Abstract

Retinal imaging working with a line scan mechanism and a line camera has the potential to image the eye with a near-confocal performance at the high frame rate, but this regime has difficulty to collect sufficient imaging light while adequately digitize the optical resolution in adaptive optics imaging. To meet this challenge, we have developed an adaptive optics line scan ophthalmoscope with an anamorphic point spread function. The instrument uses a high-speed line camera to acquire the retinal image and act as a confocal gate. Meanwhile, it employs a digital micro-mirror device to modulate the imaging light into a line of point sources illuminating the retina. The anamorphic mechanism ensures adequate digitization of the optical resolution and increases light collecting efficiency. We demonstrate imaging of the living human retina with cellular level resolution at a frame rate of 200 frames/second (FPS) with a digitization of 512 × 512 pixels over a field of view of 1.2° × 1.2°. We have assessed cone photoreceptor structure in images acquired at 100, 200, and 800 FPS in 2 normal human subjects, and confirmed that retinal images acquired at high speed rendered macular cone mosaic with improved measurement repeatability.

Highlights

  • The introduction of adaptive optics (AO) to ophthalmoscopy has enabled a revolutionary ability for studying retinal structure and function in the living human eye [1], for investigating photoreceptor spatial packing structure due to the capability of resolving individual photoreceptor cells and rendering the photoreceptor mosaic [2,3,4,5,6,7,8,9]

  • We have developed an AO line scan ophthalmoscope with an anamorphic imaging mechanism that generates an elliptic point spread function (PSF) [Fig. 1(d)] thereby increasing imaging light collection efficiency

  • We demonstrate improvement of imaging fidelity of the cone photoreceptor structure achieved by this high speed near-confocal imaging system

Read more

Summary

Introduction

The introduction of adaptive optics (AO) to ophthalmoscopy has enabled a revolutionary ability for studying retinal structure and function in the living human eye [1], for investigating photoreceptor spatial packing structure due to the capability of resolving individual photoreceptor cells and rendering the photoreceptor mosaic [2,3,4,5,6,7,8,9]. With the biometrics obtained from high resolution retinal imaging [19, 20], AO ophthalmoscopy has provided quantitative microscale assessment of the photoreceptor packing structure in healthy and diseased eyes [8, 9, 21,22,23,24,25,26,27] These achievements are very promising to enabling sensitive evaluation of therapeutic efficacy at the cellular level and facilitating development of novel treatment for photoreceptor degeneration [28,29,30,31,32]. These features dictate the necessity of high speed imaging that can be resistant to the motion impact

Objectives
Methods
Findings
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call