Residue Determination of Captan and Folpet in Vegetable Samples by Gas Chromatography/Negative Chemical IonizationMass Spectrometry

Author:

Barreda Mercedes1,LÓpez Francisco J1,Villarroya Mercedes2,Beltran Joaquim1,García-Baudín Jose Mara2,HernÁndez Felix1

Affiliation:

1. Universidad Jaume I, Research Institute for Pesticides and Water, 12071, Castellón, Spain

2. Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Departamento de Protección Vegetal, Carretera de la Coruña Km 7.5, 28040 Madrid, Spain

Abstract

Abstract A gas chromatography/negative chemical ionization-mass spectrometry (GC/NCI-MS) method has been developed for the simultaneous determination of the fungicides captan and folpet in khaki (persimmon; flesh and peel) and cauliflower. Samples were extracted with acetone in the presence of 0.1 M zinc acetate solution in order to avoid degradation of fungicides and were purified using solid-phase extraction with divinylbenzene polymeric cartridges. Purified extracts were evaporated and dissolved in hexane prior to injection into the GC/NCI-MS system. Isotope-labeled captan and folpet were used as surrogate/internal standards, and quantification was performed using matrix-matched calibration. The method showed linear response in the concentration range tested (50-2500 ng/mL). The method was fully validated with untreated blank samples of khaki (flesh and peel) and cauliflower spiked at 0.05 and 0.5 mg/kg. Satisfactory recoveries between 82 and 106% and relative standard deviations lower than 11% in all cases (n = 5) were obtained. The limit of detection for both compounds were estimated to be 0.01 mg/kg. The developed method has been applied to treated and untreated samples collected from residue trials.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology,Agronomy and Crop Science,Environmental Chemistry,Food Science,Analytical Chemistry

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