谭峰

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:中国科学院大连化学物理研究所

学位:博士

所在单位:环境学院

学科:环境科学. 环境工程

办公地点:大连理工大学西部校区环境楼B623

联系方式:tanf@dlut.edu.cn

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An electrochemically enhanced solid-phase microextraction approach based on molecularly imprinted polypyrrole/multi-walled carbon nanotubes composite coating for selective extraction of fluoroquinolones in aqueous samples

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论文类型:期刊论文

发表时间:2012-05-21

发表刊物:ANALYTICA CHIMICA ACTA

收录刊物:SCIE、EI、PubMed

卷号:727

页面范围:26-33

ISSN号:0003-2670

关键字:Solid-phase microextraction; Molecularly imprinted polymer; Fluoroquinolones; High-performance liquid chromatography; Polypyrrole

摘要:In this study, an electrochemically enhanced solid-phase microextraction (EE-SPME) approach based on molecularly imprinted polypyrrole/multi-walled carbon nanotubes (MIPPy/MWCNTs) composite coating on Pt wire was developed for selective extraction of fluoroquinolone antibiotics (FQs) in aqueous samples. During the extraction, a direct current potential was applied to the MIPPy/MWCNTs/Pt fiber as working electrode in a standard three-electrode system, FQ ions suffered electrophoretic transfer to the coating surface and then entered into the shape-complimentary cavities by hydrogen-bonding and ion-exchange interactions. After EE-SPME extraction, the fiber was desorbed with desorption solvent for high-performance liquid chromatography (HPLC) analysis. Some parameters influencing EE-SPME extraction such as applied potential, extraction time, solution pH, ionic strength, and desorption solvent were optimized. EE-SPME showed good selectivity and higher extraction efficiency to FQs compared with that of traditional solid-phase microextraction. EE-SPME coupled with HPLC to determine FQs in water samples, the limits of detection (S/N = 3) for the selected FQs are 0.5-1.9 mu g L-1. The proposed method was successfully used to the analysis of FQs spiked urine and soil samples, with recoveries of 85.1-94.2% for the urine samples and 89.8-95.5% for the soil samples. (C) 2012 Elsevier B.V. All rights reserved.