Photodegradation of sulfamethoxazole in various aqueous media: Persistence, toxicity and photoproducts assessment
Nenhuma Miniatura disponível
Data
2009-11-01
Autores
Trovo, Alam G. [UNESP]
Nogueira, Raquel Fernandes Pupo [UNESP]
Agueera, Ana
Sirtori, Carla
Fernandez-Alba, Amadeo R.
Título da Revista
ISSN da Revista
Título de Volume
Editor
Pergamon-Elsevier B.V. Ltd
Resumo
The photochemical transformation of sulfa methoxazole (SMX) was investigated in different water matrices: distilled water (DW), distilled water + nitrate (10 and 20 mg L(-1)) and seawater (SW) to evaluate its persistence, toxicity and degradation pathway. A solar simulator Suntest CPS+ was used for the irradiation experiments. Identification of transformation products was performed in DW by liquid chromatography-time of flight-mass spectrometry (LC-TOF-MS). Acute toxicity of irradiated solutions was monitored by Vibrio fischeri and Daphnia magna bioassays in DW. Differences in the degradation rates were observed between DW and SW, being slower in SW. Presence of nitrate (indirect photolysis) in distilled water did not affect SMX degradation rate. No dissolved organic carbon (DOC) removal was observed in any case, thus indicating the formation of abundant transformation products (TPs). Analysis by LC-TOF-MS allowed the identification of up to nine transformation products during photolysis in DW. Only three of them had been previously reported in the literature, detected with other techniques. The cleavage of the sulfonamide bond and the photoisomerization by rearrangement of the isoxazole ring represent the main pathways, at the time that generate the most abundant and persistent intermediates. The acute toxicity of SMX solution varied according to test organisms. Daphnia magna was the most sensitive showing an increase from 60% to 100% immobilization after 30 h of irradiation when depletion of SMX was achieved, thus indicating the higher toxicity of the phototransformation products generated. (C) 2009 Elsevier Ltd. All rights reserved.
Descrição
Palavras-chave
Pharmaceuticals, Liquid chromatography, Mass spectrometry, Transformation product
Como citar
Chemosphere. Oxford: Pergamon-Elsevier B.V. Ltd, v. 77, n. 10, p. 1292-1298, 2009.