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近红外二区窗口的深度分辨局部微血管造影术

Depth-Resolved Localization Microangiography in the NIR-II Window.

作者信息

Zhou Quanyu, Nozdriukhin Daniil, Chen Zhenyue, Glandorf Lukas, Hofmann Urs A T, Reiss Michael, Tang Lin, Deán-Ben Xosé Luís, Razansky Daniel

机构信息

Institute of Pharmacology and Toxicology and Institute for Biomedical Engineering, Faculty of Medicine, University of Zurich, Zurich, 8057, Switzerland.

Institute for Biomedical Engineering, Department of Information Technology and Electrical Engineering, ETH Zurich, Zurich, 8093, Switzerland.

出版信息

Adv Sci (Weinh). 2022 Nov 20;10(1):e2204782. doi: 10.1002/advs.202204782.

Abstract

Detailed characterization of microvascular alterations requires high-resolution 3D imaging methods capable of providing both morphological and functional information. Existing optical microscopy tools are routinely used for microangiography, yet offer suboptimal trade-offs between the achievable field of view and spatial resolution with the intense light scattering in biological tissues further limiting the achievable penetration depth. Herein, a new approach for volumetric deep-tissue microangiography based on stereovision combined with super-resolution localization imaging is introduced that overcomes the spatial resolution limits imposed by light diffusion and optical diffraction in wide-field imaging configurations. The method capitalizes on localization and tracking of flowing fluorescent particles in the second near-infrared window (NIR-II, ≈1000-1700 nm), with the third (depth) dimension added by triangulation and stereo-matching of images acquired with two short-wave infrared cameras operating in a dual-view mode. The 3D imaging capability enabled with the proposed method facilitates a detailed visualization of microvascular networks and an accurate blood flow quantification. Experiments performed in tissue-mimicking phantoms demonstrate that high resolution is preserved up to a depth of 4 mm in a turbid medium. Transcranial microangiography of the entire murine cortex and penetrating vessels is further demonstrated at capillary level resolution.

摘要

微血管改变的详细特征描述需要能够提供形态学和功能信息的高分辨率三维成像方法。现有的光学显微镜工具通常用于微血管造影,但在可实现的视野和空间分辨率之间提供的权衡并不理想,生物组织中的强光散射进一步限制了可实现的穿透深度。在此,介绍了一种基于立体视觉与超分辨率定位成像相结合的体积深层组织微血管造影新方法,该方法克服了宽场成像配置中光扩散和光衍射所带来的空间分辨率限制。该方法利用在第二近红外窗口(NIR-II,≈1000-1700nm)中流动的荧光颗粒的定位和跟踪,通过对以双视图模式操作的两个短波红外相机采集的图像进行三角测量和立体匹配来添加第三(深度)维度。所提出的方法实现的三维成像能力有助于微血管网络的详细可视化和准确的血流定量。在组织模拟体模中进行的实验表明,在浑浊介质中,高达4mm的深度仍能保持高分辨率。在毛细血管水平分辨率下进一步展示了对整个小鼠皮质和穿透血管的经颅微血管造影。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53af/9811471/e8dd40e869aa/ADVS-10-2204782-g001.jpg

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