Simulation and Analysis of Solute Transport in Multi-Lymphangion Lymphatic Vessels
Abstract
The lymphatic system (LS), a body-wide network of vessels and lymphoid organs governing fluid homeostasis and immune surveillance, has so far not been investigated as a domain for diagnostic and therapeutic molecular communications (MC) applications, despite several properties that make it a promising, complementary alternative to the cardiovascular system. These favorable properties include slower flow, simpler and less dense molecular fluid composition, and direct anatomical access to lymph nodes. Realizing this potential, however, requires a quantitative understanding of how solutes propagate through the LS, a problem that, unlike lymph flow itself, remains largely unaddressed in the literature. As a first step towards narrowing this gap, we develop a particle-based simulation (PBS) framework of solute transport through a three-dimensional chain of valve-separated, concatenated vessel segments, called lymphangions. We simulate the spatiotemporal evolution of solute concentration and qualitatively validate the resulting transport dynamics against existing in vivo measurements of fluorescent tracer propagation in multi-lymphangion lymphatic vessels. Our simulations show that the valve-gated nature of solute transport in lymphatic vessels leads to bursty solute concentrations over time, a characteristic that can also be observed in vivo. Additionally, we find that, within one pumping period, peak timing is dictated by the valves' synchronizing effect rather than the particle release time, while diffusivity and receiver placement determine peak sharpness. Overall, the proposed PBS framework provides a first quantitative basis for solute transport modeling in the LS and several concrete application scenarios for MC in this underexplored domain. Supplementary video material illustrating the PBS is publicly available on Zenodo [DOI: 10.5281/zenodo.21888066].
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BibTeX
@misc{jakumeit2026simulation,
title = {{Simulation and Analysis of Solute Transport in Multi-Lymphangion Lymphatic Vessels}},
author = {Timo Jakumeit and Thiha Aung and Robert Schober and Maximilian Schäfer},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2609.25964},
eprint = {2609.25964},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2609.25964},
}
RIS
TY - UNPB
TI - Simulation and Analysis of Solute Transport in Multi-Lymphangion Lymphatic Vessels
AU - Timo Jakumeit
AU - Thiha Aung
AU - Robert Schober
AU - Maximilian Schäfer
PY - 2026
DA - 2026/09/22
PB - arXiv
DO - 10.48550/arxiv.2609.25964
UR - https://arxiv.org/abs/2609.25964
AB - The lymphatic system (LS), a body-wide network of vessels and lymphoid organs governing fluid homeostasis and immune surveillance, has so far not been investigated as a domain for diagnostic and therapeutic molecular communications (MC) applications, despite several properties that make it a promising, complementary alternative to the cardiovascular system. These favorable properties include slower flow, simpler and less dense molecular fluid composition, and direct anatomical access to lymph nodes. Realizing this potential, however, requires a quantitative understanding of how solutes propagate through the LS, a problem that, unlike lymph flow itself, remains largely unaddressed in the literature. As a first step towards narrowing this gap, we develop a particle-based simulation (PBS) framework of solute transport through a three-dimensional chain of valve-separated, concatenated vessel segments, called lymphangions. We simulate the spatiotemporal evolution of solute concentration and qualitatively validate the resulting transport dynamics against existing in vivo measurements of fluorescent tracer propagation in multi-lymphangion lymphatic vessels. Our simulations show that the valve-gated nature of solute transport in lymphatic vessels leads to bursty solute concentrations over time, a characteristic that can also be observed in vivo. Additionally, we find that, within one pumping period, peak timing is dictated by the valves' synchronizing effect rather than the particle release time, while diffusivity and receiver placement determine peak sharpness. Overall, the proposed PBS framework provides a first quantitative basis for solute transport modeling in the LS and several concrete application scenarios for MC in this underexplored domain. Supplementary video material illustrating the PBS is publicly available on Zenodo [DOI: 10.5281/zenodo.21888066].
ER -