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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Halogenated phenolic compound determination in plasma and serum by solid phase extraction, dansylation derivatization and liquid chromatography-positive electrospray ionization-tandem quadrupole mass spectrometry
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Halogenated phenolic compound determination in plasma and serum by solid phase extraction, dansylation derivatization and liquid chromatography-positive electrospray ionization-tandem quadrupole mass spectrometry

机译:固相萃取,丹磺酰衍生化和液相色谱-正电喷雾电离串联四极杆质谱法测定血浆和血清中的卤代酚类化合物

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摘要

A robust, sensitive and accurate method was developed for the simultaneous determination in plasma and serum of suite a halogenated phenolic compounds (HPCs) for which several are known to persist in the environment and analytically pure standards are available. Namely, 14 congeners of hydroxylated polybrominated diphenyl ethers (OH-PBDEs), six congeners of hydroxylated polychlorinated biphenyls (OH-PCBs), pentachlorophenol, pentabromophenol and the flame retardant tetrabromobisphenol A (TBBPA). Solid phase extraction (SPE) enriched the target compounds and cleaned up the samples as a result of efficient adsorption on a strong anion-exchange solid phase SPE cartridge (Oasis MAX). After final clean-up the HPCs were derivatized with dansyl chloride and analyzed by liquid chromatography-tandem mass spectrometry with electrospray ionization in positive mode (ESI(+)). Chromatographic separation was achieved on a Luna PFP(2) column (2. mm × 100. mm, 3. μm particle size) with mobile phases of water and acetonitrile (both containing 0.1% formic acid). The addition of the dansyl moiety to the HPCs greatly improved analyte sensitivity as the electrospray ionization efficiency was enhanced. Instrument limits of detection (ILODs) for LC-ESI(+)-MS/MS analysis of the HPCs were in the range of 0.01-0.07. ng/mL and the method limits of quantification (MLOQs) were in the range of 0.02-0.15. ng/g. Recovery efficiencies of the suite of HPCs ranged from 64% to 118% with relative standard deviations from 2% to 12% from fortified bovine serum samples. The method was successfully applied for HPC determination in representative polar bear and snapping turtle plasma samples.
机译:开发了一种健壮,灵敏,准确的方法,可同时测定血浆和血清中的卤代酚类化合物(HPC),已知其中几种在环境中仍然存在,并且有分析纯的标准品可供使用。即,有14个同类的羟基化多溴二苯醚(OH-PBDEs),6个同类的羟基化多氯联苯(OH-PCBs),五氯苯酚,五溴苯酚和阻燃四溴双酚A(TBBPA)。固相萃取(SPE)富集了目标化合物,并通过在强阴离子交换固相SPE柱(Oasis MAX)上的有效吸附而净化了样品。最终清洁后,将HPC用丹磺酰氯衍生化,并通过液相色谱-串联质谱分析和电喷雾电离以正模式(ESI(+))进行分析。色谱分离是在Luna PFP(2)色谱柱(2. mm×100. mm,3μm粒径)上进行的,流动相为水和乙腈(均含有0.1%的甲酸)。随着电喷雾电离效率的提高,将丹磺酰基部分添加到HPC中大大提高了分析物的灵敏度。 LC-ESI(+)-MS / MS分析HPC的仪器检出限(ILOD)为0.01-0.07。 ng / mL和方法的定量限(MLOQ)在0.02-0.15之间。 ng / g。整套HPC的回收效率范围为64%至118%,相对于强化牛血清样品的相对标准偏差为2%至12%。该方法已成功用于代表性北极熊和鳄龟血浆样品中的HPC测定。

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