lunduniversity.lu.se

Denna sida på svenska This page in English

Diffusive transport of multivalent ions in cartilage

Articulate cartilage is a firm gel-like complex material, composed of collagenous fibers and cells called chondrocytes. The chondrocyte cells produce proteoglycans which bind to hyaluronic acid, forming large highly hydrophilic aggregates. These aggregates are entangled with each other and with the collagen fibrils forming what can best be described as a hydrogel that sits within the collagen network. In the general accepted model of the morphology of cartilage, the collagen fibrils associate into columnar structures that extend outward from the bone. The protoeglycans are highly charged due to the presence of sulfate and carboxylic groups. The break-down of cartilage results in a lowering of the concentration of the proteoglycans. It has been suggested to use (Gd-DTPA)2- as a contrast in MRI to monitor the concentration of proteoglycans and therefore the state of the cartilage. In healthy cartilage the concentration of (Gd-DTPA)2- will be low, while in damaged cartilage it would be high leading to T1-contrast in MRI.

There are some fundamental questions in this context. What is the dynamics of the Gd-complex in cartilage? How does one quantify the T1 contrast in terms of the state of the cartilage? On the experimental side, NMR diffusometry and micro imaging techniques are applied on model system of cartilage made from gel-forming polymers as well as on actual in-vitro samples of cartilage.

In addition, computer simulations on a model system of cartilage with the aim of going beyond the use of an ideal Donnan equilibrium approach in the analysis of experimental data pertaining to distribution of (Gd-DTPA)2 from MRI-data are performed.

Finally, a theoretical framework for the transport and concentration of ions in cartilage starting from a non-equilibrium situation is developed. This forms the basis for numerical calculations based on the finite element method.

People: Jenny Algotsson, Daniel Topgaard, Olle Söderman, Peter Jönsson, Jan Forsman (Division of Theoretical Chemistry, LU), Jonas Svensson and Leif Dahlberg (Department of Radiation Physics and the Joint and Soft Tissue Unit at UMAS, Malmö)

Contact person: Olle Söderman