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    分子印迹固相萃取-高效液相色谱法测定果蔬中4种有机磷类农药的残留量

    Determination of Residues of 4 Organophosphorus Pesticides in Fruits and Vegetables by High Performance Liquid Chromatography after Solid Phase Extraction with Molecularly Imprinted Polymers

    • 摘要: 以4种目标物丙溴磷、毒死蜱、二嗪磷、辛硫磷的混合物作为模板分子,乙二醇二甲基丙烯酸酯为交联剂、甲基丙烯酸为功能单体,通过水热聚合法制备分子印迹聚合物(MIPs),将MIPs填充在聚丙烯空柱中制备MIPs固相萃取(MIPs-SPE)柱。将果蔬样品洗净、晾干、粉碎后,分取5.00 g,加入2 g无水硫酸钠,研磨均匀。加入30 mL乙腈,超声1.5 h,离心10 min。分取1 mL上清液过活化好的MIPs-SPE柱,用4 mL正己烷淋洗,6 mL体积比9∶1的甲醇-乙酸混合溶液洗脱。收集洗脱液,于35 ℃氮气吹干,用1 mL乙腈定容,用高效液相色谱法分析。结果显示:MIPs可特异性识别4种目标物,对目标物的吸附量约非分子印迹聚合物(NIPs)的2.5倍,对硫磷、马拉硫磷、甲拌磷、甲基毒死蜱的吸附量显著低于目标物的;经MIPs-SPE柱净化后,样品大部分基质成分被去除,目标物测定无干扰。4种目标物的浓度在0.005~2.0 μmol·L−1内和对应的峰面积呈线性关系,检出限(3S/N)为0.001 5~0.004 0 μmol·L−1;在0.01,0.5,1.0,2.0 mg·kg−1加标浓度水平下,4种目标物的回收率为85.9%~102%,测定值的相对标准偏差(n=5)为3.0%~7.1%。方法用于4种果蔬样品的分析,在草莓样品中检出了丙溴磷(检出量为0.07 mg·kg−1),甘蓝样品中检出了辛硫磷(检出量为0.05 mg·kg−1),其他样品中均未检出这4种目标物。

       

      Abstract: Molecular imprinted polymers (MIPs) were prepared by hydrothermal polymerization method with mixed compounds of 4 targets (profenofos, chlorpyrifos, diazinon and phoxim) as template molecule, ethylene glycol dimethacrylate as crosslinking agent, and methacrylic acid as functional monomer. The MIPs were filled in a blank polypropylene column to prepare a MIPs solid phase extraction (MIPs-SPE) column. After washing, drying, and crushing, 5.00 g of the fruit and vegetable samples were taken, and 2 g of anhydrous sodium sulfate was added. The mixture was ground evenly, and 30 mL of acetonitrile was added for ultarsound for 1.5 h, and centrifugation for 10 min. An aliquot (1 mL) of the supernatant was taken and passed through the MIPs-SPE column activated, which was washed by 4 mL of n-hexane, and eluted by 6 mL of methanol-acetic acid mixed solution at volume ratio of 9∶1. The eluate was collected, and blown to dryness by nitrogen at 35 ℃. Then 1 mL of acetonitrile was used for constant volume, and the resulting solution was analyzed by high performance liquid chromatography. It was shown that MIPs could specifically recognize 4 targets, with an adsorption capacity of about 2.5 times than that of non molecularly imprinted polymers (NIPs). The adsorption capacity of parathion, malathion, methyl parathion, and methyl chlorpyrifos was significantly lower than that of targets. After purification by MIPs-SPE column, most of the matrix components in the sample were removed, and there was no interference in the determination of targets. Linear relationships of values of the concentration and respective peak area of 4 targets were kept in the range of 0.005-2.0 μmol · L−1, with detection limits (3S/N) in the range of 0.001 5-0.004 0 μmol · L−1. At the spiked concentration levels of 0.01, 0.5, 1.0, 2.0 mg · kg−1, the recoveries of 4 targets were found in the range of 85.9%-102%, and RSDs (n=5) of the determined values ranged from 3.0% to 7.1%. The proposed method was used for the analysis of 4 samples of vegetables and fruits, profenofos was detected in the strawberry sample with detection amount of 0.07 mg · kg−1, phoxim was detected in the cabbage sample with detection amount of 0.05 mg · kg−1, and 4 targets were not detected in other samples.

       

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