{"title":"Positive promotion effect of negative potential on propanethiol degradation in microbial electrolytic cells.","authors":"Juping You, Zuxi Liu, Zeyu Li, Zhenyi Ji, Jian Yu, Miaomiao Qu","doi":"10.1016/j.bioelechem.2026.109488","DOIUrl":"https://doi.org/10.1016/j.bioelechem.2026.109488","url":null,"abstract":"<p><p>Volatile organic sulfur compounds (VOSCs) are typical odorous pollutants that are difficult to abate. The effective removal of VOSCs by microbial electrolytic cells (MECs) is a promising strategy for reducing mitigation. This work employed propanethiol (PT) as a representative contaminate and explored the performance of MEC by controlling anodic potentials at -0.4, -0.2, 0, 0.2, 0.4 V (vs. Ag/AgCl). The results indicated that the potential of -0.2 V and -0.4 V increased PT removal by 8.2% and 13.9%, while sulfate conversion rose by 6.7% and 12.6%, demonstrating the prominent enhancement of negative polarization for PT remediation. Low-negative bioanode potentials of -0.4 V and -0.2 V drove high sulfur-to-sulfate conversion of 51.2% and 45.3%, highest protein/polysaccharide ratio of 1.37 and outer-membrane c-type cytochromes content of 36.7 μmol/cm<sup>3</sup>. Moreover, microbial community analysis showed that the abundance of functional species of Acinetobacter sp. and Thiobacillus sp. were increased. Furthermore, the observed nanowires together with metagenomic evidence further demonstrated that negative potentials exerted positive effects on microbial electroactivity. Overall, this study elucidates bioanode potential driven PT degradation of in MECs, providing valuable implications for abatement of VOSCs via bioelectrochemical systems.</p>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":" ","pages":"109488"},"PeriodicalIF":4.9,"publicationDate":"2026-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149331924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-31DOI: 10.1016/j.bioelechem.2026.109484
Valentin Saunier, Fanny Volat, Camille Gironde, Benoit Chaput, Louis Renaud, Anne Bouloumié, Alain Bergel
{"title":"Mediated amperometric monitoring of redox changes during adipocyte differentiation.","authors":"Valentin Saunier, Fanny Volat, Camille Gironde, Benoit Chaput, Louis Renaud, Anne Bouloumié, Alain Bergel","doi":"10.1016/j.bioelechem.2026.109484","DOIUrl":"https://doi.org/10.1016/j.bioelechem.2026.109484","url":null,"abstract":"<p><p>Real-time monitoring of intracellular redox dynamics provides valuable insight into biological processes such as adipocyte differentiation or adipogenesis. However, assessment of these dynamic metabolic changes in living cells remains technically challenging. Here, we evaluated a DCIP-mediated amperometric sensing for monitoring intracellular redox homeostasis during adipogenesis. Human immortalized and primary adipogenic progenitors were cultured directly on the surface of carbon electrodes. Cells were maintained under adipogenic conditions for 10 days. Cell viability, density, and differentiation were assessed by imaging and cytotoxicity assays at days 0 and 10. Intracellular redox activity was monitored by chronoamperometry following electrode polarization and addition of 2,6-dichlorophenolindophenol (DCIP). DCIP at 15 μM generated a rapid and reproducible amperometric response without detectable cytotoxicity for 30 min. The current stabilized within one minute, increased proportionally with the number of adherent cells and responded to metabolic perturbations demonstrating that the signal reflected cellular metabolic activity. Most importantly, differentiated adipogenic progenitors exhibited higher currents than undifferentiated cells, reflecting associated changes of intracellular electron-transfer activity. Collectively, the findings demonstrate that this DCIP-mediated amperometric platform enables rapid, reproducible and standardized monitoring of intracellular redox changes associated with adipogenesis providing a fluorescent probe-free, sensitive, non-destructive approach for real-time investigation of cellular metabolism and differentiation.