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通过多模光纤的数字共聚焦显微镜术。

Digital confocal microscopy through a multimode fiber.

作者信息

Loterie Damien, Farahi Salma, Papadopoulos Ioannis, Goy Alexandre, Psaltis Demetri, Moser Christophe

出版信息

Opt Express. 2015 Sep 7;23(18):23845-58. doi: 10.1364/OE.23.023845.

Abstract

Acquiring high-contrast optical images deep inside biological tissues is still a challenging problem. Confocal microscopy is an important tool for biomedical imaging since it improves image quality by rejecting background signals. However, it suffers from low sensitivity in deep tissues due to light scattering. Recently, multimode fibers have provided a new paradigm for minimally invasive endoscopic imaging by controlling light propagation through them. Here we introduce a combined imaging technique where confocal images are acquired through a multimode fiber. We achieve this by digitally engineering the excitation wavefront and then applying a virtual digital pinhole on the collected signal. In this way, we are able to acquire images through the fiber with significantly increased contrast. With a fiber of numerical aperture 0.22, we achieve a lateral resolution of 1.5µm, and an axial resolution of 12.7µm. The point-scanning rate is currently limited by our spatial light modulator (20Hz).

摘要

在生物组织深部获取高对比度光学图像仍然是一个具有挑战性的问题。共聚焦显微镜是生物医学成像的重要工具,因为它通过抑制背景信号来提高图像质量。然而,由于光散射,它在深部组织中灵敏度较低。最近,多模光纤通过控制光在其中的传播,为微创内镜成像提供了一种新的范例。在此,我们介绍一种组合成像技术,即通过多模光纤获取共聚焦图像。我们通过对激发波前进行数字工程处理,然后在采集的信号上应用虚拟数字针孔来实现这一点。通过这种方式,我们能够通过光纤获取对比度显著提高的图像。使用数值孔径为0.22的光纤,我们实现了1.5μm的横向分辨率和12.7μm的轴向分辨率。目前,点扫描速率受我们的空间光调制器限制(20Hz)。

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