Sep 2026· Journal of Hazardous Materials· Vol 517, pp.
143697
· 0 citations· 34 references
Medicine
Abstract
Per- and polyfluoroalkyl substances (PFAS) require sensitive, selective, and field-compatible monitoring in aquatic environments. Perfluorooctanoic acid (PFOA) remains challenging for electrochemical detection because of its intrinsic redox inactivity and amphiphilic structure. Here, an external-probe-free electrochemical sensor was developed by constructing a ferrocene-integrated fluorinated molecularly imprinted polymer on a screen-printed electrode (Fc-F-MIP/SPE). Methacrylic acid, 2,2,2-trifluoroethyl methacrylate, and ferrocenylmethyl methacrylate were rationally combined to provide polar recognition, fluorinated affinity, and built-in redox signaling, respectively. PFOA rebinding restricted the accessibility of the embedded ferrocene units, producing a concentration-dependent signal-off response. Theoretical calculations supported cooperative interactions between PFOA and the functional monomers, while response-based Langmuir-Freundlich-type fitting was consistent with heterogeneous apparent affinities within the imprinted layer. Under optimized conditions, Fc-F-MIP/SPE exhibited a wide detection range of 4.14-4.14 × 108 ng L-1 and a low detection limit of 3.11 ng L-1. The sensor also showed good selectivity against common coexisting substances and PFAS analogues, acceptable 7-day storage stability, and satisfactory recoveries in drinking water, tap water, and river water. By integrating amphiphilic recognition with internal ferrocene-mediated signal transduction, this work provides a reagent-minimized and portable strategy for PFOA monitoring in environmental waters.
Per- and polyfluoroalkyl substances (PFAS) are persistent synthetic fluorinated contaminants that require rapid, sensitive, and field-deployable analytical technologies beyond conventional laboratory-based mass spectrometry. Here, we report a nanoMIP-metal-phenolic network (MPN) electrochemical sensing platform for hig...
P. Lasserre, Nozomi Matsudaira, Tobias Hrovat et al.· Biosensors & bioelectronics· 0 citations
The accumulation of perfluorooctanoic acid (PFOA) in environmental waters poses substantial environmental and health risks, even at trace levels, owing to its environmental persistence. Here we developed an electrochemical sensor integrating molecularly imprinted polymers with functionalized metal–organic frameworks (M...
Kai Niu, Jiu-Xing Li, Rui Zhang et al.· Chemical Science· 0 citations
The typical off-flavor compound 2-methylisoborneol (2-MIB) is widely present in water bodies which induces unpleasant odors in water even at extremely low concentrations. It is urgent to develop a simplified laboratory-based electrochemical screening workflow for trace 2-MIB quantification since the traditional detecti...
Hao-Wen Hong, Jun Wu, Jian Lu· In Analysis· 0 citations
Perfluorooctanesulfonate (PFOS) is a highly persistent and toxic per- and polyfluoroalkyl substance (PFAS) widely recognized for its serious risks to both environmental and human health. In this work, an electrochemical impedance spectroscopy (EIS)-based sensor was developed for PFOS detection by integrating a MIL-101(...
Yu-Kang Wang, Eduardo C. Atayde, Sher-Ling Lee et al.· Langmuir· 0 citations
Electrochemical sensors still suffer from challenges associated with interference caused by fouling in complex matrices. To address this issue, we designed a tailored high-performance antifouling sensor interface based on a thiol-terminated zwitterionic terpolymer, [P(MPC-CBMA-MAA)-SH, PMCM-SH], by fine-tuning the comp...
Jin-Zhi Liang, Cheng Zhang, Kun Ge et al.· Food Chemistry· 0 citations
Per- and polyfluoroalkyl substances (PFAS) are widely employed in diverse industrial applications owing to their exceptional stain resistance, thermal stability, mechanical durability, and intrinsic non-biodegradable nature. Among this class of compounds, perfluorooctanoic acid (PFOA) stands as a representative and ext...
Wei-Ting Zhao, Xue Zhang, Yun-Sheng Shang et al.· Spectrochimica Acta Part A -...· 0 citations
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