Hillman Elizabeth M C, Moore Anna
Laboratory for Functional Optical Imaging, Department of Biomedical Engineering, Columbia University, 1210 Amsterdam Avenue, New York, New York 10027, USA.
Nat Photonics. 2007;1(9):526-530. doi: 10.1038/nphoton.2007.146.
Optical molecular imaging in small animals harnesses the power of highly specific and biocompatible contrast agents for drug development and disease research1-7. However, the widespread adoption of in vivo optical imaging has been inhibited by its inability to clearly resolve and identify targeted internal organs. Optical tomography8-11 and combined X-ray and micro-computed tomography (micro-CT)12 approaches developed to address this problem are generally expensive, complex or incapable of true anatomical co-registration. Here, we present a remarkably simple all-optical method that can generate co-registered anatomical maps of a mouse's internal organs, while also acquiring in vivo molecular imaging data. The technique uses a time series of images acquired after injection of an inert dye. Differences in the dye's in vivo biodistribution dynamics allow precise delineation and identification of major organs. Such co-registered anatomical maps permit longitudinal organ identification irrespective of repositioning or weight gain, thereby promising greatly improved accuracy and versatility for studies of orthotopic disease, diagnostics and therapies.
小动物体内的光学分子成像利用高特异性和生物相容性造影剂的特性,用于药物开发和疾病研究1 - 7。然而,体内光学成像的广泛应用受到其无法清晰分辨和识别目标内部器官的限制。为解决这一问题而开发的光学断层扫描8 - 11以及联合X射线和微型计算机断层扫描(micro - CT)12方法通常昂贵、复杂,或者无法实现真正的解剖学配准。在此,我们提出一种非常简单的全光学方法,该方法可以生成小鼠内部器官的配准解剖图谱,同时还能获取体内分子成像数据。该技术使用注射惰性染料后采集的一系列时间序列图像。染料在体内生物分布动力学的差异使得能够精确描绘和识别主要器官。这种配准的解剖图谱允许在不考虑重新定位或体重增加的情况下进行纵向器官识别,从而有望大大提高原位疾病研究、诊断和治疗的准确性和通用性。