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Generating a Fractal Microstructure of Laminin-111 to Signal to Cells
Published on: September 28, 2020
A model for transit time distributions through organs that accounts for fractal heterogeneity
1Department of Pharmacology, Martin Luther University Halle-Wittenberg, D-06097 Halle, Germany. michael.weiss@medizin.uni-halle.de
Abstract:
It has been shown that density functions of organ transit time distributions of vascular markers (washout curves) are characterized by a power-law tail, reflecting the fractal nature of the vascular network. Yet, thus far, no closed-form model is available that can be fitted to such organ outflow data. Here we propose a model that accounts for the existing data. The model is a continuous mixture of inverse Gaussian densities, implying flow heterogeneity in the organ. It has been fitted to outflow data from the rabbit heart and rat liver. The power-law decay with exponent -3 observed in the heart, corresponds to an intra-organ flow distribution with a relative dispersion of about 35%.
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