</p>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":" ","pages":"109484"},"PeriodicalIF":4.9,"publicationDate":"2026-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149293540","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Precise detection of telomerase reverse transcriptase C228T mutation using label-free and magnetically induced self-assembly electrochemical biosensors.","authors":"Wentao Li, Min Liu, Zhanyi Qu, Qianqian Deng, Ruijiang Liu, Zhan-Ao Wu","doi":"10.1016/j.bioelechem.2026.109473","DOIUrl":"https://doi.org/10.1016/j.bioelechem.2026.109473","url":null,"abstract":"<p><p>Telomerase reverse transcriptase promoter C228T mutations (TERT<sub>C228T</sub>) are strongly associated with poor outcomes in papillary thyroid cancer, necessitating sensitive detection methods. In this work, a \"Signal-off\" type of label-free and magnetically induced self-assembly electrochemical biosensors based on α-Fe<sub>2</sub>O<sub>3</sub>/Fe<sub>3</sub>O<sub>4</sub>@Au magnetic nanocomposites (MNCs) were developed for TERT<sub>C228T</sub> detection. Thiolated aptamers (Apts) for specific recognition of TERT<sub>C228T</sub> were immobilized on α-Fe<sub>2</sub>O<sub>3</sub>/Fe<sub>3</sub>O<sub>4</sub>@Au MNCs via AuS bonds, and bovine serum albumins (BSA) were employed to block non-specific sites and form α-Fe<sub>2</sub>O<sub>3</sub>/Fe<sub>3</sub>O<sub>4</sub>@Au-Apt/BSA biosensors. TERT<sub>C228T</sub> specifically hybridized with Apts, forming a rigid dsDNA film on the electrode. Enhanced steric hindrance and electrostatic repulsion suppressed electron transfer of [Fe(CN)<sub>6</sub>]<sup>3-/4-</sup>, leading to decreased current signals. The biosensors were evaluated by cyclic voltammetry, electrochemical impedance spectroscopy, and differential pulse voltammetry, the results demonstrated that the biosensors exhibited a wide linear range (10<sup>2</sup> pM- 10<sup>6</sup> pM), high sensitivity (LOD of 0.67 pM), and excellent selectivity, along with high reproducibility (RSD = 1.84%) and long-term stability (signal retention above 95% within 10 days), and enabled reliable detection in diluted human serum (recoveries of 98.1%-107.3%). Overall, the electrochemical biosensors offer a simple, rapid, and ultrasensitive platform for TERT<sub>C228T</sub> detection, with promising potential for molecular diagnosis and thyroid cancer risk stratification.</p>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":" ","pages":"109473"},"PeriodicalIF":4.9,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149219731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-03-04DOI: 10.1016/j.bioelechem.2026.109264
Caio C.G. Silva , Alessandro Cacia , Hernán D. Rojas-Mantilla , Maria V.B. Zanoni , Saulo S. Garrido , Felipe Conzuelo
{"title":"Microalgae cells with extracellular gold nanoparticles for enhanced photobioelectrochemical activity","authors":"Caio C.G. Silva , Alessandro Cacia , Hernán D. Rojas-Mantilla , Maria V.B. Zanoni , Saulo S. Garrido , Felipe Conzuelo","doi":"10.1016/j.bioelechem.2026.109264","DOIUrl":"10.1016/j.bioelechem.2026.109264","url":null,"abstract":"<div><div>Photobioelectrochemical systems (PBEs) harness the machinery of photosynthetic microorganisms to convert solar energy into electricity. However, the inefficient electron transfer at the cell-electrode interface remains as the key performance limitation. Herein, we report a plasmonic biohybrid strategy to enhance extracellular electron transfer in <em>Chlorella</em>-based photobioelectrodes by integrating gold nanoparticles (AuNPs) localized on the microalgae membrane. Two approaches are investigated, consisting of physical mixing of isolated cells with AuNPs and cultivating microalgae in a growth medium supplemented with AuNPs, with the second approach allowing to obtain about significantly higher photocurrent responses. Optimized bioelectrodes yield photocurrent densities of up to 132 μA cm<sup>−2</sup>, 74% higher than bioelectrodes fabricated using unmodified cells. Spectral response analysis reveals a strong resonance at 525 nm, consistent with the plasmonic properties of AuNPs. Importantly, pigment content, growth kinetics, and membrane integrity are preserved, confirming the biocompatibility of the modification. This work presents a facile and effective route to engineer photosynthetic bioelectrodes using nanomaterials, advancing the design of high-performance PBEs for solar-to-electricity conversion.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109264"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-03-09DOI: 10.1016/j.bioelechem.2026.109279
