• DocumentCode
    2182627
  • Title

    In vivo fluorescence confocal microendoscopy

  • Author

    Gmitro, A.F. ; Rouse, A.R. ; Kano, A.

  • Author_Institution
    Dept. of Radiol., Arizona Univ., Tucson, AZ, USA
  • fYear
    2002
  • fDate
    2002
  • Firstpage
    277
  • Lastpage
    280
  • Abstract
    A catheter-based fluorescence confocal microendoscope has been developed for in vivo imaging. The catheter in this system consists of a coherent fiber-optic imaging bundle, a miniature objective, and a focus mechanism. The proximal end of the catheter is coupled to a slit-scan confocal microscope so that high-resolution fluorescence images of cells and tissue microstructure can be viewed in real-time. The performance of the microendoscope is limited by the characteristics of the fiber bundle. The lateral resolution of the system is 1.8 microns and the axial resolution is 25 microns. The field of view is 430 microns. The maximum imaging depth, is around 200 microns below the tissue surface, but this depends on the tissue properties and wavelength range of operation. The slit-scan confocal microscope allows both gray-scale imaging at 8 frames per second and multi-spectral imaging. The frame rate in the multi-spectral imaging mode is determined by the number of spectral channels. The system has been demonstrated using topically-administered exogenous fluorescence dyes in excised tissues and in vivo animal models. A new catheter is under development with a maximum diameter of 3 mm, which will allow it to be routed through the therapeutic instrument channel of a conventional clinical endoscope, making the device practical for routine clinical use.
  • Keywords
    biological tissues; biomedical optical imaging; catheters; cellular biophysics; endoscopes; fibre optic sensors; fluorescence; image resolution; optical microscopy; real-time systems; 3 mm; axial resolution; catheter-based fluorescence confocal microendoscope; coherent fiber-optic imaging bundle; conventional clinical endoscope; excised tissues; fiber bundle; field of view; focus mechanism; gray-scale imaging; high-resolution fluorescence images; in vivo animal models; in vivo fluorescence confocal microendoscopy; in vivo imaging; lateral resolution; maximum diameter; maximum imaging depth; miniature objective; multi-spectral imaging; proximal end; real-time; routine clinical use; slit-scan confocal microscope; spectral channels; therapeutic instrument channel; tissue microstructure; tissue properties; tissue surface; topically-administered exogenous fluorescence dyes; wavelength range of operation; Catheters; Fluorescence; Focusing; Gray-scale; High-resolution imaging; In vivo; Microscopy; Microstructure; Multispectral imaging; Surface waves;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Biomedical Imaging, 2002. Proceedings. 2002 IEEE International Symposium on
  • Print_ISBN
    0-7803-7584-X
  • Type

    conf

  • DOI
    10.1109/ISBI.2002.1029247
  • Filename
    1029247