Paroxetine (PRX) is one of the most used antidepressants and an emerging contaminant with potential harmful effects to the environment and human health. The present study investigates in detail the toxic potential of PRX using a battery of bioassays on fresh- and marine species, marine bacteria, and human lymphocytes. All the tested organisms and human lymphocytes were exposed at concentrations ranging from μg L-1 to mg L-1. It was found that PRX can cause toxic effects to aquatic organisms at environmental relevant concentrations (μg L-1 level). A significant effect of PRX was observed in all tested algal species especially at the first 24 h. However, differences in responses and sensitivities among the tested algal species were observed. The most sensitive organism was found to be Dunaliella tertiolecta with IC50 = 0.092 mg L-1 (72 h). In the case of Aliivibrio fischeri, EC50 values were determined to be 16.65, 14.31 and 14.41 mg L-1 for 5, 15 and 30 min of exposure, respectively. PRX also induced cytotoxic and genotoxic effects in human lymphocytes. A dose-dependent increase in micronucleus frequencies was occurred at all tested concentrations with a statistically significant increase in micronucleus frequencies at the medium to high PRX tested concentrations. The findings of the present study expand the available toxicity profile of PRX on aquatic organisms and the knowledge about the potential risk of PRX to induce genotoxic effects in cultured human lymphocytes.
Keywords: Aquatic toxicology; Ecotoxicity; Genotoxicity and cytotoxicity; Paroxetine; Pharmaceuticals.
Copyright © 2022 Elsevier B.V. All rights reserved.