Li Baoqiang, Berti Romain, Abran Maxime, Lesage Frédéric
Institute of Biomedical Engineering, École Polytechnique de Montréal, Montreal, Quebec H3C 3A7, Canada.
Rev Sci Instrum. 2014 May;85(5):053703. doi: 10.1063/1.4875256.
Ultrasound imaging, having the advantages of low-cost and non-invasiveness over MRI and X-ray CT, was reported by several studies as an adequate complement to fluorescence molecular tomography with the perspective of improving localization and quantification of fluorescent molecular targets in vivo. Based on the previous work, an improved dual-modality Fluorescence-Ultrasound imaging system was developed and then validated in imaging study with preclinical tumor model. Ultrasound imaging and a profilometer were used to obtain the anatomical prior information and 3D surface, separately, to precisely extract the tissue boundary on both sides of sample in order to achieve improved fluorescence reconstruction. Furthermore, a pattern-based fluorescence reconstruction on the detection side was incorporated to enable dimensional reduction of the dataset while keeping the useful information for reconstruction. Due to its putative role in the current imaging geometry and the chosen reconstruction technique, we developed an attenuation compensated Born-normalization method to reduce the attenuation effects and cancel off experimental factors when collecting quantitative fluorescence datasets over large area. Results of both simulation and phantom study demonstrated that fluorescent targets could be recovered accurately and quantitatively using this reconstruction mechanism. Finally, in vivo experiment confirms that the imaging system associated with the proposed image reconstruction approach was able to extract both functional and anatomical information, thereby improving quantification and localization of molecular targets.
超声成像相对于磁共振成像(MRI)和X射线计算机断层扫描(CT)具有低成本和非侵入性的优势,多项研究报告称,从改善体内荧光分子靶点的定位和定量角度来看,超声成像是荧光分子断层扫描的一种合适补充。基于之前的工作,开发了一种改进的双模态荧光-超声成像系统,并在临床前肿瘤模型的成像研究中进行了验证。分别使用超声成像和轮廓仪获取解剖学先验信息和三维表面,以精确提取样本两侧的组织边界,从而实现改进的荧光重建。此外,在检测端采用基于模式的荧光重建,以在保持重建有用信息的同时减少数据集的维度。由于其在当前成像几何结构和所选重建技术中的假定作用,我们开发了一种衰减补偿玻恩归一化方法,以在大面积收集定量荧光数据集时减少衰减效应并消除实验因素。模拟和体模研究结果均表明,使用这种重建机制可以准确、定量地恢复荧光靶点。最后,体内实验证实,与所提出的图像重建方法相关联的成像系统能够提取功能和解剖学信息,从而改善分子靶点的定量和定位。