Oxidation of atenolol, propranolol, carbamazepine and clofibric acid by a biological Fenton-like system mediated by the white-rot fungus Trametes versicolor |
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Authors: | Ernest Marco-Urrea,Gloria Caminal,Teresa Vicent,Damià Barceló |
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Affiliation: | a Departament d'Enginyeria Química and Institut de Ciència i Tecnologia Ambiental, Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain b Department of Environmental Chemistry, IDAEA-CSIC, c/Jordi Girona 18-26, 08034 Barcelona, Spain c Unitat de Biocatàlisis Aplicada associada al IQAC (CSIC-UAB), Escola Tècnica Superior d'Enginyeria, UAB, 08193 Bellaterra, Spain d Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain e Institut Català de Recerca de l'Aigua (ICRA), Parc Científic i Tecnológic de la Universitat de Girona, Pic de Peguera, 15, 17003 Girona, Spain |
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Abstract: | Biological advanced oxidation of the pharmaceuticals clofibric acid (CA), carbamazepine (CBZP), atenolol (ATL) and propranolol (PPL) is reported for the first time. Extracellular oxidizing species were produced through a quinone redox cycling mechanism catalyzed by an intracellular quinone reductase and any of the ligninolytic enzymes of Trametes versicolor after addition of the lignin-derived quinone 2,6-dimethoxy-1,4-benzoquinone (DBQ) and Fe3+-oxalate in the medium. Time-course experiments with approximately 10 mg L−1 of initial pharmaceutical concentration resulted in percent degradations above 80% after 6 h of incubation. Oxidation of pharmaceuticals was only observed under DBQ redox cycling conditions. A similar degradation pattern was observed when CBZP was added at the environmentally relevant concentration of 50 μg L−1. Depletion of DBQ due to the attack of oxidizing agents was assumed to be the main limiting factor of pharmaceutical degradation. The main degradation products, that resulted to be pharmaceutical hydroxylated derivatives, were structurally elucidated. The detected 4- and 7-hydroxycarbamazepine intermediates of CBZP degradation were not reported to date. Total disappearance of intermediates was observed in all the experiments at the end of the incubation period. |
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Keywords: | Trametes versicolor Pharmaceuticals Hydroxyl radical Carbamazepine Beta-blockers Clofibric acid |
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