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采用 81Br 标记标准品的同位素稀释气相色谱(电子轰击电离)质谱法测定优先多溴联苯醚。

Determination of priority polybrominated diphenyl ethers by isotope dilution gas chromatography(electron ionization)MS using 81Br-labeled standards.

机构信息

Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Spain.

出版信息

Anal Chem. 2011 Apr 15;83(8):3024-32. doi: 10.1021/ac103208j. Epub 2011 Mar 17.

Abstract

A mixture of (81)Br-labeled polybrominated diphenyl ethers (PBDEs), previously synthesized in our laboratory, was separated by liquid chromatography for the individual isolation of different (81)Br-labeled PBDEs containing from 3 to 6 bromine atoms. The different fractions were collected, and a mixed labeled standard was then prepared adequate for the determination of priority PBDEs (congeners 28, 47, 99, 100, 153, and 154) in environmental samples. The spike mixture was then characterized using gas chromatography(electron ionization)MS (GC(EI)MS) both in isotope composition and concentration in combination with multiple least-squares. Contamination from natural abundance BDEs 153 and 154 was detected in the spike mixture, and a new isotope dilution equation was developed to take into account the natural abundance contribution from the spike. The spike mixture was shown to be stable during at least 4 months, and no isotope exchange between natural abundance and labeled PBDEs was detected during this period of time. Finally, the (81)Br-labeled PBDEs standard was used for the determination of congeners 28 (+33), 47, 49, 99, 100, 153, and 154 in a standard reference material (Lake Michigan fish tissue SRM 1947) using three different sample to spike ratios. No methodological calibration needed to be prepared, as no isotopic effects were detected using this labeling mode. Concentrations found were in agreement with the certified concentrations (recoveries between 89% and 116%), and reproducibility was always below 7% RSD. Kragten procedure was used to calculate expanded uncertainties. Very low limits of detection were obtained for all compounds (between 0.02 and 0.9 ng·g(-1)) using the procedure developed here.

摘要

(81)Br 标记的多溴二苯醚(PBDEs)混合物,以前在我们的实验室中合成,通过液相色谱法进行分离,以实现不同含 3 至 6 个溴原子的(81)Br 标记 PBDEs 的单独分离。不同的馏分被收集起来,然后制备一个混合标记标准品,以用于环境样品中优先 PBDEs(同系物 28、47、99、100、153 和 154)的测定。该加标混合物然后使用气相色谱(电子电离)质谱(GC(EI)MS)进行了特征描述,结合同位素组成和浓度进行了多次最小二乘法拟合。在加标混合物中检测到天然丰度 BDEs 153 和 154 的污染,并且开发了一个新的同位素稀释方程,以考虑加标混合物中天然丰度的贡献。该加标混合物在至少 4 个月内是稳定的,并且在这段时间内没有检测到天然丰度和标记 PBDEs 之间的同位素交换。最后,使用(81)Br 标记的 PBDEs 标准品,通过三种不同的样品加标比,在标准参考物质(密歇根湖鱼组织 SRM 1947)中测定了同系物 28(+33)、47、49、99、100、153 和 154。由于未检测到同位素效应,因此无需制备方法校准。发现的浓度与认证浓度一致(回收率在 89%至 116%之间),重现性始终低于 7%RSD。使用 Kragten 程序计算扩展不确定度。使用这里开发的程序,对于所有化合物都获得了非常低的检测限(0.02 至 0.9 ng·g(-1))。

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