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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Ultrasound assisted combined molecularly imprinted polymer for the selective micro-solid phase extraction and determination of aflatoxins in fish feed using liquid chromatography-tandem mass spectrometry
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Ultrasound assisted combined molecularly imprinted polymer for the selective micro-solid phase extraction and determination of aflatoxins in fish feed using liquid chromatography-tandem mass spectrometry

机译:使用液相色谱 - 串联质谱法为选择性微固 - 相萃取和鱼饲法中黄曲霉毒素的辅助聚合物的超声辅助组合的分子印迹聚合物

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摘要

A combined procedure based on using ultrasounds for target isolation followed by porous membrane-protected micro solid phase extraction using a molecularly imprinted polymer as an adsorbent has been developed as a highly selective extraction and clean-up procedure for isolating aflatoxins B1, B2, G1, and G2 from fish feed before ultra-high- performance liquid chromatography tandem mass spectrometry determination. Polymeric adsorbent beads have been synthesized by the precipitation polymerization method which guarantees a homogeneous particles size distribution and the integrity of the generated imprinted cavities. In addition, polymerization was performed using a higher proportion of organic solvent (toluene) in the porogen mixture, which generates MIP particles adequate for interacting with targets dissolved in organic (hydro-organic) mixtures (extracts from fish feed). These approaches led to a selective and high efficient pre-concentration method for AFs. Ultrasound-assisted extraction (10 mL of 60:40 acetonitrile/0.1 M KH2PO4 pH 6.0, 40% amplitude, continuous sonication for 7.0 min) allowed an efficient aflatoxins isolation from fish feed. In addition, the resulting pH of the extract (pH 7.0) has been found to be the optimum for performing clean-up/pre-concentration (enrichment factor of 33.3) by molecularly imprinted polymer based micro-solid phase extraction (orbital horizontal shaking speed at 150 rpm for 10 min for loading, and 5 mL of 95:5 acetonitrile/formic acid as eluting solution using ultrasounds 35 kHz for 15 min). The current proposal was shown to be an accurate and precise method through relative standard deviation of intraday and inter-day tests below 20% and analytical recoveries in the range of 80-100%. The limits of detection were within the 0.42-1.15 mu g kg(-1) range, quite lower than those established by European Commission guidelines for aflatoxins in animal feeds. (C) 2019 Elsevier B.V. All rights reserved.
机译:基于使用超声波用于靶隔离的组合程序,然后使用分子印迹聚合物作为吸附剂的多孔膜保护的微固相萃取作为吸附剂,作为分离黄曲霉毒素B1,B2,G1的高度选择性提取和清洁程序,在超高效液相色谱前串联质谱测定,从鱼饲料中的G2。通过沉淀聚合方法合成了聚合物吸附珠,其保证了均匀颗粒尺寸分布和产生的压印腔的完整性。另外,使用孔胶混合物中的较高比例的有机溶剂(甲苯)进行聚合,其产生足以与溶解在有机(水 - 有机)混合物中的靶(来自鱼饲料的摘录)相互作用的摩托颗粒。这些方法导致了AFS的选择性和高效的预浓度方法。超声辅助萃取(10mL 60:40乙腈/ 0.1MK2PO4PH 6.0,40%振幅,连续超声检查7.0分钟)允许从鱼饲料中分离出一种有效的黄曲霉毒素。此外,已经发现所得提取物(pH7.0)的pH值是通过分子印迹基于聚合物的微固相萃取(轨道水平摇动速度)进行清洁/预浓度(富集为33.3)的最佳选择。(轨道水平摇动速度加载150分钟,加载10分钟,5毫升95:5乙腈/甲酸,作为使用超声35kHz的洗脱溶液15分钟)。目前的提议显示通过盘中的相对标准偏差和日间间试验低于20%,分析回收率在80-100%的情况下是一种准确和精确的方法。检测限率在0.42-1.15μgkg(-1)范围内,比欧洲委员会在动物饲料中的黄曲霉毒素所建立的规定的范围内。 (c)2019 Elsevier B.v.保留所有权利。

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