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Inverse focusing inside turbid media by creating an opposite virtual objective

机译:通过创建相反的虚拟物镜使浊介质内部反向聚焦

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摘要

Limited by the penetration depth, imaging of thick bio-tissues can be achieved only by epi-detection geometry. Applications based on forward-emitted signals or bidirectional illumination are restricted by lack of an opposite objective. A method for creating an opposite virtual objective inside thick media through phase conjugation was first proposed. Under forward illumination, the backward scattering light from the media was collected to generate a phase conjugate wave, which was sent back to the media and formed an inverse focusing light. Samples combined with a diffuser or a mouse skin were used as specimens. Inverse focusing was successfully demonstrated by applying holography-based optical phase conjugation with a BaTiO3. This result indicates the capability to create an opposite virtual objective inside live tissues. The proposed method is compatible with current coherent imaging and super-resolution imaging technologies. It creates a possible way for forward-emitted signals collection and bidirectional illumination in thick specimens.
机译:受穿透深度的限制,厚的生物组织的成像只能通过落射检测几何来实现。基于前向发射信号或双向照明的应用由于缺乏相反的目标而受到限制。首先提出了一种通过相位共轭在厚介质内部创建相反的虚拟物镜的方法。在前向照明下,收集了来自介质的向后散射光,以产生相位共轭波,该共轭波被发送回介质并形成反向聚焦光。与扩散器或小鼠皮肤结合的样品用作样品。通过将基于全息的光学相与BaTiO3结合成功地证明了反向聚焦。该结果表明能够在活组织内创建相反的虚拟物镜。所提出的方法与当前的相干成像和超分辨率成像技术兼容。它为厚样品中的前向发射信号收集和双向照明提供了一种可能的方式。

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