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A sensitive and validated method for determination of melamine residue in liquid milk by reversed phase high-performance liquid chromatography with solid-phase extraction.

机译:固相萃取-反相高效液相色谱法测定液态奶中三聚氰胺残留的灵敏有效方法

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摘要

A sensitive and validated method for the determination of melamine residue in liquid milk is developed using reversed phase high-performance liquid chromatography-diode array detection (RP-HPLC-DAD) with solid-phase extraction (SPE). The conditions of the extraction, SPE and HPLC were investigated and optimized. The linearity is satisfactory in the range of 0.1-50 mug/mL with a correlation coefficient of 0.9998. Under the optimal conditions, the method limit of detection (LOD) and method limit of quantification (LOQ) were 18 mug/kg and 60 mug/kg, respectively. The recovery of melamine for milk samples spiked with 0.10-3mg/kg was in the range of 85.5-99.3% with the RSDs (n=3) of 2.3-3.7%. The intra-day assay precision (RSD) was 5.6% for five replicates of quality control milk sample at 2mg/kg level. Confirmation of the identities of melamine was achieved by monitoring the two transitions in multiple-reaction monitoring (MRM) mode, and has been applied successfully for the determination of melamine residue in liquid milk samples. The confirmatory method can permit the detection of melamine residues at levels as low as 60 mug/kg in different liquid milks
机译:使用固相萃取(SPE)的反相高效液相色谱-二极管阵列检测(RP-HPLC-DAD),开发了一种灵敏且经过验证的测定液态奶中三聚氰胺残留的方法。研究了提取条件,固相萃取和高效液相色谱条件。线性在0.1-50ug / mL的范围内令人满意,相关系数为0.9998。在最佳条件下,检测方法限(LOD)和定量方法限(LOQ)分别为18杯/千克和60杯/千克。加标0.10-3mg / kg的牛奶样品中三聚氰胺的回收率在85.5-99.3%的范围内,相对标准偏差(n = 3)为2.3-3.7%。质量控制乳样品在2mg / kg浓度下重复五次,其日内测定精度(RSD)为5.6%。三聚氰胺身份的确认是通过在多反应监测(MRM)模式下监测两个转变而实现的,已成功应用于液体奶样品中三聚氰胺残留的测定。验证方法可以检测出不同液态奶中三聚氰胺残留量低至60杯/千克

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