Transboundary ecological risks and toxicological mechanisms of a fluorinated liquid crystal monomer and aged microplastics

Journal Article (2026)
Author(s)

Rui Yang (Tsinghua University)

Sanjeeb Mohapatra (TU Delft - Sanitary Engineering)

Apple Pui Yi Chui (Chinese University of Hong Kong)

Season Si Chen (Tsinghua University)

Mui-Choo Jong (Tsinghua University)

Research Group
Sanitary Engineering
DOI related publication
https://doi.org/10.1016/j.jhazmat.2026.141802 Final published version
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Publication Year
2026
Language
English
Research Group
Sanitary Engineering
Journal title
Journal of Hazardous Materials
Volume number
507
Article number
141802
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Abstract

Fluorinated liquid crystal monomers (FLCMs) have recently emerged as persistent organic pollutants, while microplastics serve as important environmental carriers of persistent organic pollutants. However, their interactions with aged microplastics and the consequent ecological risks remain a critical blind spot. This study examined the adsorption-desorption dynamics of a representative FLCM (4-ethoxy-2,3-difluoro-4′-(trans-4-propylcyclohexyl) biphenyl, EDPB) on aged polyethylene, polypropylene, polystyrene, and polyvinyl chloride under both abiotic (i.e., environmental) and biotic (i.e., simulated gastrointestinal) conditions. Surface oxidation and increased roughness of aged polymers markedly enhanced EDPB adsorption, through combined hydrophobic attraction and fluorine‑mediated dipole interactions. Desorption was strongly medium dependent. In simulated gastric fluid, pepsin facilitated partial release (12.6–24.8%) by disrupting π–π interactions and promoting surface hydration. In contrast, intestinal components induced substantial remobilization (up to 52.8%) via the formation of hydrophobic cavities and micelle-like structures, increasing dissolved EDPB concentrations by approximately 20 μg L−1. This biphasic desorption profile highlights the critical role of intestinal processes in remobilizing adsorbed FLCMs and elevating their bioaccessible fractions. Subsequent cytotoxicity assays in Caco‑2 cells showed dose‑ and time‑dependent inhibition of cell viability, with transcriptomic analysis delineating a mitochondrial dysfunction–driven cascade. EDPB acts as a metabolic disruptor that impairs mitochondrial energetics and redox homeostasis, triggering downstream genomic instability and cell cycle arrest, which ultimately implicating oxidative stress–mediated apoptosis. This work synthesizes critical insight into the coupled environmental and biological behaviors of FLCMs, revealing their potential as transboundary persistent toxic substances and advancing the understanding of their risks in microplastic‑dominated systems.

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