Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope

J Biomed Opt. 2007 Jul-Aug;12(4):044002. doi: 10.1117/1.2772311.

Abstract

Characteristic changes in the organization of fibrillar collagen can potentially serve as an early diagnostic marker in various pathological processes. Tissue types containing collagen I can be probed by pulsed high-intensity laser radiation, thereby generating second harmonic light that provides information about the composition and structure at a microscopic level. A technique was developed to determine the essential second harmonic generation (SHG) parameters in a laser scanning microscope setup. A rat-tail tendon frozen section was rotated in the xy-plane with the pulsed laser light propagating along the z-axis. By analyzing the generated second harmonic light in the forward direction with parallel and crossed polarizer relative to the polarization of the excitation laser beam, the second-order nonlinear optical susceptibilities of the collagen fiber were determined. Systematic variations in SHG response between ordered and less ordered structures were recorded and evaluated. A 500 microm-thick z-cut lithiumniobate (LiNbO(3)) was used as reference. The method was applied on frozen sections of malignant melanoma and normal skin tissue. Significant differences were found in the values of d(22), indicating that this parameter has a potential role in differentiating between normal and pathological processes.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Collagen Type I / metabolism*
  • Collagen Type I / ultrastructure*
  • Disease Susceptibility / metabolism
  • Disease Susceptibility / pathology
  • Female
  • Humans
  • Image Interpretation, Computer-Assisted / methods
  • Melanoma / metabolism*
  • Melanoma / ultrastructure*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Microscopy, Confocal / methods*
  • Nonlinear Dynamics
  • Rats
  • Rats, Sprague-Dawley
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / ultrastructure*

Substances

  • Collagen Type I