Foundation for Research and Technology-Hellas, P.O. Box 1527, Heraklion 71110, Greece.
Opt Lett. 2010 Jan 1;35(1):34-6. doi: 10.1364/OL.35.000034.
Noncontact optical tomography in reflection mode is often the only possible configuration when imaging the expression of green fluorescent protein (GFP) or other fluorescent proteins in live animals owing to the short penetration depth of visible light. When imaging in reflection mode using noncontact approaches (i.e., without the use of fibers coupled to tissue), correctly accounting for the intensity profile of the source at the surface is a difficult task, usually needing to fit for source positions and/or approximating these to point sources. In this Letter we present a rigorous theoretical approach that directly accounts for the source's intensity profile and verify it using in vivo data from GFP-expressing mice. We show how this approach improves image quality and resolution, while considerably simplifying the forward and inverse problems of the image reconstruction process.
由于可见光的穿透深度有限,当对活体动物中的绿色荧光蛋白 (GFP) 或其他荧光蛋白的表达进行成像时,非接触式反射模式的光学层析成像往往是唯一可行的配置。当使用非接触式方法(即不使用与组织耦合的光纤)进行反射模式成像时,正确地计算表面处的光源强度分布是一项艰巨的任务,通常需要拟合光源位置和/或近似为点光源。在这篇文章中,我们提出了一种严格的理论方法,可以直接考虑光源的强度分布,并使用表达 GFP 的小鼠的体内数据进行验证。我们展示了这种方法如何提高图像质量和分辨率,同时大大简化了图像重建过程的正向和逆向问题。