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Three-dimensional ionic liquid-ferrite functionalized graphene oxide nanocomposite for pipette-tip solid phase extraction of 16 polycyclic aromatic hydrocarbons in human blood sample

•PT-SPE method was developed for the enrichment of 16 PAHs in human blood.•The PT-SPE procedure was solvent-saving, reusable, and needed less blood sample.•The method provided referenced information for assessing risks of PAH exposure in China. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitousl...

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Published in:Journal of Chromatography A 2018-06, Vol.1552, p.1-9
Main Authors: Zhang, Yun, Zhao, Yong-Gang, Chen, Wei-Sheng, Cheng, He-Li, Zeng, Xiu-Qiong, Zhu, Yan
Format: Article
Language:English
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Summary:•PT-SPE method was developed for the enrichment of 16 PAHs in human blood.•The PT-SPE procedure was solvent-saving, reusable, and needed less blood sample.•The method provided referenced information for assessing risks of PAH exposure in China. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitously found in the environment and have been proved to be prospectively associated with the risk of cancer. In this study, a simple method based on pipette-tip solid phase extraction (PT-SPE) and gas chromatography-mass spectrometry (GC–MS) has been firstly developed for the determination of 16 PAHs in human whole blood. Three-dimensional ionic liquid-ferrite functionalized graphene oxide nanocomposite (3D-IL-Fe3O4-GO) was used as sorbent in PT-SPE. Compared with conventional SPE method, the PT-SPE method was solvent-saving (1.0 mL), reusable (at least 10 times) and required less blood sample (200 μL). Affecting parameters on extraction efficiency were investigated and optimized. Under the optimized conditions, a good linearity was obtained and the recoveries of 16 PAHs at three spiked levels ranged from 85.0% to 115%. The limits of quantification (LOQs) were in the range of 0.007-0.013 μg/L. Furthermore, the developed method was successfully applied to the analysis of 16 PAHs in 14 human blood samples. The results showed that the predominant PAHs in human whole blood was low-molecular-weight PAHs, with the rank order phenanthrene (PHE)> naphthalene (NAP)> fluorene (FLU)> fluoranthene (FLT)> pyrene (PYR). Because of its simplicity, accuracy and reliability, the PT-SPE method combined with GC–MS demonstrated the applicability for clinical analysis and provided more information for PAHs exposure studies.
ISSN:0021-9673
DOI:10.1016/j.chroma.2018.03.039