Department of Physics and Mathematics, University of Eastern Finland, POB 1627, 70211 Kuopio, Finland.
Med Eng Phys. 2010 Oct;32(8):878-82. doi: 10.1016/j.medengphy.2010.06.002. Epub 2010 Jul 1.
In contrast enhanced magnetic resonance imaging (MRI) and computed tomography (CT), the equilibrium distribution of anionic contrast agent is expected to reflect the fixed charged density (FCD) of articular cartilage. Diffusion is mainly responsible for the transport of contrast agents into cartilage. In osteoarthritis, cartilage composition changes at early stages of disease, and solute diffusion is most likely affected. Thus, investigation of contrast agent diffusion could enable new methods for imaging of cartilage composition. The aim of this study was to determine the diffusion coefficient of four contrast agents (ioxaglate, gadopentetate, iodide, gadodiamide) in bovine articular cartilage. The contrast agents were different in molecular size and charge. In peripheral quantitative CT experiments, penetration of contrast agent into the tissue was allowed either through the articular surface or through deep cartilage. To determine diffusion coefficients, a finite element model based on Fick's law was fitted to experimental data. Diffusion through articular surface was faster than through deep cartilage with every contrast agent. Iodide, being of atomic size, diffused into the cartilage significantly faster (q<0.05) than the other three contrast agents, for either transport direction. The diffusion coefficients of all clinical contrast agents (ioxaglate, gadopentetate and gadodiamide) were relatively low (142.8-253.7 μm(2)/s). In clinical diagnostics, such slow diffusion may not reach equilibrium and this jeopardizes the determination of FCD by standard methods. However, differences between diffusion through articular surface and deep cartilage, that are characterized by different tissue composition, suggest that diffusion coefficients may correlate with cartilage composition. Present method could therefore enable image-based assessment of cartilage composition by determination of diffusion coefficients within cartilage tissue.
与增强磁共振成像(MRI)和计算机断层扫描(CT)相比,阴离子对比剂的平衡分布预计将反映关节软骨的固定电荷密度(FCD)。扩散主要负责对比剂向软骨的运输。在骨关节炎中,软骨成分在疾病的早期阶段发生变化,溶质扩散最有可能受到影响。因此,研究对比剂的扩散可以为软骨成分成像提供新的方法。本研究的目的是确定四种对比剂(碘海醇、钆喷酸葡胺、碘化物、钆双胺)在牛关节软骨中的扩散系数。这些对比剂在分子大小和电荷上有所不同。在周围定量 CT 实验中,允许对比剂通过关节表面或深层软骨渗透到组织中。为了确定扩散系数,基于菲克定律的有限元模型拟合实验数据。每种对比剂通过关节表面的扩散速度都快于通过深层软骨的扩散速度(q<0.05)。由于原子大小,碘化物比其他三种对比剂(无论哪种运输方向)都能更快地扩散到软骨中(q<0.05)。所有临床用对比剂(碘海醇、钆喷酸葡胺和钆双胺)的扩散系数都相对较低(142.8-253.7 μm(2)/s)。在临床诊断中,这种缓慢的扩散可能无法达到平衡,这会影响标准方法测定 FCD。然而,通过关节表面和深层软骨的扩散差异,其特征是不同的组织成分,表明扩散系数可能与软骨成分相关。因此,目前的方法可以通过确定软骨组织内的扩散系数来实现基于图像的软骨成分评估。