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利用倾斜反射镜组件实现可调频率照明的传输结构光照明显微镜。

Transmission structured illumination microscopy with tunable frequency illumination using tilt mirror assembly.

机构信息

Department of Physics, Indian Institute of Technology Delhi, New Delhi, 110016, India.

Department of Physics and Technology, UiT-The Arctic University of Norway, 9037, Tromsö, Norway.

出版信息

Sci Rep. 2023 Jan 26;13(1):1453. doi: 10.1038/s41598-023-27814-x.

DOI:10.1038/s41598-023-27814-x
PMID:36702876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9879979/
Abstract

We present experimental demonstration of tilt-mirror assisted transmission structured illumination microscopy (tSIM) that offers a large field of view super resolution imaging. An assembly of custom-designed tilt-mirrors are employed as the illumination module where the sample is excited with the interference of two beams reflected from the opposite pair of mirror facets. Tunable frequency structured patterns are generated by changing the mirror-tilt angle and the hexagonal-symmetric arrangement is considered for the isotropic resolution in three orientations. Utilizing high numerical aperture (NA) objective in standard SIM provides super-resolution compromising with the field-of-view (FOV). Employing low NA (20X/0.4) objective lens detection, we experimentally demonstrate [Formula: see text] (0.56 mm[Formula: see text]0.35 mm) size single FOV image with [Formula: see text]1.7- and [Formula: see text]2.4-fold resolution improvement (exploiting various illumination by tuning tilt-mirrors) over the diffraction limit. The results are verified both for the fluorescent beads as well as biological samples. The tSIM geometry decouples the illumination and the collection light paths consequently enabling free change of the imaging objective lens without influencing the spatial frequency of the illumination pattern that are defined by the tilt-mirrors. The large and scalable FOV supported by tSIM will find usage for applications where scanning large areas are necessary as in pathology and applications where images must be correlated both in space and time.

摘要

我们展示了倾斜镜辅助传输结构光照明显微镜(tSIM)的实验演示,该技术提供了大视场超分辨率成像。一组定制设计的倾斜镜被用作照明模块,其中样品通过从相对的镜面对反射的两束光的干涉来激发。通过改变镜倾斜角来产生可调谐的频率结构图案,并且考虑了六边形对称排列以在三个方向上实现各向同性分辨率。在标准 SIM 中使用高数值孔径(NA)物镜提供超分辨率,这会牺牲视场(FOV)。采用低 NA(20X/0.4)物镜检测,我们实验证明了[公式:见文本](0.56mm[公式:见文本]0.35mm)大小的单个 FOV 图像,与衍射极限相比,分辨率提高了[公式:见文本]1.7 倍和[公式:见文本]2.4 倍(通过调整倾斜镜利用各种照明来实现)。结果在荧光珠和生物样本上都得到了验证。tSIM 几何形状解耦了照明和收集光路,因此可以在不影响由倾斜镜定义的照明图案的空间频率的情况下自由改变成像物镜。tSIM 支持的大而可扩展的 FOV 将在需要扫描大区域的应用中得到应用,例如病理学和图像必须在空间和时间上相关的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/0a185e52c8f5/41598_2023_27814_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/eafacc0027b0/41598_2023_27814_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/f58061e5d0ff/41598_2023_27814_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/549e7b483013/41598_2023_27814_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/5d55b1c41b55/41598_2023_27814_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/3d810372c096/41598_2023_27814_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/0a185e52c8f5/41598_2023_27814_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/eafacc0027b0/41598_2023_27814_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/f58061e5d0ff/41598_2023_27814_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/549e7b483013/41598_2023_27814_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/5d55b1c41b55/41598_2023_27814_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/3d810372c096/41598_2023_27814_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a9/9879979/0a185e52c8f5/41598_2023_27814_Fig6_HTML.jpg

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