Antoine Vautier, James A. Behan, Charlotte Bodin, Florence Geneste, Frédéric Barrière
{"title":"Anthraquinone disulfonate as a stable redox mediator for efficient air-cathodes at neutral pH in dual-chamber microbial fuel cells","authors":"Antoine Vautier, James A. Behan, Charlotte Bodin, Florence Geneste, Frédéric Barrière","doi":"10.1016/j.bioelechem.2026.109279","DOIUrl":"10.1016/j.bioelechem.2026.109279","url":null,"abstract":"<div><div>Microbial Fuel Cells (MFCs) are commonly developed as organic-matter oxidizing bioanodes with abiotic air cathodes. However, O<sub>2</sub> reduction requires active aeration and/or the use of expensive catalysts using noble metals. In this study, 2,7-anthraquinone disulfonate (2,7-AQDS), an organic redox mediator commonly used in aqueous redox flow battery systems (AORFBs), served as a redox-stable intermediate for oxygen reduction. Dual-chamber MFC pilots were developed with 2,7-AQDS in the catholyte under both anoxic and aerobic conditions and compared to pilots with ferricyanide catholytes. In both conditions, cyclic voltammetry studies confirmed similar and efficient electroactivity despite the proximity AQDS formal redox potential to that of acetate oxidation. Mediated air-cathodes achieved open-circuit voltage (OCV) of 510 mV and current densities of 140 μA/cm<sup>2</sup>, nearly double those of air-only cathodes (72 μA/cm<sup>2</sup>), while delivering a 33% higher power density (12 mW/m<sup>2</sup> vs. 8 mW/m<sup>2</sup>). Passive catholyte aeration enabled continuous reoxidation of reduced 2,7-AQDS at 8.8 × 10<sup>−8</sup> mol/s, exceeding the AQDS reduction rate by the bioanode (2.5 × 10<sup>−10</sup> mol/s), thus ensuring effective self-regeneration and stable AQDS concentration. These results demonstrate that AQDS coupled with passive oxygen supply sustains biofilm activity with enhances current and power, and allow long-term / low-maintenance MFC operation and organic-matter oxidation.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109279"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-03-04DOI: 10.1016/j.bioelechem.2026.109266
Terdha Narla , Uma Nudurupati, Yangguang Ou
{"title":"Developing fast scan cyclic voltammetry at carbon fiber microelectrodes to quantify short chain fatty acids in situ","authors":"Terdha Narla , Uma Nudurupati, Yangguang Ou","doi":"10.1016/j.bioelechem.2026.109266","DOIUrl":"10.1016/j.bioelechem.2026.109266","url":null,"abstract":"<div><div>Acetic, propionic, and butyric acids are short chain fatty acids (SCFAs) and the most abundant metabolites produced by gut bacteria. To uncover mechanistic insights of their function throughout the body, it is critical to measure rapid SCFA fluxes in sites of action such as brain, muscle, and skin. Current approaches have focused on fecal and plasma measurements, where SCFA levels are low and not representative of tissue-specific concentrations or fluxes. Thus, a rapid, <em>in situ</em> methodology is needed. Fast scan cyclic voltammetry (FSCV) at carbon fiber microelectrodes (CFMs) has the spatiotemporal resolution to fill this need. However, the electrochemical response of CFMs to SCFAs have not been explored until now. By coupling FSCV at CFMs with flow injection analysis of each SCFA, we demonstrate there are distinct peaks in the cyclic voltammograms for each fatty acid. Some of these peaks display faradaic behavior in scan rate, holding potential, and switching potential experiments. Interestingly, we identify several peaks that are concentration-sensitive and therefore are promising quantifiable markers of SCFA dynamics and fluxes. This work lays the foundation in understanding the response of CFMs to fatty acids and demonstrate the utility of FSCV at CFMs for the <em>in situ</em> quantitation of SCFAs.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109266"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147371938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-02-26DOI: 10.1016/j.bioelechem.2026.109260
