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Scalable Fabrication of Stretchable, Dual Channel, Microfluidic Organ Chips
Published on: October 20, 2018
A similarity scaling approach for organ-on-chip devices
James J Feng1,2, Sarah Hedtrich3,4,5
1Department of Chemical and Biological Engineering, University of British Columbia, Vancouver, BC V6T 1Z4, Canada. james.feng@ubc.ca.
Organ-on-chip devices (OoCs) offer advanced in vitro human physiology insights. A new systematic similarity scaling approach improves OoC design and clinical translatability for better predictive value.
Area of Science:
- Biomedical Engineering
- Physiology
- In Vitro Models
Background:
- Organ-on-chip (OoC) devices are promising for emulating human physiology in vitro.
- Current OoC designs face challenges in biomimicry and clinical translatability due to ad hoc scaling.
- Limited predictive value of OoCs stems from inconsistent scaling approaches.
Purpose of the Study:
- To propose a systematic approach for OoC design and scaling based on the principle of similitude.
- To evaluate the effectiveness of this similarity scaling approach using case studies.
- To enhance the biomimicry and clinical translatability of organ-on-chip devices.
Main Methods:
- Application of the principle of similitude for scaling OoC devices.
- Analysis of lung-on-a-chip, liver-on-a-chip, and gut-liver system case studies.
- Comparison of in vitro findings with clinical data to assess predictive value.
Main Results:
- Lung-on-a-chip and liver-on-a-chip models satisfying similarity criteria showed good agreement with clinical data.
- A gut-liver system failing a kinematic similarity criterion exhibited unphysiological pharmacokinetic responses.
- The similarity scaling approach demonstrated potential for improving OoC performance.
Conclusions:
- Systematic similarity scaling is crucial for maximizing biomimicry and clinical translatability in OoCs.
- This approach can significantly improve the design and operation of organ- and human-on-chip devices.
- Adherence to similarity principles enhances the predictive power of in vitro physiological models.
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