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Focal delivery during direct infusion to brain: Role of flow rate, catheter diameter, and tissue mechanics

  • Paul F. Morrison
  • , Michael Y. Chen
  • , Richard S. Chadwick
  • , Russell R. Lonser
  • , Edward H. Oldfield

Research output: Contribution to journalArticlepeer-review

Abstract

Direct interstitial infusion is a technique capable of delivering agents over both small and large dimensions of brain tissue. However, at a sufficiently high volumetric inflow rate, backflow along the catheter shaft may occur and compromise delivery. A scaling relationship for the finite backflow distance along this catheter in pure gray matter (χ(m)) has been determined from a mathematical model based on Stokes flow, Darcy flow in porous media, and elastic deformation of the brain tissue: χ(m) = constant Q(o)3R4r(c)4G-3μ-1 (Q(o) = volumetric inflow rate, R = tissue hydraulic resistance, r(c) = catheter radius, G = shear modulus, and μ = viscosity). This implies that backflow is minimized by the use of small diameter catheters and that a fixed (minimal) backflow distance may be maintained by offsetting an increase in flow rate with a similar decrease in catheter radius. Generally, backflow is avoided in rat gray matter with a 32- gauge catheter operating below 0.5 μl/min. An extension of the scaling relationship to include brain size in the resistance term leads to the finding that absolute backflow distance obtained with a given catheter and inflow rate is weakly affected by the depth of catheter tip placement and, thus, brain size. Finally, an extension of the model to describe catheter passage through a white matter layer before terminating in the gray has been shown to account for observed percentages of albumin in the corpus callosum after a 4-μl infusion of the compound to rat striatum over a range of volumetric inflow rates.

Original languageEnglish
Pages (from-to)R1218-R1229
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume277
Issue number4 46-4
DOIs
StatePublished - Oct 1999

Keywords

  • Intracerebral drug delivery
  • Mathematical model

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