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分子筛分无标记表面增强拉曼光谱法用于临床样本中痕量小分子生物标志物的灵敏检测。

Molecular-Sieving Label-Free Surface-Enhanced Raman Spectroscopy for Sensitive Detection of Trace Small-Molecule Biomarkers in Clinical Samples.

机构信息

School of Materials Science and Engineering, Central South University, Changsha, Hunan 410083, China.

出版信息

Nano Lett. 2024 Sep 18;24(37):11520-11528. doi: 10.1021/acs.nanolett.4c02890. Epub 2024 Sep 5.

Abstract

Small-molecule biomarkers are ubiquitous in biological fluids with pathological implications, but major challenges persist in their quantitative analysis directly in complex clinical samples. Herein, a molecular-sieving label-free surface-enhanced Raman spectroscopy (SERS) biosensor is reported for selective quantitative analysis of trace small-molecule trimetazidine (TMZ) in clinical samples. Our biosensor is fabricated by decorating a superhydrophobic monolayer of microporous metal-organic frameworks (MOF) shell-coated Au nanostar nanoparticles on a silicon substrate. The design strategy principally combines the hydrophobic surface-enabled physical confinement and preconcentration, MOF-assisted molecular enrichment and sieving of small molecules, and sensitive SERS detection. Our biosensor utilizes such a "molecular confinement-and-sieving" strategy to achieve a five orders-of-magnitude dynamic detection range and a limit of detection of ≈0.5 nM for TMZ detection in either urine or whole blood. We further demonstrate the applicability of our biosensing platform for longitudinal label-free SERS detection of the TMZ level directly in clinical samples in a mouse model.

摘要

小分子生物标志物广泛存在于具有病理意义的生物流体中,但在直接对复杂临床样本进行定量分析方面仍存在重大挑战。本文报道了一种用于痕量小分子曲美他嗪(TMZ)在临床样本中选择性定量分析的分子筛标记自由表面增强拉曼光谱(SERS)生物传感器。我们的生物传感器是通过在硅衬底上修饰超疏水的微孔金属有机框架(MOF)壳包裹的 Au 纳米星纳米粒子的单分子层来制备的。该设计策略主要结合了疏水面实现的物理限域和浓缩、MOF 辅助的小分子富集和筛分,以及灵敏的 SERS 检测。我们的生物传感器利用这种“分子限域和筛分”策略,实现了在尿液或全血中检测 TMZ 的五个数量级的动态检测范围和≈0.5 nM 的检测限。我们进一步证明了我们的生物传感平台在小鼠模型中直接对临床样本中 TMZ 水平进行纵向无标记 SERS 检测的适用性。

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