{"title":"Near-field and far-field competitive couplings between plasmonic nanodisk array and nanoparticles for rapid and facile heparin assay.","authors":"Shuwen Chu, Huizhen Yuan, Yuzhang Liang, Cheng Yang, Qiang Liu, Wei Peng","doi":"10.1016/j.talanta.2025.127690","DOIUrl":null,"url":null,"abstract":"<p><p>Plasmonic biosensors hold an enticing prospect for drug testing and disease diagnostics as they have demonstrated impressive superiority in ultrasensitive and label-free detection. In this paper, we demonstrate a plasmonic sensing strategy for the heparin assay by leveraging near-field and far-field competitive couplings between gold (Au) nanoparticles (NPs) and nanodisk (ND) array. Specifically, the near-field coupling of the ND array and Au NPs binding to its surface results in a spectral redshift. Meanwhile, the far-field coupling of dispersed Au NPs in mixed solution and ND array induces a spectral blueshift. As a result, heparin concentration-dependent near-field and far-field competitive couplings determine the direction and amount of the spectral shift. Compared with existing detection technologies, this sensing strategy also presents a balance point, enabling rapid assessment of heparin dosage safety. Additionally, an exceptionally wide dynamic range of 10<sup>-4</sup> μg/mL to 10<sup>3</sup> μg/mL, a low detection limit of 29 pg/mL, and excellent selectivity are demonstrated. The analysis of heparin in serum further underscores this assay approach's potential for advancing disease diagnosis and therapeutic monitoring at the point of care.</p>","PeriodicalId":435,"journal":{"name":"Talanta","volume":"287 ","pages":"127690"},"PeriodicalIF":5.6000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Talanta","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.talanta.2025.127690","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/4 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Plasmonic biosensors hold an enticing prospect for drug testing and disease diagnostics as they have demonstrated impressive superiority in ultrasensitive and label-free detection. In this paper, we demonstrate a plasmonic sensing strategy for the heparin assay by leveraging near-field and far-field competitive couplings between gold (Au) nanoparticles (NPs) and nanodisk (ND) array. Specifically, the near-field coupling of the ND array and Au NPs binding to its surface results in a spectral redshift. Meanwhile, the far-field coupling of dispersed Au NPs in mixed solution and ND array induces a spectral blueshift. As a result, heparin concentration-dependent near-field and far-field competitive couplings determine the direction and amount of the spectral shift. Compared with existing detection technologies, this sensing strategy also presents a balance point, enabling rapid assessment of heparin dosage safety. Additionally, an exceptionally wide dynamic range of 10-4 μg/mL to 103 μg/mL, a low detection limit of 29 pg/mL, and excellent selectivity are demonstrated. The analysis of heparin in serum further underscores this assay approach's potential for advancing disease diagnosis and therapeutic monitoring at the point of care.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.