ArticleJournal of the Royal Society, Interface2026
How brain pulsations drive solute transport in the cranial subarachnoid space: insights from a toy model.
Article in Journal of the Royal Society, Interface, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- How brain pulsations drive solute transport in the cranial subarachnoid space: insights from a toy model.Journal of the Royal Society, Interface · 2026Article
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3 authors.
Funding
Abstract
Cerebrospinal fluid (CSF) circulates around and through the brain, supporting neural homeostasis by regulating the extracellular chemical environment. Yet, the physical mechanisms governing CSF-driven solute transport remain poorly understood, limiting the design of diagnostic and therapeutic strategies targeting brain clearance and drug delivery. Pulsatile CSF flow in the cranial subarachnoid space (cSAS) is driven by cardiac, respiratory and sleep-related vasomotion. Over longer timescales, weaker steady flows, such as inertial steady streaming, Stokes drift and production-drainage flow, may contribute to solute transport, but their role and relative importance remain unclear. Here, we develop a simplified two-dimensional model of CSF flow and solute transport in the cSAS using lubrication theory. Through multiple-timescale and asymptotic analyses, we derive a reduced long-time transport equation in which advection is governed by the Lagrangian mean velocity, incorporating steady streaming, production-drainage flow and Stokes drift. Analysing three physiologically relevant case studies, we show that steady flows can substantially reshape concentration profiles, enhance dispersion and alter clearance efficiency. Our results clarify the mechanisms underlying CSF-mediated transport, predict distinct regimes in humans and mice and highlight the importance of subject-specific physiological parameters when interpreting contrast-agent and intrathecal drug-delivery studies.
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