Tissue Barrier-on-Chip: A Technology for Reproducible Practice in Drug Testing
Eugen V Koch1,2, Verena Ledwig2,3, Sebastian Bendas2,3
1Institute of Microtechnology, TU Braunschweig, Alte Salzdahlumer Str. 203, 38124 Braunschweig, Germany.
Pharmaceutics
|July 27, 2022
Summary
This study introduces an innovative organ-on-chip platform for drug transport studies. The new system overcomes limitations of previous models, enabling more accurate drug permeation testing across biological barriers like the blood-brain barrier.
Area of Science:
- Biomedical Engineering
- Pharmacology
- Cell Biology
Background:
- Organ-on-chip systems are crucial for studying drug transport across biological barriers, such as the blood-brain barrier.
- Existing systems face challenges with static cell culture transfer and material limitations (polydimethylsiloxane - PDMS).
Purpose of the Study:
- To present an improved organ-on-chip platform for drug permeation testing.
- To overcome limitations in transferring static cell culture protocols and material constraints in microfluidic drug testing.
Main Methods:
- Developed a chip platform enabling tissue transfer post-seeding on membranes (polymer or Si3N4).
- Utilized a microscopable glass chip with two fluid compartments and embedded electrodes, minimizing PDMS contact.
- Incorporated features for automated fluid control, inertness, and air bubble trapping.
Main Results:
- The new design allows seamless transfer of established static cell models into microfluidic systems.
- The glass chip design minimizes PDMS-related issues, improving quantitative measurements of hydrophobic drugs.
- The system facilitates reproducible microfluidic perfusion studies of tissue barriers.
Conclusions:
- The presented organ-on-chip platform offers a practical and versatile solution for drug permeation testing.
- It enhances the study of in vitro tissue barrier models under reproducible microfluidic conditions.
- This innovation addresses key limitations, paving the way for more reliable drug development research.


