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利用光热激发的快照相衬测量实现宽场中红外高光谱成像。

Wide-Field Mid-Infrared Hyperspectral Imaging by Snapshot Phase Contrast Measurement of Optothermal Excitation.

机构信息

School of Medicine, Center for Translational Cancer Research (TranslaTUM), Chair of Biological Imaging, Technical University of Munich, D-81675 Munich, Germany.

Institute of Biological and Medical Imaging, Helmholtz Zentrum München (GmbH), D-85764 Neuherberg, Germany.

出版信息

Anal Chem. 2021 Nov 23;93(46):15323-15330. doi: 10.1021/acs.analchem.1c02805. Epub 2021 Nov 12.

Abstract

Vibrational microscopy methods based on Raman scattering or infrared absorption provide a label-free approach for chemical-contrast imaging, but employ point-by-point scanning and impose a compromise between the imaging speed and field-of-view (FOV). Optothermal microscopy has been proposed as a promising imaging modality to avoid this compromise, although at restrictively small FOVs capable of imaging only few cells. Here, we present wide-field optothermal mid-infrared microscopy (WOMiM) for wide-field chemical-contrast imaging based on snapshot pump-probe detection of optothermal signal, using a custom-made condenser-free phase contrast microscopy to capture the phase change of samples after mid-infrared irradiation. We achieved chemical contrast for FOVs up to 180 μm in diameter, yielding 10-fold larger imaging areas than the state-of-the-art, at imaging speeds of 1 ms/frame. The maximum possible imaging speed of WOMiM was determined by the relaxation time of optothermal heat, measured to be 32.8 μs in water, corresponding to a frame rate of ∼30 kHz. This proof-of-concept demonstrates that vibrational imaging can be achieved at an unprecedented imaging speed and large FOV with the potential to significantly facilitate label-free imaging of cellular dynamics.

摘要

基于拉曼散射或红外吸收的振动显微镜方法为化学对比成像提供了一种无标记的方法,但采用逐点扫描,并在成像速度和视场(FOV)之间做出妥协。光热显微镜已被提出作为一种有前途的成像方式来避免这种妥协,尽管其 FOV 非常小,只能成像少数几个细胞。在这里,我们提出了基于快照泵浦探测光热信号的宽场光热中红外显微镜(WOMiM),用于基于中红外辐射的宽场化学对比成像,使用定制的无聚光镜相差显微镜来捕获样品的相位变化。我们实现了直径达 180 μm 的 FOV 的化学对比,获得了比现有技术大 10 倍的成像面积,成像速度为 1 ms/帧。WOMiM 的最大可能成像速度由光热热的弛豫时间决定,在水中测量为 32.8 μs,对应于约 30 kHz 的帧率。该概念验证表明,振动成像可以以前所未有的成像速度和大视场实现,具有显著促进细胞动力学无标记成像的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd6/8613735/cc57587dae16/ac1c02805_0002.jpg

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