2016
DOI: 10.1016/j.envpol.2016.03.018
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Environmental fate and effect assessment of thioridazine and its transformation products formed by photodegradation

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Cited by 22 publications
(9 citation statements)
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“…Toxicity (measured with the use of V. fisheri ) was decreasing in parallel with thioridazine phototransformation. QSAR analysis revealed that carbazole derivatives formed during phototreatment may possess mutagenic or genotoxic properties (Wilde et al 2016 ).
Fig.
…”
Section: Photodegradation Studies On Psychotropic Drugsmentioning
confidence: 99%
“…Toxicity (measured with the use of V. fisheri ) was decreasing in parallel with thioridazine phototransformation. QSAR analysis revealed that carbazole derivatives formed during phototreatment may possess mutagenic or genotoxic properties (Wilde et al 2016 ).
Fig.
…”
Section: Photodegradation Studies On Psychotropic Drugsmentioning
confidence: 99%
“…[ 46 , 47 ], a phototransformation pathway being proposed for TZ (simulated sunlight irradiation via UV-Vis xenon lamp, initial conditions: 800 mL ultrapure water solutions, 0.5 and 50 mg/L concentrations, 6.5 pH, 20 ± 2 °C temperature) in Ref. [ 48 ]. Wilde et al reported that the primary elimination of TZ follows the two-steps first-order exponential kinetic model.…”
Section: Resultsmentioning
confidence: 99%
“…Wilde et al reported that the primary elimination of TZ follows the two-steps first-order exponential kinetic model. The molecular structure of the identified photoproducts was clarified by liquid chromatography-mass spectrometry (LC-MS), where the degradation pathway included hydroxylation, sulfoxidation, dehydroxylation, as well as S- and N-dealkylation, TZ-2-sulfoxide and TZ-5-sulfoxide being the two main occurring products known as the pharmacologically active human metabolites of TZ [ 48 ]. Out of the nine photoproducts, visualized by previous TLC analysis [ 28 ], four were identified following the irradiation of TZ under the same conditions as in the present study (4 h 266 nm laser exposure, 2 mg/mL concentration, 20–25 °C temperature), namely: mesoridazine (TZ-2-sulfoxide) which suffers further 2-oxidation to sulforidazine (TZ-2-sulphone), TZ-5-sulfoxide and TZ-N-desmethyl [ 28 ].…”
Section: Resultsmentioning
confidence: 99%
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“…Photodegradation, as an abiotic process, may have an important effect on the persistence of MPs. 19,20 Photochemical degradation is reported to be the dominant attenuation pathway for sulfonamides, opioids and organophosphorus flame retardants in surface water. [21][22][23] It is therefore necessary to understand the phototransformation processes of MPs in water.…”
Section: Introductionmentioning
confidence: 99%