Computational Assessment of Unsteady Flow Effects on Magnetic Nanoparticle Targeting Efficiency in a Magnetic Stented Carotid Bifurcation Artery.

IF 1.6 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Engineering and Technology Pub Date : 2023-10-01 Epub Date: 2023-09-18 DOI:10.1007/s13239-023-00681-3
Rodward L Hewlin, Michael Smith, John P Kizito
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The drug delivery scheme presented in this paper functions via placement of a faintly magnetizable stent at a diseased location in the carotid artery, followed by delivery of magnetically susceptible drug carriers guided by the local magnetic field. Using this method, the magnetic stent can apply high localized magnetic field gradients within the diseased artery, while only exposing the neighboring tissues, arteries, and organs to a modest magnetic field. The localized field gradients also produce the forces needed to attract and hold drug-containing magnetic nanoparticles at the implant site for delivering therapeutic agents to treat in-stent restenosis.</p><p><strong>Methods: </strong>The multi-physics computational model used in this work is from our previous work and has been slightly modified for the case scenario presented in this paper. The computational model is used to analyze pulsatile blood flow, particle motion, and particle capture efficiency in a magnetic stented region using the magnetic properties of magnetite (Fe<sub>3</sub>O<sub>4</sub>) and equations describing the magnetic forces acting on particles produced by an external cylindrical electromagnetic coil. The electromagnetic coil produces a uniform magnetic field in the computational arterial flow model domain, while both the particles and the implanted stent are paramagnetic. A Eulerian-Lagrangian technique is adopted to resolve the hemodynamic flow and the motion of particles under the influence of a range of magnetic field strengths (B<sub>r</sub> = 2T, 4T, 6T, and 8T). Particle diameter sizes of 10 nm-4 µm in diameter were evaluated. 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引用次数: 1

Abstract

Purpose: Worldwide, cardiovascular disease is the leading cause of hospitalization and death. Recently, the use of magnetizable nanoparticles for medical drug delivery has received much attention for potential treatment of both cancer and cardiovascular disease. However, proper understanding of the interacting magnetic field forces and the hydrodynamics of blood flow is needed for effective implementation. This paper presents the computational results of simulated implant assisted medical drug targeting (IA-MDT) via induced magnetism intended for administering patient specific doses of therapeutic agents to specific sites in the cardiovascular system. The drug delivery scheme presented in this paper functions via placement of a faintly magnetizable stent at a diseased location in the carotid artery, followed by delivery of magnetically susceptible drug carriers guided by the local magnetic field. Using this method, the magnetic stent can apply high localized magnetic field gradients within the diseased artery, while only exposing the neighboring tissues, arteries, and organs to a modest magnetic field. The localized field gradients also produce the forces needed to attract and hold drug-containing magnetic nanoparticles at the implant site for delivering therapeutic agents to treat in-stent restenosis.

Methods: The multi-physics computational model used in this work is from our previous work and has been slightly modified for the case scenario presented in this paper. The computational model is used to analyze pulsatile blood flow, particle motion, and particle capture efficiency in a magnetic stented region using the magnetic properties of magnetite (Fe3O4) and equations describing the magnetic forces acting on particles produced by an external cylindrical electromagnetic coil. The electromagnetic coil produces a uniform magnetic field in the computational arterial flow model domain, while both the particles and the implanted stent are paramagnetic. A Eulerian-Lagrangian technique is adopted to resolve the hemodynamic flow and the motion of particles under the influence of a range of magnetic field strengths (Br = 2T, 4T, 6T, and 8T). Particle diameter sizes of 10 nm-4 µm in diameter were evaluated. Two dimensionless numbers were evaluated in this work to characterize relative effects of Brownian motion (BM), magnetic force induced particle motion, and convective blood flow on particle motion.

Results: The computational simulations demonstrate that the greatest particle capture efficiency results for particle diameters within the micron range of 0.7-4 µm, specifically in regions where flow separation and vortices are at a minimum. Similar to our previous work (which did not involve the use of a magnetic stent), it was also observed that the capture efficiency of particles decreases substantially with particle diameter, especially in the superparamagnetic regime. Contrary to our previous work, using a magnetic stent tripled the capture efficiency of superparamagnetic particles. The highest capture efficiency observed for superparamagnetic particles was 78% with an 8 T magnetic field strength and 65% with a 2 T magnetic field strength when analyzing 100 nm particles. For 10 nm particles and an 8 T magnetic field strength, the particle capture efficiency was 55% and for a 2 T magnetic field strength the particle capture efficiency was observed to be 43%. Furthermore, it was found that larger magnetic field strengths, large particle diameter sizes (1 µm and above), and slower blood flow velocity improves the particle capture efficiency. The distribution of captured particles on the vessel wall along the axial and azimuthal directions is also discussed. Results for captured particles on the vessel wall along the axial flow direction showed that the particle density decreased along the axial direction, especially after the stented region. For the entrance section of the stented region, the captured particle density distribution along the axial direction is large, corresponding to the center-symmetrical distribution of the magnetic force in that section.