Yuanmo Wang , Ajay Pradhan , Pankaj Gupta , Jörg Hanrieder , Henrik Zetterberg , Ann-Sofie Cans
{"title":"Nanotip acetylcholine biosensor reveals cholinergic differentiated SH-SY5Y cells release partial vesicle content during exocytosis","authors":"Yuanmo Wang , Ajay Pradhan , Pankaj Gupta , Jörg Hanrieder , Henrik Zetterberg , Ann-Sofie Cans","doi":"10.1016/j.bioelechem.2026.109260","DOIUrl":"10.1016/j.bioelechem.2026.109260","url":null,"abstract":"<div><div>Acetylcholine (ACh) is a central neurotransmitter in cognitive function, motor control, and synaptic modulation, yet its electrochemical inactivity and the rapid kinetics of exocytosis have hindered real-time quantal measurements. Micrometer-scale enzymatic ACh biosensors previously enabled sub-millisecond extracellular recordings but were too large for synaptic positioning and intracellular recordings. Here we present a short, ultrafast and low-noise amperometric ACh biosensor based on a needle-shaped carbon fiber nanotip electrode functionalized with gold nanoparticles and enzymes. The miniaturized geometry allows precise placement at neurite release sites and minimally invasive insertion into the cell cytoplasm, enabling high-temporal resolution monitoring of presynaptic exocytosis together with quantification of intracellular ACh vesicle content. We applied this platform to differentiated human cholinergic SH-SY5Y neuroblastoma cells, an established yet underutilized cell model for cholinergic signaling. The nanotip sensor successfully captured amperometric spikes from both intracellular vesicle burst events and presynaptic ACh release. Intracellular events released a larger amount of ACh than presynaptic exocytosis events, indicating a predominance of partial exocytosis mode in these cells. These results demonstrate the nanotip ACh biosensor as a unique tool for probing fusion pore dynamics at subcellular resolution and for providing quantitative insight into the quantal nature of cholinergic signaling in human neuronal models.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109260"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-03-04DOI: 10.1016/j.bioelechem.2026.109265
A. Guessab, I. Mazurenko, E. Lojou, A. de Poulpiquet
{"title":"Electrochemistry of redox enzymes: from functional enzyme immobilization to enzymatic bio-electrochemical devices (tutorial)","authors":"A. Guessab, I. Mazurenko, E. Lojou, A. de Poulpiquet","doi":"10.1016/j.bioelechem.2026.109265","DOIUrl":"10.1016/j.bioelechem.2026.109265","url":null,"abstract":"<div><div>Electrochemistry of redox enzymes is a multidisciplinary field, and students who join labs specialized in bio-electrochemistry have various backgrounds: chemistry, biology, biotechnologies, nanotechnologies, physics, etc., so that their level in the involved disciplines is often heterogeneous, and they sometimes lack the basic knowledge about either of the fields concerned by their project (physical chemistry, electrochemistry, enzymology, etc.). Projects that gather experienced researchers from these different areas also sometimes suffer from a lack of understanding between the partners. This tutorial, which follows a lecture given at the first winter school of the French group of bio-electrochemistry (GFB), aims at guiding newcomers in the field and provides advice for more in-depth and specialized literature. It seeks to provide a solid theoretical and experimental foundation. Redox enzymes and the basic methods of immobilization at the electrode are introduced. The mechanisms of direct and mediated electron transfers are explained. An important electrochemical method, cyclic voltammetry, is explained, and the article describes how to extract information about enzyme/electrode and catalytic reactions. Finally, the tutorial presents two enzymatic bio-electrochemical devices, enzymatic fuel cells and enzymatic biosensors, and provides a guide for their electrochemical characterization.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109265"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-03-09DOI: 10.1016/j.bioelechem.2026.109277
Sunday Olakunle Oguntomi , Abhipsa Sahu , Yili Yang , Enrico Marsili
