If you are a drug discovery firm dealing with high failure rates in human clinical trials — this project developed a vascularized mini-heart that allows for in vitro measurement of pumping function. This helps predict how a drug affects the heart's pressure and flow before testing on people.
3D Bioprinted Human Heart Models for Drug Testing and Environmental Toxicity Screening
Imagine growing a tiny, working version of a human heart in a lab that can actually pump fluid. This allows scientists to test new medicines on real human-like tissue instead of relying on animals or flat petri dishes. They are also making a tiny swimming robot made of heart cells to detect poisons in the water.
What needed solving
Pharmaceutical companies face high drug failure rates because current heart models cannot pump blood or mimic human clinical parameters. This leads to increased expenditure and reliance on animal models that do not accurately reflect human physiology.
What was built
A vascularized, pumping human mini-heart and a self-propelling swimming bio-robot made from human cardiac cells.
Who needs this
Who can put this to work
If you are a toxicity testing lab dealing with the lack of specific hazard classes for cardiotoxicity in pesticides — this project developed a swimming bio-robot. This tool can be used to assess the presence of cardiotoxicants in environmental settings.
If you are a bioprinting provider dealing with the inability to create functional, pumping organs — this project developed sacrificial molding and high-resolution 3D printing techniques. This enables the production of 3D tissue constructs with multiple cardiac cell types.
Quick answers
What is the cost or price of these mini-hearts?
Based on available project data, there is no specific unit price mentioned; however, the project received an EU contribution of EUR 4,475,946 for development.
Can this be produced at an industrial scale?
Based on available project data, the project focuses on developing the technology using 3D bioprinting and molding, but industrial scaling capacity is not yet specified.
How is the IP and licensing handled?
Based on available project data, specific licensing terms are not provided, though the consortium includes 3 SMEs and 2 universities.
What is the timeline for market availability?
The project period runs from 2022-11-01 to 2027-10-31, suggesting the technology is still in the development phase.
How does this integrate with existing clinical parameters?
The mini-heart is designed to measure pressure and volume output, which are the same outputs assessed in the clinic.
Who built it
The consortium is heavily weighted toward commercial application, with a 60% industry ratio consisting of 3 SMEs. This suggests a strong drive toward commercialization, supported by the academic expertise of 2 universities across 4 countries (NL, DE, ES, PT).
Contact Universiteit Twente (NL)
Talk to the team behind this work.
Contact us to explore licensing opportunities for 3D cardiac bioprinting.