Airy light-sheet Raman imaging

被引:11
作者
Subedi, N. R. [1 ]
Yaraghi, S. [2 ]
Jung, P. S. [2 ,3 ]
Kukal, G. [4 ]
McDonald, A. G. [4 ]
Christodoulides, D. N. [2 ]
Vasdekis, A. E. [1 ]
机构
[1] Univ Idaho, Dept Phys, Moscow, ID 83844 USA
[2] Univ Cent Florida, CREOL Coll Opt & Photon, Orlando, FL 32816 USA
[3] Warsaw Univ Technol, Fac Phys, Warsaw, Poland
[4] Univ Idaho, Dept Forest Rangeland & Fire Sci, Forest & Sustainable Prod Program, Moscow, ID 83844 USA
关键词
FLUORESCENCE MICROSCOPY; ILLUMINATION; RESOLUTION; EMBRYOS;
D O I
10.1364/OE.435293
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Light-sheet fluorescence microscopy has greatly improved the speed and overall photostability of optically sectioning cellular and multi-cellular specimens. Similar gains have also been conferred by light-sheet Raman imaging; these schemes, however, rely on diffraction limited Gaussian beams that hinder the uniformity and size of the imaging field-of-view, and, as such, the resulting throughput rates. Here, we demonstrate that a digitally scanned Airy beam increases the Raman imaging throughput rates by more than an order of magnitude than conventional diffraction-limited beams. Overall, this, spectrometer-less, approach enabled 3D imaging of microparticles with high contrast and 1 mu m axial resolution at 300 msec integration times per plane and orders of magnitude lower irradiation density than coherent Raman imaging schemes. We detail the apparatus and its performance, as well as its compatibility with fluorescence light-sheet and quantitative-phase imaging towards rapid and low phototoxicity multimodal imaging. (C) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:31941 / 31951
页数:11
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