PMID- 28153235 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20180222 LR - 20180222 IS - 1873-3573 (Electronic) IS - 0039-9140 (Linking) VI - 165 DP - 2017 Apr 1 TI - Fabrication of a polymeric ionic liquid-based adsorbent for multiple monolithic fiber solid-phase microextraction of endocrine disrupting chemicals in complicated samples. PG - 152-160 LID - S0039-9140(16)30993-6 [pii] LID - 10.1016/j.talanta.2016.12.043 [doi] AB - A multiple monolithic fiber solid-phase microextraction (MMF-SPME) utilizing polymeric ionic liquid-based adsorbent was prepared. The adsorbent was obtained by in situ copolymerization of an ionic liquid, 1-trimethyl-(4-vinylbenzyl) aminium chloride and dual cross-linkers (divinylbenzene and ethylenedimethacrylate). The effect of preparation conditions including the content of ionic liquid and porogen in the polymerization mixture on extraction performance was studied in detail. Infrared spectroscopy, elemental analysis, scanning electron microscopy and mercury intrusion porosimetry were used to inspect the physicochemical properties of the new adsorbent. The applicability of the new MMF-SPME was demonstrated by the extraction of trace endocrine disrupting chemicals (EDCs). Results indicated that the prepared MMF-SPME could extract EDCs effectively through multi-interactions such as ion-exchange, pi-pi and hydrophobic interactions. After optimization of extraction parameters, a method of MMF-SPME coupled to high performance liquid chromatography/diode array detection was conducted to detect trace EDCs in complicated samples including environmental water and human urine. The limits of detection (S/N=3) and quantification (S/N=10) for targeted compounds were 0.011-0.065mug/L and 0.036-0.21mug/L, respectively. Satisfactory precision was also achieved by evaluating the repeatability and intermediate precision with relative standard deviations (RSDs) of less than 9% and 10%, respectively. At the same time, the proposed method was successfully applied for the determination of EDCs in water and human urine with spiking recoveries ranged from 70.6% to 119%. CI - Copyright (c) 2016 Elsevier B.V. All rights reserved. FAU - Pei, Miao AU - Pei M AD - State Key Laboratory of Marine Environmental Science, Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, The Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, College of the Environment and Ecology, Xiamen University, Xiamen 361005, China. FAU - Zhang, Zirui AU - Zhang Z AD - State Key Laboratory of Marine Environmental Science, Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, The Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, College of the Environment and Ecology, Xiamen University, Xiamen 361005, China. FAU - Huang, Xiaojia AU - Huang X AD - State Key Laboratory of Marine Environmental Science, Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, The Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, College of the Environment and Ecology, Xiamen University, Xiamen 361005, China. Electronic address: hxj@xmu.edu.cn. FAU - Wu, Yuanfei AU - Wu Y AD - College of Chemistry and Chemical Engineering, Xiamen University, China. Electronic address: yfw@xmu.edu.cn. LA - eng PT - Journal Article DEP - 20161221 PL - Netherlands TA - Talanta JT - Talanta JID - 2984816R OTO - NOTNLM OT - Adsorbent OT - Endocrine disrupting chemicals OT - Multiple monolithic fiber solid-phase microextraction OT - Polymeric ionic liquid OT - Urine EDAT- 2017/02/06 06:00 MHDA- 2017/02/06 06:01 CRDT- 2017/02/04 06:00 PHST- 2016/11/02 00:00 [received] PHST- 2016/12/09 00:00 [revised] PHST- 2016/12/20 00:00 [accepted] PHST- 2017/02/04 06:00 [entrez] PHST- 2017/02/06 06:00 [pubmed] PHST- 2017/02/06 06:01 [medline] AID - S0039-9140(16)30993-6 [pii] AID - 10.1016/j.talanta.2016.12.043 [doi] PST - ppublish SO - Talanta. 2017 Apr 1;165:152-160. doi: 10.1016/j.talanta.2016.12.043. Epub 2016 Dec 21.