文献类型：期刊文献

英文题名：A magnetic solid phase extraction microfluidic chip coupled with gas chromatography-mass spectrometry for the determination of polycyclic aromatic hydrocarbons in aqueous samples

作者：Sun, Yangkun[1];Ruan, Shengli[1];Zhou, Yuanyuan[1];Zhao, Linhao[1];Xiong, Wenjing[1];Lin, Chuhui[1];Kuang, Jingjing[1];Ning, Fanghong[2];Zhang, Min[3];Zhang, Hongyang[1];Hu, Ping[1]

机构：[1]East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Biotechnol, Shanghai 200237, Peoples R China;[3]East China Univ Sci & Technol, Sch Pharm, Shanghai Frontiers Sci Ctr Optogenet Tech Cell Met, State Key Lab Bioreactor Engn,Optogenet & Synthet, Shanghai 200237, Peoples R China

年份：2023

卷号：1708

外文期刊名：JOURNAL OF CHROMATOGRAPHY A

收录：;EI(收录号：20233714724512);WOS:【SCI-EXPANDED(收录号:WOS:001075878200001)】；

基金：Acknowledgments This research was funded by the National Natural Science Founda-tion of China (Grant number 81973285) .

语种：英文

外文关键词：Microfluidic chip; Magnetic solid phase extraction; GC-MS; Polycyclic aromatic hydrocarbon; Bi-functional magnetic nanoparticle

摘要：In this paper, we designed and manufactured a reliable magnetic solid phase extraction (MSPE) microfluidic chip for determination of polycyclic aromatic hydrocarbons (PAHs) in water combined with gas chromatographymass spectrometry. Sample loading, washing and elution are implemented with microinjection pump and integrated on a single chip, which reduced manual operation. Magnets were used to fix octadecyl/phenyl bifunctional Fe3O4@SiO2 extractant to avoid the design of weir structure in extraction chamber. The whole microfluidic chip was simple and low cost. Based on the microfluidic chip extraction platform, the on-chip MSPE method for the determination of PAHs was optimized and established. The results showed that this method required only 2 mL of sample, 2 mg of extractant, and 50 mu L of elution organic solvent for whole on-chip MSPE process, which was environmentally friendly and consistent with green chemistry. Method verification results were displayed which the linear range of five PAHs was between 1-100 ng/mL with good linearity (R2 >= 0.9985), and the detection limits (S/N = 3) were 0.08-0.26 ng/mL. The RSDs of intra-day precision (n=6) and inter-day precision (n=9) for PAHs were less than 6.1 % and 7.2 %, respectively. Enrichment factors were determined to be 31.3-37.7. The recoveries of river water, tap water, bottle water, waste water and urine at three spiked levels were in the range of 89.9% to 113.7% and the matrix effect values were between 83.8% to 109.6%. The extraction platform has the advantages of accurate analysis, simple design and cost-effective, which is conducive to the widespread use of microfluidic chips