Tan Weirui, Hang Yingjie, Wang Anyang, Wang Jiacheng, Wigginton Jane G, Muehlschlegel Susanne, Wu Nianqiang
Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01002, United States.
Center for BrainHealth and Texas Biomedical Device Center, The University of Texas at Dallas, Richardson, Texas 75080, United States.
ACS Omega. 2024 Aug 26;9(36):37965-37972. doi: 10.1021/acsomega.4c04685. eCollection 2024 Sep 10.
Paper lateral flow immunoassays combined with surface-enhanced Raman scattering (SERS) technology have gained increasing attention due to their high sensitivity characteristics resulting from the amplified SERS signals of the plasmon-enhanced optical probes. In contrast to conventional colorimetric lateral flow strips, SERS paper lateral flow strips (SERS-PLFSs) are currently not commercially available for widespread use. Analytical validation is the key step for commercialization. In this work, we have developed a PLFS with a hierarchical SERS probe (gold-silver nanoparticle@Raman reporter@silica) for detection of the US Food and Drug Administration (FDA)-approved traumatic brain injury (TBI) protein biomarker, ubiquitin C-terminal hydrolase-L1 (UCH-L1), in blood plasma samples. Analytical validation has been performed on this SERS-PLFS in terms of the limit of detection (LOD), limit of quantification (LOQ), accuracy, precision, selectivity, and stability. The SERS-PLFS exhibits a reportable range of 0.2-100 ng/mL with a LOD of 0.08 ng/mL toward measurement of UCH-L1 in blood plasma. The SERS-PLFS has been applied to clinical TBI samples. The test results were compared with those from enzyme-linked immunosorbent assay (ELISA), demonstrating a strong correlation between the two analytical methods. This study has important implications in the commercialization of SERS-PLFSs for rapid TBI detection in clinical practice.
结合表面增强拉曼散射(SERS)技术的纸质侧向流动免疫分析因其等离子体增强光学探针的SERS信号放大而具有高灵敏度特性,受到了越来越多的关注。与传统的比色侧向流动试纸条不同,SERS纸质侧向流动试纸条(SERS-PLFSs)目前尚未商业化广泛使用。分析验证是商业化的关键步骤。在这项工作中,我们开发了一种带有分级SERS探针(金-银纳米颗粒@拉曼报告分子@二氧化硅)的PLFS,用于检测美国食品药品监督管理局(FDA)批准的创伤性脑损伤(TBI)蛋白质生物标志物泛素C末端水解酶-L1(UCH-L1)在血浆样本中的含量。已对该SERS-PLFS在检测限(LOD)、定量限(LOQ)、准确性、精密度、选择性和稳定性方面进行了分析验证。该SERS-PLFS在检测血浆中UCH-L1时,报告范围为0.2-100 ng/mL,LOD为0.08 ng/mL。该SERS-PLFS已应用于临床TBI样本。将测试结果与酶联免疫吸附测定(ELISA)的结果进行了比较,证明这两种分析方法之间具有很强的相关性。这项研究对SERS-PLFS在临床实践中快速检测TBI的商业化具有重要意义。