Fast determination of sulfonamides and their acetylated metabolites from environmental water based on magnetic molecularly imprinted polymers

被引:38
作者
Chen, Haiyan [1 ]
Zhang, Yiqun [1 ]
Gao, Bo [2 ,3 ]
Xu, Yang [1 ]
Zhao, Qi [1 ]
Hou, Juan [1 ]
Yan, Jin [1 ]
Li, Guijie [1 ]
Wang, Hui [1 ]
Ding, Lan [1 ]
Ding, Jie [4 ]
Zhao, Chun [2 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Jilin Univ, Joint State Key Lab Integrated Optoelect, Changchun 130012, Peoples R China
[3] Jilin Agr Univ, Coll Resources & Environm Sci, Changchun 130018, Peoples R China
[4] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
关键词
Sulfonamides; Acetylated metabolites; Environmental water; Molecularly imprinted polymer; Magnetic; Scatchard analysis; Matrix effect; Liquid chromatography-tandem mass spectrometry; SOLID-PHASE EXTRACTION; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; SURFACE-WATER; MULTIRESIDUE DETERMINATION; GROUND-WATER; TRACE LEVELS; ANTIBIOTICS; SAMPLES; ANTIMICROBIALS;
D O I
10.1007/s11356-013-1795-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Group-selective magnetic molecularly imprinted polymers (MMIPs) that can extract four widely used sulfonamide antibiotics and their acetylated metabolites from environmental water were synthesized in this study. The MMIPs with saturation magnetization value of 16.7 emu g(-1) could be separated from the environmental water samples easily by the application of an adscititious magnetic field, reducing the time consumption of pretreatment. The extraction conditions were evaluated, and optimal extraction conditions were as follows: extraction time, 25 min; amount of polymers, 90 mg; washing solvent, 30 % methanol aqueous solution; and elution solvent, methanol-acetic acid (95:5, v/v). The target analytes were detected by liquid chromatography-tandem mass spectrometry, and the detection limits of the method are in the range of 0.38-1.32 ng L-1. The relative standard deviations of intra- and inter-day are in the range of 1.3-6.8 % and 1.7-9.1 %, respectively. The proposed method is suitable for the analysis of environmental water samples.
引用
收藏
页码:8567 / 8578
页数:12
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