拉曼光谱
调色板(绘画)
拉曼散射
多路复用
纳米技术
材料科学
信号(编程语言)
鉴定(生物学)
合理设计
临床诊断
化学
计算机科学
分子探针
光电子学
分子信标
分子诊断学
作者
Hanying Wang,C. Li,Mingzhe Yan,Tuotuo Zhang,Xinwei Zhang,Ping Li,Chenyu Li,X. Rosalind Wang,Junrong Li,Yao Sun
摘要
Surface-enhanced Raman scattering (SERS) combines molecular-specific fingerprints and signal amplification, making it ideally suited for multiplexed point-of-care (POC) diagnostics. Yet, the translation of SERS into practical use has been hindered by the empirical screening of Raman reporters without rational spectral tunability and the lack of rigorous validation in large clinical cohorts using handheld instrumentation. To this end, we introduce a principle-driven molecular engineering approach to create a palette of tunable isomeric Raman reporters with clinical validation through large-scale respiratory pathogen screening. Guided by molecular symmetry principles and electronic effects, we construct an isomeric palette of 24 Raman reporters with unique vibrational signatures. These reporters are enhanced by a multilayer Ag-on-Cu reporter structures (MARS) and a sub-10 nm engineered nanogap SERS enhancer (SENSE) array to maximize signal amplification. The integrated isomeric-MARS-SENSE platform enables the simultaneous identification of six respiratory pathogens in 139 clinical nasal swab samples using a handheld Raman spectrometer, achieving satisfactory sensitivity, specificity, and accuracy comparable to RT-PCR. By combining rational molecular design with robust clinical validation, we expect this work to advance next-generation multiplexed SERS diagnostics at the POC.
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