Direct photolysis of diclofenac under simulated sunlight: Transformation pathway and biological concerns.


Journal

Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 18 04 2022
revised: 05 07 2022
accepted: 16 07 2022
pubmed: 23 7 2022
medline: 28 9 2022
entrez: 22 7 2022
Statut: ppublish

Résumé

Topical diclofenac gels are frequently applied on human skin and, consequently are exposed to sunlight during outdoor activities. The degradation of diclofenac (DCF) with sunlight exposure is known to occur but the detailed transformation characteristics and biological concerns have not been comprehensively investigated. In the present work, the transformation products during diclofenac photolysis were identified with the aid of ultra-performance liquid chromatography coupled with triple time-of-flight mass spectrometry (UPLC-TripleTOF). Biological concerns, including microtoxicity, genotoxicity, cytotoxicity and antiestrogenicity were examined with multiple in-vitro bioassays. Spearman correlation analysis was conducted to obtain further insight into the contributions of photolysis products to overall biological concerns. The results demonstrated that diclofenac was readily degraded under sunlight to form five main photolysis products via substitution, dechlorination, dehydroxylation, homodimerization and heterodimerization. Products P1, P2 and P5 were reported previously, while two dimer products (P3 and P4) are innovative products and have not been found in prior studies. A significant elevation in the microtoxicity was found during the photolysis of diclofenac, resulting mainly from the carbazole-containing photolysis products P2, P3, P4 and P5. Genotoxicity and antiestrogenicity declined along with the reduction of diclofenac, indicating that no photolysis products were genotoxic or anti-estrogenic. Modest cytotoxicity to the human skin epidermis cell line was observed and attributed to the formation of intermediate species. This outcome highlighted the biological concerns of diclofenac to human health when exposed to sunlight.

Identifiants

pubmed: 35868525
pii: S0045-6535(22)02268-8
doi: 10.1016/j.chemosphere.2022.135775
pii:
doi:

Substances chimiques

Carbazoles 0
Gels 0
Water Pollutants, Chemical 0
Diclofenac 144O8QL0L1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

135775

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Li-Ping Li (LP)

Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai, 519087, China. Electronic address: lliay@connect.ust.hk.

Yan-Chao Jin (YC)

College of Environmental Science and Engineering, Fujian Normal University, Fuzhou, 350007, China; Fujian Key Laboratory of Pollution Control & Resource Reuse, Fuzhou, 350007, China.

Le Fang (L)

Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai, 519087, China.

Cheng Zhang (C)

Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai, 519087, China.

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Classifications MeSH