Department of Mechanical and Aerospace Engineering, University of Florida, Gainesville, FL, USA.
Microvasc Res. 2012 Nov;84(3):306-13. doi: 10.1016/j.mvr.2012.09.001. Epub 2012 Sep 13.
The solid tumor is an abnormal environment that is resistant to systemically delivered drugs. Increased plasma leakiness and extracellular matrix density along with poor lymphatic function can result in interstitial flow that attenuates the effectiveness of therapeutics. This study expands upon a previously presented magnetic resonance (MR) imaging-based porous media model by investigating low permeability tumors, where interstitial flow may have increased effect on systemically delivered solutes. The solute transport of the porous media model is compared to that of experiment and the two-compartment model. Small non-necrotic tumors (n=3) were MR-imaged, serially, for 90 min after a bolus injection of Gd-based contrast agent (CA). These data provided for the calculation of experimental CA concentration over 90 min, while only early time points (15 min) were used to create vascular permeability, K(trans), maps for the porous media model. A K(trans) scale factor (range=1.3-2.5) in the porous media model was found to account for the reduction of permeability (measured by two-compartment model) due to interstitial flow. The optimized porous media simulations showed: 1) better dynamic CA behavior agreement with the experimental data than the two-compartment model (>33% reduction of RMS error); 2) similar spatial CA distribution trends across tumor with increased uptake at the tumor boundary.
实体瘤是一种对全身给药药物有抵抗力的异常环境。血浆通透性增加和细胞外基质密度增加以及淋巴功能不良会导致间质流,从而降低治疗药物的疗效。本研究通过研究低渗透性肿瘤,扩展了之前提出的基于磁共振(MR)成像的多孔介质模型,其中间质流可能对全身给药的溶质产生更大的影响。将多孔介质模型的溶质传输与实验和双室模型进行了比较。对 3 个小非坏死肿瘤(n=3)进行了 MR 成像,在注射 Gd 基造影剂(CA)后 90 分钟内进行了连续成像。这些数据可用于计算 90 分钟内的实验 CA 浓度,而仅使用早期时间点(15 分钟)来创建多孔介质模型的血管通透性 K(trans)图。在多孔介质模型中发现,K(trans)比例因子(范围为 1.3-2.5)可解释由于间质流导致的渗透性降低(通过双室模型测量)。优化后的多孔介质模拟显示:1)与双室模型相比,与实验数据的 CA 动态行为更吻合(RMS 误差降低了 33%以上);2)在肿瘤边界处摄取增加的情况下,肿瘤内的 CA 分布趋势相似。