Abstract
In this study, we developed a new method for the accurate quantification of eugenol in fish samples based on stable isotope dilution assay (SIDA) and solid-phase extraction (SPE) coupled gas chromatography–triple quadrupole mass spectrometry (SIDA-SPE-GC-MS/MS). Due to the difference of matrix effect (ME), it was difficult to determine accurately the level of eugenol residue in different fish and shrimp samples based on external standard calibration method. SIDA was applied to compensate matrix effect (ME) that eugenol-d3 was used as internal standard (IS). Freshwater fish (carp, channel catfish), marine fish (turbot), and shrimp (Penaeus vannawei) were used for the method validation. The average recoveries of eugenol were in the range of 94.7 to 109.78 % when the spiking levels were 10, 50, and 200 μg kg−1. The inter-day and intra-day precisions were in the range of 1.15–8.19 and 0.71–8.45 %. The limit of detection (LOD) and the limit of quantification (LOQ) were approximately 2.5 and 5.0 μg kg−1. This method was applied to the real fish samples assay obtained from aquaculture markets in Beijing, China. Eugenol residue was found in two fish samples with the levels at 6.2 and 7.7 μg kg−1, respectively.
Similar content being viewed by others
References
Popovic NT, Strunjak-Perovic I, Coz-Rakovac R, Barisic J, Jadan M, Berakovic AP, et al. Tricaine methane-sulfonate (MS-222) application in fish anaesthesia. J Appl Ichthyol. 2012;28:553–64.
Weber RA, Peleteiro JB, García Martín LO, Aldegunde M. The efficacy of 2-phenoxyethanol, metomidate, clove oil and MS-222 as anaesthetic agents in the Senegalese sole (Solea senegalensis Kaup 1858). Aquaculture. 2009;288:147–50.
Kildea MA, Allan GL, Kearney RE. Accumulation and clearance of the anaesthetics clove oil and AQUI-STM from the edible tissue of silver perch (Bidyanus bidyanus). Aquaculture. 2004;232(1–4):265–77.
Li JC, Zhang J, Yang L. Optimization of solid-phase-extraction cleanup and validation of quantitative determination of eugenol in fish samples by gas chromatography–tandem mass spectrometry. Anal Bioanal Chem. 2015;407(21):6563–8.
Wang CF, Fan A, Zhu X, Lu Y, Deng SH, Gao WC, et al. Trace quantification of 1-triacontanol in beagle plasma by GC-MS/MS and its application to a pharmacokinetic study. Biomed Chromatogr. 2015;29(5):749–55.
Dagan L, Reillon F, Roland A, Schneider R. Development of a routine analysis of 4-mercapto-4-methylpentan-2-one in wine by stable isotope dilution assay and mass tandem spectrometry. Anal Chim Acta. 2014;821:48–53.
Chen Y, Guo Z, Wang X, Qiu C. Sample preparation. J Chromatogr A. 2008;1184:191–219.
Song S, Ma X, Li C. Multi-residue determination method of pesticides in leek by gel permeation chromatography and solid phase extraction followed by gas chromatography with mass spectrometric detector. Food Control. 2007;18(5):448–53.
Angioni A, Pintore GA, Caboni P. Determination of wine aroma compounds by dehydration followed by GC/MS. J AOAC INTERNATIONAL. 2012;95(3):813–9.
Nielsen KF, Madsen JØ. Determination of ergosterol on mouldy building materials using isotope dilution and gas chromatography–tandem mass spectrometry. J Chromatogr A. 2000;898(2):227–34.
European Commission Decision 2002/657/EC. Implementing council directive 96/23/EC concerning the performance of analytical methods and the interpretation of results. Off J Eur Commun (2002), L221.
Chatterjee NS, Utture S, Banerjee K, Shabeerb TPA, Kamble N, Mathewa S, et al. Multiresidue analysis of multiclass pesticides and polyaromatic hydrocarbons in fatty fish by gas chromatography tandem mass spectrometry and evaluation of matrix effect. Food Chem. 2016;196:1–8.
Meinertz JR, Schreier TM, Porcher ST, Smerud JR. Evaluation of a method for quantifying eugenol concentrations in the fillet tissue from freshwater fish species. J AOAC Int. 2016;99(2):558–64.
Japanese positive list system for agricultural chemical residues in foods—maximum residue limits (MRLs) list of agricultural chemicals in foods. http://www.m5.ws001.squarestart.ne.jp/foundation/agrdtl.php?a_inq=51100.
US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM): guidance for industry, bioanalytical method validation, 2001. Available from: http://www.fda.gov/cder/guidance/index.htm.
Acknowledgments
This research was supported by the Special Scientific Research Funds for Central Non-profit Institutes, Chinese Academy of Fishery Sciences (2016ZD1104).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
All animal procedures were approved and conducted under the guidelines of the Chinese Academy of Fishery Sciences (Beijing, China).
Conflict of interest
The authors declare that they have no competing interests.
Rights and permissions
About this article
Cite this article
Li, J., Liu, H., Wang, C. et al. Determination of eugenol in fish and shrimp muscle tissue by stable isotope dilution assay and solid-phase extraction coupled gas chromatography–triple quadrupole mass spectrometry. Anal Bioanal Chem 408, 6537–6544 (2016). https://doi.org/10.1007/s00216-016-9850-z
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00216-016-9850-z