Preparation of molecularly imprinted polymer for use as SPE adsorbent for the simultaneous determination of five sulphonylurea herbicides by HPLC

被引:46
作者
Tang, Kaijie [1 ]
Gu, Xiaohong [2 ]
Luo, Qiushui [1 ]
Chen, Shangwei [2 ]
Wu, Leiyan [1 ]
Xiong, Jianhua [1 ]
机构
[1] Jiangxi Agr Univ, Coll Food Sci & Engn, Jiangxi Key Lab Nat Prod & Funct Food, Nanchang 330045, Jiangxi, Peoples R China
[2] Jiangnan Univ, State Key Lab Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
Molecularly imprinted polymers; Solid-phase extraction; Pyrazosulphuron ethyl; Rice grain; Sulphonylurea herbicides; SOLID-PHASE EXTRACTION; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; ENVIRONMENTAL WATER; SELECTIVE EXTRACTION; SAMPLES; CLEANUP; SILICA; RICE; ACID;
D O I
10.1016/j.foodchem.2013.10.152
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A high selective pre-treatment method for the analysis of sulphonylurea herbicides (SUHs) in rice grain samples based on molecularly imprinted solid-phase extraction (MISPE) was developed. The molecularly imprinted polymers (MIPs) were synthesised with high adsorption capacity and suitable particle size using pyrazosulphuron ethyl (PS) as the template and by screening three porogens and porogen volumes. The resulting MIPs showed high selectivity for PS. The MISPE procedure was developed for the purification and enrichment of PS, bensulphuron methyl (BSM), tribenuron methyl (TBM), metsulphuron methyl (MSM) and nicosulphuron (NS) from a rice grain sample prior to reversed-phase high-performance liquid chromatography (HPLC) analysis. Average recoveries of the PS, NS, MSM and BSM were 95.6%, 88.6%, 87.8% and 89.4%, respectively, but the recovery of TBM was lower (48.2%). This pre-treatment methodology for extracting SUHs was simple and cleaner extractions. The limits of detection ranged from 10.1 to 50.0 ng L-1. Five local rice grain samples were analysed by HPLC-MISPE, and PS was detected in all five samples, while BSM was detected in one sample. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:106 / 112
页数:7
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