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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Multi-dye residue analysis of triarylmethane, xanthene, phenothiazine and phenoxazine dyes in fish tissues by ultra- performance liquid chromatography-tandem mass spectrometry
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Multi-dye residue analysis of triarylmethane, xanthene, phenothiazine and phenoxazine dyes in fish tissues by ultra- performance liquid chromatography-tandem mass spectrometry

机译:高效液相色谱-串联质谱法分析鱼组织中的三芳基甲烷,an吨,吩噻嗪和吩恶嗪染料

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摘要

Beside the possible illegal use of malachite green in aquaculture, other familiar dyes could also been applied by fraudulent producers due to their antiseptic and antibacterial activity. In this contribution, a new sensitive multi-residue method was developed to determine triarylmethane, xanthene, phenothiazine and phenoxazine dyes in fish by ultra-performance liquid chromatography-tandem mass spectrometry. Samples were extracted with acetonitrile, followed by an oxidation step using 2,3-dichloro- 5,6-dicyanobenzoquinone. Further clean-up was performed by tandem solid phase extraction using weak and strong cation exchange cartridges. Extracts were analysed by UPLC-MS~n operating in the positive electrospray ionisation mode (ESI+). The fourteen dyes were separated within only 12 min on a C_(18) BEH column using 1 mM ammonium acetate in water at pH 4.5 and acetonitrile as mobile phases at a flowrate of 0.4 mL min~(-1). The presented method was validated as defined by the European Union and scientific literature. Good linearity (R ≥0.99 and goodness-of-fit (g) ≤10%) was achieved over the tested concentration range (0.25-2 ng g~(-1)). Limit of quantification was 0.25 ng g~(-1) for all dyes, with a signal-to-noise ratio of at least 10/1. This is at least 5 to 10 times lower than previous published methods. Limits of detection were all<0.1 ng g~(-1). Precision and trueness fell within the criteria requested by the EC requirements for this concentration range. Decision limit (CC_α) and detection capability (CC_β) were all<1 and<0.25 ng g~(-1), respectively. Due to background levels of the xanthene dyes, the two rhodamine dyes could only be determined above 0.75 ng g~(-1). For these dyes, the method can only be used for screening purposes. To show the applicability of the method, a monitoring study was performed to investigate the occurrence of artificial dyes in wildlife European eel in Flemish rivers
机译:除了可能在水产养殖中非法使用孔雀石绿外,欺诈性生产者还可能因其抗菌和抗菌活性而使用其他熟悉的染料。在这一贡献中,开发了一种新的灵敏的多残留方法,通过超高效液相色谱-串联质谱法测定鱼中的三芳基甲烷,x吨,吩噻嗪和吩恶嗪染料。用乙腈萃取样品,然后使用2,3-二氯-5,6-二氰基苯并醌进行氧化步骤。使用弱阳离子交换盒和强阳离子交换盒通过串联固相萃取进行进一步的净化。提取物通过在正电喷雾电离模式(ESI +)下运行的UPLC-MS分析。在C_(18)BEH色谱柱上,使用1 mM乙酸铵的pH 4.5水溶液和乙腈作为流动相,在0.4 mL min〜(-1)的流速下,仅在12分钟内即可分离出14种染料。所提出的方法已经过欧盟和科学文献的验证。在测试浓度范围(0.25-2 ng g〜(-1))内,具有良好的线性度(R≥0.99,拟合度(g)≤10%)。所有染料的定量限为0.25 ng g〜(-1),信噪比至少为10/1。这至少比以前发布的方法低5到10倍。检出限均<0.1 ng g〜(-1)。精确度和真实性均在EC要求的浓度范围内。决策极限(CC_α)和检测能力(CC_β)分别<1和<0.25 ng g〜(-1)。由于x吨染料的背景水平,两种罗丹明染料只能测定高于0.75 ng g〜(-1)。对于这些染料,该方法只能用于筛选目的。为了证明该方法的适用性,进行了一项监测研究,以调查佛兰德斯河野生欧洲鳗鱼中人工染料的存在

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