Analysis and Stability Study of Isoeugenol in Aquaculture Products by Headspace Solid-Phase Microextraction Coupled to Gas Chromatography–Mass Spectrometry

异丁醇 丁香酚 色谱法 固相微萃取 化学 质谱法 气相色谱-质谱法 气相色谱法 检出限 样品制备 有机化学
作者
Jessica P. Rafson,Sherri B. Turnipseed,Christine R. Casey,Amanda De Bono,Mark R. Madson
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:72 (25): 14411-14418 被引量:2
标识
DOI:10.1021/acs.jafc.4c02318
摘要

Headspace solid-phase microextraction coupled to gas chromatography–mass spectrometry (HS-SPME-GC-MS) offers an alternative analysis method for isoeugenol (an active ingredient in fish sedatives) that avoids the use of organic solvents, simplifies sample preparation, and can be fully automated. This work focuses on developing and evaluating an HS-SPME-GC-MS method for isoeugenol in aquaculture samples and testing the stability of isoeugenol itself. Because of isoeugenol's relatively low volatility, more polar SPME fiber coatings (polyacrylate and polydimethylsiloxane/divinylbenzene) had better performance and the headspace extractions took over 30 min to reach equilibrium. Additionally, it was found that isoeugenol was relatively unstable compared to a deuterated standard (d3-eugenol) in the presence of water. To address this, after the fish samples were homogenized with water, they were heated at 50 °C for 1 h prior to analysis for equilibration. By using the method developed in this work, isoeugenol's detection limits in multiple aquaculture matrices (shrimp, tilapia, and salmon) were in the low ng/g range (<15 ng/g), well below the target testing level (200 ng/g). Additionally, by adding d3-eugenol as an internal standard, excellent linearity (R2 > 0.98), accuracy (97–99% recoveries), and precision (5–13% RSDs) were all achieved.

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