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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

机译:用改性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药物中所选新烟碱杀虫剂的多残余方法

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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.
机译:使用复杂矩阵中的改性Quechers的提取方法开发了用于测定多颞霉素的可靠和经济效率的方法,即Hedyotis Diffusa(传统中草药的代表,其中包含大量颜料,皂苷和萜烯)和半流体鹿胎儿的提取物(用几种不同草药制作的中药专利药物的代表,除了其他干扰组件外,特别含有大量的蛋白质)。超级性能液相色谱串联质谱(UPLC-MS / MS)用于量化和确认五种化合物。除了通过MRM模式获得的两个转变,离子无线电进一步进行识别。提出了每个选定的产物离子和所提出的热解方式的所提出的化学结构。特别优化提取,清理,UPLC分离和MS / MS参数,以获得更好的回收率。五种杀虫剂的检测(LODS)的低限制范围为0.04至0.81μgkg-1。 Matrix匹配在0.05-50μgkG-1的浓度范围内的校准来补偿基质效应,并且合理的回收率80.2-105.4%的五种化合物的不同掺入水平均以1.7%至10.6%的速度。该方法是一种替代方法,用于分析中药中的新烟白素,与其他检测方法相比更可靠和有前途。

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