Periodic Reporting for period 1 - DBSBOT (Deep brain stimulation based on the wireless magnetically localised and ultrasonically actuated micro-robot)
Reporting period: 2023-04-01 to 2025-03-31
The project aligns with the EU’s Brain Research Strategy, which utilizes innovative technologies to advance understanding and treatment of neurological diseases. By integrating robotics, material science, and biomedical engineering, the microrobots aim to reduce surgical risks, improve patient quality of life, and lower healthcare costs.
1. Device Development
(1)Designed and fabricated micro-scale piezoelectric robots using two-photon lithography, which are capable of converting ultrasonic energy into electrical stimulation pulses.
(2)Integrated magnetic nanoparticles to enable precise spatial control under the guidance of an external magnetic field.
2. In Vitro Validation
(1)Demonstrated effective responses in human SH-SY5Y neural cells under ultrasound stimulations.
(2)Maintained stable performance for more than 30 days without material degradation.
These technical achievements represent a significant advance over conventional DBS systems, eliminating the risks of invasive operations. The project has generated two drafted journal article manuscripts and paved the road for future development of in vivo investigations and foundation for clinical translation.
(1)Successfully developed ultrasound-powered piezoelectric microrobots (50-80μm scale) using two-photon lithography, demonstrating precise energy conversion from ultrasonic waves to electrical stimulation pulses.
(2)Achieved sub-millimeter positioning accuracy (≤10 μm) through integrated magnetic nanoparticle guidance.
(3)Validated neural stimulation capability in human SH-SY5Y cell models, showing biocompatibility after 3-day cell viability tests.
2. Potential Impacts:
(1)Clinical Transformation: Could improve DBS therapy by eliminating risks associated with implanted needles to reduce infection rates.
(2)Research Advancement: Enables new neuromodulation studies through minimally invasive and precise positioning.
3. Key Research Needs for Further Development:
(1)In vivo validation in Parkinson's disease animal models.
(2)Long-term biocompatibility studies (6-12 months).
(3)Optimization for different brain regions/targets.
(4)Preclinical safety/efficacy data package for regulatory submission.
4. Commercialization Support Requirements:
(1)Partnership development with neurotech manufacturers.
(2)Regulatory affairs expertise for medical device approval.
These results demonstrate progress toward showing the possibility of replacing current DBS systems. Successful translation could benefit an estimated 3-5 million potential patients worldwide.