首页> 外文期刊>International journal of environmental analytical chemistry >High-performance liquid chromatography tandem mass spectrometry for simultaneous detection of aflatoxins B_1, B_2, G_1 and G_2 in Indian medicinal herbs using QuEChERS-based extraction procedure
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High-performance liquid chromatography tandem mass spectrometry for simultaneous detection of aflatoxins B_1, B_2, G_1 and G_2 in Indian medicinal herbs using QuEChERS-based extraction procedure

机译:高效液相色谱串联质谱法,使用基于QuEChERS的提取方法同时检测印度草药中的黄曲霉毒素B_1,B_2,G_1和G_2

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Since the discovery of aflatoxins (AFs) in the 1960s, much research has focused on detecting the toxins in contaminated food and feedstuffs. But the quality determination in medicinal plant matrices with respect to AFs is scare. Hence, a simple, accurate and sensitive high-performance liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method was developed for simultaneous determination of AFs AFB(1), AFB(2), AFG(1) and AFG(2) in two Indian popular medicinal herbs i.e. senna (Cassia angustifolia) and kalmegh (Andrographis paniculata). AFs have been extracted from herb matrix using a QuEChERS (quick, easy, cheap, effective, rugged and safe)-based extraction procedure followed by applying primary secondary amine and C18 for further clean-up step and then were quantified under the multiple reaction monitoring together with positive ionisation modes. Matrix-matched calibration was used for quantification in order to reduce the matrix effect. Validation of the method was carried out in herbs by recovery experiments. Recoveries of the spiked samples were in the range of 61.9-111.5% with an inter-day and intraday relative standard deviation lower than 20.0%. Limits of detection and quantification ranged from 0.41 to 0.95ngmL(-1) and 1.2 to 3.8gkg(-1), respectively. The expanded uncertainty of the method was 21% for all the toxins in both the herbs. Finally, the proposed method was successfully applied to determine AF residues in real field samples of senna and kalmegh obtained from different locations in India.
机译:自从1960年代发现黄曲霉毒素(AFs)以来,许多研究都集中在检测受污染的食品和饲料中的毒素。但是,关于AF的药用植物基质的质量确定是令人恐惧的。因此,开发了一种简单,准确,灵敏的高效液相色谱-串联质谱(LC-MS / MS)方法,用于同时测定AF的AFB(1),AFB(2),AFG(1)和AFG( 2)在两种印度流行的草药中,即番泻叶(Cassia angustifolia)和卡尔梅​​(Andrographis paniculata)。已经使用基于QuEChERS(快速,简便,廉价,有效,坚固耐用和安全)的提取程序从草药基质中提取了AF,随后应用伯仲胺和C18进行进一步的纯化,然后在多反应监测下进行了定量加上正电离模式。基质匹配的校准用于定量,以减少基质效应。通过回收实验在草药中对该方法进行了验证。加标样品的回收率在61.9-111.5%的范围内,日间和日内相对标准偏差低于20.0%。检出限和定量限分别为0.41至0.95ngmL(-1)和1.2至3.8gkg(-1)。对于两种草药中的所有毒素,该方法的扩展不确定度均小于21%。最后,该方法成功地用于测定从印度不同地点获得的番泻叶和卡尔梅的真实样品中的AF残留。

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