J Biomed Opt. 2010 Jan-Feb;15(1):010506. doi: 10.1117/1.3299321.
We introduce a noncontact imaging method utilizing multifrequency structured illumination for improving lateral and axial resolution and contrast of fluorescent molecular probes in thick, multiple-scattering tissue phantoms. The method can be implemented rapidly using a spatial light modulator and a simple image demodulation scheme similar to structured light microscopy in the diffraction regime. However, imaging is performed in the multiple-scattering regime utilizing spatially modulated scalar photon density waves. We demonstrate that by increasing the structured light spatial frequency, fluorescence from deeper structures is suppressed and signals from more superficial objects enhanced. By measuring the spatial frequency dependence of fluorescence, background can be reduced by localizing the signal to a buried fluorescent object. Overall, signal-to-background ratio (SBR) and resolution improvements are dependent on spatial frequency and object depth/dimension with as much as sevenfold improvement in SBR and 33% improvement in resolution for approximately 1-mm objects buried 3 mm below the surface in tissue-like media with fluorescent background.
我们介绍了一种利用多频结构光照相的非接触成像方法,以提高在厚的、多散射组织体模中的荧光分子探针的横向和轴向分辨率和对比度。该方法可以使用空间光调制器和类似于结构光显微镜在衍射模式下的简单图像解调方案快速实现。然而,成像在多散射区域中利用空间调制的标量光子密度波来进行。我们证明,通过增加结构光的空间频率,可以抑制来自较深结构的荧光,并增强来自更浅层物体的信号。通过测量荧光的空间频率依赖性,可以将信号定位到埋置的荧光物体上来减少背景。总的来说,信号与背景比(SBR)和分辨率的提高取决于空间频率和物体的深度/尺寸,对于埋置于类似组织的介质中深度为 3mm 的约 1mm 物体,SBR 提高了七倍,分辨率提高了 33%,荧光背景下的分辨率提高了七倍,而分辨率提高了 33%。