August 2019
Volume 60, Issue 11
Free
ARVO Imaging in the Eye Conference Abstract  |   August 2019
Visible-light sensorless adaptive optics optical coherence tomography of retinal response to laser exposure
Author Affiliations & Notes
  • Ryne Watterson
    Engineering Science, Simon Fraser University, Burnaby, British Columbia, Canada
  • Daniel Wahl
    Engineering Science, Simon Fraser University, Burnaby, British Columbia, Canada
  • Myeong Jin Ju
    Engineering Science, Simon Fraser University, Burnaby, British Columbia, Canada
  • Marinko V. Sarunic
    Engineering Science, Simon Fraser University, Burnaby, British Columbia, Canada
  • Footnotes
    Commercial Relationships   Ryne Watterson, None; Daniel Wahl, None; Myeong Jin Ju, Seymour Vision (E); Marinko Sarunic, Seymour Vision (I)
  • Footnotes
    Support  CIHR - Canadian Institutes of Health Research, NSERC - Natural Sciences and Engineering Research Council of Canada, Innovate BC, and MSFHR - Michael Smith Foundation for Health Research
Investigative Ophthalmology & Visual Science August 2019, Vol.60, PB028. doi:
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    • Get Citation

      Ryne Watterson, Daniel Wahl, Myeong Jin Ju, Marinko V. Sarunic; Visible-light sensorless adaptive optics optical coherence tomography of retinal response to laser exposure. Invest. Ophthalmol. Vis. Sci. 2019;60(11):PB028.

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

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Abstract

Purpose : In vivo visualization of cellular-level retinal structure with adaptive optics optical coherence tomography enables studies of retinal changes in mouse models of diseases causing blindness. We present our work on visible-light sensorless adaptive optics (VIS-SAO) OCT for structural and fluorescence imaging in the small eyes of mice. The response of the retina to laser exposures is studied in mice with the VIS-SAO OCT.

Methods : The VIS-SAO OCT system shown in Fig 1 was constructed based on our previous reports using a supercontinuum laser and tunable filter. Red light with a central wavelength of 635 nm and a bandwidth of 35 nm was delivered at 100 µW into the mouse eye. The system also provided GFP excitation for fluorescence imaging. The system used two deformable elements including a Variable Focus Lens (VFL), and segmented Deformable Mirror (DM). The Adaptive Optics was performed using image-based optimization algorithm, driven by the en face VIS-SAO OCT images. A dichroic mirror was used to co-align a retinal exposure laser with the OCT light, such that higher power light could be focused onto the retina while simultaneously recording images.

Results : VIS-SAO OCT images were acquired in pigmented mice. Representative images of mouse retina are shown in Fig 2 demonstrating the high-resolution imaging capability of our system. The B-scan in Fig 2a demonstrates VIS-SAO OCT imaging with the red light. The image in Fig 2b shows the ability to visualize the GFP emission and the effect of SAO optimization from the same system. We have done experiments to investigate retinal response with VIS-SAO OCT during and after laser exposure. The retinal response to different exposures will be presented.

Conclusions : We present a VIS-SAO OCT system for small animal retinal imaging, which enables wavefront sensorless aberrations correction for user-selected layers. In vivo retinal imaging of pigmented mice is presented, and the image quality improvement resulting from AO correction is demonstrated.

This abstract was presented at the 2019 ARVO Imaging in the Eye Conference, held in Vancouver, Canada, April 26-27, 2019.

 

Fig. 1: Multimodal VIS-SAO OCT and fluorescence imaging system. DM, deformable mirror; GM, galvanometer scanner; VFL, variable focus lens; PMT, photo multiplier tube; FC, fiber coupler; MEB, multi-edge beam splitter; DCM, dichroic mirror.

Fig. 1: Multimodal VIS-SAO OCT and fluorescence imaging system. DM, deformable mirror; GM, galvanometer scanner; VFL, variable focus lens; PMT, photo multiplier tube; FC, fiber coupler; MEB, multi-edge beam splitter; DCM, dichroic mirror.

 

Fig. 2: (a) VIS-SAO OCT B-scan of mouse retina with 635nm center wavelength. (b) Comparison of before and after SAO is applied to GFP fluorescence images of microglia.

Fig. 2: (a) VIS-SAO OCT B-scan of mouse retina with 635nm center wavelength. (b) Comparison of before and after SAO is applied to GFP fluorescence images of microglia.

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