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Issue title: 2nd International Symposium on Mechanobiology: Cartilage and Chondrocyte. Paris, France, April 2001
Article type: Research Article
Authors: Wang, Christopher C.‐B. | Guo, X. Edward | Sun, Dongning | Mow, Van C. | Ateshian, Gerard A. | Hung, Clark T.
Affiliations: Department of Biomedical Engineering, Columbia University, New York, NY 10027, USA
Note: [] Address for correspondence: Dr. Clark T. Hung, Cellular Engineering Laboratory, Department of Biomedical Engineering, Columbia University, 3513 Engineering Terrace, M.C. 8904, 1210 Amsterdam Avenue, New York, NY 10027, USA. Tel.: +1 212 854 6542; Fax: +1 212 854 8725; E‐mail: [email protected].
Abstract: A non‐invasive methodology (based on video microscopy, optimized digital image correlation and thin plate spline smoothing technique) has been developed to determine the intrinsic tissue stiffness (Ha) and the intrinsic fixed charge density (c0F) distribution for hydrated soft tissues such as articular cartilage. Using this technique, the depth‐dependent inhomogeneous parameters Ha(z) and c0F(z) were determined for young bovine cartilage and incorporated into a triphasic mixture model. This model was then used to predict the mechanical and electrochemical events (stress, strain, fluid/osmotic pressure, and electrical potentials) inside the tissue specimen under a confined compression stress relaxation test. The integration of experimental measurements with theoretical analyses can help to understand the unique material behaviors of articular cartilage. Coupled with biological assays of cell‐scale biosynthesis, there is also a great potential in the future to study chondrocyte mechanotransduction in situ with a new level of specificity.
Journal: Biorheology, vol. 39, no. 1-2, pp. 11-25, 2002
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