食品科学 ›› 2025, Vol. 46 ›› Issue (10): 274-281.doi: 10.7506/spkx1002-6630-20240730-298

• 安全检测 • 上一篇    下一篇

QuEChERS-超高效液相色谱-串联质谱法同时测定果蔬中新型甲氧基丙烯酸酯类杀菌剂Mandestrobin和Metyltetraprole残留

周文静,王卢燕,周昌瑜,方楠,张昌朋,蒋金花   

  1. (1.宁波大学食品科学与工程学院,农产品质量安全全国重点实验室,浙江 宁波 315800;2.浙江省农业科学院农产品质量安全与营养研究所,农产品质量安全全国重点实验室,浙江 杭州 310021)
  • 出版日期:2025-05-25 发布日期:2025-05-07
  • 基金资助:
    国家自然科学基金面上项目(32272577)

Simultaneous Determination of Residues of New Quinone Outside Inhibitor Fungicides Mandestrobin and Metyltetraprole in Fruits and Vegetables by QuEChERS Coupled with Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry

ZHOU Wenjing, WANG Luyan, ZHOU Changyu, FANG Nan, ZHANG Changpeng, JIANG Jinhua   

  1. (1. State Key Laboratory for Quality and Safety of Agro-products, College of Food Science and Engineering, Ningbo University, Ningbo 315800, China; 2. State Key Laboratory for Quality and Safety of Agro-products, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China)
  • Online:2025-05-25 Published:2025-05-07

摘要: 基于QuEChERS结合超高效液相色谱-串联质谱法建立6 种常见果蔬中新型甲氧基丙烯酸酯类杀菌剂Mandestrobin和Metyltetraprole残留的检测方法。芹菜、黄瓜、玉米、葡萄、草莓、桃样品分别经10 mL乙腈提取,25 mg N-丙基乙二胺、2.5 mg聚碳酸酯及150 mg无水硫酸镁净化后,以0.1%甲酸溶液-乙腈为流动相,经Waters Acquity UPLC® BEH C18色谱柱(2.1 mm×100 mm,1.7 µm)分离,采用基质标准曲线进行定量。结果表明:Mandestrobin和Metyltetraprole在0.005~0.5 mg/L质量浓度范围内线性关系良好,相关系数在0.995 2~0.999 9之间,定量限均为0.01 mg/kg。在0.01、0.1、0.5 mg/kg 3 个加标水平下,Mandestrobin和Metyltetraprole平均加标回收率分别为84.0%~107.0%、84.0%~104.0%,相对标准偏差分别为3.7%~18.3%、3.9%~14.7%。该方法快速、准确、灵敏度高,适用于同时定量分析常见果蔬中的Mandestrobin和Metyltetraprole残留,可为国内外农产品中新型甲氧基丙烯酸酯类杀菌剂Mandestrobin和Metyltetraprole检测和残留风险评估提供技术支持。

关键词: Mandestrobin;Metyltetraprole;QuEChERS;超高效液相色谱-串联质谱;残留

Abstract: A method for the detection of the residues of two new quinone outside inhibitor (QoI) fungicides, mandestrobin and metyltetraprole, in six common types of fruits and vegetables (celery, cucumber, corn, grape, strawberry and peach) was developed by quick, easy, cheap, effective, rugged and safe (QuEChERS) combined with ultra-high performance liquid chromatography-tandem mass spectrometry. Samples were extracted with acetonitrile and further purified with a mixture of 25 mg of N-propylethylenediamine, 2.5 mg of polycarbonate and 150 mg of anhydrous magnesium sulfate. The chromatographic separation was accomplished on a Waters Acquity UPLC® BEH C18 column (2.1 mm × 100 mm, 1.7 μm) using a mobile phase consisting of 0.1% formic acid and acetonitrile. The results showed that the calibration curves of mandestrobin and metyltetraprole exhibited a good linear relationship in the concentration range of 0.005–0.5 mg/L, with correlation coefficients ranging from 0.995 2 to 0.999 9, and the limit of quantification (LOQ) was 0.01 mg/kg for both analytes. At three spiked levels of 0.01, 0.1 and 0.5 mg/kg, the average spiked recovery rates of mandestrobin and metyltetraprole ranged from 84.0% to 107.0% and 84.0% to 104.0%, respectively, with relative standard deviations (RSDs) ranging from 3.7% to 18.3% and 3.9% to 14.7%, respectively. This method is rapid, accurate, sensitive, and suitable for simultaneous quantification of mandestrobin and metyltetraprole residues in fruits and vegetables, providing technical support for the detection and risk assessment of the novel QoI fungicides mandestrobin and metyltetraprole in agricultural products.

Key words: mandestrobin; metyltetraprole; QuEChERS; ultra-high performance liquid chromatography-tandem mass spectrometry; residue

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