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由带有周围布拉格镜的纳米孔阵列实现的亚微米分辨率表面等离子体共振成像,以提高灵敏度和隔离度。

Sub-micron resolution surface plasmon resonance imaging enabled by nanohole arrays with surrounding Bragg mirrors for enhanced sensitivity and isolation.

作者信息

Lindquist Nathan C, Lesuffleur Antoine, Im Hyungsoon, Oh Sang-Hyun

机构信息

Department of Electrical and Computer Engineering, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Lab Chip. 2009 Feb 7;9(3):382-7. doi: 10.1039/b816735d. Epub 2008 Dec 19.

Abstract

We present nanohole arrays in thin gold films as sub-micron resolution surface plasmon resonance (SPR) imaging pixels in a microarray format. With SPR imaging, the resolution is not limited by diffraction, but by the propagation of surface plasmon waves to adjacent sensing areas, or nanohole arrays, causing unwanted interference. For ultimate scalability, several issues need to be addressed, including: (1) as several nanohole arrays are brought close to each other, surface plasmon interference introduces large sources of error; and (2) as the size of the nanohole array is reduced, i.e. fewer holes, detection sensitivity suffers. To address these scalability issues, we surround each biosensing pixel (a 3-by-3 nanohole array) with plasmonic Bragg mirrors, blocking interference between adjacent SPR sensing pixels for high-density packing, while maintaining the sensitivity of a 50 x larger footprint pixel (a 16-by-16 nanohole array). We measure real-time, label-free streptavidin-biotin binding kinetics with a microarray of 600 sub-micron biosensing pixels at a packing density of more than 10(7) per cm(2).

摘要

我们展示了在薄金膜中的纳米孔阵列,其作为微阵列形式的亚微米分辨率表面等离子体共振(SPR)成像像素。对于SPR成像,分辨率不受衍射限制,而是受表面等离子体波传播到相邻传感区域或纳米孔阵列导致不必要干扰的限制。为了实现最终的可扩展性,需要解决几个问题,包括:(1)当几个纳米孔阵列彼此靠近时,表面等离子体干扰会引入大量误差源;(2)随着纳米孔阵列尺寸减小,即孔数减少,检测灵敏度会受到影响。为了解决这些可扩展性问题,我们用等离子体布拉格镜围绕每个生物传感像素(一个3×3纳米孔阵列),在保持50倍更大尺寸像素(一个16×16纳米孔阵列)灵敏度的同时,阻挡相邻SPR传感像素之间的干扰以实现高密度封装。我们用一个由600个亚微米生物传感像素组成的微阵列,以每平方厘米超过10⁷的封装密度测量了实时、无标记的链霉亲和素-生物素结合动力学。

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