Institute for Biomedical Engineering, University and ETH Zurich, Wolfgang-Pauli-Strasse 10, 8093 Zurich, Switzerland.
Pharmaceutics. 2011 Apr 26;3(2):229-74. doi: 10.3390/pharmaceutics3020229.
Fluorescence microscopic imaging is widely used in biomedical research to study molecular and cellular processes in cell culture or tissue samples. This is motivated by the high inherent sensitivity of fluorescence techniques, the spatial resolution that compares favorably with cellular dimensions, the stability of the fluorescent labels used and the sophisticated labeling strategies that have been developed for selectively labeling target molecules. More recently, two and three-dimensional optical imaging methods have also been applied to monitor biological processes in intact biological organisms such as animals or even humans. These whole body optical imaging approaches have to cope with the fact that biological tissue is a highly scattering and absorbing medium. As a consequence, light propagation in tissue is well described by a diffusion approximation and accurate reconstruction of spatial information is demanding. While in vivo optical imaging is a highly sensitive method, the signal is strongly surface weighted, i.e., the signal detected from the same light source will become weaker the deeper it is embedded in tissue, and strongly depends on the optical properties of the surrounding tissue. Derivation of quantitative information, therefore, requires tomographic techniques such as fluorescence molecular tomography (FMT), which maps the three-dimensional distribution of a fluorescent probe or protein concentration. The combination of FMT with a structural imaging method such as X-ray computed tomography (CT) or Magnetic Resonance Imaging (MRI) will allow mapping molecular information on a high definition anatomical reference and enable the use of prior information on tissue's optical properties to enhance both resolution and sensitivity. Today many of the fluorescent assays originally developed for studies in cellular systems have been successfully translated for experimental studies in animals. The opportunity of monitoring molecular processes non-invasively in the intact organism is highly attractive from a diagnostic point of view but even more so for the drug developer, who can use the techniques for proof-of-mechanism and proof-of-efficacy studies. This review shall elucidate the current status and potential of fluorescence tomography including recent advances in multimodality imaging approaches for preclinical and clinical drug development.
荧光显微镜成像是广泛应用于生物医学研究,以研究细胞培养或组织样本中的分子和细胞过程。这是由荧光技术的固有灵敏度高,与细胞尺寸相比具有良好的空间分辨率,所使用的荧光标记的稳定性以及已开发用于选择性标记靶分子的复杂标记策略所驱动的。最近,二维和三维光学成像方法也已应用于监测完整生物生物体(如动物甚至人类)中的生物过程。这些全身光学成像方法必须应对生物组织是高度散射和吸收介质的事实。因此,组织中的光传播很好地由扩散近似描述,并且对空间信息的准确重建是有要求的。虽然体内光学成像是一种高度敏感的方法,但信号强烈地受表面加权影响,即,从相同光源检测到的信号随着其在组织中嵌入的深度变深而变弱,并且强烈依赖于周围组织的光学特性。因此,定量信息的推导需要诸如荧光分子断层扫描(FMT)之类的层析技术,其映射荧光探针或蛋白质浓度的三维分布。FMT 与结构成像方法(如 X 射线计算机断层扫描(CT)或磁共振成像(MRI))的组合将允许在高清晰度解剖参考上绘制分子信息,并能够利用组织光学特性的先验信息来提高分辨率和灵敏度。如今,许多最初为细胞系统研究开发的荧光测定法已成功地转化为动物实验研究。从诊断的角度来看,在完整的生物体中非侵入性地监测分子过程的机会非常吸引人,但对于药物开发者来说更是如此,他们可以使用这些技术进行机制证明和疗效证明研究。这篇综述将阐明荧光层析成像的现状和潜力,包括用于临床前和临床药物开发的多模态成像方法的最新进展。