13)C_3,~(15)N_3)-labeled compound enables selective and confirmatory detection. Acquisition was performed sequentially in the negative ion mode for cyanuric acid, while in the positive mode for melamine within the same run. Validation of the method was conducted according to European Union criteria (CD 2002/657/EC). Internal standard-corrected recoveries were within the 99-116% range for both analytes in the two matrix types, along with repeatability and intermediate reproducibility values of <12.3 and <31.2%, respectively. LODs were 0.025 and 0.050 mg/kg for melamine and cyanuric acid, respectively, whereas LOQs, set arbitrarily at the lowest fortification level, were 0.05 and 0.10 mg/kg for melamine and cyanuric acid, respectively. CCa and CCβ, at the 1 mg/kg maximum limit (ML) for infant formula powder endorsed by WHO, were respectively 1.03 and 1.05 mg/kg for melamine and 1.04 and 1.09 mg/kg for cyanuric acid.
机译:同位素稀释液相色谱 - 电喷雾电离串联质谱法,用于同时测定牛奶(0-6.3mg / kg)和牛奶基婴儿配方中的三聚氰胺和氰尿酸(0-0.3和0-2.0的范围描述了mg / kg)。这种定量方法需要简单的样品制备,限于乙酰纤维/水中的蛋白质沉淀,然后是离心和直接注射上清液。对每个分析物的两个诊断转变反应的选择反应监测,每种分析物和每个相应的(〜(13)C_3,〜(15)N_3) - 标记化合物可以选择性和确认检测。在氰尿酸的负离子模式中顺序地进行采集,同时在同一运行中的三聚氰胺的阳性模式。根据欧盟标准进行该方法的验证(CD 2002/657 / EC)进行。内部标准校正的回收率在两种矩阵类型中的分析物的99-116%范围内,以及重复性和中间再现性分别为<12.3和<31.2%。对于三聚氰胺和氰尿酸分别为0.025和0.050mg / kg的LOD,而LOQs,在最低强化水平下任意设定的LOQs,分别为三聚氰胺和氰尿酸的0.05和0.10mg / kg。 CCA和CCβ,在婴儿配方粉末的1mg / kg最大限制(ml),致幼儿配方粉末,分别为三聚氰胺和1.04和1.04和1.09mg / kg用于氰尿酸的1.03和1.05mg / kg。

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