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一种通过液相色谱-串联质谱法同时测定虹鳟鱼中三苯甲烷染料残留量的快速简便方法。

A rapid and simple method for simultaneous determination of triphenylmethane dye residues in rainbow trouts by liquid chromatography-tandem mass spectrometry.

作者信息

Kaplan Muammer, Olgun Elmas O, Karaoglu Oznur

机构信息

Tubitak Marmara Research Centre, Food Institute, P.O. Box 21, 41470 Gebze, Kocaeli, Turkey.

Tubitak Marmara Research Centre, Food Institute, P.O. Box 21, 41470 Gebze, Kocaeli, Turkey.

出版信息

J Chromatogr A. 2014 Jul 4;1349:37-43. doi: 10.1016/j.chroma.2014.04.091. Epub 2014 May 6.

Abstract

A rapid and simple LC-MS/MS method was developed and optimized for screening and confirmation of triphenylmethane dyes including malachite green (MG), leucomalachite green (LMG), crystal violet (CV), leucocrystal violet (LCV) and brilliant green (BG) in fish muscle with skin. Leucocrystal violet D6 (LCV-D6) and leucomalachite green-D5 (LMG D5) was used as internal standards. Sample preparation is a simple procedure based on solid-liquid extraction with acetonitrile containing 1% acetic acid, followed by centrifugation and evaporation of the supernatant. The residue was dissolved in acetonitrile with 0.1% acetic acid and centrifuged prior to LC-MS/MS analysis. Chromatographic separation of analytes was performed on an Inertsil ODS-4 C18 column with ammonium acetate buffer in acetonitrile gradient. The mass detection was performed on a triple-quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) mode via electrospray ionization (ESI+). The developed method was validated according to the criteria set in Commission Decision 2002/657/EC. The decision limit (CCα) was 0.43, 0.24, 0.33, 0.28 and 0.17μgkg(-1) for MG, LMG, CV, LCV and BG respectively. The detection capability (CCβ) values obtained were 0.56, 0.31, 0.43, 0.37 and 0.22μgkg(-1), respectively. The precision of the method, expressed as relative standard deviation (RSD) values for the within-day and inter-day laboratory reproducibility, for MG, LMG, CV, LCV and BG at the four levels of fortification (0.3, 0.5, 1, and 2μgkg(-1)), was less than 16 and 19% respectively. Accuracy of the method was confirmed by successful participation of a proficiency test organized by FAPAS. The method has been used for the analysis of 208 fish samples of which seven samples were found to be non-compliant containing low residues of LMG and LCV.

摘要

建立并优化了一种快速简便的液相色谱-串联质谱法,用于筛查和确证带皮鱼肉中包括孔雀石绿(MG)、无色孔雀石绿(LMG)、结晶紫(CV)、无色结晶紫(LCV)和亮绿(BG)在内的三苯甲烷类染料。以无色结晶紫-D6(LCV-D6)和无色孔雀石绿-D5(LMG D5)作为内标。样品制备是一个基于用含1%乙酸的乙腈进行固液萃取的简单程序,随后进行离心并蒸发上清液。残渣用含0.1%乙酸的乙腈溶解,并在进行液相色谱-串联质谱分析前离心。分析物的色谱分离在Inertsil ODS-4 C18柱上进行,采用乙腈梯度的乙酸铵缓冲液。质量检测通过电喷雾电离(ESI+)在三重四极杆串联质谱仪上采用多反应监测(MRM)模式进行。所建立的方法根据欧盟委员会第2002/657/EC号决定中规定的标准进行了验证。MG、LMG、CV、LCV和BG的决策限(CCα)分别为0.43、0.24、0.33、0.28和0.17μg/kg(-1)。获得的检测能力(CCβ)值分别为0.56、0.31、0.43、0.37和0.22μg/kg(-1)。该方法的精密度,以日内和日间实验室重现性的相对标准偏差(RSD)值表示,对于MG、LMG、CV、LCV和BG在四个加标水平(0.3、0.5、1和2μg/kg(-1))下分别小于16%和19%。通过成功参加由FAPAS组织的能力验证试验确认了该方法的准确性。该方法已用于分析208份鱼类样品,其中7份样品被发现不符合标准,含有低残留的LMG和LCV。

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