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http://dx.doi.org/10.13103/JFHS.2017.32.2.89

Development and Validation of an Analytical Method for Glucuronolactone in Energy Drinks by Hydrophilic Interaction Liquid Chromatography-electrospray Tandem Mass Spectrometry  

Oh, Mi Hyune (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Lim, Moo Song (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Chai, Jeung Young (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Kim, Eun Jung (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Cho, Joong Hoon (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Lim, Chul Joo (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Choi, Sun Ok (Hazardous Substances Analysis Team, Gyeongin Regional Food & Drug Administration)
Publication Information
Journal of Food Hygiene and Safety / v.32, no.2, 2017 , pp. 89-95 More about this Journal
Abstract
A rapid, sensitive analytical method for glucuronolactone in beverages was developed and validated using hydrophilic interaction liquid chromatography coupled to electrospray ionization tandem mass spectrometry (HILIC-ESI-MS/MS). To determine the optimum analytical conditions for glucuronolactone, three different kinds of HILIC columns and two mobile phases with different pH values were examined. An amide-bonded stationary phase with a pH 9 acetonitrile-rich mobile phase was the best condition in terms of column retention, ESI-MS/MS response area, and signal-to-noise ratio. After extraction, glucuronolactone was separated through the HILIC amide column and detected by negative ESI-MS/MS in selected reaction monitoring (SRM) mode. Nine energy drinks sold in Korea were spiked with glucuronolactone at a concentration of 5 ng/mL; the Monster $Energy^{TM}$ sample showed the smallest peak area and its signal-to-noise ratio was used for method validation. Good linearity was obtained in the concentration range from 20 to 1500 ng/mL with a correlation coefficient > 0.998. The developed method had a limit of detection (LOD) of 6 ng/mL and a limit of quantitation (LOQ) of 20 ng/mL. The recovery of this method at concentration of 20, 100, 500, and 1000 ng/mL was 96.3%-99.2% with relative standard deviations (RSD) of 1.6%-14.0%. A reproducibility precision assessment at concentration of 100 and 500 ng/mL was carried out among three laboratories. The recovery of that evaluation was 95.1%-102.3% with RSD of 2.7%-7.0%. An analysis of variance indicated that there was no difference between the recovery results of the three laboratories at the 5% significance level. The validated method is applicable to inspecting beverages adulterated with glucuronolactone in Korea.
Keywords
Glucuronolactone; Energy drink; Analysis method; HILIC; ESI-MS/MS;
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