用于光片光场计算荧光脑成像的光子神经探针微内窥镜。

IF 4.8 2区 医学 Q1 NEUROSCIENCES Neurophotonics Pub Date : 2024-09-01 Epub Date: 2024-02-06 DOI:10.1117/1.NPh.11.S1.S11503
Peisheng Ding, Hannes Wahn, Fu-Der Chen, Jianfeng Li, Xin Mu, Andrei Stalmashonak, Xianshu Luo, Guo-Qiang Lo, Joyce K S Poon, Wesley D Sacher
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引用次数: 0

摘要

意义重大:光片荧光显微镜被广泛用于高速、高对比度、容积成像。由于传统光片显微镜需要正交的荧光激发和收集目标,其几何尺寸限制了该技术在非透明生物体内大脑成像中的应用。我们最近展示了植入式光子神经探针,它能在脑组织深处发射可寻址的光片,使激发光学元件微型化。在此,我们提出了一种微内窥镜,它由光片神经探针和基于图像光纤束的小型化荧光收集光学器件组成,用于无镜头、光场、计算荧光成像。目的:代工制造的硅基光片神经探针可与市售图像光纤束封装在一起,形成微内窥镜,用于脑组织深度光片光场荧光成像:方法:使用带有五个可寻址光片的光片神经探针和图像光纤束开发了微型内窥镜原型。用悬浮在琼脂糖中的荧光珠和固定的小鼠脑组织对微内窥镜进行了荧光成像测试:结果:利用微内窥镜展示了体积光片光场荧光成像。与仅使用纤维束的外延照明光场成像相比,成像深度增加,重建精度提高:我们的工作为脑组织的体积荧光成像提供了一种解决方案,它体积小、对比度高。本文中的概念验证演示说明了成像方法的工作原理和方法,为今后研究光子神经探针微内窥镜在体内进行深层脑荧光成像奠定了基础。
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Photonic neural probe enabled microendoscopes for light-sheet light-field computational fluorescence brain imaging.

Significance: Light-sheet fluorescence microscopy is widely used for high-speed, high-contrast, volumetric imaging. Application of this technique to in vivo brain imaging in non-transparent organisms has been limited by the geometric constraints of conventional light-sheet microscopes, which require orthogonal fluorescence excitation and collection objectives. We have recently demonstrated implantable photonic neural probes that emit addressable light sheets at depth in brain tissue, miniaturizing the excitation optics. Here, we propose a microendoscope consisting of a light-sheet neural probe packaged together with miniaturized fluorescence collection optics based on an image fiber bundle for lensless, light-field, computational fluorescence imaging.

Aim: Foundry-fabricated, silicon-based, light-sheet neural probes can be packaged together with commercially available image fiber bundles to form microendoscopes for light-sheet light-field fluorescence imaging at depth in brain tissue.

Approach: Prototype microendoscopes were developed using light-sheet neural probes with five addressable sheets and image fiber bundles. Fluorescence imaging with the microendoscopes was tested with fluorescent beads suspended in agarose and fixed mouse brain tissue.

Results: Volumetric light-sheet light-field fluorescence imaging was demonstrated using the microendoscopes. Increased imaging depth and enhanced reconstruction accuracy were observed relative to epi-illumination light-field imaging using only a fiber bundle.

Conclusions: Our work offers a solution toward volumetric fluorescence imaging of brain tissue with a compact size and high contrast. The proof-of-concept demonstrations herein illustrate the operating principles and methods of the imaging approach, providing a foundation for future investigations of photonic neural probe enabled microendoscopes for deep-brain fluorescence imaging in vivo.

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来源期刊
Neurophotonics
Neurophotonics Neuroscience-Neuroscience (miscellaneous)
CiteScore
7.20
自引率
11.30%
发文量
114
审稿时长
21 weeks
期刊介绍: At the interface of optics and neuroscience, Neurophotonics is a peer-reviewed journal that covers advances in optical technology applicable to study of the brain and their impact on the basic and clinical neuroscience applications.
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