Measurement of diffusion of uncharged molecules in articular cartilage.
Abstract: The diffusion of glucose (180 M.W.), inulin (5,000 M.W.) and dextran (20,000 M.W.) into mature bovine and equine articular cartilage was studied. Concentration profiles were determined using a one-dimensional experimental configuration and the diffusion coefficient and partition coefficient calculated from a theoretical model. Glucose was found to diffuse the fastest, followed by inulin and dextran. The partition coefficient was similarly ordered. The rate of diffusion was found to decrease with increasing diffusion time, indicating a dependence on solute concentration. No time variation was evident in the partition coefficient. In addition, no difference was found between species or between the location sites within the animal joint.
Publication Date: 1984-04-01 PubMed ID: 6205821
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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The research investigates the diffusion rate of different uncharged molecules in the joint (articular) cartilage of mature bovines and horses. The study finds that the diffusion rate varies depending on the molecular weight of the substance and does not depend on the species or the specific location in the joint.
Research Methodology
- Three substances were used for the study: glucose (180 M.W.), inulin (5,000 M.W.) and dextran (20,000 M.W.). The molecular weight (M.W.) of these substances were varied to understand the impact of molecular size on diffusion.
- The concentration profiles of these substances in the cartilage were determined using a one-dimensional experimental configuration.
- The researchers used a theoretical model to calculate the diffusion and partition coefficients, which reveal the speed and extent of diffusion respectively.
Key Findings
- Glucose – the lightest molecule among the three – was found to diffuse the fastest, followed by medium-weight inulin and heavy dextran. Thus, the speed of diffusion appears to be inversely related to the molecular weight of the substance.
- The partition coefficient, which indicates how widespread the substances are within the cartilage, was ordered similarly: highest for glucose and lowest for dextran.
- The rate of diffusion was found to decrease as more molecules entered the cartilage (as diffusion time increased), suggesting a concentration dependence of the diffusion rate.
- There were no observed temporal changes in the partition coefficient, suggesting it is not influenced by changes in the concentration of the substance in the cartilage.
- No difference in diffusion or partitioning was observed between bovines and horses, or between different parts of the joint, indicating that these factors do not significantly affect the diffusion of uncharged molecules in joint cartilage.
Cite This Article
APA
Allhands RV, Torzilli PA, Kallfelz FA.
(1984).
Measurement of diffusion of uncharged molecules in articular cartilage.
Cornell Vet, 74(2), 111-123.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cartilage, Articular / metabolism
- Cattle
- Dextrans / metabolism
- Diffusion
- Glucose / metabolism
- Horses
- Inulin / metabolism
- Molecular Weight
- Time Factors
Grant Funding
- AM05778 / NIADDK NIH HHS
- AM19849 / NIADDK NIH HHS
Citations
This article has been cited 13 times.- Kodama J, Wilkinson KJ, Otsuru S. Nutrient metabolism of the nucleus pulposus: A literature review. N Am Spine Soc J 2023 Mar;13:100191.
- Shoga JS, Graham BT, Wang L, Price C. Direct Quantification of Solute Diffusivity in Agarose and Articular Cartilage Using Correlation Spectroscopy. Ann Biomed Eng 2017 Oct;45(10):2461-2474.
- McMurtrey RJ. Analytic Models of Oxygen and Nutrient Diffusion, Metabolism Dynamics, and Architecture Optimization in Three-Dimensional Tissue Constructs with Applications and Insights in Cerebral Organoids. Tissue Eng Part C Methods 2016 Mar;22(3):221-49.
- Spitters TW, Mota CM, Uzoechi SC, Slowinska B, Martens DE, Moroni L, Karperien M. Glucose gradients influence zonal matrix deposition in 3D cartilage constructs. Tissue Eng Part A 2014 Dec;20(23-24):3270-8.
- Jackson A, Gu W. TRANSPORT PROPERTIES OF CARTILAGINOUS TISSUES. Curr Rheumatol Rev 2009 Feb 1;5(1):40.
- Ceelen KK, Gawlitta D, Bader DL, Oomens CW. Numerical analysis of ischemia- and compression-induced injury in tissue-engineered skeletal muscle constructs. Ann Biomed Eng 2010 Mar;38(3):570-82.
- Zhang L, Szeri AZ. Transport of neutral solute in articular cartilage: effect of microstructure anisotropy. J Biomech 2008;41(2):430-7.
- Evans RC, Quinn TM. Dynamic compression augments interstitial transport of a glucose-like solute in articular cartilage. Biophys J 2006 Aug 15;91(4):1541-7.
- Mauck RL, Hung CT, Ateshian GA. Modeling of neutral solute transport in a dynamically loaded porous permeable gel: implications for articular cartilage biosynthesis and tissue engineering. J Biomech Eng 2003 Oct;125(5):602-14.
- Gonsalves M, Barker AL, Macpherson JV, Unwin PR, O'Hare D, Winlove CP. Scanning electrochemical microscopy as a local probe of oxygen permeability in cartilage. Biophys J 2000 Mar;78(3):1578-88.
- Peng SX, VonBargen EC, Bornes DM, Pikul S. Permeability of articular cartilage to matrix metalloprotease inhibitors. Pharm Res 1998 Sep;15(9):1414-8.
- Macpherson JV, O'Hare D, Unwin PR, Winlove CP. Quantitative spatially resolved measurements of mass transfer through laryngeal cartilage. Biophys J 1997 Nov;73(5):2771-81.
- Torzilli PA. Effects of temperature, concentration and articular surface removal on transient solute diffusion in articular cartilage. Med Biol Eng Comput 1993 Jul;31 Suppl:S93-8.
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