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The natural anthraquinone dye emodin: Eco/genotoxicological characterization for aquatic organisms.

Authors :
de Farias, Natália Oliveira
Rodrigues, Amanda Rocha
Botelho, Marina Tenório
Magalhães, Gabriel Rampazzo
Räisänen, Riikka
Freeman, Harold S.
Umbuzeiro, Gisela de Aragão
Source :
Food & Chemical Toxicology. Jul2024, Vol. 189, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Emodin is an anthraquinone secondary metabolite produced by several species of plants and fungi. Emodin is known for its pharmacological versatility, and, in the textile industry, for its good dyeing properties. However, its use in the textile industry can result in the formation and disposal of large volumes of wastewater. Emodin mutagenicity has been shown in bacteria and in human cells, but little is known about its possible toxic, genotoxic, or mutagenic effects in aquatic organisms. We have evaluated the eco/genotoxicity of emodin to aquatic organisms. Emodin was toxic to Daphnia similis (EC 50 = 130 μg L−1) and zebrafish embryos (LC 50 = 25 μg L−1). No toxicity was observed for Raphidocelis subcapitata , Ceriodaphnia dubia , or Parhyale hawaiensis. Additional biochemistry/molecular studies are needed to elucidate the toxic/mutagenic pathways of emodin in aquatic organisms. The PNEC value for emodin was 0.025 μg L−1. In addition to mutagenicity in the Salmonella /microsome assay, emodin was mutagenic in the micronucleus assay in the amphipod P. hawaiensis. Among the anthraquinone dyes tested to date, natural or synthetic, emodin was the most toxic to aquatic species. • Emodin is toxic to Daphnia similis and Danio rerio embryos. • Among the organisms studied, Danio rerio embryo was the most sensitive to emodin. • Emodin is mutagenic to Parhyale hawaiensis. • Emodin is more toxic than dermorubin and dermocybin to aquatic species. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02786915
Volume :
189
Database :
Academic Search Index
Journal :
Food & Chemical Toxicology
Publication Type :
Academic Journal
Accession number :
177885420
Full Text :
https://doi.org/10.1016/j.fct.2024.114749