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Tissue Compatibility of Silicon Microfabricated Probes Inserted into the Brain

Published online by Cambridge University Press:  02 July 2020

J. N. Turner
Affiliation:
Wadsworth Center, New York State Department of Health, Albany, NY12201
William Shain
Affiliation:
Wadsworth Center, New York State Department of Health, Albany, NY12201
D. H. Szarowski
Affiliation:
Wadsworth Center, New York State Department of Health, Albany, NY12201
M. Anderson
Affiliation:
Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY12180
S. Martins
Affiliation:
Applied and Engineering Physics, Cornell University, Ithaca, NY14853
R. Davis
Affiliation:
Applied and Engineering Physics, Cornell University, Ithaca, NY14853
H. G. Craighead
Affiliation:
Applied and Engineering Physics, Cornell University, Ithaca, NY14853
M. Isaacson
Affiliation:
Applied and Engineering Physics, Cornell University, Ithaca, NY14853
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Extract

The application of nano- and microfabricated devices based on silicon electronics technology is an emerging interdisciplinary area combining engineering and biology. The placement of electrically active probes in damaged or diseased tissues of the central nervous system could have enormous impact on the health and quality of life of large numbers of individuals by restoring lost function, or by treating or controlling disease states. Such probes have been fabricated at a high level of engineering sophistication. Unfortunately, when inserted into the brain a tissue reaction is initiated forming a scar that surrounds and electrically isolates the probe within a few weeks. This reaction is thought to primarily involve glial cells, and is undoubtedly dominated by the bulk surface of the probes which have a silicon oxide layer on top of single crystal silicon.

Model probes (Fig. 1) were microfabricated by photolithography with a 1×1mm tab used for gripping and inserting probes.

Type
Shared Resources: Access to Critical Instrumentation
Copyright
Copyright © Microscopy Society of America 1997

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References

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3. Support: NIH RR R01 10957Google Scholar