Department of Chemistry, University of Otago, Dunedin, New Zealand.
J Chromatogr A. 2011 Oct 14;1218(41):7242-7. doi: 10.1016/j.chroma.2011.08.052. Epub 2011 Aug 22.
Pressurized liquid extraction (PLE) combined with in-cell clean-up of co-extracts, so-called selective-PLE (S-PLE), is a fast and accepted method for the analysis of halogenated organic contaminants in fish. However, many of the existing methods were optimized for use with single classes of contaminants. The main objective of this research was to develop an S-PLE method that elutes a minimal amount of fats while simultaneously extracting halogenated pesticides, polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) from fat-rich fish. The optimized method uses n-hexane:dichloromethane (75:25, v/v) as the extraction solvent, a 0.0078 fat to fat-retainer ratio (FFR) with Florisil as the fat retainer, three individual 5-min extractions with flush volumes of 150% and a selection of labeled surrogate standards (isotope dilution). This method resulted in a mean recovery of 77% for all target analytes in spiked samples and an average relative standard deviation of 6.3%. The method was validated with a certified reference material; the mean measured analyte concentrations agreed with the reference values except in the case of individual endosulfan isomers. It is likely that interconversion from the beta- to alpha-endosulfan isomer had occurred in the CRM, resulting in low measured concentrations for beta-endosulfan and high measured concentrations for alpha-endosulfan when compared with the reference values. Finally, the method was tested on three fish species with varying fat content. Different contaminant patterns were observed in the various species.
加压液体萃取(PLE)与共提取物的细胞内净化相结合,即所谓的选择性 PLE(S-PLE),是一种快速且被接受的用于分析鱼类中卤代有机污染物的方法。然而,许多现有的方法都是针对单一类污染物进行优化的。本研究的主要目的是开发一种 S-PLE 方法,该方法在洗脱最少脂肪的同时,从富含脂肪的鱼类中同时提取卤代农药、多氯联苯(PCBs)和多溴二苯醚(PBDEs)。优化后的方法使用正己烷:二氯甲烷(75:25,v/v)作为萃取溶剂,脂肪与 Florisil 之比为 0.0078(FFR),Florisil 作为脂肪保留剂,三个单独的 5 分钟萃取,冲洗体积为 150%,并选择标记的替代标准品(同位素稀释)。该方法在加标样品中所有目标分析物的平均回收率为 77%,平均相对标准偏差为 6.3%。该方法用一种经过认证的参考物质进行了验证;除个别硫丹异构体外,测得的分析物浓度平均值与参考值一致。在 CRM 中,β-硫丹异构体很可能发生向α-硫丹异构体的转化,导致β-硫丹的测量浓度较低,而α-硫丹的测量浓度较高,与参考值相比。最后,该方法在三种脂肪含量不同的鱼类物种上进行了测试。在不同的物种中观察到不同的污染物模式。