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采用低温净化的固液萃取法并结合气相色谱-质谱联用技术测定燕麦样品中的唑虫酰胺。

Determining tolfenpyrad in oat samples using solid-liquid extraction with low-temperature purification and analysis by gas chromatography coupled with mass spectrometry.

作者信息

Rocha Teófilo Karine, Alves Costa Lucélio Marques, Figueiredo Gustavo Rodrigues Amarante, Sicupira Lázaro Chaves, Silvério Flaviano Oliveira

机构信息

Department of Chemistry, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Diamantina, Minas Gerais, Brazil.

Institute of Agricultural Sciences, Universidade Federal de Minas Gerais, Montes Claros, Minas Gerais, Brazil.

出版信息

Anal Methods. 2025 Jun 19;17(24):5018-5026. doi: 10.1039/d5ay00287g.

Abstract

Tolfenpyrad is an insecticide classified as highly toxic to humans, and was recently approved for use in oat cultivation in Brazil. This approval has raised concerns about potential food safety risks in the country. Thus, the present study aims to optimize and validate solid-liquid extraction with low-temperature purification followed by analysis by gas chromatography coupled with mass spectrometry to quantify tolfenpyrad in oats to facilitate monitoring and inspection for tolfenpyrad use in oat samples. The method consisted of adding 4 g of oats, 4 mL of water, and 8 mL of pure acetonitrile to a bottle with a cap. The mixture was shaken, centrifuged, and refrigerated at -20 °C for 1 h. The supernatant obtained was then transferred to a Falcon tube with 500 mg of NaSO and 150 mg of C18 sorbent. The mixture was again shaken and centrifuged, and the supernatant was subsequently removed for chromatographic analysis. Under optimized conditions, the method showed selectivity, accuracy, and precision with a recovery of 99.25% and a relative standard deviation of 2.70%. The validated linear range was 3.0 to 150 μg kg, with detection and quantification limits of 0.5 and 3.0 μg kg, respectively. The calculated matrix effect was 89.23%. The optimized and validated technique was applied to 19 real samples and three samples presented tolfenpyrad at concentrations of 11 to 45 μg kg. These results demonstrate the method's potential as a practical tool for routine monitoring of pesticide residues, contributing to strengthening food safety control.

摘要

唑虫酰胺是一种对人类具有高毒性的杀虫剂,最近在巴西被批准用于燕麦种植。这一批准引发了该国对潜在食品安全风险的担忧。因此,本研究旨在优化和验证低温净化的固液萃取方法,随后通过气相色谱-质谱联用进行分析,以定量燕麦中的唑虫酰胺,便于对燕麦样品中唑虫酰胺的使用进行监测和检查。该方法包括向一个带盖的瓶子中加入4克燕麦、4毫升水和8毫升纯乙腈。将混合物振荡、离心,并在-20℃下冷藏1小时。然后将得到的上清液转移至含有500毫克无水硫酸钠和150毫克C18吸附剂的离心管中。再次振荡并离心混合物,随后取出上清液进行色谱分析。在优化条件下,该方法具有选择性、准确性和精密度,回收率为99.25%,相对标准偏差为2.70%。验证后的线性范围为3.0至150微克/千克,检测限和定量限分别为0.5和3.0微克/千克。计算得出的基质效应为89.23%。将优化和验证后的技术应用于19个实际样品,有3个样品中唑虫酰胺的浓度为11至45微克/千克。这些结果证明了该方法作为农药残留常规监测实用工具的潜力,有助于加强食品安全控制。

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