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    GENG Jin-pei, CAO Peng, LIANG Jun-ni, XU Ying-jiang, LI Xiao-yu, LI Jin-qiang, SHA Mei-lan, MU Yan. UHPLC-MS/MS Determination of Residual Amounts of 8 Estrogens in Meat Products[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2012, 48(12): 1398-1402.
    Citation: GENG Jin-pei, CAO Peng, LIANG Jun-ni, XU Ying-jiang, LI Xiao-yu, LI Jin-qiang, SHA Mei-lan, MU Yan. UHPLC-MS/MS Determination of Residual Amounts of 8 Estrogens in Meat Products[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2012, 48(12): 1398-1402.

    UHPLC-MS/MS Determination of Residual Amounts of 8 Estrogens in Meat Products

    • UHPLC-MS/MS was applied to the determination of residual amounts of 8 kinds of estrogens, including octylphenol, 4-nonylphenol, bishphenol A, diethylstilbestrol, estrone, 17β-estradiol, 17α-ethinylestradiol and estriol, in meat products. The sample was extracted twice with acetic ether, which was concentrated and purified by HLB solid-phase extraction column. The eluate was evaporated to near dryness by N2-blowing and the residue was dissolved with methanol-water (1+9). ACQUITYTM BEH C18 chromatographic column was used for separation, using the mixed solutions of 5 mmol·L-1 ammonium acetate (containing φ 0.1% formic acid) and methanol as mobile phase in the gradient elution. ESI with negative ionization mode and multi-reactions monitoring mode were used in the MS/MS analysis. Values of detection limits (3S/N) found were in the range of 0.2-0.3 μg·kg-1. Values of recovery and RSD′s (n=6) were found in the ranges of 76.2%-108.3% and 4.3%-11.7%, respectively.
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