April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Observation of Porcine Corneal Stroma at the Cellular Level by Full-Field Oct
Author Affiliations & Notes
  • K. Yumikake
    Ophthalmology, Osaka Univ Medical School, Tokyo, Japan
  • M. Akiba
    TOPCON Adv Biomed Imaging Lab,
    Topcon Medical Systems, Paramus, New Jersey
  • K. Chan
    TOPCON Adv Biomed Imaging Lab,
    Topcon Medical Systems, Paramus, New Jersey
  • A. Sekine
    TOPCON Corporation, Tokyo, Japan
  • Y. Fukuma
    TOPCON Advanced Biomedical Imaging Lab,
    Topcon Medical Systems, Paramus, New Jersey
  • N. Maeda
    Ophthalmology, Osaka Univ Medical School, Suita, Japan
  • Footnotes
    Commercial Relationships  K. Yumikake, None; M. Akiba, TOPCON, E; K. Chan, TOPCON, E; A. Sekine, TOPCON, E; Y. Fukuma, TOPCON, E; N. Maeda, TOPCON, F.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 5773. doi:
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      K. Yumikake, M. Akiba, K. Chan, A. Sekine, Y. Fukuma, N. Maeda; Observation of Porcine Corneal Stroma at the Cellular Level by Full-Field Oct. Invest. Ophthalmol. Vis. Sci. 2010;51(13):5773.

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

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Abstract

Purpose: : Full-field OCT (FF-OCT) is an ultra-high resolution OCT technique which is considered to be suitable for imaging of cornea at a cellular level. This study was conducted to verify the feasibility of FF-OCT in the imaging of stroma of ex vivo porcine cornea.

Methods: : The FF-OCT setup used in the study was based on a Linnik type interference microscope where a horizontal cross-sectional image is detected with a two-dimensional CCD camera. A Halogen lamp is used as the broadband source which offers a 2µm depth resolution in tissue. The lateral resolution is limited by the objective lens (NA=0.5) as 1µm. Images were obtained through the stroma in ex vivo porcine cornea. The area ratio (%) of keratocyte and the density of fibrillar structure in the FF-OCT image are compared between the superficial layer and deep layer of the stroma.

Results: : Different from that observed with a confocal microscope, the nucleus of keratocyte was observed as low-intensity area and cytoplasm was observed as high-intensity area. The area ratio (%) of keratocyte was significantly larger at superficial stroma (53.0±19.5) than that at the deep layer (27.1±14.4; p=0.031, paired-t test) Moreover, a well defined fibrillar structure which might possibly be associated with the arrangement of collagen was observed as well. There was a significant difference in the density (line/mm2) of fibrillar structure between the superficial layer (14.7±20.3) and the deep layer (580.0±109.5; p=0.001, paired-t test).

Conclusions: : FF-OCT might be used as the OCT microscope for the observation of corneal stroma, where it may offer additional information that is different from that observed with a confocal microscope such as a high-intensity cytoplasm of the keratocyte and fibrillar structure.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • imaging/image analysis: non-clinical 
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