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采用改进的分散固相萃取结合超高效液相色谱串联质谱法测定中药中多种新烟碱类杀虫剂的多残留方法

Multi-residue Method for Determination of Selected Neonicotinoid Insecticides in Traditional Chinese Medicine Using Modified Dispersive Solid-phase Extraction Combined with Ultra-performance Liquid Chromatography Tandem Mass Spectrometry.

作者信息

Qin Yao, Chen Lina, Yang Xiaojing, Li Sainan, Wang Yumeng, Tang Ying, Liu Chunming

机构信息

Central Laboratory, Changchun Normal University.

出版信息

Anal Sci. 2015;31(8):823-30. doi: 10.2116/analsci.31.823.

Abstract

A reliable and cost-effective method for the determination of multiple neonicotinoids was developed using a modified QuEChERS-based extraction procedure in complex matrices, namely Hedyotis diffusa (a representative of the Traditional Chinese herb which contains lots of pigment, saponin and terpene) and Semifluid extract of deer foetus (a representative of the Chinese traditional patent medicine that was produced with several different herbs, and especially containing lots of protein, except for other interference components). Ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) was used for the quantification and confirmation of five compounds. Except for two transitions obtained by the MRM mode, identification was further carried out by the ion radios. The proposed chemical structure of every selected product ion and the proposed pyrolysis way were presented. The extraction, clean-up, UPLC separation and MS/MS parameters were especially optimized in order to obtain better recoveries. The low limits of detection (LODs) of five insecticides ranged from 0.04 to 0.81 μg kg(-1). Matrix matched calibration in the concentration range of 0.05 - 50 μg kg(-1) were used to compensate the matrix effect, and reasonable recoveries 80.2 - 105.4% of five compounds were demonstrated in different spiked levels with inter-RSD from 1.7 to 10.6%. The proposed method is an alternative approach to make an analysis of neonicotinoids in Chinese medicine, which is more reliable and promising compared with other detection methods.

摘要

采用改良的基于QuEChERS的萃取方法,开发了一种可靠且经济高效的测定多种新烟碱类化合物的方法,该方法适用于复杂基质,即白花蛇舌草(一种含有大量色素、皂苷和萜类化合物的传统中草药代表)和鹿胎膏(一种由多种不同草药制成的传统中成药代表,尤其含有大量蛋白质以及其他干扰成分)。采用超高效液相色谱串联质谱法(UPLC-MS/MS)对五种化合物进行定量和确证。除了通过多反应监测(MRM)模式获得的两个离子跃迁外,还通过离子比率进一步进行确证。给出了每个选定产物离子的化学结构推测以及热解方式推测。对萃取、净化、UPLC分离和MS/MS参数进行了特别优化,以获得更好的回收率。五种杀虫剂的低检测限(LOD)范围为0.04至0.81 μg kg⁻¹。采用浓度范围为0.05 - 50 μg kg⁻¹的基质匹配校准来补偿基质效应,在不同加标水平下五种化合物的回收率为80.2 - 105.4%,相对标准偏差(RSD)为1.7至10.6%。所提出的方法是一种分析中药中新烟碱类化合物的替代方法,与其他检测方法相比,该方法更可靠且更具前景。

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