Investigation of Inlet Conditions in The Mixing Process of Nanoparticles and Blood in a T-Shaped Microfluidic Reactor with Small Rectangular Cavities

Yale J Biol Med. 2023 Mar 31;96(1):43-55. doi: 10.59249/FUAH2942. eCollection 2023 Mar.

Abstract

During the metastasis of cancer cells, circulating tumor cells (CTCs) are released from the primary tumor, reach the bloodstream, and colonize new organs. A potential reduction of metastasis may be accomplished through the use of nanoparticles in micromixers in order to capture the CTCs that circulates in blood. In the present study, the effective mixing of nanoparticles and the blood that carries the CTCs are investigated. The mixing procedure was studied under various inlet velocity ratios and several T-shaped micromixer geometries with rectangular cavities by using computational fluid dynamics techniques. The Navier-Stokes equations were solved for the blood flow; the discrete motion of particles is evaluated by a Lagrangian method while the diffusion of blood substances is studied by using a scalar transport equation. Results showed that as the velocity ratio between the inlet streams increases, the mixing rate of nanoparticles with the blood flow is increased. Moreover, nanoparticles are uniformly distributed across the mixing channel while their concentration is decreased along the channel. Furthermore, the evolution in time of the blood substances in the mixing channel increases with the increase of the velocity ratio between the two streams. On the other hand, the concentration of both the blood substances and the nanoparticles is decreased in the mixing channel as the velocity ratio increases. Finally, the differences in the dimensions of the rectangular cavities seems to have an insignificant effect both in the evolution in time of the blood substances and the concentration of nanoparticles in the mixing channel.

Keywords: CTCs; Computational Fluid; Discrete Element Method; Dynamics; Microfluidics; Mixing reactor; Nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bays
  • Humans
  • Microfluidics* / methods
  • Nanoparticles*