Key result
An algorithmic approach using a 3D-1D coupled blood flow and oxygen transport model generated surrogate microvascular networks with similar stochastic properties to original networks.
Why the study?
Reconstructing fine-scale microvascular network components causes significant segmentation errors and is time- and cost-intensive, creating a need for fast and reliable reconstruction algorithms generating surrogate networks.
This computational model provides a fast and reliable method to generate surrogate microvascular networks that mimic the morphological and physiological properties of real networks.
May aid surrogate microvascular modeling in simulations; leaves open empirical validation before clinical use.
In this work, we introduce an algorithmic approach to generate microvascular networks starting from larger vessels that can be reconstructed without noticeable segmentation errors. Contrary to larger vessels, the reconstruction of fine‐scale components of microvascular networks shows significant segmentation errors, and an accurate mapping is time and cost intense. Thus there is a need for fast and reliable reconstruction algorithms yielding surrogate networks having similar stochastic properties as the original ones. The microvascular networks are constructed in a marching way by adding vessels to the outlets of the vascular tree from the previous step. To optimise the structure of the vascular trees, we use Murray's law to determine the radii of the vessels and bifurcation angles. In each step, we compute the local gradient of the partial pressure of oxygen and adapt the orientation of the new vessels to this gradient. At the same time, we use the partial pressure of oxygen to check whether the considered tissue block is supplied sufficiently with oxygen. Computing the partial pressure of oxygen, we use a 3D‐1D coupled model for blood flow and oxygen transport. To decrease the complexity of a fully coupled 3D model, we reduce the blood vessel network to a 1D graph structure and use a bi‐directional coupling with the tissue which is described by a 3D homogeneous porous medium. The resulting surrogate networks are analysed with respect to morphological and physiological aspects.
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Köppl et al. (2020) studied this question. 3D-1D coupled blood flow and oxygen transport model was evaluated on Generation of surrogate microvascular networks. An algorithmic approach using a 3D-1D coupled blood flow and oxygen transport model generated surrogate microvascular networks with similar stochastic properties to original networks.
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