The present application relates to the technical field of determination of nifursol
metabolite content, and particularly relates to a method for determining the residual amount of nifursol
metabolite in
royal jelly. The method comprises the following steps: the
royal jelly sample is sequentially subjected to
trichloroacetic acid hydrolysis, o-nitrobenzaldehyde
derivatization and
ethyl acetate purification, and is treated with
acetonitrile aqueous solution to constant volume, the pretreated sample is subjected to
gradient elution using 5 mmol / L
ammonium acetate
aqueous solution-
acetonitrile as a mobile phase, and is determined by liquid
chromatography-
tandem mass spectrometry, and the isotopic
internal standard method is used for qualitative and quantitative analysis during determination. The
royal jelly sample is hydrolyzed using a
trichloroacetic acid solution before
derivatization treatment, so that the to-be-measured component is well separated from the sample matrix, the matrix influence is reduced, and then the liquid
chromatography-
tandem mass spectrometry analysis is performed in combination with the selection of the mobile phase and the isotopic
internal standard method, thereby improving the qualitative and
quantitative accuracy of the residual amount of nifursol
metabolite in royal jelly.