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A Fully Biological Gas-Exchange Membrane toward a Biofabricated, Booster Lung
Erica M Comber1, Kalliope G Roberts1, Isabel M Joyce1,2
1Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States of America.
ACS Biomaterials Science & Engineering
|April 13, 2026
Summary
Researchers engineered a biological tissue to mimic the lung's gas-exchange barrier for long-term respiratory support, paving the way for biofabricated implantable lungs and improved patient outcomes.
Area of Science:
- Biomaterials Engineering
- Regenerative Medicine
- Respiratory Physiology
Background:
- Chronic lung disease necessitates long-term respiratory support, but current extracorporeal membrane oxygenation (ECMO) is limited by clotting and bleeding complications.
- Permanent respiratory support requires biocompatible materials that prevent clot formation and bleeding, a challenge not yet met by artificial devices.
- Engineering a biofabricated tissue mimicking the alveolar-capillary barrier is crucial for developing long-term, implantable support lungs.
Purpose of the Study:
- To engineer a preliminary, fully biological tissue that replicates the alveolar-capillary barrier.
- To assess the potential of this tissue as a gas-exchange membrane for an implantable, biofabricated support lung.
- To evaluate the mechanical strength, permeability, and cellular viability of the engineered tissue.
Main Methods:
- Fabrication of high-concentration, type I collagen membranes (18.8 ± 3.6 μm-thick).
- Characterization of mechanical strength, water permeability, and oxygen transfer under static, air-liquid conditions.
- Coculture of membranes with human umbilical vein endothelial cells (HUVECs) and A549 lung epithelial cells, followed by assessment of tissue viability and permeability to 70 kDa-FITC dextran.
Main Results:
- The collagen I hydrogel membranes exhibited mechanical strength (≥120 mmHg) and significant oxygen transfer (75% of a silicone sheet).
- Cocultured cells remained viable in air-liquid conditions, demonstrating biocompatibility.
- Dextran permeability indicated the necessity of an alveolar epithelium for enhanced barrier function.
Conclusions:
- A biofabricated collagen I tissue shows promise as a gas-exchange membrane for implantable support lungs.
- Further optimization, including thinner membranes and advanced cell sourcing, is needed for a functional, intracorporeal support lung.
- This approach offers a potential solution for long-term respiratory support in chronic lung disease patients.
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