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  • Title: Stereoselective dissipation of epoxiconazole in grape (Vitis vinifera cv. Kyoho) and soil under field conditions.
    Author: Liang H, Qiu J, Li L, Li W, Zhou Z, Liu F, Qiu L.
    Journal: Chemosphere; 2012 May; 87(8):982-7. PubMed ID: 22414382.
    Abstract:
    Stereoselective dissipation of epoxiconazole had been studied in grape and soil during plant growing under field conditions in this paper. A sensitive and rapid chiral method was developed and validated for the determination of epoxiconazole stereoisomers in grape and soil based on liquid chromatography coupled with triple quadrupole mass spectrometry (LC-MS/MS). Phenomenex Lux Cellulose-1 column was used for enantioseparation with a mixture of acetonitrile/water (90/10, v/v) as mobile phase at flow rate of 0.3 mL min(-1). Fortified recoveries in grape and soil samples ranged from 76.0% to 91.9% and relative standard deviations were less than 11.4% with fortified levels of 0.025-1.0 mg kg(-1). The limits of detection and quantification were 0.005 mg kg(-1) and 0.025 mg kg(-1), respectively, with linear calibration curves extending up to 5.0 mg kg(-1). The field experimental results showed that dissipations of epoxiconazole stereoisomers in grape followed first-order kinetics (R(2)>0.92) and stereoselectivity occurred in 2 h after spraying. The (-)-stereoisomer with half-life of 9.3 d degraded faster than (+)-stereoisomer with that of 13.2 d, and resulted in relative enrichment of (+)-stereoisomer. However, the stereoisomeric dissipations in soil were triphasic ("increase-decrease-steady") with lower dissipation rates, and also occurred with preferential degradation of (-)-stereoisomer under field condition. The results for stereoselective dissipations can be applied for food and environmental assessments of chiral pesticides.
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