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A multi-residue method for GC-MS determination of selected endocrine disrupting chemicals in fish and seafood from European and North African markets

机译:来自欧洲和北非市场的鱼类和海鲜中所选内分泌的GC-MS测定的多残基方法

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摘要

An integrated study was conducted to determine the presence of six types of endocrine disrupting chemicals (bisphenol A, triclosan, two alkylphenols, two phenylphenols, eleven organophosphorus pesticides and seven parabens) in the fish and seafood samples from Europe and North Africa. The proposed method involves ultrasound-assisted extraction followed by continuous solid-phase extraction prior to GC-MS analysis. Analytical quality parameters such as linearity, accuracy, precision, sensitivity and selectivity were all good. Limits of detections ranged from 0.5 to 20.0 ng/kg. The relative standard deviation was lower than 7.5% and recoveries ranged from 84 to 105%. The method was successfully used to determine the target analytes in 20 fish and seafood samples from different fish shops and supermarkets in Europe and North Africa. Analyte contents spanned the range 4.6-730 ng/kg and were all below the maximum legally allowed limits. EDCs most frequently found in the samples analysed were dichlorvos, 2-phenylphenol and nonylphenol.
机译:进行了综合研究以确定鱼类和北非的鱼类和海鲜样品中六种类型的内分泌破坏化学物质(双酚A,三丙烷,两种烷基酚,两种羟基苯甲酸盐)和七种羟基苯磺酯。所提出的方法涉及超声辅助提取,然后在GC-MS分析之前连续固相萃取。分析质量参数,如线性,准确性,精度,灵敏度和选择性都很好。检测限范率范围为0.5至20.0 ng / kg。相对标准偏差低于7.5%,回收率范围为84至105%。该方法成功地用于确定来自欧洲和北非的不同鱼类商店和超市的20条鱼类和海鲜样品中的靶分析物。分析物内容截止了4.6-730 ng / kg的范围,并且均低于合法允许的限制。在分析的样品中最常发现的EDC是DhloLvos,2-苯基苯酚和壬基酚。

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