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STTR Phase I: Development High-throughput Screening System for Glaucoma Therapeutics Using a Bioengineered Human Eye Tissue

Award Information
Agency: National Science Foundation
Branch: N/A
Contract: 1448900
Agency Tracking Number: 1448900
Amount: $225,000.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: BT
Solicitation Number: N/A
Timeline
Solicitation Year: 2014
Award Year: 2015
Award Start Date (Proposal Award Date): 2015-01-01
Award End Date (Contract End Date): 2015-12-31
Small Business Information
347 Shaker Run
Albany, NY 12205
United States
DUNS: 079405061
HUBZone Owned: No
Woman Owned: Yes
Socially and Economically Disadvantaged: No
Principal Investigator
 Dhruba Bharali
 (631) 559-2727
 djbharali@yahoo.com
Business Contact
 Dhruba Bharali
Phone: (631) 559-2727
Email: djbharali@yahoo.com
Research Institution
 SUNY Polytechnic Institute
 Magnus Bergkvist
 
257 Fuller Rd.
Albany, NY 12203
United States

 Nonprofit College or University
Abstract

The broader impact/commercial potential of this Small Business Technology Transfer (STTR) project will be the development of a testing system that will facilitate glaucoma drug development in a more cost-effective manner. This will enable better treatment of glaucoma and ultimately prevention of vision loss. This work will overcome a major limiting factor for glaucoma drug discovery, and provide scientists and doctors with a unique tool to understand the physiology of the human eye as related to glaucoma. Commercially, this project will allow for high-throughput testing of new glaucoma therapies, making this technology highly desirable to the pharmaceutical industry. Longer term, this technology has the potential to provide a healthy transplantable tissue that can cure glaucoma. This STTR Phase I project proposes to address the lack of effective in vitro model for testing targeted glaucoma therapies. This work will be the first-of-its-kind, exploring the feasibility to bioengineer a physiologically-relevant 3D human trabecular outflow tract utilizing co-culture and cell differentiation methods along with microfabrication techniques. It is based on the development of a custom-built system that will incorporate the bioengineered tissue into a platform that mimics the flow of aqueous humor and pressure changes in the human eye. At the conclusion of this project, it is anticipated that the bioengineered tissue will behave similarly to its in vivo counterpart, and be usable as higher throughput testing platform for drugs affecting the outflow physiology of the human trabecular outflow tract. In addition, this project will lead to a platform that could be used by other scientists to study and understand the biology of the human trabecular outflow tract.

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

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