太赫兹辐射
生物传感器
纳米技术
生物分子
材料科学
生物芯片
信号(编程语言)
纳米传感器
光电子学
钥匙(锁)
探测理论
光学传感
光子学
等离子体子
可扩展性
太赫兹光谱与技术
表面等离子共振
分子生物物理学
纳米生物技术
化学
生物标志物
作者
Hao Bi,Xiaomeng Bian,Zongyu Zhang,Tianshu Li,Rui You
标识
DOI:10.1021/acsanm.5c03780
摘要
Direct detection of biomolecules using terahertz (THz) waves remains challenging due to their inherently weak signal responses. While metasurface-enhanced interactions offer a common solution, achieving scalable, nondestructive, and controllable molecular capture remains a key challenge. To address this challenge, we designed two complementary nanoprobes, AuNPs and Au@Fe 3 O 4, for incorporation into a THz metasurface-based sensing platform. AuNPs efficiently enrich target molecules in high-field resonance regions for signal amplification. Au@Fe 3 O 4 probes enable magnetic targeting and spatial localization under an external field. Using neuron-specific enolase (NSE), a key neuroendocrine biomarker, as the target analyte, our platform demonstrated strong linear detection from 0.01 to 50 ng/mL. It achieved ultralow limits of detection (LODs) of 0.007 ng/mL (AuNPs) and 0.003 ng/mL (Au@Fe 3 O 4 )─among the lowest reported for NSE via THz sensing. Significantly, the dual-probe strategy achieved synergistic enhancement. This synergistic dual-probe platform provides a promising strategy for highly sensitive and spatially controllable THz biosensing, facilitating high-precision, scalable biomarker detection in clinical diagnostics and point-of-care personalized medicine.
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