Elucidation of phototransformation reactions of the X‐ray contrast medium iopromide under simulated solar radiation using UPLC‐ESI‐QqTOF‐MS |
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Authors: | Sandra Pérez Peter Eichhorn Vanesa Ceballos Damià Barceló |
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Institution: | 1. IDAEA‐CSIC, Department of Environmental Chemistry, Jordi Girona 18‐26, Barcelona 08034, Spain;2. Catalan Institute for Water Research (ICRA), Parc Científic i Tecnològic de la Universitat de Girona, Edifici Jaume Casademont, Porta A, Planta 1 ‐ Despatx 13C/Pic de Peguera, 15E‐17003 Girona, Spain |
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Abstract: | The highly polar, nonionic X‐ray contrast agent iopromide (C18H24N3O8I3; 791 Da) is resistant to microbial degradation during the activated sludge process in wastewater treatment plants and hence is released into the aquatic environment. Against this background, the present study was conducted to evaluate the phototransformation, potentially constituting the most relevant removal mechanism in rivers and streams. The photolysis of the iodinated aromatic compound was investigated in a Suntest solar simulator using aqueous solutions. Following a 120‐min irradiation period, an almost complete primary degradation of iopromide gave rise to a series of photoproducts that were chromatographed on a reversed‐phase UPLC and subsequently characterized by a combination of accurate mass measurements on a ESI‐QqToF‐MS instrument and H/D‐exchange experiments. This analytical approach facilitated confident identification of eight prominent products with the following elemental compositions and molecular weights: C18H25N3O9I2 (681 Da); C18H25N3O8I2 (665 Da); C17H23N3O8I2 (651 Da); C18H24N3O9I (553 Da); C17H24N3O8I (525 Da); C15H20N3O6I (465 Da); C14H18N3O6I (451 Da); and C18H25N3O9 (427 Da). Their formation was the result of four principal photoreactions: (1) gradual, and eventually complete, deiodination of the aromatic ring; (2) substitution of the halogen by a hydroxyl group; (3) N‐dealkylation of the amide in the hydroxylated side chain; and (4) oxidation of a methylene group in the hydroxylated side chain to the corresponding ketone. In conclusion, the findings of the artificial sunlight irradiation experiments indicated that in real environmental settings iopromide might suffer partial or even complete deiodination. Copyright © 2009 John Wiley & Sons, Ltd. |
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Keywords: | X‐ray contrast agent iopromide photolysis ESI‐QqToF‐MS photoproducts identification |
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