High-speed low-frequency chirped coherent anti-Stokes Raman scattering microscopy using an ultra-steep long-pass filter

被引:5
作者
Ren, Liqing [1 ,2 ]
Raanan, Dekel [2 ]
Hurwitz, Ilan [2 ]
Oron, Dan [2 ]
机构
[1] Yulin Univ, Coll Energy Engn, 51 Chongwen Rd, Yulin 719000, Peoples R China
[2] Weizmann Inst Sci, Dept Phys Complex Syst, 234 Herzl St, IL-76100 Rehovot, Israel
关键词
CARS MICROSCOPY; SPECTROSCOPY; MOTIONS;
D O I
10.1364/OE.27.035993
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Coherent anti-Stokes Raman scattering (CARS) microscopy is becoming a more common tool in biomedical research. High-speed CARS microscopy has important applications in live cell imaging and in label-free pathology. However, only a few realizations exist of CARS imaging applied in the few terahertz spectral range (<300 cm(-1)), in which much is unknown to date. Although single-beam CARS microscopy proved to be robust in this low-frequency region, pixel-dwell time using presently available schemes is still relatively long, in the millisecond scale. Single-beam notch-shaped chirped-CARS (C-CARS) microscopy in the fingerprint region can be performed without using lock-in detection, yet it necessitates double-notch shaping, resulting in a relatively complex system. Here, we demonstrate that C-CARS in the low-frequency regime can be achieved using a sharp-edge, which is created by an ultra-steep long-pass filter (ULPF). Furthermore, we demonstrate that this variant of C-CARS spectroscopy can be performed without post-processing analyses. This is used to image collagen in a biological sample with a pixel dwell time of 200 microseconds. This sharp-edge C-CARS method may find important application in rapid low-frequency CARS imaging of live cells or for imaging of fast flowing objects such as in microfluidic channels. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:35993 / 36001
页数:9
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