Abstract

This work presents an optospectroscopic characterization technique for soft tissue microstructure using site-matched confocal Raman microspectroscopy and polarized light microscopy. Using the technique, the microstructure of soft tissue samples is directly observed by polarized light microscopy during loading while spatially correlated spectroscopic information is extracted from the same plane, verifying the orientation and arrangement of the collagen fibers. Results show the response and orientation of the collagen fiber arrangement in its native state as well as during tensile and compressive loadings in a porcine sclera model. An example is also given showing how the data can be used with a finite element program to estimate the strain in individual collagen fibers. The measurements demonstrate features that indicate microstructural reorganization and damage of the sclera’s collagen fiber arrangement under loading. The site-matched confocal Raman microspectroscopic characterization of the tissue provides a qualitative measure to relate the change in fibrillar arrangement with possible chemical damage to the collagen microstructure. Tests and analyses presented here can potentially be used to determine the stress-strain behavior, and fiber reorganization of the collagen microstructure in soft tissue during viscoelastic response.

Highlights

  • Collagen fibers are the main constituent of the extracellular matrix of most soft tissues

  • The results show movement patterns of the collagen microstructure while a larger sample of tissue is loaded and unloaded

  • Further investigation to elaborate these findings could shed light on the relationships between a tissue’s microstructural and global behaviors. This optospectroscopic characterization technique could benefit from some improvements including using an electron multiplying charged coupled camera to increase image sensitivity and a piezo-electric fixture mechanism to refine the mechanical loading methods

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Summary

Introduction

Collagen fibers are the main constituent of the extracellular matrix of most soft tissues. An opto-mechanical characterization technique for collagenous tissue is demonstrated using scleral tissue as a model. Sclera is a complex tissue composed predominantly of water (72.2%) and collagen (22.1%) along with trace amounts of mucoid (2.3%), elastin (1.4%) and other proteinous constituents [1]. It is layered tissue and its underlying collagen microstructure has been found to vary greatly in specific fibrillar arrangement from region to region of the globe [2, 3]. The assembly and structure of collagen fibrils in sclera has been well-

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