在流体存在的情况下,磁性纳米颗粒在肿瘤球体中捕获的计算机模型。

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Barbara Wirthl, Christina Janko, Stefan Lyer, Bernhard A. Schrefler, Christoph Alexiou, Wolfgang A. Wall
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引用次数: 0

摘要

提高常规化疗药物疗效的主要挑战之一是,它们不能以足够高的剂量到达癌细胞,同时影响健康组织,并对癌症患者造成严重的副作用和痛苦。为了克服这一缺陷,磁性纳米颗粒作为转运系统已经成为一种有希望实现更特异性肿瘤靶向的方法。负载药物的磁性纳米颗粒可以通过施加外部磁场引导到目标组织。然而,施加在纳米颗粒上的磁力随着距离的增加而迅速下降,使得靶向肿瘤具有挑战性,在有流动血液或间质液的情况下更是如此。因此,我们提出了一个在测试装置中捕获磁性纳米颗粒的计算模型:我们的模型包括肿瘤周围的流动、引导纳米颗粒的磁力以及肿瘤内的运输。我们展示了磁性纳米颗粒在外磁场中运输的模型如何与基于多孔介质理论的多相肿瘤模型相结合。我们的方法基于潜在的物理机制,可以为无法在实验研究中得出结论的机制提供重要的见解。这样的计算模型能够对纳米颗粒设计空间进行有效和系统的探索,首先是在受控的测试设置中,然后是在更复杂的体内场景中。作为一种有效的工具,它可以最大限度地减少昂贵的试错设计方法,加速转化为临床实践,以改善治疗效果并限制癌症患者的不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An in silico model of the capturing of magnetic nanoparticles in tumour spheroids in the presence of flow

An in silico model of the capturing of magnetic nanoparticles in tumour spheroids in the presence of flow

One of the main challenges in improving the efficacy of conventional chemotherapeutic drugs is that they do not reach the cancer cells at sufficiently high doses while at the same time affecting healthy tissue and causing significant side effects and suffering in cancer patients. To overcome this deficiency, magnetic nanoparticles as transporter systems have emerged as a promising approach to achieve more specific tumour targeting. Drug-loaded magnetic nanoparticles can be directed to the target tissue by applying an external magnetic field. However, the magnetic forces exerted on the nanoparticles fall off rapidly with distance, making the tumour targeting challenging, even more so in the presence of flowing blood or interstitial fluid. We therefore present a computational model of the capturing of magnetic nanoparticles in a test setup: our model includes the flow around the tumour, the magnetic forces that guide the nanoparticles, and the transport within the tumour. We show how a model for the transport of magnetic nanoparticles in an external magnetic field can be integrated with a multiphase tumour model based on the theory of porous media. Our approach based on the underlying physical mechanisms can provide crucial insights into mechanisms that cannot be studied conclusively in experimental research alone. Such a computational model enables an efficient and systematic exploration of the nanoparticle design space, first in a controlled test setup and then in more complex in vivo scenarios. As an effective tool for minimising costly trial-and-error design methods, it expedites translation into clinical practice to improve therapeutic outcomes and limit adverse effects for cancer patients.

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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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