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Per- and polyfluoroalkyl substances (PFAS) comprise many chemicals with strong carbon-carbon and carbon-fluorine bonds and have extensive industrial applications in manufacturing several consumer products. The solid covalent bonding makes them more persistent in the environment and stays away from all types of degradation, naming them 'forever chemicals.' Zebrafish (Danio rerio) was used to evaluate the genotoxic and cytotoxic effects of legacy PFAS, Perfluorooctane sulfonate (PFOS), and its alternatives, such as Perfluoro-2-methyl-3-oxahexanoic acid ammonium (GenX) and 7H-Perfluoro-3,6-dioxa-4-methyl-octane-1-sulfonic acid (Nafion by-product 2 [NBP2]) upon single and combined exposure at an environmental concentration of 10 µg/L for 48-h. Erythrocyte micronucleus cytome assay (EMNCA) revealed an increased frequency of micronuclei (MN) in fish erythrocytes with a significant increase in NBP2-treated fish. The order of genotoxicity noticed was NBP2 > PFOS > Mixture > GenX in D. rerio. Fish exposed to PFOS and its alternatives in single and combined experiments did not cause any significant difference in nuclear abnormalities. However, PFOS and combined exposure positively inhibit cytokinesis, resulting in an 8.16 and 7.44-fold-change increase of binucleated cells. Besides, statistically, increased levels of reactive oxygen species (ROS) and malondialdehyde (MDA) content indicate oxidative stress in D. rerio. In addition, 'forever chemicals' resulted in cytotoxicity, as evident through changes in nucleus width to the erythrocyte length in NBP2 and mixture exposure groups. The findings revealed that PFAS alternative NBP2 is more toxic than PFOS in inducing DNA damage and cytotoxicity. In addition, all three tested 'forever chemicals' induced ROS and lipid peroxidation after individual and combined exposure. The present work is the first to concern the genotoxicity and cytotoxicity of 'forever chemicals' in the aquatic vertebrate D. rerio.
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http://dx.doi.org/10.1016/j.mrgentox.2024.503788 | DOI Listing |
Environ Sci Pollut Res Int
September 2025
Data Forward Analytics, LLC, Principal, Las Cruces, NM, 88011, USA.
Per- and poly-fluoroalkyl substances (PFAS) are fluorinated organic compounds known as forever chemicals that are used in many materials, from cooking appliances to industrial detergents. Given their high chemical stability due to their lipophilic properties and widespread use, PFAS tend to bioaccumulate in the cardiac, hepatic, renal, gastrointestinal, and neural tissues, resulting in a variety of malignant and non-malignant diseases. Depression is a prevalent mental health condition that affects an individual's activities of daily living.
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science and Engineering, Fudan University, Shanghai 200433, People's Republic of China.
The exceptional stability of carbon-fluorine (C-F) bonds in perfluorooctanoic acid (PFOA) presents a fundamental challenge in environmental remediation as traditional degradation methods struggle to break these bonds under mild conditions. Here, we demonstrate that the air-water interface in microdroplets can be strategically utilized to dramatically enhance PFOA ( = 20 mg L) degradation through a simple Fe(III)-Oxalate photochemical system, achieving complete destruction with 99% defluorination within 4 h at room temperature - a rate 2 orders of magnitude faster than conventional methods. Through comprehensive spectroscopic and computational investigations, we reveal that this remarkable enhancement stems from three synergistic interfacial effects: concentrated generation of superoxide radicals (O) from earth-abundant Fe(III)-Oxalate complexes, significantly enhanced O nucleophilicity due to disrupted solvation shells, and a strong interfacial electric field that catalyzes C-F bond activation.
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
Institute of Environment and Ecology, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, P. R. China.
Recognized as a "forever chemical", perfluorooctanoic acid (PFOA) calls for urgent environmental cleanup. Photocatalytic degradation emerged as a sustainable solution, but it still suffers from sluggish reaction kinetics and insufficient C-F bond cleavage. Addressing the above bottlenecks, we strategically constructed frustrated Lewis acid-base pairs (FLP) on InO photocatalyst, which theoretically reduces the PFOA decarboxylation energy by 2.
View Article and Find Full Text PDFCommun Chem
August 2025
Department of Chemistry, Shantou University, Shantou, PR China.
The recalcitrance of fluorinated organic pollutants-featuring robust Csp²-F and Csp³-F bonds-poses critical challenges to aquatic ecosystems due to their extreme persistence and bioaccumulation. Whereas current destruction strategies suffer from high energy consumption and non-selective, here we present a solar-powered mineralization strategy utilizing cerium oxide/mesoporous silica (CeO/mSiO) heterojunction photocatalysts for complete defluorination of organofluorine contaminants, including fluorinated e-waste, fluoro-antibiotics and perfluorinated surfactant. Under visible light irradiation, the optimized 5%CeO/mSiO achieved 91.
View Article and Find Full Text PDFEnviron Res
August 2025
MOE Key Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing, 100871, China. Electronic address:
Legacy organochlorine pesticides (OCPs) persist as global environmental threats despite international bans, while novel OCPs have been widely adopted as alternatives; however, the spatiotemporal dynamics and regulatory drivers of both legacy and novel OCPs in river systems remain poorly quantified. This study revealed the spatiotemporal distribution, source contributions, drivers, and historical trends of traditional and novel OCPs in 131 river sediment samples. Total OCP concentrations (42.
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