Multimodal triple-mode probe with colorimetric-fluorescence-SERS (CFSERS) for sensitive and quantitative detection of C-reactive protein in clinical diagnostics.

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-10-01 Epub Date: 2025-04-07 DOI:10.1016/j.talanta.2025.128100
Wei Li, Xinrui Wang, Mingze Zhu, Xin Huang, Pacifique Hirwa Umutoni, Ting-Hsuan Chen, Jian Lu, Shih-Chi Chen, Guangming Tan, Bryan P Yan, Bee Luan Khoo
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引用次数: 0

Abstract

Chronic inflammation remains a major global health concern, necessitating the development of advanced tools for continuous, precise monitoring. This study introduces a novel, clinically impactful triple-mode probe that integrates colorimetric, fluorescence, and surface-enhanced Raman scattering (SERS) signals, offering unparalleled multimodal detection capabilities. The probe's design leverages europium chelate-doped polystyrene nanoparticles (ECNPs), ensuring minimal signal cross-interference through a long Stokes shift. A key innovation is the development of a multimodal mapping algorithm that seamlessly integrates these optical signals, providing a sensitive and robust platform for biomarker detection with broad dynamic ranges. The probe's clinical relevance is demonstrated by its application in lateral flow assays (LFAs) for detecting C-reactive protein (CRP) levels, achieving a detection limit of 6.31 ng/mL and dynamic ranges from 23.13 to 2000 ng/mL, significantly outperforming single-mode detection methods. In clinical validation using urine samples from 31 patients, the triple-mode LFA showed excellent correlation (0.9377) and agreement (93.55 %) with gold standard enzyme-linked immunosorbent assay (ELISA) results. This demonstrates that the proposed multimodal platform offers a highly sensitive, cost-effective, and versatile tool for monitoring inflammation and other disease biomarkers, with substantial potential for clinical applications in diagnostics and disease management.

比色-荧光- sers (CFSERS)多模态三模探针用于临床诊断中c反应蛋白的敏感和定量检测。
慢性炎症仍然是一个主要的全球健康问题,需要开发先进的工具来进行连续、精确的监测。本研究介绍了一种新型的、具有临床影响力的三模探针,它集成了比色、荧光和表面增强拉曼散射(SERS)信号,提供了无与伦比的多模态检测能力。探针的设计利用了铕螯合物掺杂的聚苯乙烯纳米颗粒(ECNPs),通过长斯托克斯位移确保最小的信号交叉干扰。一个关键的创新是开发了一种多模态映射算法,该算法无缝地集成了这些光学信号,为生物标志物检测提供了一个敏感而强大的平台,具有广泛的动态范围。该探针在检测c反应蛋白(CRP)水平的横向流动试验(LFAs)中的应用证明了其临床意义,检测限为6.31 ng/mL,动态范围为23.13至2000 ng/mL,显著优于单模检测方法。在31例患者尿样的临床验证中,三模LFA与金标准酶联免疫吸附试验(ELISA)结果具有良好的相关性(0.9377)和一致性(93.55%)。这表明,所提出的多模式平台为监测炎症和其他疾病生物标志物提供了一种高度敏感、成本效益高、用途广泛的工具,在诊断和疾病管理方面具有巨大的临床应用潜力。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
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.
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