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Solute Transport of Negatively Charged Contrast Agents Across Articular Surface of Injured Cartilage.

Authors :
Kokkonen HT
Chin HC
Töyräs J
Jurvelin JS
Quinn TM
Source :
Annals of biomedical engineering [Ann Biomed Eng] 2017 Apr; Vol. 45 (4), pp. 973-981. Date of Electronic Publication: 2016 Nov 08.
Publication Year :
2017

Abstract

Solute transport through the extracellular matrix (ECM) is crucial to chondrocyte metabolism. Cartilage injury affects solute transport in cartilage due to alterations in ECM structure and solute-matrix interactions. Therefore, cartilage injury may be detected by using contrast agent-based clinical imaging. In the present study, effects of mechanical injury on transport of negatively charged contrast agents in cartilage were characterized. Using cartilage plugs injured by mechanical compression protocol, effective partition coefficients and diffusion fluxes of iodine- and gadolinium-based contrast agents were measured using high resolution microCT imaging. For all contrast agents studied, effective diffusion fluxes increased significantly, particularly at early times during the diffusion process (38 and 33% increase after 4 min, P < 0.05 for iodine and Gd-DTPA; and 76% increase after 10 min for diatrizoate, P < 0.05). Effective partition coefficients were unaffected in mechanically injured cartilage. Mechanical injury reduced PG content and collagen integrity in cartilage superficial zone. This study suggests that alterations in contrast agent diffusion flux, a non-equilibrium transport parameter, provides a more sensitive indicator for assessment of cartilage matrix integrity than partition coefficient and the equilibrium distribution of solute. These findings may help in developing clinical methods of contrast agent-based imaging to detect cartilage injury.

Details

Language :
English
ISSN :
1573-9686
Volume :
45
Issue :
4
Database :
MEDLINE
Journal :
Annals of biomedical engineering
Publication Type :
Academic Journal
Accession number :
27826673
Full Text :
https://doi.org/10.1007/s10439-016-1756-6