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凝胶渗透色谱和两步微型柱净化后,采用氮磷检测和火焰光度检测气相色谱法测定蔬菜中含氮和含磷农药残留量

Determination of nitrogen- and phosphorus-containing pesticide residues in vegetables by gas chromatography with nitrogen-phosphorus and flame photometric detection after gel permeation chromatography and a two-step minicolumn cleanup.

作者信息

Ueno Eiji, Oshima Harumi, Saito Isao, Matsumoto Hiroshi

机构信息

Aichi Prefectural Institute of Public Health, Tsuji-machi, Kita-ku, Nagoya 462-8576, Japan.

出版信息

J AOAC Int. 2003 Nov-Dec;86(6):1241-51.

Abstract

An efficient and reliable multiresidue method for determining pesticide residues in a large number of vegetable samples was studied. First, the important target compounds for monitoring, 52 nitrogen- and/or phosphorus-containing pesticides, were selected. The sample was extracted with acetonitrile, and the separated acetonitrile layer was cleaned up by a salting-out step. The acetonitrile extract was purified by gel permeation chromatography that divided the pesticide eluate into 2 fractions; the pesticide fractions were respectively purified by a 2-step minicolumn cleanup in which the second pesticide fraction was loaded on a silica-gel minicolumn. After a Florisil minicolumn was inserted on the silica-gel minicolumn, the first pesticide fraction was loaded on the tandem minicolumn, which was eluted with acetone-petroleum ether (3 + 7). The combined eluate was subjected to dual-column gas chromatography (GC) with nitrogen-phosphorus and flame photometric detection. By application of the optimum cleanup conditions to the 52 pesticides selected, good resolution and low breakdown levels of the pesticides during GC were maintained. Recoveries of the 52 pesticides from fortified cabbage, lettuce, spring onion, and spinach ranged from 72 to 108% with relative standard deviations of 2-17%, except for the recoveries of methamidophos and chlorothalonil. The detection limits of the pesticides were satisfactory (0.001-0.009 mg/kg) for monitoring pesticide residues in vegetables.

摘要

研究了一种高效可靠的多残留方法,用于测定大量蔬菜样品中的农药残留。首先,选择了52种含氮和/或含磷的农药作为监测的重要目标化合物。样品用乙腈提取,分离出的乙腈层通过盐析步骤进行净化。乙腈提取物通过凝胶渗透色谱法进行纯化,该方法将农药洗脱液分为2个馏分;农药馏分分别通过两步微型柱净化,其中第二个农药馏分加载到硅胶微型柱上。在硅胶微型柱上插入弗罗里硅土微型柱后,将第一个农药馏分加载到串联微型柱上,用丙酮 - 石油醚(3 + 7)洗脱。合并的洗脱液采用带氮磷和火焰光度检测的双柱气相色谱法(GC)进行分析。通过将最佳净化条件应用于所选的52种农药,在气相色谱分析过程中保持了良好的分离度和较低的农药分解水平。除甲胺磷和百菌清的回收率外,52种农药在强化的卷心菜、生菜、葱和菠菜中的回收率为72%至108%,相对标准偏差为2%至17%。这些农药的检测限对于监测蔬菜中的农药残留是令人满意的(0.001 - 0.009 mg/kg)。

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