June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Imaging retina in rodent eyes with high resolution polarization sensitive optical coherence tomography
Author Affiliations & Notes
  • Stanislava Fialová
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
    Medical Imaging Cluster, Medical University of Vienna, Vienna, Austria
  • Marco Augustin
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
    Medical Imaging Cluster, Medical University of Vienna, Vienna, Austria
  • Roberto Plasenzotti
    Division of Biomedical Research, Medical University of Vienna, Vienna, Austria
  • Michael Pircher
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
    Medical Imaging Cluster, Medical University of Vienna, Vienna, Austria
  • Christoph K Hitzenberger
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
    Medical Imaging Cluster, Medical University of Vienna, Vienna, Austria
  • Bernhard Baumann
    Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
    Medical Imaging Cluster, Medical University of Vienna, Vienna, Austria
  • Footnotes
    Commercial Relationships Stanislava Fialová, None; Marco Augustin, None; Roberto Plasenzotti, None; Michael Pircher, None; Christoph Hitzenberger, None; Bernhard Baumann, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 5939. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Stanislava Fialová, Marco Augustin, Roberto Plasenzotti, Michael Pircher, Christoph K Hitzenberger, Bernhard Baumann; Imaging retina in rodent eyes with high resolution polarization sensitive optical coherence tomography. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):5939.

      Download citation file:


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

      ×
  • Supplements
Abstract
 
Purpose
 

Animal models play an important role in studies of ocular diseases such as age-related macular degeneration and glaucoma. The purpose of this study is to develop high-resolution polarization sensitive OCT (HR-PS-OCT) for imaging the eyes of rodents and to demonstrate in vivo imaging in rats and mice.

 
Methods
 

Spectral domain HR-PS-OCT with an axial resolution of 5.1 µm in air (3.8 µm in tissue) was developed. The central wavelength of the used light source (superluminescent diode) was 840 nm, acquisition speed was 83 kHz. Due to the high scan speed, a whole 3D data set can be acquired in few seconds (1024x200x1536 in 3.44 s) which reduces motion artifacts. In addition to standard OCT images that show sample reflectivity, phase retardation and fast axis orientation images were calculated. PS-OCT images enable the identification of birefringent tissues (such as sclera) and depolarizing tissues (such as retinal pigment epithelium - RPE, choroid).

 
Results
 

Healthy non-pigmented/pigmented rats as well as pigmented mice were imaged with the system. On the high-resolution reflectivity images, all retinal layers were observed in all animals. On the phase retardation images, the birefringent properties of the sclera and depolarization properties of the RPE-choroid were observed.

 
Conclusions
 

A dedicated HR-PS-OCT system for ocular imaging in rodents was developed and was demonstrated in vivo on rats and mice. On the high-resolution images all retinal layers could be identified. From polarization sensitive images birefringent and depolarizing tissues were identified. OCT represents a non-lethal and non-invasive alternative to histology. Our results demonstrate the feasibility of the system for high speed and high-resolution imaging of the rodent retina in longitudinal studies.  

 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×