体内
小RNA
材料科学
红外线的
临床前影像学
各向异性
纳米技术
光学
化学
物理
生物
生物化学
基因
生物技术
作者
Yutian Lei,Chusheng Liu,Yakun Shi,Ping Li,Yanfei Zhang,Si‐Yang Liu,Xing Han,Jiuxin Qu,Jianhe Guo,Zong Dai
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-04-25
卷期号:25 (18): 7543-7552
被引量:4
标识
DOI:10.1021/acs.nanolett.5c01375
摘要
Near-infrared surface-enhanced Raman scattering (NIR-SERS) probes are promising for in vivo molecular imaging, but they face challenges in balancing plasmonic activity and signal reproducibility. We designed target-zippable anisotropic NIR gold nanorod (ani-NIR-AuNR) SERS probes, whose end and side regions are decorated with catalytic hairpin assembly (CHA) DNA hairpins and Raman reporters, respectively. These ani-NIR-AuNR monomers maintain a near-zero background until triggered by targets to form uniform side-by-side dimers with an average gap of 0.88 nm, synergistically amplifying electromagnetic enhancement and chemical enhancement. The CHA allows one target to zip numerous dimers, boosting hotspot density. These effects endow the SERS probes with good reproducibility (RSD = 8.56%), superior sensitivity (LOD = 0.15 fM), and a broad linear range (1 fM to 1 nM) for let-7d detection. Compared to fluorescence probes, they offer higher brightness, better spatial resolution, and longer signal persistence in in vivo miRNA imaging, demonstrating substantial potential in bioapplications.
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