Nusz Gregory J, Marinakos Stella M, Rangarajan Srinath, Chilkoti Ashutosh
Department of Biomedical Engineering, Duke University, Pratt School of Engineering, Box 90271, Durham, North Carolina 27708, USA.
Appl Opt. 2011 Jul 20;50(21):4198-206. doi: 10.1364/AO.50.004198.
The development of truly scalable, multiplexed optical microarrays requires a detection platform capable of simultaneous detection of multiple signals in real-time. We present a technique we term dual-order snapshot spectroscopic imaging (DOSSI) and demonstrate that it can be effectively used to collect spectrally resolved images of a full field of view of sparsely located spots in real time. Resonant peaks of plasmonic gold nanoparticles were tracked as a function of their surrounding refractive index. Measurement uncertainty analysis indicated that the spectral resolution of DOSSI in the described configuration is approximately 0.95 nm. Further, real-time measurements by DOSSI allowed discrimination between optically identical nanoparticles that were functionalized with two homologous small molecule ligands that bound to the same protein, albeit with different affinity, based purely on their different molecular interaction kinetics-a feat not possible with slower raster-type hyperspectral imaging systems, or other dark-field optical detection systems that solely rely on end point measurements. Kinetic measurements of plasmon bands by DOSSI can be performed with a relatively simple optical system, thereby opening up the possibility of developing low-cost detectors for arrayed plasmonic diagnostics.
真正可扩展的多路复用光学微阵列的发展需要一个能够实时同时检测多个信号的检测平台。我们提出了一种我们称之为双阶快照光谱成像(DOSSI)的技术,并证明它可以有效地用于实时收集稀疏分布斑点全视野的光谱分辨图像。追踪了等离子体金纳米颗粒的共振峰与其周围折射率的函数关系。测量不确定度分析表明,在所述配置中DOSSI的光谱分辨率约为0.95nm。此外,通过DOSSI进行的实时测量能够区分用两种同源小分子配体功能化的光学上相同的纳米颗粒,这两种配体与同一种蛋白质结合,尽管亲和力不同,这纯粹是基于它们不同的分子相互作用动力学——这是较慢的光栅型高光谱成像系统或其他仅依赖终点测量的暗场光学检测系统无法实现的壮举。通过DOSSI对等离激元带进行动力学测量可以用一个相对简单的光学系统来完成,从而为开发用于阵列等离子体诊断的低成本探测器开辟了可能性。