Photonics Research Laboratory, Center of Excellence on Applied Electromagnetic Systems, School of Electrical and Computer Engineering, College of Engineering, University of Tehran, Tehran 1439957131, Iran.
Canary Center at Stanford for Cancer Early Detection, Bio-Acoustic MEMS in Medicine (BAMM) Laboratory, Department of Radiology, Stanford School of Medicine, Stanford University, Palo Alto, California 94304, United States.
ACS Nano. 2020 Jul 28;14(7):8518-8527. doi: 10.1021/acsnano.0c02797. Epub 2020 Jul 8.
Plasmonic sensors provide real-time and label-free detection of biotargets with unprecedented sensitivity and detection limit. However, they usually lack the ability to estimate the thickness of the target layer formed on top of the sensing surface. Here, we report a sensing modality based on reflection spectroscopy of a nanoplasmonic Fabry-Perot cavity array, which exhibits characteristics of both surface plasmon polaritons and localized plasmon resonances and outperforms its conventional counterparts by providing the thickness of the surface-adsorbed layers. Through numerical simulations, we demonstrate that the designed plasmonic surface resembles two entangled Fabry-Perot cavities excited from both ends. Performance of the device is evaluated by studying sensor response in the refractive index (RI) measurement of aqueous glycerol solutions and during formation of a surface-adsorbed layer consisting of protein (, NeutrAvidin) molecules. By tracking the resonance wavelengths of the two modes of the nanoplasmonic surface, it is therefore possible to measure the thickness of a homogeneous adsorbed layer and RI of the background solution with precisions better than 4 nm and 0.0001 RI units. Using numerical simulations, we show that the thickness estimation algorithm can be extended for layers consisting of nanometric analytes adsorbed on an antibody-coated sensor surface. Furthermore, performance of the device has been evaluated to detect exosomes. By providing a thickness estimation for adsorbed layers and differentiating binding events from background RI variations, this device can potentially supersede conventional plasmonic sensors.
等离子体激元传感器提供了实时、无标记的生物靶标检测,具有空前的灵敏度和检测极限。然而,它们通常缺乏估计传感表面上形成的目标层厚度的能力。在这里,我们报告了一种基于纳米等离子体法布里-珀罗腔阵列反射光谱的传感模式,它具有表面等离子体激元和局域等离子体共振的特性,通过提供表面吸附层的厚度,优于其传统对应物。通过数值模拟,我们证明了设计的等离子体表面类似于从两端激发的两个纠缠的法布里-珀罗腔。通过研究水甘油溶液的折射率(RI)测量和由蛋白质(NeutrAvidin)分子组成的表面吸附层形成过程中的传感器响应,评估了器件的性能。通过跟踪纳米等离子体表面的两种模式的共振波长,因此可以测量均匀吸附层的厚度和背景溶液的 RI,精度优于 4nm 和 0.0001 RI 单位。通过数值模拟,我们表明厚度估计算法可以扩展到吸附在抗体涂覆的传感器表面上的纳米级分析物组成的层。此外,还评估了该器件检测外泌体的性能。通过提供吸附层的厚度估计并区分结合事件与背景 RI 变化,该器件有可能取代传统的等离子体传感器。