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Toward Sustainable Antifouling Solutions: Degradation Profile of Promising Nature-Inspired Flavonoids

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  • Daniela Pereira

    (LSRE-LCM, ALiCE, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal
    Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal
    These authors contributed equally to this work.)

  • Sofia Duarte

    (Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal
    These authors contributed equally to this work.)

  • Cátia Vilas-Boas

    (Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal)

  • Joana R. Almeida

    (CIIMAR/CIMAR LA—Interdisciplinary Center of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, 4450-208 Matosinhos, Portugal)

  • Maria J. Sampaio

    (LSRE-LCM, ALiCE, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal)

  • Honorina Cidade

    (Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal
    CIIMAR/CIMAR LA—Interdisciplinary Center of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, 4450-208 Matosinhos, Portugal)

  • Alexandra S. Maia

    (Associate Laboratory i4HB—Institute for Health and Bioeconomy, University Institute of Health Sciences—CESPU, 4585-116 Gandra, Portugal
    UCIBIO—Applied Molecular Biosciences Unit, Translational Toxicology Research Laboratory, University Institute of Health Sciences (1H-TOXRUN, IUCS-CESPU), 4585-116 Gandra, Portugal)

  • Maria Elizabeth Tiritan

    (Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal
    CIIMAR/CIMAR LA—Interdisciplinary Center of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, 4450-208 Matosinhos, Portugal)

  • Marta Correia-da-Silva

    (Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal
    CIIMAR/CIMAR LA—Interdisciplinary Center of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, 4450-208 Matosinhos, Portugal)

Abstract

The accumulation of aquatic organisms on submerged surfaces causes major economic and environmental impacts in marine ecosystems. Conventional antifouling biocides pose risks due to toxicity to non-target species and bioaccumulation. Nature-inspired compounds such as flavonoids have emerged as more sustainable alternatives. Aiming to assess the environmental impact of new antifouling flavonoids and to evaluate the toxicity of their transformation products, this study investigates the degradation of three promising antifouling flavonoids (chalcone CC345G and dihydrochalcones DH345 and DH345P) in aqueous matrices. Comprehensive abiotic and biotic degradation assays (hydrolysis, photodegradation, and biodegradation) were conducted. Appropriate liquid chromatography with UV detection methods were developed and validated to monitor the studies. The glycosylated chalcones bearing a triazole moiety CC345G revealed no detectable degradation under any of the experimental conditions. In contrast, both dihydrochalcones underwent significant abiotic degradation; DH345 was more susceptible to hydrolysis at pH 7.10 (17.41% degradation), while DH345P was more prone to photolysis in sterilized natural seawater at pH 8.82 (45.82–54.52% degradation), also showing substantial degradation in hydrolysis (24.34–42.41%) and biodegradation (33.43–41.07%). Overall, the prenylated dihydrochalcone DH345P exhibited the highest degradation rate among the tested compounds. Analysis with high-resolution mass spectrometry disclosed several transformation products in degradation assays, and one chemical structure was proposed. Preliminary ecotoxicity assessment performed on the degradation products using Artemia salina indicated low toxicity, suggesting minimal environmental impact.

Suggested Citation

  • Daniela Pereira & Sofia Duarte & Cátia Vilas-Boas & Joana R. Almeida & Maria J. Sampaio & Honorina Cidade & Alexandra S. Maia & Maria Elizabeth Tiritan & Marta Correia-da-Silva, 2026. "Toward Sustainable Antifouling Solutions: Degradation Profile of Promising Nature-Inspired Flavonoids," Sustainability, MDPI, vol. 18(9), pages 1-17, April.
  • Handle: RePEc:gam:jsusta:v:18:y:2026:i:9:p:4364-:d:1930884
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