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Multispectral Depth-Resolved Fluorescence Lifetime Spectroscopy Using SPAD Array Detectors and Fiber Probes

机译:使用SPAD阵列检测器和光纤探针的多光谱深度分辨荧光寿命光谱

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摘要

Single Photon Avalanche Diode (SPAD) arrays are increasingly exploited and have demonstrated potential in biochemical and biomedical research, both for imaging and single-point spectroscopy applications. In this study, we explore the application of SPADs together with fiber-optic-based delivery and collection geometry to realize fast and simultaneous single-point time-, spectral-, and depth-resolved fluorescence measurements at 375 nm excitation light. Spectral information is encoded across the columns of the array through grating-based dispersion, while depth information is encoded across the rows thanks to a linear arrangement of probe collecting fibers. The initial characterization and validation were realized against layered fluorescent agarose-based phantoms. To verify the practicality and feasibility of this approach in biological specimens, we measured the fluorescence signature of formalin-fixed rabbit aorta samples derived from an animal model of atherosclerosis. The initial results demonstrate that this detection configuration can report fluorescence spectral and lifetime contrast originating at different depths within the specimens. We believe that our optical scheme, based on SPAD array detectors and fiber-optic probes, constitute a powerful and versatile approach for the deployment of multidimensional fluorescence spectroscopy in clinical applications where information from deeper tissue layers is important for diagnosis.
机译:单光子雪崩二极管(SPAD)阵列得到了越来越多的开发,并已在生化和生物医学研究中显示出潜力,无论是成像还是单点光谱应用。在这项研究中,我们探索了SPAD的应用以及基于光纤的传递和收集几何结构,以在375 nm激发光下实现快速,同步的单点时间,光谱和深度分辨荧光测量。光谱信息通过基于光栅的色散在阵列的各列中进行编码,而深度信息则由于探针收集光纤的线性排列而在各行中进行编码。针对分层的基于荧光琼脂糖的体模实现了初始表征和验证。为了验证该方法在生物学标本中的实用性和可行性,我们测量了从动脉粥样硬化动物模型中福尔马林固定的兔主动脉样品的荧光特征。初步结果表明,这种检测配置可以报告源自样品内不同深度的荧光光谱和寿命对比。我们相信,基于SPAD阵列检测器和光纤探头的光学方案,构成了一种强大而通用的方法,可用于在临床应用中部署多维荧光光谱法,其中来自较深组织层的信息对于诊断至关重要。

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