Multimodal Full-Field Optical Coherence Tomography on biological tissue: toward all optical digital pathology

被引:5
|
作者
Harms, F. [1 ,2 ]
Dalimier, E. [2 ]
Vermeulen, P. [3 ]
Fragola, A. [3 ]
Boccara, A. C. [1 ,2 ]
机构
[1] ESPCI, Inst Langevin, 10 Rue Vauquelin, F-75005 Paris, France
[2] LLTech, F-75008 Paris, France
[3] ESPCI, Lab Phys & Etud Mat, F-75005 Paris, France
来源
MULTIMODAL BIOMEDICAL IMAGING VII | 2012年 / 8216卷
关键词
OCT; Structured Illumination; multimodal imaging; digital pathology; MICROSCOPY; LIGHT;
D O I
10.1117/12.908459
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Optical Coherence Tomography (OCT) is an efficient technique for in-depth optical biopsy of biological tissues, relying on interferometric selection of ballistic photons. Full-Field Optical Coherence Tomography (FF-OCT) is an alternative approach to Fourier-domain OCT (spectral or swept-source), allowing parallel acquisition of en-face optical sections. Using medium numerical aperture objective, it is possible to reach an isotropic resolution of about 1x1x1 mu m. After stitching a grid of acquired images, FF-OCT gives access to the architecture of the tissue, for both macroscopic and microscopic structures, in a non-invasive process, which makes the technique particularly suitable for applications in pathology. Here we report a multimodal approach to FF-OCT, combining two Full-Field techniques for collecting a backscattered endogeneous OCT image and a fluorescence exogeneous image in parallel. Considering pathological diagnosis of cancer, visualization of cell nuclei is of paramount importance. OCT images, even for the highest resolution, usually fail to identify individual nuclei due to the nature of the optical contrast used. We have built a multimodal optical microscope based on the combination of FF-OCT and Structured Illumination Microscopy (SIM). We used x30 immersion objectives, with a numerical aperture of 1.05, allowing for sub-micron transverse resolution. Fluorescent staining of nuclei was obtained using specific fluorescent dyes such as acridine orange. We present multimodal images of healthy and pathological skin tissue at various scales. This instrumental development paves the way for improvements of standard pathology procedures, as a faster, non sacrificial, operator independent digital optical method compared to frozen sections.
引用
收藏
页数:8
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