If you are a cardiac implant manufacturer dealing with the low 35-60% efficacy of current arrhythmia therapies — this project developed CardioINK that restores cardiac signaling. This could replace or augment traditional pacing systems with a biocompatible material.
Conductive Nano-Biomaterial for Treating Heart Arrhythmias and Preventing Stroke
Imagine the heart's electrical system is like a set of wires that have frayed or broken, causing an irregular beat. This project creates a special 'conductive ink' made of tiny metal wires in a gel that can be painted onto the heart using a thin tube. This ink acts like a bridge, reconnecting the electrical paths so the heart beats in sync again.
What needed solving
Current treatments for Atrial Fibrillation and Left Bundle Branch Blocks have low efficacy (35-60%) and poor biocompatibility. This leads to high healthcare costs and severe outcomes like stroke and heart failure.
What was built
CardioINK, a composite biomaterial of noble metal nanowires in a collagen-alginate hydrogel, and a specialized minimally invasive delivery catheter.
Who needs this
Who can put this to work
If you are a clinic network dealing with high patient volumes of the 13-22 million EU citizens with impaired conductivity — this project developed a minimally invasive delivery method. This reduces the need for costly follow-up treatments associated with current therapies.
If you are a biotech firm dealing with poor biocompatibility in heart implants — this project developed a noble metal-based nanowire composite in a collagen-alginate hydrogel. This provides a blueprint for high-efficacy conductive materials in other organ systems.
Quick answers
What is the expected cost or price of the treatment?
Based on available project data, specific pricing is not mentioned, but the project aims to reduce the 2.6% of annual EU healthcare expenditure currently spent on these conditions.
Can this be produced at an industrial scale?
The project includes two industrial partners and one SME to develop a commercialization strategy, suggesting a move toward industrial scaling.
How is the IP and licensing handled?
Based on available project data, the consortium is developing a commercialization and regulatory strategy for both EU and US markets, though specific licensing terms are not listed.
What is the timeline for market entry?
The project runs from September 2025 to August 2029, with the goal of reaching first-in-human trials by the end of the period.
How does this integrate with existing surgical workflows?
CardioINK is designed to be delivered using specialized minimally invasive catheters, allowing it to fit into existing catheterization lab workflows.
Who built it
The consortium is well-balanced for commercial transition, featuring a 25% industry ratio with 2 industrial partners and 1 SME. Led by a major university hospital (Universitätsklinikum Heidelberg) and involving 8 partners across 5 countries (AT, BE, DE, IE, NL), the group combines clinical expertise with research and industrial capacity to bridge the gap between animal testing and human trials.
Contact Universitätsklinikum Heidelberg regarding the CardioINK commercialization strategy.
Talk to the team behind this work.
Contact us to connect with the NANOBEAT consortium for licensing opportunities.