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Analysis, Design, and Control of

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Analysis, Design, and Control of Movable Neuro-Probes Z. Nenadic, E. Branchaud, R. Andersen, J. Pezaris, W. Collins, and J. Burdick B. Greger, B ... – PowerPoint PPT presentation

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Title: Analysis, Design, and Control of


1
Analysis, Design, and Control of Movable
Neuro-Probes
Z. Nenadic, E. Branchaud, R.
Andersen, J. Pezaris, W. Collins, and J.
Burdick B. Greger, B. Pesaran
Engineering and Applied Science
Biology California
Institute of Technology
(Auxiliary Program Started April 1, 2001)
2
Limitations of Current Neuro-Probe Technology
Key Challenge record high quality signals from
many neurons (for months/years)
  • Fixed positioning of implant
  • Non-optimal (or wrong!) receptive fields.
  • Electrode not near cell body.
  • Low impedance (poor SNR) design required.
  • Gliosis and encapsulation

3
  • Movable Probe Concept computer controlled
    movable probes can
  • track moving neurons, find new neurons, break
    through encapsulation.
  • Project Goals
  • Short term validate concept, enable more
    complex acute experiments
  • Intermediate term Develop design specs for MEMS
    devices
  • Long term develop MEMS technology for
    implantable devices (see talk by Y.C. Tai)

4
Current Research Program Outline
  • Theory develop algorithms for probe control
    using modeled (computational) environment
  • Model extra-cellular neuron potentials
  • Characterize local field potentials (LFP)
  • Control algorithm development guided by
    computational model
  • Implementation meso-scale hardware test-beds
  • Validate concept, evaluate algorithms
  • Enable testing of Biomechanical issues of
    chronic movable probe operation

5
Single Cell Extracellular Potential Simulation
3720 compartment NEURON pyramidal cell model
(adapted from Mainen Sejnowski 96) Synaptic
inputs scattered uniformly throughout dendrites.
Laplace equation Boundary condition Since
solution nearly impossible, use line source
approximation (Holt Koch 99)
6
(No Transcript)
7
Spatial Variation of Extracellular Potential
8
Peak-to-peak amplitude Tuning curve
Added noise -- independent, Gaussian, zero-mean
Noise variance -- determined by signal-to-noise
ratio (SNR)
9
Movable Probe Feedback
10
Movie 1
Movie 2
11
Movable Probe Test-bed Development
  • Multiple development phases to maximize
    scientific gain and engineering development along
    the way.
  • Acute probes inserted in brain tissue for a
    few hours
  • Initial validation of movable probe concept and
    algorithms
  • Enable better short-term prosthetic feedback
    experiments
  • Semi-chronic electrodes remain, motors
    removed
  • Understand biophysical issues of chronic probe
    operation
  • Track neural populations over days for plasticity
    studies
  • Will set spec.s for future MEMS devices
  • Chronic movable system permanently implanted
  • Ultimate goal needs MEMS development
  • Key technology for future neural-prosthetics

12
Acute Test-Beds
  • Last time motorizing the CCMD, a pre-existing
    manual 4 probe device
  • Completed, with lessons learned
  • (need to list some lessons here)

Put diagram of Thomas system here a few words
about status
13
Semi-Chronic Test-bed
  • Phase I(a) two motor drive that fits inside head
    cap
  • Motors and electrodes stay inserted for a few
    days
  • Power, control, data wires attached at start of
    each session
  • Useful for studies in learning and plasticity
  • Phase I(b) two motor drive that fits inside head
    cap
  • motors detached at end of every
    sessionelectrodes stay implanted for long
    periods of time.
  • enables testing of long term biophysical impact
    of chronic electrode operation (inflammation,
    gliosis, etc.)
  • Phase II 12-16 motor micro-drive with removable
    motor assembly. Will enable consistent
    recordings of many cells

14
Phase 1 Design Progress
Pretty Picture
Pretty Picture
15
Conclusions
  • Developed theory for control of movable probe
    based on peak-to-peak amplitude. Future
    investigations will include
  • other wave form features, such as phase, shape,
    frequency, etc.
  • event detection algorithms to handle
    irregularity of spike trains
  • the effects of multiple units (inclusion of
    spike sorting).
  • effects of tissue dimpling and relaxation
    (easily incorporated)
  • Movable Probe Test-Beds development program
    started
  • CCMD motorization completed, with lessons
    learned.
  • 5-probe acute system developed
  • Phase I of semi-chronic system largely designed
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