Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Institut d'Imagerie Biomédicale (I2BM), Service Hospitalier Frédéric Joliot (SHFJ), 4 place du Général Leclerc, 91401, Orsay Cedex, France.
Opt Lett. 2010 Sep 15;35(18):3024-6. doi: 10.1364/OL.35.003024.
The performance of small animal photonic imaging has been considerably improved since the development of fluorescence diffuse optical tomography (fDOT), which can reconstruct fluorescent probe distribution inside tissue. However, the quantification capabilities of this new technology are still a topic of debate, especially in comparison to classical nuclear imaging techniques. Here, we present a method to in vivo calibrate the quantity and localization of a probe provided by free-space fDOT (where no plate is compressing the mouse) with positron emission tomography (PET) and x-ray computed tomography, respectively. This methodology allowed us to demonstrate a strong linear correlation (R(2)=0.95) between fDOT and PET for probe concentrations ranging from 3 nM to 1 μM in a deep-seated organ.
自荧光漫射光学断层成像(fDOT)技术发展以来,小动物的光子成像性能得到了显著提高,该技术可以重建组织内荧光探针的分布。然而,与传统的核成像技术相比,这项新技术的定量能力仍然存在争议。在这里,我们提出了一种方法,通过正电子发射断层扫描(PET)和 X 射线计算机断层扫描(CT)分别对自由空间 fDOT(小鼠未被压板压缩)提供的探针的数量和定位进行体内标定。该方法允许我们在深部器官中,在 3 nM 到 1 μM 的探针浓度范围内,证明 fDOT 和 PET 之间存在很强的线性相关性(R(2)=0.95)。