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通过固相萃取和气相色谱/质谱联用对一种简单快速测定葡萄汁和葡萄酒样品中杀菌剂的方法进行优化和验证。

Optimization and validation of a simple and fast method for the determination of fungicides in must and wine samples by SPE and GC/MS.

作者信息

Lagunas-Allué Laura, Sanz-Asensio Jesús, Martínez-Soria Maria-Teresa

机构信息

University of La Rioja, Department of Chemistry, Madre de Dios, 51, La Rioja, 26006, Spain.

出版信息

J AOAC Int. 2012 Sep-Oct;95(5):1511-9. doi: 10.5740/jaoacint.11-402.

Abstract

A rapid, simple, and low-cost method based on SPE was optimized and validated for simultaneous determination of eight fungicides belonging to different chemical classes in must and wine. The method involves extraction of 10 mL of must or wine samples with a C18 cartridge using 5 mL of dichloromethane as the elution solvent. Separation and final determination of the fungicides (vinclozolin, dichlofluanid, penconazol, captan, quinoxyfen, fluquinconazol, boscalid, and pyraclostrobin) was performed by GC coupled to single quadrupole MS. Recoveries at 10, 50, and 100 microg/L were between 71 and 106% in both matrixes for the fungicides evaluated. The calculated LOQ ranged from 1.5 to 3.4 microg/L in must and 1.1 to 3.8 microg/L in wine. Matrix effects observed for wine and must samples were overcome by using matrix-matched calibration. The developed method was linear at concentrations within the tested interval, with coefficients of determination higher than 0.999. The expanded uncertainties at 10 microg/L were <20% for all analytes. Intralaboratory precision in terms of the Horwitz ratio of the fungicides evaluated was below 0.5, suggesting the ruggedness of the method. The proposed method was applied to determine fungicide residues in must samples obtained from red grapes treated with two new commercial formulations, as well as in their corresponding final wines.

摘要

一种基于固相萃取(SPE)的快速、简便且低成本的方法得到了优化和验证,用于同时测定葡萄汁和葡萄酒中属于不同化学类别的八种杀菌剂。该方法包括使用5 mL二氯甲烷作为洗脱溶剂,用C18柱萃取10 mL葡萄汁或葡萄酒样品。杀菌剂(乙烯菌核利、百菌清、戊唑醇、克菌丹、喹氧灵、氟喹唑、啶酰菌胺和吡唑醚菌酯)的分离和最终测定通过气相色谱-单四极杆质谱联用进行。在所评估的杀菌剂中,两种基质在10、50和100 μg/L加标水平下的回收率在71%至106%之间。计算得出的葡萄汁中定量限范围为1.5至3.4 μg/L,葡萄酒中为1.1至3.8 μg/L。通过使用基质匹配校准克服了葡萄酒和葡萄汁样品中观察到的基质效应。所开发的方法在测试浓度范围内呈线性,测定系数高于0.999。所有分析物在10 μg/L时的扩展不确定度均小于20%。所评估杀菌剂的实验室内部精密度(以霍维茨比率衡量)低于0.5,表明该方法的耐用性良好。所提出的方法应用于测定用两种新商业配方处理的红葡萄所制得的葡萄汁样品及其相应最终葡萄酒中的杀菌剂残留。

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