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  • Title: An all-embracing analytical method comprising modified QuEChERS-dispersive micro-solid-phase extraction-dispersive liquid-liquid microextraction using FeGA MOF for the extraction and preconcentration of pesticides simultaneously from juice and flesh of watermelon.
    Author: Pezhhanfar S, Farajzadeh MA, Hosseini-Yazdi SA, Mogaddam MRA.
    Journal: Anal Sci; 2023 Aug; 39(8):1201-1214. PubMed ID: 37017814.
    Abstract:
    For the first time, a comprehensive analytical method based on a one-dimensional metal-organic framework comprising "quick, easy, cheap, effective, rugged, and safe-dispersive micro solid phase extraction-dispersive liquid-liquid microextraction" was introduced in this research. Moreover, the first-ever attempt was accomplished to apply the iron-gallic acid metal-organic framework in analytical method development. The goal of the research was to analyze the pesticide content of watermelon comprehensively in its flesh and juice. Based on this, comprehensive and reliable food safety monitoring can be done. Initially, pesticides of the watermelon flesh were extracted using an mL volume of acetonitrile by vortexing. At the same time, the pesticides of watermelon juice were extracted from the juice matrix onto the sorbent particles facilitated by vortexing. The obtained acetonitrile phase was also used to desorb the analytes from the sorbent surface by vortexing. As a result, the pesticide content of both juice and flesh was extracted into the acetonitrile. The pesticide-enriched acetonitrile was then used as the disperser solvent by being merged with µL level of 1,2-dibromoethane and injection into deionized water. A cloudy solution was created as the result. Centrifugation triggered extractant at the bottom of the conical glass test tube and an aliquot of it was injected into a gas chromatograph equipped with a flame ionization detector. High enrichment factors (210-400), appreciable extraction recoveries (42-80%), wide linear ranges (3.20-1000 µg kg-1), relative standard deviations in the ranges of 3.6-4.4% for intra- (n = 6) and 4.4-5.3% for inter-day (n = 3) precisions, and low limits of detection (0.43-0.97 µg kg-1), and quantification (1.42-3.20 µg kg-1) were obtained by the application of the developed method.
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