4.6 Article

Design Choices for Next-Generation Neurotechnology Can Impact Motion Artifact in Electrophysiological and Fast-Scan Cyclic Voltammetry Measurements

期刊

MICROMACHINES
卷 9, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/mi9100494

关键词

electrode; artifact; electrophysiology; electrochemistry; fast-scan cyclic voltammetry (FSCV); neurotechnology; neural interface; neuromodulation; neuroprosthetics; brain-machine interfaces

资金

  1. National Institutes of Health (NIH) National Institute of Neurological Disorders and Stroke (NINDS) [R01NS062019, R01NS094396, R01NS089688, R21NS108098]
  2. Defense Advanced Research Projects Agency (DARPA) Biological Technologies Office (BTO) Targeted Neuroplasticity Training Program under the auspices of Doug Weber and Tristan McClure-Begley through the Space and Naval Warfare Systems Command (SPAWAR) System [N66001-17-2-4010]
  3. Grainger Foundation
  4. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS108098, R01NS094396, R01NS089688, R01NS062019] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Implantable devices to measure neurochemical or electrical activity from the brain are mainstays of neuroscience research and have become increasingly utilized as enabling components of clinical therapies. In order to increase the number of recording channels on these devices while minimizing the immune response, flexible electrodes under 10 mu m in diameter have been proposed as ideal next-generation neural interfaces. However, the representation of motion artifact during neurochemical or electrophysiological recordings using ultra-small, flexible electrodes remains unexplored. In this short communication, we characterize motion artifact generated by the movement of 7 mu m diameter carbon fiber electrodes during electrophysiological recordings and fast-scan cyclic voltammetry (FSCV) measurements of electroactive neurochemicals. Through in vitro and in vivo experiments, we demonstrate that artifact induced by motion can be problematic to distinguish from the characteristic signals associated with recorded action potentials or neurochemical measurements. These results underscore that new electrode materials and recording paradigms can alter the representation of common sources of artifact in vivo and therefore must be carefully characterized.

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