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    SONG Xin, HANG Xueyu, WANG Qin, WANG Lu, FENG Xiaoqing. HPLC-MS/MS Determination of 4-Nonyl Phenol in Edible Vegetable Oils[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2018, 54(5): 611-615. DOI: 10.11973/lhjy-hx201805026
    Citation: SONG Xin, HANG Xueyu, WANG Qin, WANG Lu, FENG Xiaoqing. HPLC-MS/MS Determination of 4-Nonyl Phenol in Edible Vegetable Oils[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2018, 54(5): 611-615. DOI: 10.11973/lhjy-hx201805026

    HPLC-MS/MS Determination of 4-Nonyl Phenol in Edible Vegetable Oils

    • HPLC-MS/MS was applied to the determination of 4-nonyl phenol (4-NP) in edible vegetable oils. The sample of edible vegetable oil was dissolved in mixture of ethyl acetate-cyclohexane (1+1),and then purified by gel permeation chromatography, through collecting the fractions between 14.0 to 17.0 min, and the solution obtained was evaporated to near dryness at 30℃. The residue was taken up and diluted to 1.0 mL with methanol. In HPLC separation, Agilent Poroshell120ec-C18 chromatographic column was used as stationary phase, and the mixture of methanol and 0.1% (mass fraction) ammonia solution mixed in different ratios was used as mobile phase in gradient elution. In MS/MS determination, ESI- and multi-reactions monitor mode were adopted. 4-n-NP-D4 was used as internal standard and blank corn oil was used as matrix. Linearity range of 4-NP was found between 0.25 μg·kg-1 and 160 μg·kg-1 with detection limit (3S/N) of 1.00 μg·kg-1. Tests for recovery were made by standard addition method at 3 concentration levels of 2.00, 5.00, 10.00 μg·kg-1, giving values of recovery and RSD's (n=6) in the ranges of 99.0% to 115% and 4.3% to 8.1% respectively.
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