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arXiv · 1712.08472

A new microscopy for imaging retinal cells

Timothé Laforest·Dino Carpentras·Mathieu Künzi·Laura Kowalczuk·Francine Behar-Cohen·Christophe Moser
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Abstract

The evaluation and monitoring of cells health in the human retina is crucial and follow time course of retinal diseases, detect lesions before irreversible visual loss and to evaluate treatment effects. Towards this goal, a major challenge is to image and quantify retinal cells in human eyes in a non-invasive manner. Despite the phenomenal advances in Optical Coherence Tomography (OCT) and Adaptive Optics systems, in vivo imaging of many of these cells is limited by the fact that cell contrast in reflection is extremely low. Here, we report on a major advance by proposing and demonstrating a radically different method compared with OCT to visualize retinal cells with high contrast, resolution and an acquisition time suitable for clinical use. The method uses a transscleral illumination which provides a high numerical aperture in a dark field configuration. The light backscattered by the Retinal Pigment Epithelium (RPE) and the choroid provides a forward illumination for the upper layer of the retina, thus providing a transmission illumination condition. By collecting the scattered light through the pupil, the partially coherent illumination produces dark field images, which are combined to reconstruct a quasi-quantitative phase image with twice the numerical aperture given by the eye's pupil. The retrieved quasi-quantitative phase images (QPI) of cells in ex vivo human and pig's eyes are validated with those taken with a standard QPI system. We then apply the technique in vivo on human eye, without pupil dilation, we demonstrated the feasibility to image retinal cells up to the retinal pigment epithelium within a few seconds.

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Timothé Laforest, Dino Carpentras, Mathieu Künzi, Laura Kowalczuk, Francine Behar-Cohen, Christophe Moser. 2017-12-20. A new microscopy for imaging retinal cells. https://arxiv.org/abs/1712.08472

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