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A rapid quantitative method of ultra performance liquid chromatography (UPLC) has been developed for the analysis of 17 amino acids in fish eggs from Acipenser schrenckii, Huso dauricus and Acipenser ruthenus. The analytes were hydrolyzed with 6 0 mol/L HCI. The extraction solution was concentrated under low pressure and neutralized with NaOH solution before derivatization with 6-aminoquinolyl-N-hydroxy-succinimidyl carbamate (AQC) as derivatization agent in borate buffer solution (pH 8.8). Gradient UPLC separation was performed on a C, column (BEH C18, 100 mm x2.1 mm, 1.7 micro m) with 30 mmol/L ammonium acetate (pH 3. 5 adjusted with formic acid) and acetonitrile (containing 0. 15% (v/v) formic acid and 30 mmol/L ammonium acetate) as the mobile phases at a flow rate of 0. 7 mL/min. The detection was carried out with a photo-diode array (PDA) detector and the wavelength was set at 260 nm. The linear ranges were from 5.0 to 1000 micro mol/L with the correlation coefficients (r2) &gt; or = 0. 995 0. The method was validated by the analysis of seven replicates. The 17 amino aci standards were spiked in fish eggs at three levels of 100, 500 and 750 micro mol/L, and the averag recoveries were 75.4% - 107.3% with the relative standard deviations of 2. 19% - 12.3%. The limits of detection (LOD) for the analytes were from 0.94 micro mol/L to 4.04 micro mol/L. The method was successfully applied to the analysis of the 17 amino acids in fish eggs from Acipenser schrenckii, Huso dauricus and Acipenser ruthenus. The method is simple, rapid, precise and reliable.

Determination of 17 amino acids in fish eggs by ultra performance liquid chromatography coupled with precolumn derivatization