Several biological processes, such as convective nutrient transport and convective drug delivery in biological tissues involves the transvascular and interstitial movement of biofluids. This work addresses transvascular and interstitial transport of nutrient inside a spherical tumor. Most of the biological tissues behave like deformable porous material and show mechanical behavior towards the fluid motion, due to the fact, that the forces like the drag, which is associated with fluid flow may compress the tissue material. On the macroscopic level, transport of solutes like nutrients, drug molecules, etc. within the tumor interstitial space is modeled. The hydrodynamic problem is treated with biphasic mixture theory under steady state and spherically symmetry situation. The transvascular transport of nutrient is modeled with the modified Sterling’s equation. The present model describes the overall nutrient distribution and predicts various criteria for the necrosis formation inside the tumor. Present study justifies that the parameters, which controls the nutrient supply to the tumor interstitial space through the blood vessel network inside the tumor, competes with reversible nutrient consumption kinetics of the tumor cells. This study also finds the role of some of those parameters on the deformation of cellular phase of the tumor as a consequence of interstitial fluid flow.
The present work addresses transvascular and interstitial fluid transport inside a solid tumor surrounded by normal tissue (close to an in vivo mimicking setup). In general, biological tissues behave like a soft porous material and show mechanical behavior towards the fluid motion through the interstitial space. In general, forces like viscous drag that are associated with the fluid flow may compress the tissue material. On the macroscopic level, we try to model the motion of fluids and macromolecules through the interstitial space of solid tumor and the normal tissue layer. The transvascular fluid transport is assumed to be governed by modified Starling's law. The poroelastohydrodynamics (interstitial hydrodynamics and the deformation of tissue material) inside the tumor and normal tissue regions is modeled using linearized biphasic mixture theory. Correspondingly, the velocity distribution of fluid is coupled to the displacement field of the solid phase (mainly cellular phase and extracellular matrix) in both the normal and tumor tissue regions. The corresponding velocity field is used within the transport reaction equation for fluids and macromolecules through interstitial space to get the overall solute (e.g., nutrients, drug, and other macromolecules) distribution. This study justifies that the presence of the normal tissue layer plays a significant role in delaying/assisting necrosis inside the tumor tissue. It is observed that the exchange process of fluids and macromolecules across the interface of the tumor and normal tissue affects the effectiveness factor corresponding to the tumor tissue.
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