Early-Stage Disease Detection via Intravascular Nanomachines: Modeling and Analysis

IF 2.5 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Abdollah Rezagholi;Sergi Abadal;Filip Lemic;Eduard Alarcón;Ethungshan Shitiri
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引用次数: 0

Abstract

Early-stage disease detection remains challenging due to the low abundance of circulating biomarkers during the initial stages of disease. Among emerging technologies, intra-body nanoscale communication offers an innovative solution to identify molecular cues within the human bloodstream. This study investigates a minimally invasive approach for early-stage disease detection using nanomachines introduced into the bloodstream. To assess the feasibility of this approach, computational simulations are used to emulate the vascular environment and evaluate biomarker detection performance under different physiological conditions. Current modeling approaches often fail to capture essential vascular characteristics, including non-uniform flow structures, size-dependent particle mobility, and particle margination driven by red blood cell interactions. To address these limitations, our study incorporates these factors into the simulation framework and quantifies their individual and combined effects on biomarker detection probability. Baseline detection performance is first obtained under uniform flow assumptions, after which introducing selected vascular transport mechanisms progressively reduces detection probability for all vessel types and nanomachine sizes. Among the considered vessels, capillary-scale vessels provide the most favorable local encounter conditions across all nanomachine sizes. These findings highlight the need to include vessel-dependent transport effects when evaluating nanomachine-enabled biomarker detection in microvascular environments.
通过血管内纳米机器进行早期疾病检测:建模和分析
由于在疾病的初始阶段循环生物标志物的丰度较低,早期疾病检测仍然具有挑战性。在新兴技术中,体内纳米级通信为识别人体血液中的分子线索提供了一种创新的解决方案。本研究探讨了一种微创方法,用于早期疾病的检测,将纳米机器引入血液。为了评估该方法的可行性,我们使用计算模拟来模拟血管环境,并评估不同生理条件下生物标志物的检测性能。目前的建模方法往往不能捕捉基本的血管特征,包括不均匀的流动结构,大小依赖的颗粒迁移率,以及由红细胞相互作用驱动的颗粒边缘。为了解决这些限制,我们的研究将这些因素纳入模拟框架,并量化它们对生物标志物检测概率的单个和组合影响。首先在均匀流动假设下获得基线检测性能,然后引入选定的血管运输机制,逐步降低所有血管类型和纳米机器尺寸的检测概率。在考虑的血管中,毛细血管在所有纳米机器尺寸中提供了最有利的局部相遇条件。这些发现强调了在评估微血管环境中纳米机器支持的生物标志物检测时,需要包括血管依赖的运输效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.90
自引率
13.60%
发文量
23
期刊介绍: As a result of recent advances in MEMS/NEMS and systems biology, as well as the emergence of synthetic bacteria and lab/process-on-a-chip techniques, it is now possible to design chemical “circuits”, custom organisms, micro/nanoscale swarms of devices, and a host of other new systems. This success opens up a new frontier for interdisciplinary communications techniques using chemistry, biology, and other principles that have not been considered in the communications literature. The IEEE Transactions on Molecular, Biological, and Multi-Scale Communications (T-MBMSC) is devoted to the principles, design, and analysis of communication systems that use physics beyond classical electromagnetism. This includes molecular, quantum, and other physical, chemical and biological techniques; as well as new communication techniques at small scales or across multiple scales (e.g., nano to micro to macro; note that strictly nanoscale systems, 1-100 nm, are outside the scope of this journal). Original research articles on one or more of the following topics are within scope: mathematical modeling, information/communication and network theoretic analysis, standardization and industrial applications, and analytical or experimental studies on communication processes or networks in biology. Contributions on related topics may also be considered for publication. Contributions from researchers outside the IEEE’s typical audience are encouraged.
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