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Digital micromirror device as a spatial illuminator for fluorescence lifetime and hyperspectral imaging

机译:数字微镜设备作为空间照明器,用于荧光寿命和高光谱成像

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摘要

Time-domain fluorescence lifetime imaging (FLIM) and hyper-spectral imaging (HSI) are two advanced microscopy techniques widely used in biological studies. Typically both FLIM and HSI are performed with either a whole-field or raster-scanning approach, which often prove to be technically complex and expensive, requiring the user to accept a compromise among precision, speed, and spatial resolution. We propose the use of a digital micromirror device (DMD) as a spatial illuminator for time-domain FLIM and HSI with a laser diode excitation source. The rather unique features of the DMD allow both random and parallel access to regions of interest (ROIs) on the sample, in a very rapid and repeatable fashion. As a consequence both spectral and lifetime images can be acquired with a precision normally associated with single-point systems but with a high degree of flexibility in their spatial construction. In addition, the DMD system offers a very efficient way of implementing a global analysis approach for FLIM, where average fluorescence decay parameters are first acquired for a ROI and then used as initial estimates in determining their spatial distribution within the ROI. Experimental results obtained on phantoms employing fluorescent dyes clearly show how the DMD method supports both spectral and temporal separation for target identification in HSI and FLIM, respectively. (c) 2008 Optical Society of America.
机译:时域荧光寿命成像(FLIM)和高光谱成像(HSI)是在生物学研究中广泛使用的两种先进的显微技术。通常,FLIM和HSI都是通过全场扫描或光栅扫描方法执行的,这通常被证明在技术上既复杂又昂贵,要求用户接受精度,速度和空间分辨率之间的折衷。我们建议使用数字微镜设备(DMD)作为时域FLIM和HSI的空间照明器,并带有激光二极管激励源。 DMD相当独特的功能允许以非常快速和可重复的方式随机和并行访问样品上的感兴趣区域(ROI)。结果,可以以通常与单点系统相关联的精度获得光谱和寿命图像,但是在其空间构造上具有高度的灵活性。另外,DMD系统提供了一种非常有效的方式来实现FLIM的全局分析方法,其中首先为ROI获取平均荧光衰减参数,然后将其用作初始估计,以确定其在ROI中的空间分布。在使用荧光染料的体模上获得的实验结果清楚地表明,DMD方法如何同时支持光谱和时间分离,以分别在HSI和FLIM中进行目标识别。 (c)2008年美国眼镜学会。

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