Cucurbit(n)uril-functionalized magnetic composite for the dispersive solid-phase extraction of perfluoroalkyl and polyfluoroalkyl substances in environmental samples with determination by ultra-high performance liquid chromatography coupled to Orbitrap high-resolution mass spectrometry

化学 检出限 萃取(化学) 轨道轨道 固相萃取 自来水 色谱法 高效液相色谱法 质谱法 吸附 环境化学 有机化学 环境工程 工程类
作者
Zhenzhen Huang,Peng Liu,Xia Lin,Yudong Xing,Yan Zhou,Yuehua Luo,Hian Kee Lee
出处
期刊:Journal of Chromatography A [Elsevier BV]
卷期号:1674: 463151-463151 被引量:18
标识
DOI:10.1016/j.chroma.2022.463151
摘要

• Magnetic composite Fe 3 O 4 @CB(7) was for the first time investigated for SPE. • Surface modification by CB(7) enhanced separation and enrichment of trace PFASs. • The method was successfully applied to environmental water and fish samples. Perfluoroalkyl and polyfluoroalkyl substances (PFASs) have raised serious public health concerns because of their potential adverse effects in humans as revealed by toxicological and epidemiological research. However, routine monitoring of PFASs is still challenging due to their trace levels in various environmental and biological matrices. In this study, magnetic composite materials based on iron (II, III) oxide (Fe 3 O 4) with surface functionalization by cucurbit(n)uril (CB(n)) (Fe 3 O 4 @CB(n)) (n = 6, 7, 8), were prepared and evaluated as new adsorbents for the magnetic solid-phase extraction of nine PFASs in lake water, tap water and fish muscle samples. The Fe 3 O 4 @CB(n) was characterized to examine their surface morphologies, sizes magnetism and thermal stability. Featuring good aqueous solution dispersibility, the macrocyclic structure of Fe 3 O 4 @CB(n) was also endowed with strong host-guest interactions, allowing extraction and enrichment capability towards the PFASs in complex matrices. MSPE using Fe 3 O 4 @CB(7) combination with ultra-high performance liquid chromatography coupled to Orbitrap high-resolution mass spectrometry, gave satisfactory quantitative analytical performance with low limits of detection of 0.004-0.04 μg L −1 and limits of quantification of 0.005-0.1 μg L −1 , linearities ranging from 0.01 to 10 μg L −1 with high coefficients of determination (R 2 ≥ 0.993), and enrichment factors (15-76) for the nine target PFASs. The method proved to be effective for the enrichment and analysis of trace levels of PFASs in genuine environmental water and fish muscle samples, indicating that Fe 3 O 4 @CB(7) has promising applicability as an adsorbent for these contaminants.
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