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Combined Environmental Impacts and Toxicological Interactions of Per- and Polyfluoroalkyl Substances (PFAS) and Microplastics (MPs)
Summary
This review examines how microplastics and per- and polyfluoroalkyl substances (PFAS) frequently co-occur in the environment and interact to alter each other's environmental fate and biological effects. Researchers found that co-exposure can enhance PFAS bioaccumulation by up to 2.5-fold compared to PFAS alone, accompanied by amplified oxidative stress, immune disruption, and reproductive impairment in aquatic organisms. The magnitude and direction of combined effects depend heavily on polymer type, particle size, surface aging, and biological context.
Pervasive microplastics (MPs) and per- and polyfluoroalkyl substances (PFAS) frequently co-occur across aquatic and terrestrial environments due to shared sources, transport pathways, and persistence, yet their interaction-driven effects on environmental fate, bioavailability, and toxicity remain incompletely resolved. This review critically synthesizes current knowledge on the environmental co-occurrence of MPs and PFAS, the physicochemical mechanisms governing their interactions, and the resulting ecological and toxicological consequences across aquatic, terrestrial, and biological systems. Emphasis is placed on sorption and desorption processes; environmental modifiers such as pH, salinity, dissolved organic matter (DOM), and aging; and biological responses under combined exposure scenarios. Across laboratory and field studies, MPs–PFAS co-exposure is frequently associated with altered PFAS partitioning and enhanced organismal uptake, with reported bioaccumulation increases of up to ~2.5-fold relative to PFAS-only exposures. These changes are often accompanied by amplified oxidative stress, immune dysregulation, metabolic disturbance, and reproductive impairment, particularly in aquatic invertebrates and early life stages of fish. Evidence further indicates that the magnitude and direction of combined effects depend on polymer type, particle size, surface aging, and biological context, underscoring the highly system-specific nature of MPs–PFAS interactions. By integrating findings from environmental monitoring, laboratory toxicology, and mechanistic and modeling studies, this review identifies key knowledge gaps related to nanoplastics detection, environmentally realistic exposure conditions, sorption reversibility, and mixture toxicity assessment. Collectively, these insights highlight limitations in current single-contaminant risk frameworks and underscore the importance of incorporating MPs-mediated PFAS transport and bioavailability into exposure assessment and regulatory evaluation.
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