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Simultaneous Mechanical Loading and Confocal Reflection Microscopy for Three-Dimensional Microbiomechanical Analysis of Biomaterials and Tissue Constructs

Published online by Cambridge University Press:  31 January 2003

Sherry L. Voytik-Harbin
Affiliation:
Department of Basic Medical Sciences, Purdue University, 1515 Hansen Hall, West Lafayette, IN 47907-1515, USA Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47907-1296, USA
Blayne A. Roeder
Affiliation:
School of Mechanical Engineering, Purdue University, West Lafayette, IN 47907-1288, USA
Jennifer E. Sturgis
Affiliation:
Department of Basic Medical Sciences, Purdue University, 1515 Hansen Hall, West Lafayette, IN 47907-1515, USA
Klod Kokini
Affiliation:
Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47907-1296, USA School of Mechanical Engineering, Purdue University, West Lafayette, IN 47907-1288, USA
J. Paul Robinson
Affiliation:
Department of Basic Medical Sciences, Purdue University, 1515 Hansen Hall, West Lafayette, IN 47907-1515, USA Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47907-1296, USA
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Abstract

At present, mechanisms by which specific structural and mechanical properties of the three-dimensional extracellular matrix microenvironment influence cell behavior are not known. Lack of such knowledge precludes formulation of engineered scaffolds or tissue constructs that would deliver specific growth-inductive signals required for improved tissue restoration. This article describes a new mechanical loading–imaging technique that allows investigations of structural–mechanical properties of biomaterials as well as the structural–mechanical basis of cell–scaffold interactions at a microscopic level and in three dimensions. The technique is based upon the integration of a modified, miniature mechanical loading instrument with a confocal microscope. Confocal microscopy is conducted in a reflection and/or fluorescence mode for selective visualization of load-induced changes to the scaffold and any resident cells, while maintaining each specimen in a “live,” fully hydrated state. This innovative technique offers several advantages over current biomechanics methodologies, including simultaneous visualization of scaffold and/or cell microstructure in three dimensions during mechanical loading; quantification of macroscopic mechanical parameters including true stress and strain; and the ability to perform multiple analyses on the same specimen. This technique was used to determine the structural–mechanical properties of three very different biological materials: a reconstituted collagen matrix, a tissue-derived biomaterial, and a tissue construct representing cells and matrix.

Type
Biological Applications
Copyright
© 2003 Microscopy Society of America

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