...
首页> 外文期刊>Iranian polymer journal >Hydrophilic molecularly imprinted dispersive solid-phase extraction coupled with liquid chromatography for determination of azoxystrobin residues in cucumber
【24h】

Hydrophilic molecularly imprinted dispersive solid-phase extraction coupled with liquid chromatography for determination of azoxystrobin residues in cucumber

机译:亲水性分子印迹分散固相萃取-液相色谱法测定黄瓜中嘧菌酯残留

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The hydrophilic molecularly imprinted dispersive solid-phase extraction (HMIDSPE) coupled with liquid chromatography (LC) for the separation and the determination of azoxystrobin in cucumber was exploited. Hydrophilic molecularly imprinted microspheres (HMIMs) for azoxystrobin were synthesized through precipitation polymerization that hydroxypropyl methacrylate (HPMA) as functional monomer, ethylene glycol dimethacrylate (EGDMA) as cross-linker, azobisisobutyronitrile (AIBN) as initiator, a mixture solution of butanone (MEK) and n-heptane (V:V 7:3) as solvent. The microspheres were determined by Fourier-transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM). Under the optimum DSPE conditions, the HMIMs could extract and enrich azoxystrobin very efficiently. Comparing HMIMs with C-18, the average recoveries of azoxystrobin from blank cucumber samples spiked at 0.1, 0.5, and 1 mg mL(-1), ranged between 85.93 and 88.89% with relative standard deviations (RSD), were 2.10-4.91%. The average recoveries of azoxystrobin that used C-18 as sorbent were 56.20-60.66% with relative standard deviations (RSD) of 3.22-5.18%. The limit of detection (LOD) and the limit of quantification (LOQ) of azoxystrobin were 3.24 x 10(-4) mg kg(-1) and 0.005 mg kg(-1), respectively. The method of HMIDSPE-LC exhibited highly efficient separation and the enrichment of azoxystrobin. The actual samples were detected free of azoxystrobin.
机译:利用亲水性分子印迹分散固相萃取(HMIDSPE)结合液相色谱(LC)分离和测定黄瓜中的过氧化氧合酶。通过沉淀聚合反应合成了用于唑固酮的亲水分子印迹微球(HMIM),其中甲基丙烯酸羟丙酯(HPMA)为功能单体,乙二醇二甲基丙烯酸酯(EGDMA)作为交联剂,偶氮二异丁腈(AIBN)作为引发剂,丁酮(MEK)的混合溶液和正庚烷(V:V 7:3)作为溶剂。通过傅里叶变换红外光谱法(FTIR)和扫描电子显微镜(SEM)确定微球。在最佳DSPE条件下,HMIMs可以非常有效地提取和富集嘧菌酯。将HMIM与C-18进行比较,从空白黄瓜样品中加标分别为0.1、0.5和1 mg mL(-1)的嘧菌酯的平均回收率在2.10-4.91%之间,范围在85.93至88.89%之间,相对标准偏差(RSD)为2.10-4.91% 。使用C-18作为吸附剂的嘧菌酯的平均回收率为56.20-60.66%,相对标准偏差(RSD)为3.22-5.18%。嘧菌酯的检出限(LOD)和定量限(LOQ)分别为3.24 x 10(-4)mg kg(-1)和0.005 mg kg(-1)。 HMIDSPE-LC的方法显示出高效的分离作用和对三氧化氮的富集。检测到的实际样品中不含嘧菌酯。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号