1 demonstration of cortical recording and reduced inflammatory response using flexible polymer...
Post on 20-Dec-2015
217 views
TRANSCRIPT
1
DEMONSTRATION OF CORTICAL RECORDING AND REDUCED INFLAMMATORY RESPONSE USING FLEXIBLE POLYMER NEURAL PROBES
LIGA and Biophotonics Lab
André Mercanzini, Karen Cheung, Derek Buhl, Marc Boers, Anne Maillard, Philippe, Colin, Jean-Charles Bensadoun, Arnaud Bertsch, Alan Carleton and Philippe RenaudEcole Polytechnique Fédérale de Lausanne, EPFL, SwitzerlandUniversity of British Columbia, Vancouver, CanadaMassachusetts Institute of Technology, USA
NTHUInstitute of NanoEngineering and MicroSystem Speaker:Wen Cheng Yang
2
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
LIGA and Biophotonics Lab
3
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
4
Introduction
Neural interfaces currently help neuroscientists in their study of the brain’s functions and promise to introduce new solutions for conditions such as Parkinson’s and paralysis.
In order to decrease this response, flexible probes have been designed by several groups in order to comply with brain tissue motion.
Polyimide probes and parylene probes have been developed in order to decrease brain-device compliance mismatch.
5
Introduction
Ref: Leigh R. Hochberg, Mijail D. Serruya, Gerhard M. Friehs, Jon A. Mukand, Maryam Saleh,Abraham H. Caplan, Almut Branner, David Chen, Richard D. Penn & John P. Donoghue. “Neuronal ensemble control of prosthetic devices by a human with tetraplegia”. Nature Vol 442.13 July 2006
6
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
LIGA and Biophotonics Lab
7
Device fabrication
LIGA and Biophotonics Lab
Step 1:A 500 nm TiW and a 1000 nm sacrificial aluminum layer are deposited on a silicon wafer.
Step 2:Polyimide is spun to a thickness of 15 µm
Step 3:Ti/Pt/Ti metal sandwich is deposited atthicknesses of 50nm/200nm/50nm respectively.
8
Device fabrication
LIGA and Biophotonics Lab
Step 4:A second polyimide layer is spun to a thickness of 2 µm
Step 5:A second polyimide Ti/Pt/Ti sandwich is then deposited and etched thus defining the second layer of electrodes. The finalpolyimide layer is spun to a thickness of 2um
9
Device fabrication
LIGA and Biophotonics Lab
Step 6:The three layers of polyimide are then etched in an O2 plasma using the Ti and sacrificial Al as etch stops. The oxide hard mask is dry etched and the wafer is ready for packaging and device release
10
Outline
LIGA and Biophotonics Lab
SEM image of the fabricated device.
11
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
LIGA and Biophotonics Lab
12
Device packaging
LIGA and Biophotonics Lab
Microscope image demonstrating crossover of metal layers and electrode sites.
A packaged flexible neural probe device
13
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
LIGA and Biophotonics Lab
14
Electrical characterization
LIGA and Biophotonics Lab
Impedance magnitude and phase for one electrode site
Figure shows the typical impedance spectrum of devices .There was no apparent difference in impedance between the bottom and top metal layers.
15
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
16
Acute recordings
EEG recordings from 16 electrode sites distinguishing 2 single units
Demonstrates local field potential recordingsidentifying two single units in the mouse cortex. All 16 electrode sites were active.
17
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
18
Histology
General staining for cells with DAPI Staining for microglia, CD11b (green) and astrocytes, GFAP (red).
19
Outline
Introduction Device fabrication Device packaging Electrical characterization Acute recordings Histology Conclusion
20
Conclusion
Due to the smaller neural probe size, and brain-probe compliance match, we have demonstrated reduced insertion and chronic damage using polyimide
microfabricated probes.
21
LIGA and Biophotonics Lab
Thanks for your attendance .