Single Input Multi Output Model of Molecular Communication via Diffusion With Spheroidal Receivers

IF 2.3 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Ibrahim Isik;Mitra Rezaei;Adam Noel
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引用次数: 0

Abstract

Spheroids are aggregates of cells that can mimic the cellular organization often found in tissues. Spheroids can be created from various cell types, including cancer cells, stem cells, and primary cells, and they serve as valuable tools in biological research. Although there are initial results on how a molecular signal can propagate between a pair of spheroids, practical experiments typically use clusters of spheroids and there isn’t a good understanding of how neighboring spheroids impact the spatiotemporal dynamics of local molecule propagation. This paper simulates a series of scenarios to gain intuition about propagation in such multi-spheroid systems for applications such as transport and drug delivery. The spheroids are modeled as porous media with a corresponding effective diffusion coefficient. System variations are considered with a higher spheroid porosity (i.e., with a higher effective diffusion coefficient) and molecule uptake by the spheroid cells (approximated as a first-order degradation reaction while molecules diffuse within the spheroid). Results show that a local crowd of spheroids will eventually slow overall propagation, such that molecules stay in the vicinity of the transmitter for longer. The results demonstrate that a single-spheroid receiver model is insufficient to accurately model propagation under these conditions.
球面接收器扩散分子通信的单输入多输出模型
球状体是细胞的聚集体,可以模仿组织中经常发现的细胞组织。球体可以从各种细胞类型中产生,包括癌细胞、干细胞和原代细胞,它们在生物学研究中是有价值的工具。虽然对分子信号如何在一对球体之间传播有初步的结果,但实际实验通常使用球体簇,并且对相邻球体如何影响局部分子传播的时空动力学还没有很好的理解。本文模拟了一系列场景,以直观地了解这种多球体系统在运输和药物输送等应用中的传播。球体被模拟为具有相应有效扩散系数的多孔介质。系统变化被认为具有更高的球体孔隙率(即具有更高的有效扩散系数)和球体细胞的分子摄取(近似为分子在球体内扩散时的一级降解反应)。结果表明,局部的球状体群最终会减慢整体传播速度,这样分子在发射器附近停留的时间就更长了。结果表明,单球面接收器模型不足以准确地模拟这些条件下的传播。
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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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