个人膳食样品中碱/中性和氨基甲酸酯类农药的测定方法。

L S Sheldon, J T Keever, J M Roberds, J B Beach, J N Morgan
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引用次数: 0

摘要

饮食摄取可能是接触污染物的一个重要途径。因此,饮食暴露评估应被视为总暴露评估过程的重要组成部分。这项工作的目的是开发可靠的方法,适用于广泛的碱性/中性和氨基甲酸盐型农药在作为膳食暴露评估研究的一部分收集的重复饮食样本中。所得到的方法需要对低于1 ng/g的浓度敏感,准确和精确,并且尽可能简单和经济有效。作为第一步,收集了目前测量食品中农药含量的方法的信息。虽然文献方法可以作为一个起点,但很少应用于重复的饮食样本,检出限通常很高(10至100 ng/g)。进行实验工作以评估单个提取、清理和分析程序;将最有前途的程序链接到分析方法中;并在最后的方法上生成性能数据。最后采用索氏萃取-溶剂分馏-凝胶渗透色谱法清洗。采用气相色谱/质谱法分析碱/中性农药。采用高效液相色谱法对氨基甲酸酯类农药进行分析。性能测试结果表明,该方法对大部分农药具有良好的准确度(回收率> 70%)、精密度(% RSD < 25%)和灵敏度(方法检出限< 1.0 ng/g)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Method for measuring base/neutral and carbamate pesticides in personal dietary samples.

Dietary uptake may be a significant pathway of exposure to contaminants. As such, dietary exposure assessments should be considered an important part of the total exposure assessment process. The objective of this work was to develop reliable methods that are applicable to a wide range of base/neutral and carbamate-type pesticides in duplicate diet samples collected as part of dietary exposure assessment studies. The resulting method needed to be sensitive to concentrations below 1 ng/g, accurate and precise, and as simple and cost effective as possible. As a first step, information was gathered on current methods for measuring pesticides in foods. Although the literature methods could serve as a starting point, few had been applied to duplicate diet samples and detection limits were generally high (10 to 100 ng/g). Experimental work was performed to evaluate individual extraction, cleanup, and analysis procedures; link the most promising procedures into analysis methods; and generate performance data on the final method. The final method used Soxhlet extraction with solvent partitioning and gel permeation chromatography cleanup. Gas chromatography/mass spectrometry was used for the analysis of base/neutral pesticides. High performance liquid chromatography analysis was used for the analysis of carbamate pesticides. Results of performance testing showed good accuracy (recovery > 70%), precision (% RSD < 25%), and sensitivity (method detection limits < 1.0 ng/g) for most pesticides targeted for study.

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