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Spatial Filter Based Bessel-Like Beam for Improved Penetration Depth Imaging in Fluorescence Microscopy

机译:基于空间滤波器的贝塞尔样光束,用于荧光显微镜中改进的穿透深度成像

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摘要

Monitoring and visualizing specimens at a large penetration depth is a challenge. At depths of hundreds of microns, several physical effects (such as, scattering, PSF distortion and noise) deteriorate the image quality and prohibit a detailed study of key biological phenomena. In this study, we use a Bessel-like beam in-conjugation with an orthogonal detection system to achieve depth imaging. A Bessel-like penetrating diffractionless beam is generated by engineering the back-aperture of the excitation objective. The proposed excitation scheme allows continuous scanning by simply translating the detection PSF. This type of imaging system is beneficial for obtaining depth information from any desired specimen layer, including nano-particle tracking in thick tissue. As demonstrated by imaging the fluorescent polymer-tagged-CaCO3 particles and yeast cells in a tissue-like gel-matrix, the system offers a penetration depth that extends up to 650 mu m. This achievement will advance the field of fluorescence imaging and deep nano-particle tracking.
机译:在大的穿透深度下监视和可视化标本是一个挑战。在数百微米的深度,几种物理效应(例如散射,PSF失真和噪声)会降低图像质量,并禁止对关键生物学现象进行详细研究。在这项研究中,我们使用贝塞尔样光束共轭与正交检测系统来实现深度成像。通过对激发物镜的后孔径进行设计,可以生成类似贝塞尔的穿透式无衍射光束。提出的激励方案允许通过简单地转换检测PSF进行连续扫描。这种类型的成像系统有益于从任何所需的标本层获得深度信息,包括在厚组织中跟踪纳米粒子。正如通过荧光荧光标记的CaCO3颗粒和酵母细胞在组织状凝胶基质中成像所证明的那样,该系统的穿透深度可扩展到650微米。这一成就将推动荧光成像和深纳米粒子跟踪领域的发展。

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