Label-free CARS microscopy through a multimode fiber endoscope

被引:54
|
作者
Tragardh, Johanna [1 ]
Pikalek, Tomas [1 ]
Sery, Mojmir [1 ]
Meyer, Tobias [2 ,3 ,4 ]
Popp, Juergen [2 ,3 ,4 ]
Cizmar, Tomas [1 ,2 ,5 ]
机构
[1] CAS, Inst Sci Instruments, Vvi, Kralovopolska 147, Brno 61264, Czech Republic
[2] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[3] Friedrich Schiller Univ Jena, Inst Phys Chem, Helmholtzweg 4, D-07743 Jena, Germany
[4] Abbe Ctr Photon, Helmholtzweg 4, D-07743 Jena, Germany
[5] Friedrich Schiller Univ Jena, Inst Appl Opt, Frobelstieg 1, D-07743 Jena, Germany
来源
OPTICS EXPRESS | 2019年 / 27卷 / 21期
基金
欧洲研究理事会;
关键词
IMAGING IN-VIVO; LIGHT; TISSUE;
D O I
10.1364/OE.27.030055
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Multimode fibres have recently been employed as high-resolution ultra-thin endoscopes, capable of imaging biological structures deep inside tissue in vivo. Here, we extend this technique to label-free non-linear microscopy with chemical contrast using coherent anti-Stokes Raman scattering (CARS) through a multimode fibre endoscope, which opens up new avenues for instant and in-situ diagnosis of potentially malignant tissue. We use a commercial 125 mu m diameter, 0.29 NA GRIN fibre, and wavefront shaping on an SLM is used to create foci that are scanned behind the fibre facet across the sample. The chemical selectivity is demonstrated by imaging 2 mu m polystyrene and 2.5 mu m PMMA beads with per pixel integration time as low as 1 ms for epi-detection. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:30055 / 30066
页数:12
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