Department of Hydromechanics and Modeling of Hydrosystems, Institute for Modelling Hydraulic and Environmental Systems, University of Stuttgart, Stuttgart, Germany.
PLoS One. 2012;7(3):e31966. doi: 10.1371/journal.pone.0031966. Epub 2012 Mar 12.
We propose a computational simulation framework for describing cancer-therapeutic transport in the lung. A discrete vascular graph model (VGM) is coupled to a double-continuum model (DCM) to determine the amount of administered therapeutic agent that will reach the cancer cells. An alveolar cell carcinoma is considered. The processes in the bigger blood vessels (arteries, arterioles, venules and veins) are described by the VGM. The processes in the alveolar capillaries and the surrounding tissue are represented by a continuum approach for porous media. The system of equations of the coupled discrete/continuum model contains terms that account for degradation processes of the therapeutic agent, the reduction of the number of drug molecules by the lymphatic system and the interaction of the drug with the tissue cells. The functionality of the coupled discrete/continuum model is demonstrated in example simulations using simplified pulmonary vascular networks, which are designed to show-off the capabilities of the model rather than being physiologically accurate.
我们提出了一个用于描述肺部癌症治疗输送的计算模拟框架。一个离散的血管图模型(VGM)与双连续体模型(DCM)耦合,以确定到达癌细胞的治疗药物的量。考虑了肺泡细胞癌。较大血管(动脉、小动脉、小静脉和静脉)中的过程由 VGM 描述。肺泡毛细血管和周围组织中的过程通过多孔介质的连续体方法表示。耦合离散/连续模型的方程组包含用于治疗药物降解过程、通过淋巴系统减少药物分子数量以及药物与组织细胞相互作用的术语。使用简化的肺血管网络进行的示例模拟演示了耦合离散/连续模型的功能,这些模拟旨在展示模型的功能,而不是生理上的准确性。