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[采用在线固相萃取-超高效液相色谱-高分辨质谱联用法同时测定杨梅中29种农药残留]

[Simultaneous determination of 29 pesticides residues in bayberry by pass-through solid-phase extraction and ultra-performance liquid chromatography-high resolution mass spectrometry].

作者信息

Pan Shengdong, Guo Yanbo, Wang Li, Zhang Dandan

机构信息

Key Laboratory of Health Risk Appraisal for Trace Toxic Chemicals of Zhejiang Province,Ningbo Municipal Center for Disease Control and Prevention, Ningbo 315010, China.

出版信息

Se Pu. 2021 Jun;39(6):614-623. doi: 10.3724/SP.J.1123.2020.11011.

Abstract

A rapid and accurate analysis method based on PRiME HLB pass-through solid-phase extraction (SPE) and ultra-performance liquid chromatography-high resolution mass spectrometry (UPLC-HRMS) was developed for the determination of 29 pesticide residues in bayberry samples. The bayberry samples were first extracted using acetonitrile by vortexing; then, the extract solution was salted out and purified by PRiME HLB pass-through solid-phase extraction (SPE) cartridges. Chromatographic separation was subsequently carried out on a Waters ACQUITY UPLC HSS T column (100 mm×2.1 mm, 1.8 μm) using 5 mmol/L ammonium acetate in water and acetonitrile as the elution solvent. The electrospray ion source in positive (ESI) mode and full mass-data-dependent MS (full mass-ddMS) mode were used for quantification by the matrix-matched external standard method. The LC conditions were first optimized, and two analytical columns, Waters ACQUITY UPLC HSS T and Waters ACQUITY UPLC BEH C, were investigated for the 29 pesticides. The results indicated that the Waters ACQUITY UPLC HSS T column showed better chromatographic retention. Moreover, composites of the mobile phase were also studied. Compared to the acetonitrile-formic acid aqueous solution system and acetonitrile-formic acid-ammonium acetate aqueous solution system, the acetonitrile-ammonium acetate aqueous solution system used as the mobile phase exhibited much better chromatographic behavior for most of the 29 pesticides. In particular, the MS responses of some of the target pesticides were significantly improved when using the ammonium acetate-acetonitrile system as the mobile phase. In addition, the sample pretreatment conditions for the 29 pesticides in bayberry samples were systematically optimized. The matrix effect (ME) for three different types of purification methods were applied to evaluate the purification efficiency for the 29 pesticides in the bayberry samples. The following results were obtained from the post-spiking experiments: (1) For graphitized carbon (GCB) SPE, the post-spiking recoveries of 29 pesticides in the bayberry samples were generally low, less than 60%. (2) For the QuEChERS method, the recoveries of most target pesticides improved. The pesticide ratio with recoveries ranging from 70% to 120% was found to be 41%; however, the pesticide ratio with recoveries of less than 60% was still high (35%). (3) For the PRiME HLB-based pretreatment method, the recoveries of the 29 pesticides obviously improved. The pesticide ratio with recoveries between 70% and 120% was up to 76%, while the pesticide ratios were only 14% and 10% for post-spiking recoveries of 60%-70% and >120%, respectively. Meanwhile, the recoveries of all 29 pesticides were found to be more than 60%. Therefore, the PRiME HLB-based method was better than the GCB SPE and QuEChERS methods for pretreatment of the 29 pesticides in the bayberry samples. In addition, the PRiME HLB-based pretreatment process does not require tedious operation processes such as activation, balance, and elution, and thus, the sample pretreatment time is greatly shortened. Under the optimal conditions, the 29 target pesticides showed good linearity in the range of 1.0-200.0 μg/L, with correlation coefficients () higher than 0.999. The limits of detection (LODs) were 2.0 μg/kg for the 29 target pesticides. The recoveries of the pesticides spiked in the bayberry samples were in the range of 69.2%-135.6% at 6, 200, and 400 μg/kg, respectively, while the relative standard deviations (RSDs) in the range of 0.7%-14.6%. The proposed method based on PRiME HLB-pass through SPE-UPLC-HRMS was adopted to determine these 29 pesticides in 30 bayberry samples purchased from local and online markets. According to the results, pesticides such as methamidamine, difenoconazole, and tebuconazole were frequently detected in the bayberry samples. However, the maximum residue limits (MRLs) of methamidamine, difenoconazole, and tebuconazole in bayberry samples were not provided in GB 2763-2019. In summary, the developed method is fast, simple, sensitive, and accurate, and it can be applied for daily monitoring of pesticides in bayberry samples.

