Silicone Coatings for Biostable Chronic Neural Prostheses

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: 2R44NS060377-02A2
Agency Tracking Number: R44NS060377
Amount: $2,078,683.00
Phase: Phase II
Program: SBIR
Solicitation Topic Code: NINDS
Solicitation Number: PA10-050
Solicitation Year: 2011
Award Year: 2011
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
45 Spinelli Place, CAMBRIDGE, MA, -
DUNS: 085502958
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 (617) 661-0060
Business Contact
Phone: (617) 661-0060
Research Institution
DESCRIPTION (provided by applicant): The miniaturization of neuroprosthetic technology has led to an urgent need for thin, conformal, insulating coatings that retain their biocompatibility and stability over long periods. Silicone coatings have long been used in the medical device industry for their biocompatibility and electrically insulating properties. However, conventional silicone encapsulation technologies are unfit for many miniature medical devices including implantable, chronic microelectrode arrays used in some neuroprosheses. Initiated Chemical Vapor Deposition (iCVD) is an attractive alternative to conventional polymer coatings applied using solvent-based techniques such as dip/spray and curing. iCVD has the benefits of thinness, conformality(conforms very well to complex shapes) and high purity. The goal of this work is to produce electrically insulating, biostable iCVD coatings for chronic neural prosthetic devices. In Phase I, we have demonstrated that iCVD silicone coatings exhibit prolonged stability in simulated in-vivo environments under constant sweeping voltage bias (6+ years under soak without any loss in resistivity), show excellent adhesion and flexibility, are bioinert, and meet USP Plastic Class VI requirements. Furthermore, we have demonstrated a three folds increase in deposition rate via the codeposition of a linear siloxane spacer molecule, making the process even more economically viable for commercialization. In Phase II, GVD will qualify promising deposition conditions andde-insulation methods for neural probe coatings. A serives of in-vitro tests will allow us to downselect the most promising conditions. GVD will partner with Dr. William Shain (Seattle Children's Research Institute) to confirm the suitability of selected probe coating methods through staggered in vivo studies. Upon successful performance demonstrated during the in vivo studies, GVD will design an upgraded coating system optimized for cost-effective commercial production of successful coatings. The ultimategoal of this work is to achieve single step encapsulation of three-dimensional neural probe arrays and of neural prosthetic assemblies. The development of a stable, durable, biocompatible insulating coating under this Phase II will enable that goal to be achieved. PUBLIC HEALTH RELEVANCE: The success of this Phase II will allow GVD to offer to researchers and manufacturers a proven, effective tool for the biocompatible insulation and encapsulation of neuroprosthetic devices capable of augmentingimpaired function of the nervous system. The coating developed under this work will overcome shortfalls of other encapsulants and provide greater flexibility in the design of devices, the choice of materials used, and the minimum dimensions which can be achieved in neuroprosthetic devices. Therapeutically, the coating will provide safe and effective protection and enhanced reliability of devices in chronic applications. The long-term impact will be to de-bottleneck the development of devices and acceleratetheir proliferation as treatments for neurological disorders.

* Information listed above is at the time of submission. *

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