Meyer Heiko, Garofalakis Anikitos, Zacharakis Giannis, Psycharakis Stylianos, Mamalaki Clio, Kioussis Dimitris, Economou Eleftherios N, Ntziachristos Vasilis, Ripoll Jorge
Institute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, Heraklion Crete, Greece.
Appl Opt. 2007 Jun 10;46(17):3617-27. doi: 10.1364/ao.46.003617.
During the past decade, optical imaging combined with tomographic approaches has proved its potential in offering quantitative three-dimensional spatial maps of chromophore or fluorophore concentration in vivo. Due to its direct application in biology and biomedicine, diffuse optical tomography (DOT) and its fluorescence counterpart, fluorescence molecular tomography (FMT), have benefited from an increase in devoted research and new experimental and theoretical developments, giving rise to a new imaging modality. The most recent advances in FMT and DOT are based on the capability of collecting large data sets by using CCDs as detectors, and on the ability to include multiple projections through recently developed noncontact approaches. For these to be implemented, we have developed an imaging setup that enables three-dimensional imaging of arbitrary shapes in fluorescence or absorption mode that is appropriate for small animal imaging. This is achieved by implementing a noncontact approach both for sources and detectors and coregistering surface geometry measurements using the same CCD camera. A thresholded shadowgrammetry approach is applied to the geometry measurements to retrieve the surface mesh. We present the evaluation of the system and method in recovering three-dimensional surfaces from phantom data and live mice. The approach is used to map the measured in vivo fluorescence data onto the tissue surface by making use of the free-space propagation equations, as well as to reconstruct fluorescence concentrations inside highly scattering tissuelike phantom samples. Finally, the potential use of this setup for in vivo small animal imaging and its impact on biomedical research is discussed.
在过去十年中,光学成像与层析成像方法相结合已证明其在提供体内发色团或荧光团浓度的定量三维空间图谱方面的潜力。由于其在生物学和生物医学中的直接应用,扩散光学层析成像(DOT)及其荧光对应物荧光分子层析成像(FMT)受益于专门研究的增加以及新的实验和理论发展,从而产生了一种新的成像模式。FMT和DOT的最新进展基于使用电荷耦合器件(CCD)作为探测器收集大量数据集的能力,以及通过最近开发的非接触方法纳入多个投影的能力。为了实现这些,我们开发了一种成像装置,该装置能够在荧光或吸收模式下对任意形状进行三维成像,适用于小动物成像。这是通过对光源和探测器都采用非接触方法,并使用同一台CCD相机对表面几何测量进行配准来实现的。一种阈值化阴影测量方法应用于几何测量以检索表面网格。我们展示了该系统和方法在从体模数据和活体小鼠中恢复三维表面方面的评估。该方法用于通过利用自由空间传播方程将测量的体内荧光数据映射到组织表面,以及重建高度散射的组织样体模样品内部的荧光浓度。最后,讨论了该装置在体内小动物成像中的潜在用途及其对生物医学研究的影响。