Conclusion: The simulation results presented in this work have shown to yield favorable capture efficiencies for micron range particles and superparamagnetic particles using magnetized implants such as the stent discussed in this work. The results presented in this work justify further investigation of MDT as a treatment technique for cardiovascular disease.

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磁支架颈动脉分叉中非恒定流对磁性纳米粒子靶向效率影响的计算评估。
目的:在世界范围内,心血管疾病是导致住院和死亡的主要原因。近年来,可磁化纳米颗粒用于药物递送在潜在的癌症和心血管疾病治疗方面受到了广泛关注。然而,为了有效地实施,需要正确理解相互作用的磁场力和血流的流体动力学。本文介绍了通过诱导磁性模拟植入辅助医疗药物靶向(IA-MDT)的计算结果,旨在向心血管系统中的特定部位给予患者特定剂量的治疗剂。本文提出的药物递送方案的作用是在颈动脉病变部位放置一个弱磁化支架,然后在局部磁场的引导下递送磁敏感药物载体。使用这种方法,磁性支架可以在患病动脉内施加高的局部磁场梯度,同时仅将邻近的组织、动脉和器官暴露在适度的磁场中。局部场梯度还产生将含药物的磁性纳米颗粒吸引并保持在植入部位所需的力,用于递送治疗剂以治疗支架内再狭窄。方法:本工作中使用的多物理计算模型来自我们之前的工作,并针对本文提出的情况进行了轻微修改。该计算模型用于利用磁铁矿(Fe3O4)的磁性和描述由外部圆柱形电磁线圈产生的作用在颗粒上的磁力的方程来分析磁支架区域中的脉动血流、颗粒运动和颗粒捕获效率。电磁线圈在计算动脉流模型域中产生均匀的磁场,而粒子和植入的支架都是顺磁性的。采用欧拉-拉格朗日技术来求解在一系列磁场强度(Br = 2T、4T、6T和8T)。评估了直径为10 nm-4µm的颗粒直径大小。在这项工作中,评估了两个无量纲数,以表征布朗运动(BM)、磁力诱导的粒子运动和对流血流对粒子运动的相对影响。结果:计算模拟表明,颗粒直径在0.7-4µm微米范围内,特别是在流分离和涡流最小的区域,颗粒捕获效率最高。与我们之前的工作(不涉及磁性支架的使用)类似,还观察到颗粒的捕获效率随着颗粒直径的增加而显著降低,尤其是在超顺磁性状态下。与我们之前的工作相反,使用磁性支架将超顺磁性颗粒的捕获效率提高了两倍。当分析100nm颗粒时,在8T磁场强度下观察到的超顺磁性颗粒的最高捕获效率为78%,在2T磁场强度下为65%。对于10nm颗粒和8T磁场强度,颗粒捕获效率为55%,而对于2T磁场强度,观察到颗粒捕获效率是43%。此外,研究发现,较大的磁场强度、较大的粒径(1µm及以上)和较慢的血流速度可以提高颗粒捕获效率。还讨论了捕获颗粒在血管壁上沿轴向和方位角方向的分布。沿轴向流动方向在血管壁上捕获的颗粒的结果表明,颗粒密度沿轴向方向降低,尤其是在支架区域之后。对于支架区域的入口截面,沿轴向捕获的颗粒密度分布较大,对应于该截面中磁力的中心对称分布。结论:本工作中的模拟结果表明,使用磁化植入物(如本工作中讨论的支架)对微米级颗粒和超顺磁性颗粒产生了良好的捕获效率。这项工作中的结果证明了MDT作为心血管疾病治疗技术的进一步研究是合理的。
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来源期刊
Cardiovascular Engineering and Technology
Cardiovascular Engineering and Technology Engineering-Biomedical Engineering
CiteScore
4.00
自引率
0.00%
发文量
51
期刊介绍: Cardiovascular Engineering and Technology is a journal publishing the spectrum of basic to translational research in all aspects of cardiovascular physiology and medical treatment. It is the forum for academic and industrial investigators to disseminate research that utilizes engineering principles and methods to advance fundamental knowledge and technological solutions related to the cardiovascular system. Manuscripts spanning from subcellular to systems level topics are invited, including but not limited to implantable medical devices, hemodynamics and tissue biomechanics, functional imaging, surgical devices, electrophysiology, tissue engineering and regenerative medicine, diagnostic instruments, transport and delivery of biologics, and sensors. In addition to manuscripts describing the original publication of research, manuscripts reviewing developments in these topics or their state-of-art are also invited.
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