Authors
Amal Tlili, Farah Ibrahim, Armand Fahs, Catherine Branger
Published in
Mikrochimica acta. Volume 193. Issue 12. Nov 09, 2026. Epub Nov 09, 2026.
Abstract
An electrochemical sensor for the selective detection of perfluorooctanoic acid (PFOA), a highly persistent and hazardous per- and polyfluoroalkyl substances (PFAS), was developed using a molecularly imprinted polymer (MIP) approach. The sensing layer was fabricated through surface-initiated controlled photopolymerization (via a "grafting from" strategy) directly from a commercial screen-printed gold electrode that was first functionalized with a tailor-made photoiniferter. Upon UV irradiation, acrylamide (AAm) and ethylene glycol dimethacrylate (EGDMA) were copolymerized in the presence of PFOA, generating specific recognition sites within the polymer network. Optimization was performed on the polymerization time and the extraction procedure of PFOA from the MIP layer, with morphological and chemical characterization via atomic force microscopy (AFM) and energy-dispersive X-ray spectroscopy (EDX), respectively. Sensor performances were assessed using square wave voltammetry (SWV). It could detect PFOA over a wide concentration range, from 8 pM to 80 µM, with a limit of detection (LOD) of 8 pM (3.31 ng/L). Selectivity was evaluated against structurally similar non-fluorinated compounds, as well as short- and long-chain PFAS, showing good recognition of PFOA even in competitive mixtures (ratios of 1:1, 1:5, and 1:10). Applicability was further confirmed through successful detection in tap water, surface freshwater, and river water demonstrating good correlation between electrochemical measurements and high-performance liquid chromatography (HPLC-MS/MS) results. The controlled grafting strategy developed enables the formation of a robust and selective MIP layer, offering a promising platform for sensitive PFAS detection in natural waters.
PMID:
43000466
Bibliographic data and abstract were imported from PubMed on 09 Nov 2026.
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