3D cellular imaging of the cornea with Gabor-domain optical coherence microscopy

A Gabor-domain optical coherence microscope (GDOCM) with 2-micrometer invariant lateral and axial resolutions and a working distance of 15 mm was developed for 3D imaging of corneal tissue over a 1 mm2 field of view. The increased working distance over the previous in-contact implementation enables imaging of corneal tissue inside the viewing chamber in which corneas are stored after recovery from donors. The GDOCM system was used to image excised human corneas. 3D images of the cornea were acquired by imaging through the PMMA viewing chamber. The images achieved cellular resolution in the volume being imaged. Due to the curvature of the cornea, the endothelium, a single layer of cells lining the posterior surface of the cornea, cannot be viewed in a single en face image. A flattening algorithm was implemented to obtain an en face view of the endothelium. The GDOCM images were compared with those acquired with a specular microscope commonly used in eye banks for endothelial evaluation, and the endothelial cell density was assessed for both sets of images. A key advantage of GDOCM is the capability to image the entire thickness of the cornea in 3D with cellular resolution over a large field of view.

[1]  Kye-Sung Lee,et al.  Parallelized multi–graphics processing unit framework for high-speed Gabor-domain optical coherence microscopy , 2014, Journal of biomedical optics.

[2]  Changsik Yoon,et al.  Quantitative assessment of human donor corneal endothelium with Gabor domain optical coherence microscopy , 2019, Journal of biomedical optics.

[3]  Leopold Schmetterer,et al.  Anterior segment optical coherence tomography , 2018, Progress in Retinal and Eye Research.

[4]  Panomsak Meemon,et al.  Gabor-based fusion technique for Optical Coherence Microscopy. , 2010, Optics express.

[5]  Beth Ann Benetz,et al.  An evaluation of image quality and accuracy of eye bank measurement of donor cornea endothelial cell density in the Specular Microscopy Ancillary Study. , 2005, Ophthalmology.

[6]  A. Fercher,et al.  Measurement of intraocular distances by backscattering spectral interferometry , 1995 .

[7]  M. Fink,et al.  In vivo high resolution human corneal imaging using full-field optical coherence tomography. , 2018, Biomedical optics express.

[8]  Supraja Murali,et al.  Three-dimensional adaptive microscopy using embedded liquid lens. , 2009, Optics letters.

[9]  Jonathan H. Lass,et al.  Introduction: Current and New Technologies in Corneal Donor Tissue Evaluation: Comparative Image Atlas. , 2018, Cornea.

[10]  Patrice Tankam,et al.  Assessing microstructures of the cornea with Gabor-domain optical coherence microscopy: pathway for corneal physiology and diseases. , 2015, Optics letters.

[11]  Virgil-Florin Duma,et al.  MEMS-based handheld scanning probe with pre-shaped input signals for distortion-free images in Gabor-domain optical coherence microscopy. , 2016, Optics express.

[12]  W. Marsden I and J , 2012 .

[13]  Kostadinka Bizheva,et al.  250 kHz, 1.5 µm resolution SD-OCT for in-vivo cellular imaging of the human cornea. , 2018, Biomedical optics express.

[14]  Danna Zhou,et al.  d. , 1934, Microbial pathogenesis.

[15]  O Stachs,et al.  In vivo three-dimensional confocal laser scanning microscopy of corneal surface and epithelium , 2008, British Journal of Ophthalmology.