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姜黄素在蜂蜜样品中几种多环芳烃的气相色谱-质谱测定前的深共晶溶剂分散微固相萃取中的应用。

Application of curcumin as a green and new sorbent in deep eutectic solvent-based dispersive micro-solid phase extraction of several polycyclic aromatic hydrocarbons from honey samples prior to gas chromatography-mass spectrometry determination.

机构信息

Food and Drug Safety Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Pharmaceutical Analysis Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

J Sep Sci. 2021 Nov;44(21):4037-4047. doi: 10.1002/jssc.202100354. Epub 2021 Sep 9.

DOI:10.1002/jssc.202100354
PMID:34459084
Abstract

A green, simple, and efficient dispersive micro-solid phase extraction method was developed for the extraction of polycyclic aromatic hydrocarbons from honey samples. In this method, for the first time, curcumin was used as an efficient and green sorbent to extract the analytes from the sample. After that the adsorbed analytes were eluted using a deep eutectic solvent prepared by mixing tetrabutylammonium chloride: ethylene glycol and analyzed by gas chromatography-mass spectrometry. Important experimental factors affecting adsorption and desorption steps of the method were optimized and under optimal experimental conditions, low limits of detection (0.14-0.37 ng/g) and quantification (0.49-1.3 ng/g), wide linear range (1.3-500 ng/g) with a coefficient of determination ≥0.994 were obtained. Relative standard deviation values for intra- and interday precisions were ≤7.5% for all of the analytes at a concentration of 2 ng/g for each analyte (n = 6). Extraction recovery of the method was in the range of 72-81%. Finally, 20 honey samples were analyzed and the analytes were successfully detected. The method is environment friendly because of the use of curcumin as a sorbent. Also, biodegradability of the used deep eutectic solvent components is another advantage of the method.

摘要

建立了一种绿色、简单、高效的分散微固相萃取方法,用于从蜂蜜样品中提取多环芳烃。在该方法中,首次使用姜黄素作为高效、绿色的吸附剂从样品中提取分析物。然后,使用由四丁基氯化铵:乙二醇混合制备的深共晶溶剂洗脱吸附的分析物,并通过气相色谱-质谱法进行分析。优化了影响方法吸附和解吸步骤的重要实验因素,在最佳实验条件下,该方法的检测限(0.14-0.37ng/g)和定量限(0.49-1.3ng/g)较低,线性范围较宽(1.3-500ng/g),相关系数≥0.994。对于每个分析物浓度为 2ng/g 的所有分析物,日内和日间精密度的相对标准偏差值均≤7.5%(n=6)。该方法的萃取回收率在 72-81%之间。最后,分析了 20 个蜂蜜样品,并成功检测到了分析物。由于使用姜黄素作为吸附剂,该方法对环境友好。此外,所使用的深共晶溶剂成分的可生物降解性是该方法的另一个优点。

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