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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Environmental photochemical fate and UVC degradation of sodium levothyroxine in aqueous medium

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Author(s):
Silva Parizi, Marcela Prado [1] ; Lastre Acosta, Arlen Mabel [2] ; Ishiki, Hamilton Mitsugu [3] ; Rossi, Renata Calciolari [3] ; Mafra, Renata Cristina [3] ; Silva Costa Teixeira, Antonio Carlos [2]
Total Authors: 6
Affiliation:
[1] Sao Paulo State Univ UNESP, Energy Engn Dept, Barrageiros Av 1881, Rosana, SP - Brazil
[2] Univ Sao Paulo, Dept Chem Engn, Chem Syst Engn Ctr, Res Grp Adv Oxidat Proc, Av Prof Luciano Gualberto Tr 3, 380, Sao Paulo, SP - Brazil
[3] Univ Western Sao Paulo Unoeste, Environm & Reg Dev, Presidente Prudente, SP - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Environmental Science and Pollution Research; v. 26, n. 5, p. 4393-4403, FEB 2019.
Web of Science Citations: 0
Abstract

The synthetic hormone sodium levothyroxine (LTX) is one of the most prescribed drugs in the world and the most effective in hypothyroidism treatment. The presence of LTX in the environment has become a matter of major concern due to the widespread use of this hormone and by the fact that it is only partially removed in conventional water and sewage treatment plants. However, information regarding the photochemical fate of this hormone in environmental or engineered systems is scarce in the literature. In this work, the sunlight-driven direct and indirect LTX degradation was investigated by determining the photolysis quantum yield, I broken vertical bar (LTX) = 3.80 (+/- 0.02) x 10(-5), as well as the second-order kinetic constants of the reactions with hydroxyl radicals, k (LTX,aEuro cent OH) = 1.50 (+/- 0.01) x 10(10) L mol(-1) s(-1) and singlet oxygen, k (LTX,1O2) = 1.47 (+/- 0.66) x 10(8) L mol(-1) s(-1). Mathematical simulations indicate that LTX photodegradation is favored in shallow, nitrite-rich, and dissolved organic matter (DOM)-poor environments, with LTX half-life times varying from less than 10 days to about 80 days. LTX removals of 85 and 95% were achieved by UVC photolysis and UVC/H2O2 after 120 min, respectively. Three transformation products, triiodothyronine, diiodothyronine, and diiodotyrosine, were identified during LTX degradation by the UVC-based processes studied. The results herein regarding photo-induced kinetics coupled with environmental fate simulations may help evaluate LTX persistence and also the design of water and wastewater treatment processes. (AU)

FAPESP's process: 13/50218-2 - CEPEMA - Cooperative Center of Environmental Engineering
Grantee:Claudio Augusto Oller do Nascimento
Support Opportunities: Research Projects - Thematic Grants