From Geometry to Flow Allocation: A Physics-Based Framework for Interpretable Microvascular Hemodynamics.

IF 4.4 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Alexander Fiedler, Marius Drysch, Sonja Verena Schmidt, Pia Weskamp, Felix Reinkemeier, Flemming Puscz, Alexander Sogorski, Marcus Lehnhardt, Christoph Wallner
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引用次数: 0

Abstract

Anastomotic angle and flow allocation change together in end-to-side junctions, complicating interpretation of angle-dependent wall shear. We used MITOS Flow Lab, a two-dimensional D2Q9 two-relaxation-time lattice-Boltzmann environment, to examine this coupling in steady, rigid-walled, Newtonian models at Re ≈ 91. Angles of 30-120° were compared under equal outlet pressures and at approximately matched branch-flow fractions of 0.25 and 0.21, achieved with angle-specific static outlet-pressure offsets. Under equal outlet pressures, the branch-flow fraction decreased from 0.356 to 0.151 across this angle range, while the minimum normalized signed recipient-floor shear increased from 0.140 to 0.450. Matching flow allocation substantially reduced angle-associated variation in this endpoint and in the sub-toe response, whereas sub-heel and sub-ostial responses remained angle dependent under the adjusted boundary conditions. This qualitative contrast persisted when the lumen resolution was increased from 32 to 64 nodes for the 0.25 target, although minimum-shear attenuation changed from approximately 83% to 74%. The 0.21 target was examined only on the production grid. These experiments demonstrate that the interpretation of angle-associated shear depends on the flow-allocation condition used for comparison. They do not identify a boundary-independent geometric effect or a causal mediation fraction. Absolute values and attenuation magnitudes remain sensitive to discretization and have not been independently validated. These controlled comparisons provide a framework for interpreting angle-associated shear together with achieved flow allocation and the specified outlet conditions.

从几何到血流分配:一个基于物理的可解释微血管血流动力学框架。
吻合角和流动分配在端侧连接处一起改变,使角度依赖性壁剪切的解释复杂化。我们使用MITOS Flow Lab,一个二维D2Q9双弛豫时间晶格-玻尔兹曼环境,在Re≈91的稳定、刚性壁、牛顿模型中检验了这种耦合。在相同的出口压力和0.25和0.21的分支流动分数近似匹配的情况下,通过特定角度的静态出口压力偏移来比较30-120°的角度。在出口压力相等的情况下,分支流动分数从0.356下降到0.151,而最小归一化签名接收层剪切从0.140增加到0.450。匹配的流动分配大大减少了该端点和趾下响应的角度相关变化,而在调整后的边界条件下,足跟下和口下响应仍然依赖于角度。当流腔分辨率从32个节点增加到64个节点时,这种定性对比仍然存在,尽管最小剪切衰减从大约83%变化到74%。0.21目标仅在生产网格上进行了检查。这些实验表明,角相关剪切的解释取决于用于比较的流量分配条件。他们没有确定一个边界无关的几何效应或因果中介分数。绝对值和衰减幅度仍然对离散化很敏感,尚未独立验证。这些可控的比较提供了一个框架来解释与角度相关的剪切,以及实现的流量分配和指定的出口条件。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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