{"title":"One-Step Label-Free Electrochemical Lateral Flow Immunosensor for SARS-CoV‑2 Antigen Detection.","authors":"Jakkaphan Kumsab, Wanwisa Deenin, Kanokwan Charoenkitamorn, Abdulhadee Yakoh, Gastón A Crespo, Sudkate Chaiyo","doi":"10.1021/acsmeasuresciau.5c00096","DOIUrl":null,"url":null,"abstract":"<p><p>Rapid and ultrasensitive diagnostic tests for COVID-19 remain crucial, yet conventional lateral flow antigen kits are limited by their reliance on labeled probes and suboptimal sensitivity at low viral loads. Here, we present a label-free electrochemical antigen test kit (free-EATK) that enables one-step detection of the SARS-CoV-2 N protein without the need for conjugate pads, covalently labeled redox probes, or signal normalization schemes. The system integrates a nitrocellulose-coated electrode, a redox pad preloaded with [Ru-(NH<sub>3</sub>)<sub>6</sub>]<sup>3+</sup>, and a sample inlet. Upon sample application, the immunocomplex forms directly at the sensing zone, followed by diffusion of the redox mediator toward the electrode surface. Signal generation is achieved through direct anodic square wave voltammetry, offering sharp oxidation peaks without additional surface modification or multistep protocols. The method achieves a detection limit of 0.69 pg/mL, with high reproducibility (RSD < 10%, <i>n</i> = 10), sensitivity of 91.7%, and specificity of 100% across clinical samples (<i>n</i> = 24). The free-EATK offers a simple, robust, and reproducible alternative for early stage infectious disease screening, particularly in settings where conventional labels or complex assay formats are impractical.</p>","PeriodicalId":29800,"journal":{"name":"ACS Measurement Science Au","volume":"5 5","pages":"760-770"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12532048/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Measurement Science Au","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acsmeasuresciau.5c00096","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/15 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Rapid and ultrasensitive diagnostic tests for COVID-19 remain crucial, yet conventional lateral flow antigen kits are limited by their reliance on labeled probes and suboptimal sensitivity at low viral loads. Here, we present a label-free electrochemical antigen test kit (free-EATK) that enables one-step detection of the SARS-CoV-2 N protein without the need for conjugate pads, covalently labeled redox probes, or signal normalization schemes. The system integrates a nitrocellulose-coated electrode, a redox pad preloaded with [Ru-(NH3)6]3+, and a sample inlet. Upon sample application, the immunocomplex forms directly at the sensing zone, followed by diffusion of the redox mediator toward the electrode surface. Signal generation is achieved through direct anodic square wave voltammetry, offering sharp oxidation peaks without additional surface modification or multistep protocols. The method achieves a detection limit of 0.69 pg/mL, with high reproducibility (RSD < 10%, n = 10), sensitivity of 91.7%, and specificity of 100% across clinical samples (n = 24). The free-EATK offers a simple, robust, and reproducible alternative for early stage infectious disease screening, particularly in settings where conventional labels or complex assay formats are impractical.
期刊介绍:
ACS Measurement Science Au is an open access journal that publishes experimental computational or theoretical research in all areas of chemical measurement science. Short letters comprehensive articles reviews and perspectives are welcome on topics that report on any phase of analytical operations including sampling measurement and data analysis. This includes:Chemical Reactions and SelectivityChemometrics and Data ProcessingElectrochemistryElemental and Molecular CharacterizationImagingInstrumentationMass SpectrometryMicroscale and Nanoscale systemsOmics (Genomics Proteomics Metabonomics Metabolomics and Bioinformatics)Sensors and Sensing (Biosensors Chemical Sensors Gas Sensors Intracellular Sensors Single-Molecule Sensors Cell Chips Arrays Microfluidic Devices)SeparationsSpectroscopySurface analysisPapers dealing with established methods need to offer a significantly improved original application of the method.