May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Ultrafast all–solid–state lasers for non–invasive ocular tissue imaging
Author Affiliations & Notes
  • M. Han
    Kirchhoff Institut fuer Physik, Heidelberg, Germany
  • L. Zickler
    Kirchhoff Institut fuer Physik, Heidelberg, Germany
  • H. Sun
    Kirchhoff Institut fuer Physik, Heidelberg, Germany
  • G. Giese
    Max Planck Institute for Medical Research, Heidelberg, Germany
  • J. Bille
    Kirchhoff Institut fuer Physik, Heidelberg, Germany
  • Footnotes
    Commercial Relationships  M. Han, None; L. Zickler, None; H. Sun, None; G. Giese, None; J. Bille, None.
  • Footnotes
    Support  BMBF Project
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 1140. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      M. Han, L. Zickler, H. Sun, G. Giese, J. Bille; Ultrafast all–solid–state lasers for non–invasive ocular tissue imaging . Invest. Ophthalmol. Vis. Sci. 2004;45(13):1140.

      Download citation file:


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

      ×
  • Supplements
Abstract

Abstract: : Purpose: All–solid–state ultrafast lasers are not only attractive for therapeutic applications in refractive surgery, keratoplasty and glaucoma treatment, but also promising for diagnostic purpose for non–invasive high resolution ocular tissue imaging. Multi–harmonic generation from corneal tissue and autofluorescence imaging of retinal tissue are of our main interests. Methods: Excised porcine eye samples were probed with a homemade Nd:glass femtosecond laser with regenerative amplifier and a commercial Ti:sapphire femtosecond laser. Cornea multi–harmonic imaging and retina two photon autofluorescence imaging were conducted with a ZEISS multiphoton laser scanning microscopy. Results: Femtosecond laser induced multi–harmonic generation enabled a diffraction limited high resolution corneal tissue imaging with strong contrast and large sensing depth. Staining or slicing was not required for sample preparation. Two–photon autofluorescence imaging of retinal tissue demonstrated high sensitivity with satisfactory resolution, which could be used as a complementary imaging mode for confocal retina tomography and optical coherent tomography. Conclusions: Based on the nonlinear phenomenon induced by the ultrafast laser pulse including multi–harmonic generation and two photon autofluorescence, ultrafast lasers may lead to new imaging methods for non–invasive ocular tissue diagnostics and in–vivo clinical study.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • laser • microscopy: light/fluorescence/immunohistochemistry 
×
×

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.

×