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Explant Analysis of Utah Electrode Arrays Implanted in Human Cortex for Brain-Computer-Interfaces
Kevin Woeppel1,2, Christopher Hughes1,2,3, Angelica J Herrera1,2,3
1Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.
Longer implantation of brain-computer interfaces (BCIs) in humans leads to increased tissue encapsulation and material degradation, impacting recording quality. New biomaterials are needed for stable, long-term BCI performance.
Area of Science:
- Neuroscience
- Biomaterials Science
- Clinical Engineering
Background:
- Brain-computer interfaces (BCIs) offer therapeutic potential for paralysis but require long-term stability for clinical use.
- Factors influencing BCI performance, such as electrode material integrity and host tissue response, are critical but understudied in human implants.
Purpose of the Study:
- To characterize material integrity and tissue encapsulation of explanted human intracortical BCI arrays.
- To identify factors influencing electrophysiological performance and long-term stability of BCI devices.
Main Methods:
- Explant analysis of six Utah arrays (platinum and iridium oxide) from two human participants with varying implantation durations (182 and 980 days).
- Utilized optical microscopy, two-photon microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy.
Main Results:
- Recording quality initially increased then declined, correlating with longer implantation times.
- Arrays implanted longer showed greater tissue encapsulation and material degradation (platinum arrays).
- Iridium oxide coating showed some degradation upon stimulation, but performance was initially unaffected.
Conclusions:
- Both tissue encapsulation and material degradation increase with longer BCI implantation durations.
- These factors correlate with reduced signal amplitude and impedance, compromising electrophysiological performance.
- Development of novel biomaterials is essential to minimize encapsulation and enhance stability for sustained BCI function.
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