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Related Concept Videos

iChip01:24

iChip

The cultivation of environmental microorganisms has long been hindered by the inability to replicate complex native conditions in vitro. The isolation chip (iChip) addresses this limitation by facilitating the growth of previously uncultivable microorganisms through in situ incubation. Designed for high-throughput microbial cultivation, the iChip comprises hundreds of microchambers, each capable of housing a single microbial cell. These microchambers are loaded with a mixture of molten agar and...

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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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Updated: Jun 12, 2026

Combining Human Organoids and Organ-on-a-Chip Technology to Model Intestinal Region-Specific Functionality
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Intestinal Cells-on-Chip for Permeability Studies.

Marit Keuper-Navis1, Hossein Eslami Amirabadi2,3, Joanne Donkers1

  • 1Department of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), 2333 BE Leiden, The Netherlands.

Micromachines
|January 8, 2025
PubMed
Summary
This summary is machine-generated.

A new intestine-on-chip system with a 3D-printed disc enables accurate measurement of intestinal permeability. This flexible model improves preclinical testing of drug compounds by mimicking the human small intestinal barrier.

Keywords:
cell monolayerin vitro modelintestinal absorptionintestinal barrierintestine-on-chippermeability

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Area of Science:

  • Biomedical Engineering
  • Drug Discovery
  • In Vitro Modeling

Background:

  • Accurate preclinical in vitro models are needed to assess intestinal permeability.
  • Existing intestine-on-chip systems require further optimization for specificity, integrity, and complexity.

Purpose of the Study:

  • To develop and validate a novel intestine-on-chip system for improved intestinal permeability studies.
  • To enhance preclinical testing platforms for drug compound evaluation.

Main Methods:

  • Adapted an established intestine-on-chip model for cell monolayer culture using a 3D-printed disc.
  • Investigated membrane characteristics and standardized read-outs under static and dynamic flow conditions.
  • Compared results to traditional static permeability studies.

Main Results:

  • The 3D-printed disc supported accurate Caco-2 and human enteroid monolayer formation.
  • The chip accurately detected barrier integrity and compound permeability under laminar flow.
  • Both flow dynamics and membrane properties significantly influenced permeability outcomes.

Conclusions:

  • The novel intestinal cell-on-chip system offers high flexibility for permeability studies.
  • Further validation with diverse compounds is necessary to realize the system's full potential.
  • This model advances preclinical assessment of the human small intestinal barrier.