材料科学
生物传感器
移动设备
纳米技术
光电子学
计算机科学
操作系统
作者
Ming‐Qing Li,Bo Cao,Yanling Wang,Hang Zhou,H.H. Yao,Yuan Gao,Xu-Li Zhuang,Jianlei Liu,Chijia Zeng,H. Susan Zhou,Dandan Zhu,Jian Ma,Feiyun Cui
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2025-06-30
卷期号:44 (9): 6442-6455
标识
DOI:10.1007/s12598-025-03408-6
摘要
Abstract The intrinsic property of MXenes to adsorb dyes with high Raman scattering cross‐sections makes them promising candidates for surface‐enhanced Raman scattering (SERS) biosensors. In the study, we report a vanadium carbide MXene (V 2 CT x )‐based SERS biosensor tag, V 2 CT x @Thi (thionine)@Au NPs (gold nanoparticles)‐Ab (antibody), owing to its large interlayer spacing and superior dye adsorption capacity. The tag V 2 CT x @Thi@Au NPs‐Ab was fully characterized and validated, demonstrating a significantly enhanced Raman signal through both electromagnetic and chemical enhancement mechanisms. Using a handheld Raman spectrometer as a readout tool, the developed handheld SERS biosensor was successfully applied for the detection of viral antigens. The biosensor exhibited excellent linearity (1.562–100 nM) and achieved a low limit of detection (LOD) 1.562 nM. Moreover, the biosensor demonstrated good selectivity and stability for detecting the target S protein in saliva samples. Our study highlights the potential of V 2 CT x MXene as a powerful material for handheld SERS biosensors, paving the way for portable and efficient viral diagnostics.
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