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Microfluidic design for in-vitro liver zonation-a numerical analysis using COMSOL Multiphysics.

Reza Mahdavi1, Sameereh Hashemi-Najafabadi2, Mohammad Adel Ghiass3

  • 1Biotechnology Department, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, P.O. Box 14115-114, Iran.

Medical & Biological Engineering & Computing
|September 21, 2023
PubMed
Summary

This study introduces a novel microfluidic chip design to replicate liver zonation in vitro. The optimized chip ensures proper oxygen and glucose distribution for accurate disease modeling and drug toxicity research.

Keywords:
COMSOLLiver zonationMicrofluidicsNumerical simulationOrgan-on-a-chip

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Area of Science:

  • Biomedical Engineering
  • Cell Biology
  • Organ-on-a-Chip Technology

Background:

  • Current in vitro models lack accuracy for liver disease and toxicity studies.
  • Liver zonation, a key physiological feature, is challenging to replicate in vitro.
  • Organ-on-a-chip technology offers controlled environments for cell culture.

Purpose of the Study:

  • To propose and validate a microfluidic device for creating oxygen gradients to mimic liver zonation.
  • To identify optimal parameters for cell density and flow rate for physiological relevance.
  • To provide a tool for advanced in vitro liver studies and other gas-gradient-dependent cell research.

Main Methods:

  • Development of a microfluidic chip with an integrated gas channel for oxygen gradient generation.
  • Numerical simulation using COMSOL Multiphysics, incorporating cell-specific oxygen and glucose consumption rates.
  • Analysis of various flow rates and cell densities to determine optimal distribution.

Main Results:

  • Identification of optimal cell density and flow rate for uniform oxygen and glucose distribution.
  • Demonstration of achieving physiologically relevant oxygen and glucose concentrations within 24 hours and 30 minutes, respectively.
  • Validation of the microfluidic design's capability to establish controlled oxygen gradients.

Conclusions:

  • The proposed microfluidic design effectively recreates liver zonation in vitro.
  • This technology serves as a valuable tool for liver disease modeling, drug toxicity testing, and hypoxia studies.
  • The adaptable design is applicable to various cell studies requiring controlled gas concentration gradients.