摘要

建立了一种基于PRiME HLB直通式固相萃取(SPE)和超高效液相色谱-高分辨率质谱(UPLC-HRMS)的快速准确分析方法,用于测定杨梅样品中的29种农药残留。杨梅样品首先用乙腈涡旋提取;然后,提取液经盐析并用PRiME HLB直通式固相萃取(SPE)小柱纯化。随后在Waters ACQUITY UPLC HSS T柱(100 mm×2.1 mm,1.8 μm)上进行色谱分离,以5 mmol/L醋酸铵水溶液和乙腈作为洗脱溶剂。采用电喷雾离子源正离子(ESI)模式和全质量数据依赖型质谱(全质量-ddMS)模式,通过基质匹配外标法进行定量。首先对液相色谱条件进行了优化,并考察了Waters ACQUITY UPLC HSS T和Waters ACQUITY UPLC BEH C两种分析柱对29种农药的分离效果。结果表明,Waters ACQUITY UPLC HSS T柱具有更好的色谱保留性能。此外,还研究了流动相的组成。与乙腈-甲酸水溶液体系和乙腈-甲酸-醋酸铵水溶液体系相比,以乙腈-醋酸铵水溶液体系作为流动相时,29种农药中的大多数表现出更好的色谱行为。特别是,当使用醋酸铵-乙腈体系作为流动相时,一些目标农药的质谱响应显著提高。此外,系统地优化了杨梅样品中29种农药的样品预处理条件。应用三种不同净化方法的基质效应(ME)来评估杨梅样品中29种农药的净化效率。加标后实验得到以下结果:(1)对于石墨化碳(GCB)固相萃取,杨梅样品中29种农药的加标后回收率普遍较低,低于60%。(2)对于QuEChERS方法,大多数目标农药的回收率有所提高。回收率在70%至120%之间的农药比例为41%;然而,回收率低于60%的农药比例仍然较高(35%)。(3)对于基于PRiME HLB的预处理方法,29种农药的回收率明显提高。回收率在70%至120%之间的农药比例高达76%,而加标后回收率在60%-70%和>120%时的农药比例分别仅为14%和10%。同时,29种农药的回收率均超过60%。因此,基于PRiME HLB的方法在杨梅样品中29种农药的预处理方面优于GCB固相萃取和QuEChERS方法。此外,基于PRiME HLB的预处理过程不需要活化、平衡和洗脱等繁琐的操作步骤,因此大大缩短了样品预处理时间。在最佳条件下,29种目标农药在1.0-200.0 μg/L范围内呈现良好的线性关系,相关系数()高于0.999。29种目标农药的检出限(LOD)为2.0 μg/kg。在杨梅样品中添加6、200和400 μg/kg农药时,回收率分别在69.2%-135.6%范围内,相对标准偏差(RSD)在0.7%-14.6%范围内。采用基于PRiME HLB-直通式SPE-UPLC-HRMS的方法测定了从当地和网上市场购买的30个杨梅样品中的这29种农药。结果表明,杨梅样品中经常检测到甲胺磷、苯醚甲环唑和戊唑醇等农药。然而,GB 2763-2019中未规定杨梅样品中甲胺磷、苯醚甲环唑和戊唑醇的最大残留限量(MRL)。综上所述,所建立的方法快速、简便、灵敏、准确,可用于杨梅样品中农药的日常监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2654/9404219/88e711f30938/cjc-39-06-614-img_1.jpg

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