首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of eugenol, isoeugenol and methyleugenol in fish fillet using gas chromatography coupled to tandem mass spectrometry
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Simultaneous determination of eugenol, isoeugenol and methyleugenol in fish fillet using gas chromatography coupled to tandem mass spectrometry

机译:气相色谱-串联质谱法同时测定鱼片中的丁香酚,异丁香酚和甲基丁香酚

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Gas chromatography (GC) coupled with triple quadrupole tandem mass spectrometry (MS/MS) operated in electron ionization mode (El) has been shown to have advantages in the trace analysis of chemical compounds. Employing the instrument, a method has been built to simultaneously determine eugenol, isoeugenol' and methyleugenol, which have been widely used as fish anesthetic, in the fish fillet. Procedure for the sample preparation was achieved by using hexane extraction followed by phenyl solid phase extraction (SPE) cleanup, which was free of such steps as rotary evaporation and nitrogen blowing by taking the volatility of eugenol and its isomers into consideration. The method was validated by conducting recovery studies on fortified fish fillet samples at four concentrations. The linearity in the range of 5-500 mu g-L-1 was forced through the origin giving a coefficient of determination (r(2)) greater than 0.9982. Limits of detection (LODs) for eugenol, isoeugenol' and methyleugenol were 0.4, 1.2' and 0.2 mu g.kg(-1), respectively. The limits of quantification (LOQs) were 1.2, 4' and 0.7 mu g.kg(-1) for eugenol, isoeugenol` and methyleugenol, respectively. The recoveries for eugenol and its isomers ranged from 76.4 to 99.9% with relative standard deviations (RSD) in a range from 2.18 to 15.5%. This method is quick, simple and suitable for determining the residues of eugenol, isoeugenol and methyleugenol simultaneously in batch samples of fish fillet. (C) 2016 Elsevier B.V. All rights reserved.
机译:气相色谱(GC)结合以电子电离模式(El)操作的三重四极杆串联质谱(MS / MS)在化合物的痕量分析中具有优势。利用该仪器,已建立了一种同时测定鱼片中丁香酚,异丁香酚和甲基丁香酚的方法,丁香酚,异丁香酚和甲基丁香酚被广泛用作鱼的麻醉剂。通过使用己烷萃取,然后进行苯固相萃取(SPE)净化来实现样品制备的程序,该步骤无需考虑旋香酚及其异构体的挥发性,而无需进行旋转蒸发和吹氮等步骤。通过对四种浓度的强化鱼片样品进行回收率研究验证了该方法的有效性。通过原点强制进行5-500μg-L-1范围内的线性,得出的测定系数(r(2))大于0.9982。丁香酚,异丁香酚和甲基丁香酚的检出限分别为0.4、1.2'和0.2μg.kg(-1)。丁子香酚,异丁子香酚和甲基丁子香酚的定量限(LOQs)分别为1.2、4'和0.7μg.kg(-1)。丁香酚及其异构体的回收率在76.4%至99.9%之间,相对标准偏差(RSD)在2.18%至15.5%之间。该方法快速,简便,适用于同时测定鱼片批次样品中的丁香酚,异丁香酚和甲基丁香酚的残留。 (C)2016 Elsevier B.V.保留所有权利。

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