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Focused fluorescence excitation with time-reversed ultrasonically encoded light and imaging in thick scattering media

机译:用时间反向超声编码的光进行聚焦荧光激发,并在厚散射介质中成像

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摘要

Scattering dominates light propagation in biological tissue, and therefore restricts both resolution and penetration depth in optical imaging within thick tissue. As photons travel into the diffusive regime, typically 1 mm beneath human skin, their trajectories transition from ballistic to diffusive due to the increased number of scattering events, which makes it impossible to focus, much less track, photon paths. Consequently, imaging methods that rely on controlled light illumination are ineffective in deep tissue. This problem has recently been addressed by a novel method capable of dynamically focusing light in thick scattering media via time reversal of ultrasonically encoded (TRUE) diffused light. Here, using photorefractive materials as phase conjugate mirrors, we show a direct visualization and dynamic control of optical focusing with this light delivery method, and demonstrate its application for focused fluorescence excitation and imaging in thick turbid media. These abilities are increasingly critical for understanding the dynamic interactions of light with biological matter and processes at different system levels, as well as their applications for biomedical diagnosis and therapy.
机译:散射控制着生物组织中的光传播,因此限制了厚组织内光学成像的分辨率和穿透深度。当光子进入通常在人类皮肤下方1毫米的扩散区时,由于散射事件数量的增加,它们的轨迹从弹道转变为扩散,这使得不可能聚焦,而更不用说跟踪光子路径了。因此,依赖于受控光照明的成像方法在深部组织中无效。最近,已经通过一种新颖的方法解决了这个问题,该方法能够通过超声编码的(TRUE)散射光的时间反转将光动态聚焦在厚散射介质中。在这里,使用光折变材料作为相位共轭镜,我们展示了这种光传输方法对光学聚焦的直接可视化和动态控制,并展示了其在浓浊介质中聚焦荧光激发和成像的应用。这些能力对于理解光与生物物质和过程在不同系统级别上的动态相互作用以及它们在生物医学诊断和治疗中的应用越来越重要。

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