| Literature DB >> 29885499 |
Francisco E R Gomes1, Patricia L S Bergo2, Marília A Trap3, Mariângela Spadoto4, Carlos A Galinaro5, Edson Rodrigues-Filho3, Andrei Leitão6, Germano Tremiliosi-Filho6.
Abstract
Degradation studies of the propylparaben (PrP), butylparaben (BuP) and of the propylparaben-butylparaben mixture (PrP-BuP) in deionized water and surface river water was investigated as a function of pH and initial concentration of the reactants using a medium-pressure mercury lamp. The photolysis of parabens (concentration ranging from 5 to 30 mg L-1) followed apparent pseudo-first-order kinetics, with rate constants (k) in deionized water and surface river water changed from 1.80 × 10-1 to 3.68 × 10-2 min-1 and 1.43 × 10-1 to 1.45 × 10-2 min-1, respectively. Degradation reaction was faster at pH 5 in comparison with pH 7 or 11. The photolysis of parabens was greater than 91%, with low mineralization (26.15%) observed in acidic medium after 95 min. Analysis by chromatography coupled to mass spectrometry (LC-MS/MS) showed that only one product was generated during the degradation reaction and has UV bands similar to 3,4-dihydroxybenzoic acid. Estrogenic activity tests showed that non-degraded parabens stimulated the growth of breast adenocarcinoma (MCF-7) cells and this effect was evaluated after the photolysis. Cytotoxicity assays using fibroblasts cells (Balb/C 3T3 clone A31) indicated that the parental compounds and degradation products were not cytotoxic. On the contrary, non-degraded parabens were toxic to Ceriodaphnia dubia, but the product of photolysis was not. Overall, the photolytic method presented was able to degrade these parabens providing safe and non-estrogenic reaction product.Entities:
Keywords: Ceriodaphnia dubia.; Cytotoxicity assays; Estrogenic activity; Parabens; Photolysis
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Year: 2018 PMID: 29885499 DOI: 10.1016/j.chemosphere.2018.05.135
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086