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The Blood-brain Barrier00:49

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Correction: Kang et al. Fluid Flow to Electricity: Capturing Flow-Induced Vibrations with Micro-Electromechanical-System-Based Piezoelectric Energy Harvester. <i>Micromachines</i> 2024, <i>15</i>, 581.

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In Vitro Blood-Brain Barrier-Integrated Neurological Disorder Models Using a Microfluidic Device.

Jin-Ha Choi1, Mallesh Santhosh2, Jeong-Woo Choi1,2

  • 1Department of Chemical and Biomolecular Engineering, Sogang University, 35 Baekbeom-ro (Sinsu-dong), Mapo-gu, 121-742 Seoul, Korea.

Micromachines
|December 28, 2019
PubMed
Summary
This summary is machine-generated.

Researchers developed advanced in vitro blood-brain barrier (BBB) models using microfluidic and organ-on-a-chip systems. These models aid neurological disorder research and personalized therapy development.

Keywords:
blood–brain barrier (BBB)in vitro modelmicrofluidic deviceneuroinflammationneurological disorders

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Area of Science:

  • Neuroscience
  • Biomedical Engineering
  • Pharmacology

Background:

  • The blood-brain barrier (BBB) is crucial for central nervous system (CNS) protection against harmful substances.
  • Neurological disorders necessitate realistic in vitro models for effective research and treatment development.
  • Existing models often lack the dynamic physiological conditions of the in vivo BBB.

Purpose of the Study:

  • To introduce advanced in vitro blood-brain barrier (BBB) models for neurological disorder research.
  • To leverage microfluidic and organ-on-a-chip technologies for enhanced BBB modeling.
  • To establish a platform for improved drug screening and personalized neurological therapies.

Main Methods:

  • Development of a microfluidic system to mimic BBB fluidic flow and shear stress.
  • Integration of human organ-on-a-chip technology for a more realistic BBB model.
  • Utilizing these systems to simulate physiological conditions relevant to neurological disorders.

Main Results:

  • The developed models effectively replicate key aspects of the in vivo BBB, including shear stress and nutrient supply.
  • These advanced models offer a more accurate representation of the BBB compared to traditional methods.
  • The systems facilitate the study of drug interactions and transport across the BBB.

Conclusions:

  • Microfluidic and organ-on-a-chip BBB models represent a significant advancement in neurological disorder research.
  • These models provide a powerful platform for drug screening and the development of personalized therapeutic strategies.
  • This technology holds promise for accelerating the translation of research findings into clinical applications for neurological diseases.