Gabor domain optical coherence microscopy combined with laser scanning confocal fluorescence microscopy

被引:7
作者
Yoon, Changsik [1 ]
Qi, Yue [2 ]
Mestre, Humberto [3 ]
Canavesi, Cristina [4 ]
Marola, Olivia J. [5 ]
Cogliati, Andrea [4 ]
Nedergaard, Maiken [3 ]
Libby, Richard T. [5 ]
Rolland, Jannick P. [1 ,2 ,4 ]
机构
[1] Univ Rochester, Inst Opt, Wilmot Bldg, Rochester, NY 14627 USA
[2] Univ Rochester, Dept Biomed Engn, Robert B Goergen Hall, Rochester, NY 14627 USA
[3] Univ Rochester, Ctr Translat Neuromed, Dept Neurosurg, Med Ctr, Rochester, NY 14642 USA
[4] LighTopTech Corp, 150 Lucius Gordon Dr,Ste 201, West Henrietta, NY 14586 USA
[5] Univ Rochester, Flaum Eye Inst, Dept Ophthalmol, Med Ctr, Rochester, NY 14642 USA
关键词
EARLY BLADDER-CANCER; SWEPT SOURCE; DELAY-LINE; LABEL-FREE; TOMOGRAPHY; OCT; SENSITIVITY; ASTROCYTES; PLATFORM; PROBE;
D O I
10.1364/BOE.10.006242
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report on the development of fluorescence Gabor domain optical coherence microscopy (Fluo GD-OCM), a combination of GD-OCM with laser scanning confocal fluorescence microscopy (LSCFM) for synchronous micro-structural and fluorescence imaging. The dynamic focusing capability of GD-OCM provided the adaptive illumination environment for both modalities without any mechanical movement. Using Fluo GD-OCM, we imaged ex vivo DsRed-expressing cells in the brain of a transgenic mouse, as well as Cy3-labeled ganglion cells and Cy3-labeled astrocytes from a mouse retina. The self-registration of images taken by the two different imaging modalities showed the potential for a correlative study of subjects and double identification of the target. (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:6242 / 6257
页数:16
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