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Uptake and depuration kinetics of dicofol metabolite 4,4_-dichlorobenzophenone, in the edible Asiatic clam Meretrix meretrix
Date Issued
2019
Author(s)
Ivorra, Lucia
Cruzeiro, Catarina
Chan, Shek Kiu
Cardoso, Patricia G.
DOI
10.1016/j.chemosphere.2019.06.155
Abstract
Uptake and depuration kinetics of 4,4_-dichlorobenzophenone (main metabolite of dicofol) in the edible clam Meretrix meretrix were evaluated through a mesocosm experiment. M.�meretrix was exposed to different dicofol concentrations (environmental concentration, D1_=_50_ng/L; supra-environmental concentration, D2_=_500_ng/L) for 15 days, followed by the same depuration period. To accomplish this goal, an analytical method was successfully optimized for 4,4_-DCBP using QuEChERS as extraction method with a range of concentrations 0.3�76.8_ng/g ww quantified by gas chromatography coupled to tandem mass spectrometry. Our results demonstrated different kinetics of accumulation depending on the two dicofol treatments. For D1, the uptake kinetic was best fitted using a plateau followed by one phase association kinetic model, while for D2 a one phase association kinetic model suited better. Similar bioconcentration factors were obtained for both concentrations but only animals exposed to D2, showed 4,4_-DCBP levels above the limits of quantification after 24_h exposure. These animals also showed lower uptake rate (ku) than organisms exposed to D1. During the depuration period, only organisms exposed to D1 successfully depurated after 24_h. On the other hand, although animals exposed to D2 presented higher elimination factor, they did not reach the original levels after depuration. Moreover, values detected in these clams were higher than the Maximum Residue Level (10_ng/g) established by the European legislation. This indicates that longer periods of depuration time than the ones used in this study, may be needed in order to reach safe levels for human consumption. This work also demonstrated that studies on metabolite kinetics during uptake/depuration experiments, could be a new alternative to understand the impact and metabolism of pesticides in the marine environment.
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