Volume 93, Issue S255
ABS15-0652
Free Access

Assessing the microstructures of the human cornea using Gabor-Domain optical coherence microscopy with large field of view and high resolution

G. Thuret

G. Thuret

Corneal Graft Biology, Engineering and Imaging Laboratory, EA 2521, SFR143, Faculty of Medicine, University Jean Monnet, Saint Etienne, France

Institut Universitaire de France-Paris, Saint Etienne, France

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P. Tankam

P. Tankam

The Institute of Optics and Center for Visual Science, University of Rochester, Rochester, NY, United States

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Z. He

Z. He

Corneal Graft Biology, Engineering and Imaging Laboratory, EA 2521, SFR143, Faculty of Medicine, University Jean Monnet, Saint Etienne, France

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M. Lanis

M. Lanis

Department of Biomedical Engineering, University of Rochester, Rochester, NY, United States

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C. Canavesi

C. Canavesi

LighTopTech Corp., R&D, West Henrietta, NY, United States

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T. Lepinet

T. Lepinet

Laboratoire Hubert Curien UMR-CNRS 5516 and Biology, Engineering and Imaging of the Corneal Graft Laboratory EA2521, University Jean Monnet, Saint Etienne, France

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H. Hindman

H. Hindman

School of Medicine and Dentistry, Ophthalmology, University of Rochester Medical Center, Rochester, NY, United States

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D. Topham

D. Topham

Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY, United States

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P. Gain

P. Gain

Corneal Graft Biology, Engineering and Imaging Laboratory, EA 2521, SFR143, Faculty of Medicine, University Jean Monnet, Saint Etienne, France

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J.P. Rolland

J.P. Rolland

The Institute of Optics and Center for Visual Science, University of Rochester, Rochester, NY, United States

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First published: 23 September 2015

Abstract

Purpose

To investigate the performances of a new large field of view and high volumetric-resolution Gabor-Domain Optical Coherence Microscope (GD-OCM) in imaging human corneal microstructures

Methods

The GD-OCM combined the high sectioning capability of optical coherence tomography with the high lateral resolution of confocal microscopy. We developed a system that achieved high-contrast imaging with a field of view of 1 ± 1 mm2 and volumetric cellular resolution of 2 μm across a thickness of up to 2 mm in tissue. The system fitted on a movable cart and the handheld scanning probe was attached to an articulated arm that may be adjusted to image different locations of the cornea without contact. For real time visualization, we implemented a parallelized Multi-Graphic Processing Units architecture to speed up the processing of data. In this investigation, we focused on imaging the microanatomy of the corneal stroma keratocytes as well as corneal endothelial cells of ex vivo human corneas maintained in an innovative bioreactor

Results

The overall time to 3D visualization, including acquisition that is 1.5 minutes, processing and rendering of a 1000 × 1000 × 400 voxels, was <2 minutes compared to 2 hours on a conventional CPU. The system produced 3D high-resolution images of the distribution of epithelial cells, stromal keratocytes and endothelial cells, comparable to standard in vivo confocal microscopy

Conclusions

This innovative GD-OCM allows pseudo histology of the cornea in an unprecedented wide field and a short acquisition time compatible with analysis of ex vivo living corneas

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