{"title":"Proof-of-concept bioelectrochemical characterization of Mycolicibacterium smegmatis for diagnostic applications","authors":"Sunday Olakunle Oguntomi , Abhipsa Sahu , Yili Yang , Enrico Marsili","doi":"10.1016/j.bioelechem.2026.109277","DOIUrl":"10.1016/j.bioelechem.2026.109277","url":null,"abstract":"<div><div>Elevated urease activity in tuberculosis-infected individuals is often suggestive of bacterial virulence by promoting survivability and establishment of the causative pathogen (<em>Mycobacterium tuberculosis</em>) in the host. Thus, heightened urease activity could be a promising biomarker for screening pathogenic mycobacterial strains<em>.</em> In this proof-of-concept study, we evaluate the suitability of electrochemical techniques for direct screening of mycobacterial strains based on urease activity. <em>Mycolicibacterium smegmatis</em> wildtype (WT), a derived knockout mutant of the LCP protein family (<em>∆0107</em>) with high urease activity, and its complement strain (<em>c-0107</em>) were coated in polydopamine (PDA) and immobilized on a screen-printed electrode (SPE) for microscopy and electrochemical characterization, in presence of exogenous redox mediators: potassium ferricyanide, anthraquinone, and riboflavin. Microscopy showed compatibility of PDA as a coating material for mycobacterial cells. Electrochemical analysis results indicated enhanced <em>M. smegmatis</em> electroactivity in the presence of anthraquinone, with higher current output in the strain with high urease activity. Experiments at different urea concentrations suggest that urea is not required for this screening approach. This work shows that electrochemical data can potentially distinguish mycobacterial strains based on urease activity. It also lays a groundwork in the model mycobacteria <em>M. smegmatis</em>, which could facilitate development of assays for pathogenic mycobacterial species.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109277"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147388331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BioelectrochemistryPub Date : 2026-10-01Epub Date: 2026-02-28DOI: 10.1016/j.bioelechem.2026.109258
Jiaru Fu , Dewei Huang , Bolu Sun , Chengwen Li , Yuqiong Wu , Huajie Li , Jiali Kang , Haiying He , Xiangdong Wang , Yaru Zhang , Xuanxiu Da , Mian Chen , Lin Yang
{"title":"Optimization of a MWCNTs-AuNPs composite-modified electrochemical immunosensor with anti-fouling property for highly sensitive and rapid detection of BNP in myocardial infarction-induced heart failure diagnosis","authors":"Jiaru Fu , Dewei Huang , Bolu Sun , Chengwen Li , Yuqiong Wu , Huajie Li , Jiali Kang , Haiying He , Xiangdong Wang , Yaru Zhang , Xuanxiu Da , Mian Chen , Lin Yang","doi":"10.1016/j.bioelechem.2026.109258","DOIUrl":"10.1016/j.bioelechem.2026.109258","url":null,"abstract":"<div><div>Brain natriuretic peptide (BNP) is a sensitive biomarker for acute heart failure (AHF). Rapid, sensitive, and anti-fouling BNP detection in serum remains clinically unmet. Herein, a novel electrochemical immunosensor with synergistic signal amplification and anti-fouling ability was constructed via layered AuNPs/MWCNTs-AuNPs modification. Bottom AuNPs mitigate MWCNTs agglomeration and enable stable Anti-BNP immobilization via Au<img>S bonds, MWCNTs enhance conductivity, and top AuNPs amplify signals, forming an efficient electron-transport network. A nitrocellulose (NC) membrane was laminated for anti-fouling via rapid contaminant sieving. Under optimization, the sensor shows a linear range of 7.81–8 × 10<sup>3</sup> pg/mL for BNP, with a detection limit of 8.14 × 10<sup>−2</sup> pg/mL (3σ, <em>n</em> = 11), outperforming ELISA. It exhibits excellent selectivity (vs. cTn-I, glucose, IL-6), repeatability (RSD = 2.3%), and stability (92.4% retention over 30 days). Serum recovery rates of 102–105% confirm anti-fouling reliability. This cost-effective platform promises POCT for AHF and underpins anti-fouling biosensor development.</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"171 ","pages":"Article 109258"},"PeriodicalIF":4.5,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147363735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}