首页> 外文期刊>Food Chemistry >Determination of pyridaphenthion in soybean sprout samples by gas chromatography mass spectrometry with matrix matching calibration strategy after metal sieve linked double syringe based liquid-phase microextraction
【24h】

Determination of pyridaphenthion in soybean sprout samples by gas chromatography mass spectrometry with matrix matching calibration strategy after metal sieve linked double syringe based liquid-phase microextraction

机译:用气相色谱质谱法测定大豆萌发样品中的吡啶脱硫,用基质匹配校准校正金属筛基于双注射器基于液相微萃取后的基质匹配校准

获取原文
获取原文并翻译 | 示例
           

摘要

A novel analytical strategy for the trace determination of pyridaphenthion pesticide was developed in this study. Gas chromatography-mass spectrometry (GC-MS) was used for the accurate, feasible and precise determination of this analyte. Liquid phase microextraction (LPME) was performed with a metal sieve linked double syringe (MSLDS) system, which eliminated the need for a disperser solvent. In order to increase extraction efficiency for the analyte, all variable parameters were optimized and the system analytical performance of the proposed method was determined. Limit of detection and quantification (LOD and LOQ) values of pyridaphenthion were found to be 0.8 and 2.7 mu g L-1, respectively. Compared to GC-MS system's analytical performance, the developed method provided approximately 273-folds improvement in the detection limit of the analyte. Applicability/accuracy of the developed analytical strategy was checked by recovery experiments carried out with soybean sprouts, and the results obtained were satisfactory.
机译:本研究开发了一种新的微量测定吡啶硫代硫代西硫代硫代硫代硫代硫代硫酮的分析策略。气相色谱 - 质谱(GC-MS)用于该分析物的精确,可行和精确的测定。用金属筛网连接的双注射器(MSLDS)系统进行液相微萃取(LPME),这消除了对分散器溶剂的需要。为了提高分析物的提取效率,优化所有可变参数,并确定所提出的方法的系统分析性能。发现吡啶病的检测和定量(LOD和LOQ)值分别为0.8和2.7μg1-1。与GC-MS系统的分析性能相比,开发方法提供了大约273倍的改善分析物的检测限。通过用大豆发芽进行的恢复实验检查了发育的分析策略的适用性/准确性,得到的结果令人满意。

著录项

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