Department of Civil and Environmental Engineering, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Alfred Benesch & Company, Lincoln, Nebraska, USA.
Ann Biomed Eng. 2024 Jun;52(6):1693-1705. doi: 10.1007/s10439-024-03482-4. Epub 2024 Mar 19.
Convection-enhanced drug delivery (CED) directly infuses drugs with a large molecular weight toward target cells as a therapeutic strategy for neurodegenerative diseases and brain cancers. Despite the success of many previous in vitro experiments on CED, challenges still remain. In particular, a theoretical predictive model is needed to form a basis for treatment planning, and developing such a model requires well-controlled injection tests that can rigorously capture the convective (advective) and diffusive transport of an infusate. For this purpose, we investigated the advection-diffusion transport of an infusate (bromophenol blue solution) in the brain surrogate (0.2% w/w agarose gel) at different injection rates, ranging from 0.25 to 4 μL/min, by closely monitoring changes in the color intensity, propagation distance, and injection pressures. One dimensional closed-form solution was examined with two variable sets, such as the mathematically calculated coefficient of molecular diffusion and average velocity, and the hydraulic dispersion coefficient and seepage velocity by the least squared method. As a result, the seepage velocity was greater than the average velocity to some extent, particularly for the later infusion times. The poroelastic deformation in the brain surrogate might lead to changes in porosity, and consequently, slight increases in the actual flow velocity as infusion continues. The limitation of efficiency of the single catheter was analyzed by dimensionless analysis. Lastly, this study suggests a simple but robust approach that can properly capture the convective (advective) and diffusive transport of an infusate in an in vitro brain surrogate via well-controlled injection tests.
经颅超声促渗给药(CED)作为治疗神经退行性疾病和脑癌的一种策略,可将大分子量的药物直接递送至靶细胞。尽管CED 的许多先前的体外实验都取得了成功,但仍存在挑战。特别是,需要建立一个理论预测模型作为治疗计划的基础,而开发这样的模型需要经过严格控制的注射测试,以严格捕捉递注物的对流(平流)和扩散传输。为此,我们通过密切监测颜色强度、传播距离和注射压力的变化,研究了在不同注射速率(0.25 至 4 μL/min)下,脑替代物(0.2%w/w 琼脂糖凝胶)中递注物(溴酚蓝溶液)的对流-扩散传输。通过最小二乘法,我们用两个变量集检验了一维封闭解,如数学计算的分子扩散系数和平均速度、水力弥散系数和渗流速度。结果表明,在一定程度上,渗流速度大于平均速度,特别是在后期的注入时间。脑替代物中的多孔弹性变形可能导致孔隙率发生变化,进而导致随着注入的持续进行,实际流速略有增加。通过无量纲分析,研究还分析了单导管效率的局限性。最后,本研究提出了一种简单而稳健的方法,可以通过严格控制的注射测试,在体外脑替代物中适当捕捉递注物的对流(平流)和扩散传输。