In its first year, the BLOOD2POWER project has laid a strong foundation by achieving technical milestones that demonstrate the feasibility and potential impact of the under development technology. This highlights promising avenues for both clinical and economic impact.
Results Overview
Validation of Energy-Harvesting TENG: Successfully created and tested in vitro, the triboelectric nanogenerator (TENG) meets performance criteria for converting body motion into electrical energy.
PMIC and Antenna Design: Initial designs for a low-energy Power Management Integrated Circuit (PMIC) and wireless communication antenna provide the foundation for real-time data transmission, a key feature of the iGraft’s IoMT integration.
Potential Impacts
Sustainable Technology: The TENG’s ability to operate without batteries highlights a sustainable path for implantable electronic medical devices, reducing environmental impact and maintenance needs.
Improved Patient Outcomes: By enabling continuous, self-powered monitoring, the iGraft will provide early alerts on potential graft issues, potentially reducing the need for complex medical interventions and improving patient recovery.
Healthcare Cost Savings: The early detection of complications could reduce hospitalizations and long-term care costs associated with vascular graft failure, addressing a substantial healthcare burden.
Key Needs for Further Uptake and Success
To fully realize these impacts and transition from research to market, essential development and support areas have been identified and are actively being addressed:
Continued Research and Demonstrative Trials: Within the project, further in vitro and in vivo studies are planned to assemble and validate the iGraft’s performance
IPR and Commercialization: Securing intellectual property rights for the energy-harvesting and data transmission technology is essential for market competitiveness. A PCT to project the IP of energy-harvesting system has been filed with the support of a patent attorney.
Market Access and Funding: Initial steps, including the development of a business plan, have been undertaken. In the future, establishing connections with investors and medical device companies and securing additional funding will be essential for scaling production in the next phases beyond this BLOOD2POWER project.
Regulatory Approvals and Standards: Establishing a clear regulatory pathway is essential to bring the iGraft to market. We have scouted and benchmarked Contract Research Organizations (CROs) to identify a suitable partner for collaboration. This CRO will mediate interactions with regulatory bodies and focus on standardization efforts to ensure safety and quality compliance.
Stakeholder Engagement and Market Alignment: Insights from medical doctors, patients, and the public will guide the final stages of development, ensuring the iGraft meets end-user expectations. A survey is underway, and ongoing engagement with our stables clinical consultancy board will help to align the technology with ethical considerations and market needs.
Through these strategic actions, the BLOOD2POWER team aims to bring the iGraft to fruition, providing a breakthrough in vascular graft technology and improving patient outcomes.