A Parylene Ribbon Cable for Neural Prosthetic Applications

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$101,100.00
Award Year:
2010
Program:
SBIR
Phase:
Phase I
Contract:
1R43DC011675-01
Award Id:
95997
Agency Tracking Number:
DC011675
Solicitation Year:
n/a
Solicitation Topic Code:
NIDCD
Solicitation Number:
n/a
Small Business Information
BLACKROCK MICROSYSTEMS, 391 CHIPETA WAY, STE G, SALT LAKE CITY, UT, 84108
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
827132015
Principal Investigator:
RICK VANWAGENEN
(801) 582-5533
RICKVW@BLACKROCKMICRO.COM
Business Contact:
WAGENEN VAN
() -
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): This project addresses the process development and evaluation of an extremely flexible, Parylene C, micro-ribbon cable that is both biocompatible and biostable. Such a cable would be employed to link micro-electrode arr ays with percutaneous connectors as well as with other in vivo micro-electronic arrays and modules. The key innovation is the approach utilized to form a monolithic structure with the array and connector directly incorporated into the ribbon cable. Thus th ere is no need to connect the cable to the array and connector after its synthesis. The primary advantages are extreme flexibility and low modulus resulting in easy placement of the electrode array and minimal to no residual tethering forces exerted on the array in vivo. A third advantage is the wide range of cable designs that can be easily and inexpensively fabricated using MEMs photolithographic processes. After process development validations will focus on designs for enhanced flexibility and stress rel ief as well as in vitro testing of electrical and mechanical properties. The key criteria for success are to develop a method of manufacturing a monolithic ribbon cable structure followed by evaluation, of the cable in terms of acceptable flexibility (as d etermined by key neuroscience researchers), mechanical and electrical stability in accelerated in vitro testing and finally feasibility and ease of manufacture at an acceptable cost.

* information listed above is at the time of submission.

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