Investigative Ophthalmology & Visual Science Cover Image for Volume 61, Issue 7
June 2020
Volume 61, Issue 7
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ARVO Annual Meeting Abstract  |   June 2020
Non-contact phase-gradient corneal microscopy with asymmetric transillumination
Author Affiliations & Notes
  • Timothy Weber
    Boston University, Brookline, Massachusetts, United States
  • Jerome Mertz
    Boston University, Brookline, Massachusetts, United States
  • Footnotes
    Commercial Relationships   Timothy Weber, None; Jerome Mertz, None
  • Footnotes
    Support  NIH Grant EY029486
Investigative Ophthalmology & Visual Science June 2020, Vol.61, 4744. doi:
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      Timothy Weber, Jerome Mertz; Non-contact phase-gradient corneal microscopy with asymmetric transillumination. Invest. Ophthalmol. Vis. Sci. 2020;61(7):4744.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : There is great interest in non-contact, cellular-scale corneal imaging for diagnostics and disease monitoring. Existing techniques derive image contrast from reflected light and therefore require a high degree of optical sectioning in order to reject much stronger reflections originating at other surfaces, such as the air-cornea interface. Here we present an alternative approach based on obliquely transmitted light, which produces phase-gradient contrast images of the cornea across a 1-mm field of view.

Methods : Like the slit lamp technique known as retroillumination, our method uses reflected light from the fundus to transilluminate the cornea. However, our method differs in two important aspects: 1) we use a single long working distance objective lens for both illumination and imaging. This design enables the use of much larger numerical aperture (tantamount to higher resolving power). 2) We tailor the illumination pattern on the fundus to emphasize features of interest. For instance, in our prototype system (Fig. 1), we use an asymmetric illumination pattern to reveal phase-gradient contrast. To demonstrate the principle, we imaged the posterior corneal surface of a realistic model eye (Ocular Instruments OEMI-7).

Results : With asymmetric transillumination, we can visualize the posterior surface of the model eye cornea. Specifically, we saw small scratches at the cornea-aqueous interface (see Fig. 2). When the illumination pattern was altered to be symmetric, no such scratches could be detected in single frames.

Conclusions : We have introduced a new technique for corneal microscopy based on fundus reflection. Unlike other reflection-based corneal microscopy techniques, our method uses transmitted light. Transmission and reflection imaging geometries are known to produce qualitatively different image contrast. Future work should establish which corneal structures the method is sensitive to and compare sensitivity to reflection techniques.

This is a 2020 ARVO Annual Meeting abstract.

 

The magnified image of an LED is projected onto the retina/fundus (blue inset). The back reflected light asymmetrically obliquely transilluminates the cornea. The microscopy field of view (indicated with a white dashed box in the green inset) is 10x magnified onto the sensor of a CMOS camera. We use crossed polarization and a central block to eliminate strong back reflections from intermediate objective lens surfaces.

The magnified image of an LED is projected onto the retina/fundus (blue inset). The back reflected light asymmetrically obliquely transilluminates the cornea. The microscopy field of view (indicated with a white dashed box in the green inset) is 10x magnified onto the sensor of a CMOS camera. We use crossed polarization and a central block to eliminate strong back reflections from intermediate objective lens surfaces.

 

Phase gradient image of model eye cornea-aqueous interface.

Phase gradient image of model eye cornea-aqueous interface.

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