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May 18, 2026Chemosphere0 citationsOpen Access

Elucidation of colchicine degradation pathways under UVC, UVC/H2O2 and UVC/S2O82− processes: proposed transformation products identification, mechanistic insights and in silico evaluation

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EMEduardo O. MarsonGSG Martins dos SantosLCLucas Ezequiel Morais Costa

Key Points

  • This research aims to elucidate the pathways and mechanisms of colchicine degradation under various UVC-based processes.
  • Evaluated colchicine degradation under UVC, UVC/H2O2, and UVC/S2O82− processes.
  • Identified six transformation products (TPs) with focus on degradation kinetics and mechanisms.
  • Conducted in silico (Q)SAR assessments for TPs to evaluate mobility and persistence.
  • Over 90% colchicine removal achieved within 12 minutes with UVC (k = 0.22 min−1).
  • Oxidant-assisted processes enhanced degradation rates by 2.3–2.6 times.
  • Some TPs retained carcinogenic potential and were predicted to be non-biodegradable.

Abstract

Colchicine (COL), an alkaloid widely consumed during the COVID-19 pandemic, is inefficiently removed by conventional wastewater treatment plants, leading to environmental exposure to the parent compound and its transformation products (TPs). This study evaluated the degradation of COL under UVC, UVC/H 2 O 2 , and UVC/S 2 O 8 2− processes, focusing on degradation kinetics, TPs formation, degradation mechanisms, and toxicological and environmental relevance. Use of UVC achieved over 90% COL removal within 12 min (k = 0.22 min −1 ), while the oxidant-assisted processes enhanced degradation rates by 2.3 and 2.6 times, involving sulfate (SO 4 •– ) and hydroxyl (HO • ) radicals, respectively. Six TPs were identified, including process-specific and isomeric species, some reported for the first time, predominantly formed via O -demethylation, ether bond cleavage, and sulfate radical-mediated oxidation at the amide nitrogen. Photolytic, electron transfer, and hydrogen abstraction mechanisms were proposed. In silico (Q)SAR assessments revealed that all the TPs exhibited higher mobility and similar persistence, compared to COL, suggesting an increased potential for groundwater contamination. Most of the TPs were predicted to be non-biodegradable and inefficiently removed by conventional activated sludge treatment. Several TPs retained carcinogenic potential comparable to COL, particularly those formed under UVC/H 2 O 2 and UVC/S 2 O 8 2− . Overall, oxidant-assisted UVC processes promoted more effective degradation of both COL and its TPs, compared to photolysis alone. • UVC, UVC/H 2 O 2 , and UVC/S 2 O 8 2− generated distinct transformation products (TPs). • Identification of six proposed TPs, with two new compounds (TP 304 and TP 416). • Degradation involved O -demethylation, ether cleavage, and amide N -oxidation. • UVC formed one low-toxicity TP, but did not promote its degradation. • UVC/H 2 O 2 and UVC/S 2 O 8 2− formed TPs of higher concern, but degraded them.

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Cite This Study

Marson et al. (2026) studied this question.

synapsesocial.com/papers/6a0aac6d5ba8ef6d83b6fcfahttps://doi.org/10.1016/j.chemosphere.2026.144959
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