基于原子超薄等离子纳米材料的奇异相位增强横向位置移动无标记生物传感技术

IF 23.4 Q1 OPTICS
Shaodi Zhu, Rodolphe Jaffiol, Aurelian Crunteanu, Cyrille Vézy, Sik-To Chan, Wu Yuan, Ho-Pui Ho, Shuwen Zeng
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引用次数: 0

摘要

在早期疾病诊断和分子生物学研究中,快速等离子体生物传感受到广泛关注。然而,对于传统的角度干涉型质子传感器来说,如果没有质子纳米粒子等辅助放大标签,要获得更高的灵敏度仍是一个挑战。为了解决这个问题,我们开发了一种基于相位奇异性增强横向位置移动的质子生物传感器。这种奇异性表现为共振质子基底反射暗点处的突然相位延迟,导致反射光束的巨大位置偏移。在此,我们首次证明了银纳米薄膜上的原子级 Ge2Sb2Te5(GST)薄层是一种新型相位响应增强质子材料。GST 层不仅能精确地实现奇异相变,还能作为活性纳米银薄膜的保护层。这种新配置在校准实验中测得了破纪录的最大位置偏移 439.3 μm,灵敏度超高,达到 1.72 × 108 nm RIU-1(折射率单位)。探测极限为 6.97 × 10-7 RIU,位置分辨率为 0.12 μm。此外,这种位置偏移检测的优点系数(FOM)高达 4.54 × 1011 μm(RIU∙°)-1,实现了对痕量生物分子的无实验室检测。在有针对性的生物传感实验中,优化后的传感器成功检测到了最低浓度为 1 × 10-16 M 的小细胞因子生物标记物(TNF-α 和 IL-6)。这两种分子是临床诊断中关键的促炎性癌症标志物,而目前的临床技术无法对其进行直接筛查。为了进一步验证我们传感系统的选择性,我们还测量了整合素与精氨酰甘天冬氨酸(RGD)肽(细胞粘附中的一种关键蛋白相互作用)结合的亲和力,Mn2+离子浓度从 1 nM 到 1 mM 不等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Label-free biosensing with singular-phase-enhanced lateral position shift based on atomically thin plasmonic nanomaterials

Label-free biosensing with singular-phase-enhanced lateral position shift based on atomically thin plasmonic nanomaterials

Rapid plasmonic biosensing has attracted wide attention in early disease diagnosis and molecular biology research. However, it was still challenging for conventional angle-interrogating plasmonic sensors to obtain higher sensitivity without secondary amplifying labels such as plasmonic nanoparticles. To address this issue, we developed a plasmonic biosensor based on the enhanced lateral position shift by phase singularity. Such singularity presents as a sudden phase retardation at the dark point of reflection from resonating plasmonic substrate, leading to a giant position shift on reflected beam. Herein, for the first time, the atomically thin layer of Ge2Sb2Te5 (GST) on silver nanofilm was demonstrated as a novel phase-response-enhancing plasmonic material. The GST layer was not only precisely engineered to singularize phase change but also served as a protective layer for active silver nanofilm. This new configuration has achieved a record-breaking largest position shift of 439.3 μm measured in calibration experiments with an ultra-high sensitivity of 1.72 × 108 nm RIU−1 (refractive index unit). The detection limit was determined to be 6.97 × 10−7 RIU with a 0.12 μm position resolution. Besides, a large figure of merit (FOM) of 4.54 × 1011 μm (RIU∙°)−1 was evaluated for such position shift interrogation, enabling the labelfree detection of trace amounts of biomolecules. In targeted biosensing experiments, the optimized sensor has successfully detected small cytokine biomarkers (TNF-α and IL-6) with the lowest concentration of 1 × 10−16 M. These two molecules are the key proinflammatory cancer markers in clinical diagnosis, which cannot be directly screened by current clinical techniques. To further validate the selectivity of our sensing systems, we also measured the affinity of integrin binding to arginylglycylaspartic acid (RGD) peptide (a key protein interaction in cell adhesion) with different Mn2+ ion concentrations, ranging from 1 nM to 1 mM.

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来源期刊
Light-Science & Applications
Light-Science & Applications 数理科学, 物理学I, 光学, 凝聚态物性 II :电子结构、电学、磁学和光学性质, 无机非金属材料, 无机非金属类光电信息与功能材料, 工程与材料, 信息科学, 光学和光电子学, 光学和光电子材料, 非线性光学与量子光学
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