分辨率增强介观成像与圆柱透镜校正斜平面光片显微镜。

IF 2.3
Yao Zhou, Mengmeng Li, Shimeng Gao, Fenghe Zhong, Peng Fei
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引用次数: 0

摘要

单物镜光片荧光显微镜(LSFM)具有高速大样本成像的优点,但其有限的荧光采集角度在低倍率下会造成荧光损失,从而降低系统分辨率。为了解决这个问题,我们引入了一种使用同轴调制模块的新方法。通过将两组圆柱形镜头与相机的滚动快门相结合,我们在低倍率模式下以优化的荧光收集角度实现了3D成像。与先进的单物镜LSFM相比,我们的方法为低NA斜平面显微镜(NA 0.5)提供了实用的解决方案,并将沿光传播轴的分辨率提高了约30%。我们用荧光微球验证了该系统的分辨率,实现了亚微米横向和亚细胞轴向分辨率。此外,我们已经证明了使用gfp标记的神经元和Siha宫颈癌细胞样本进行细胞计数的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resolution-Enhanced Mesoscopic Imaging With Cylindrical Lens-Corrected Oblique Plane Light-Sheet Microscopy.

Single-objective light sheet fluorescence microscopy (LSFM) excels in high-speed imaging of large samples, but its limited fluorescence collection angle would degrade system resolution due to the fluorescence loss at low magnifications. To address this issue, we introduce a new method using a coaxial modulation module. By combining two sets of cylindrical lenses with the camera's rolling shutter, we achieve 3D imaging with an optimized fluorescence collection angle in low-magnification mode. Compared to advanced single-objective LSFM, our method provides a practical solution for low-NA oblique plane microscopy (NA 0.5) and enhances resolution by ~30% along the light propagation axis. We validated the system's resolution with fluorescent microspheres, achieving sub-micron lateral and sub-cellular axial resolutions. Furthermore, we have demonstrated its feasibility using GFP-labeled neurons and Siha cervical cancer cell samples for cell counting.

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