Interface self-referenced dynamic full-field optical coherence tomography

被引:5
|
作者
Monfort, Tual [1 ,2 ]
Azzollini, Salvatore [1 ]
Ben Yacoub, Tasnim [1 ]
Audo, Isabelle [1 ]
Reichman, Sacha [1 ]
Grieve, Kate [1 ,2 ]
Thouvenin, Olivier [3 ]
机构
[1] Sorbonne Univ, Inst Vis, INSERM, CNRS, 17 rue Moreau, F-75012 Paris, France
[2] CHNO Quinze Vingts, INSERM DGOS CIC 1423, 28 rue Charenton, F-75012 Paris, France
[3] Univ PSL, Inst Langevin, ESPCI Paris, CNRS, F-75005 Paris, France
基金
欧洲研究理事会;
关键词
SPATIALLY INCOHERENT ILLUMINATION; IN-VIVO; RESOLUTION; CONTRAST; OCT; SENSITIVITY; MICROSCOPY;
D O I
10.1364/BOE.488663
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dynamic full-field optical coherence tomography (D-FFOCT) has recently emerged as an invaluable live label-free and non-invasive imaging modality able to image subcellular biological structures and their metabolic activity within complex 3D samples. However, DFFOCT suffers from fringe artefacts when imaging near reflective surfaces and is highly sensitive to vibrations. Here, we present interface Self-Referenced (iSR) D-FFOCT, an alternative configuration to D-FFOCT that takes advantage of the presence of the sample coverslip in between the sample and the objective by using it as a defocused reference arm, thus avoiding the aforementioned artefacts. We demonstrate the ability of iSR D-FFOCT to image 2D fibroblast cell cultures, which are among the flattest mammalian cells.
引用
收藏
页码:3491 / 3505
页数:15
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