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An MAE-GPC-RRLC-MS/MS Method for Quantitative Determination of Rhodamine B Residue in Salted Pork |
LIU Hong-hua,ZHANG Li-kang,WU Wei,ZHANG Jing-xuan,ZHANG Yan |
1. The Sixteenth Secondary School of Tangshan, Tangshan 063000, China;
2. Hebei Key Laboratory of Food Security, Hebei Institute of Food Quality Supervision Inspection and Research, Shijiazhuang
050091, China;3. Department of Life Sciences, Tangshan Normal University, Tangshan 063000, China |
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Abstract A new method is developed for the determination of rhodamine B residue in salted pork by microwave extraction- gel permeation chromatography-rapid resolution liquid chromatography-tandem mass spectrometry (MAE-GPC-RRLC-MS/ MS) with multiple reaction monitoring (MRM) in positive ionization mode. Samples were extracted with tert-butyl methyl ether under microwave assistance and then cleaned up by gel permeation chromatography. The chromatographic separation was performed on an Agilent Plus C18 column using a mobile phase consisting of 0.1% aqueous formic acid and methanol. The limit of quantification (LOQ) of the RRLC-MS/MS method was 0.25 lag/kg and the linear range was between 1.0 μg/L and 100 μg/L with a correlation coefficient of 0.9998. The recovery rates of rhodamine B at the spike levels of 1.0, 3.0 μ g/kg and 5.0 μ g/kg were in the range of 71.1% to 102.0% with relative standard deviation between 5.1% and 17.1%. This method had the advantages of rapidity, accuracy and specificity and allowed sensitive and accurate qualification and quantification of rhodamine B.
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