4.7 Article

Exploring the phototransformation and assessing the in vitro and in silico toxicity of a mixture of pharmaceuticals susceptible to photolysis

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 756, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.144079

Keywords

Ecotoxicity; HRMS; Pharmaceuticals; Photolysis; Transformation products

Funding

  1. General Secretariat for Research and Technology (GSRT)
  2. Hellenic Foundation for Research and Innovation (H.F.R.I.) [429]
  3. COST (European Cooperation in Science and Technology)
  4. 2014-2020 Interreg IPA Cross Border Cooperation Programme [CCI 2014 TC 16 I5CB 009]
  5. Greece Republic of North Macedonia, Research Project: Aqua-M II: Sustainable management of cross-border water resources [5030774]

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The study comprehensively investigated the phototransformation and ecotoxicity of a mixture of twelve pharmaceutically active compounds susceptible to photolysis. A total of 166 transformation products were identified, including twelve novel ones. The results demonstrated that photolysis of the target mixture leads to a decrease of the observed toxicity.
The present study comprehensively investigates the phototransformation and ecotoxicity of a mixture of twelve pharmaceutically active compounds (PhACs) susceptible to photolysis. Namely, three antibiotics (ciprofloxacin, levofloxadn, moxifloxacin), three antidepressants (bupropion, duloxetine, olanzapine), three anti-inflammatory drugs (diclofenac, ketoprofen, nimesulide), two beta-blockers (propranolol, timolol) and the antihistamine ranitidine were treated under simulated solar irradiation in ultra-pure and river water. A total of 166 different transformation products (TPs) were identified by ultra-high performance liquid chromatography coupled with Orbitrap high resolution mass spectrometry (UHPLC-Orbitrap HRMS), revealing the formation of twelve novel TPs and forty-nine not previously described in photolytic studies. The kinetic profiles of the major TPs resulting from a series of chemical reactions involving hydroxylation, cleavage and oxidation, dehalogenation, decarboxylation, dealkylation and photo substitution have been investigated and the transformation pathways have been suggested. Additionally, an in vitro approach to the toxicity assessment of daphnids was contrasted with ecotoddty data based on the Ecological Structure Activity Relationships (ECOSAR) software comprising the in silico tool to determine the adverse effects of the whole mixture of photolabile parent compounds and TPs. The results demonstrated that photolysis of the target mixture leads to a decrease of the observed toxicity. (C) 2020 Published by Elsevier B.V.

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