显微镜
共焦
共焦显微镜
显微镜
光学
材料科学
荧光显微镜
分辨率(逻辑)
光学显微镜
光学切片
图像分辨率
超分辨显微术
薄层荧光显微镜
扫描共焦电子显微镜
计算机科学
荧光
物理
扫描电子显微镜
人工智能
作者
Bingying Zhao,Minoru Koyama,Jérôme Mertz
摘要
There has been recent interest in the development of fluorescence microscopes that provide high-speed volumetric imaging for life-science applications. For example, multi-z confocal microscopy enables simultaneous optically-sectioned imaging at multiple depths over relatively large fields of view. However, to date, multi-z microscopy has been hampered by limited spatial resolution owing to its initial design. Here we present a variant of multi-z microscopy that recovers the full spatial resolution of a conventional confocal microscope while retaining the simplicity and ease of use of our initial design. By introducing a diffractive optical element in the illumination path of our microscope, we engineer the excitation beam into multiple tightly focused spots that are conjugated to axially distributed confocal pinholes. We discuss the performance of this multi-z microscope in terms of resolution and detectability and demonstrate its versatility by performing in-vivo imaging of beating cardiomyocytes in engineered heart tissues and neuronal activity in c. elegans and zebrafish brains.
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