SBIR-STTR Award

Biointegrated Synthetic Grafts for Reconstruction of Vascular Tissue
Award last edited on: 12/9/2015

Sponsored Program
SBIR
Awarding Agency
DOD : DHA
Total Award Amount
$1,149,668
Award Phase
2
Solicitation Topic Code
DHP14-009
Principal Investigator
Andrew Marshall

Company Information

Healionics Corporation

2121 North 35th Street Suite 200
Seattle, WA 98103
   (206) 432-9060
   info@healionics.com
   www.healionics.com
Location: Single
Congr. District: 07
County: King

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2014
Phase I Amount
$149,978
Current vascular repair and replacement grafts made from synthetic biomaterials, typically expanded polytetrafluoroethylene (ePTFE), have poor functionality for use with smaller vessels in the extremities. We propose using ?STAR? synthetic biomaterial, a well developed microporous tissue scaffold, already in human device use, to construct grafts that potentially overcome the issues with stenosis and infection that limit use of existing prosthetic graft materials. When implanted, STAR biomaterial exhibits large reductions in foreign body response, enhances angiogenesis, and concentrates natural immune cells to resist infections. These biological responses are regulated by the tightly controlled and optimized porous geometry, and do not require use of added biologics. By significantly reducing foreign body encapsulation around the graft exterior, ?STARgraft? reduces capsular contraction, a significant contributor to lumen narrowing. Use of STAR biomaterial on the inner blood-contacting surfaces offers potential to use the pore structure?s inherent proangiogenicity to facilitate capillary ingrowth and support spontaneous endothelialization. Since the biological responses to STAR biomaterial are largely independent of material chemistry, STARgraft can be constructed from well-characterized high-compliance elastomeric silicones highly suited for vascular graft use. Preliminary in vivo feasibility data in an arteriovenous shunt model suggests the approach has promise for the vascular reconstruction application.

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
2016
Phase II Amount
$999,690
Use ofexisting smaller prosthetic grafts for vascular repair and reconstruction after severetrauma to the extremities is greatly limited by issues with stenosis and infection.We propose treating the exterior of ePTFE vascular grafts with STAR biomaterial, a well-developed microporous synthetic tissue scaffold already in human use.STAR prevents the usual formation of a constrictive fibrotic perigraft tissue capsule.Mechanical constriction effects areeliminated, permitting greater freedom for natural pulsatile and vibratory motion of the graft wall.This suppresses progression of neointimal hyperplasia by alleviating compliance mismatch and providing more favorable stress conditions at the ePTFE-neointima interface.The STAR biointerface also addresses the infection risk of ePTFE grafts; STAR biomaterial harnesses the bodys natural antimicrobial defenses by concentrating immune cells to resist infections.These biological responses are regulated by the tightly controlled and optimized porous geometry and do not require use of added biologics.Promising preliminary results suggest that this approach can lead to a major improvementin clinical performance and reliability.Phase II technical objectives aredemonstrating advantages of superior patency and infection control in an ovine arterial bypass model with controlled bacterial challenge, and performing neededbench testingtowards qualifyingthe novel graft design for human use.