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    CHU Xiao-na, JIAO Xiu-yan, MU A-li, WU Yan, GENG Xun, LI Hui, FU Hong-lei, LI yan. Determination of Melamine Residue in Milk by HPLC-MS/MS[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2015, 51(3): 394-397.
    Citation: CHU Xiao-na, JIAO Xiu-yan, MU A-li, WU Yan, GENG Xun, LI Hui, FU Hong-lei, LI yan. Determination of Melamine Residue in Milk by HPLC-MS/MS[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2015, 51(3): 394-397.

    Determination of Melamine Residue in Milk by HPLC-MS/MS

    • HPLC-MS/MS was applied to measure melamine residue in milk. The sample was extracted with acetonitrile-water,purified by Waters Oasis MCX solid phase extraction column,dried by nitrogen at 50 ℃,dissolved with 1 mL of acetonitrile and used for HPLC-MS/MS analysis. Waters Hilic column (100 mm×2.1 mm,3 μm) was used as stationary phase,and a mixture (95+5) of acetonitrile and 5 mmol·L-1 of ammonium acetate as mobile phase. ESI+ and MRM were adopted in MS/MS. Internal standard method was used for quantization. Linearity range of melamine was within 10.0 μg·L-1,the detection limit (3S/N) was 0.5 μg·kg-1. Tests for recovery and precision were made by addition of melamine,giving values of recovery in the range of 99.8%-103% and values of RSD′s (n=10) in the range of 1.9%-3.2%.
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