Small Diameter (3-5mm), Nanofibrous Biomimetic Vascular Graft Prosthesis

Information

  • Research Project
  • 7930557
  • ApplicationId
    7930557
  • Core Project Number
    R44HL096170
  • Full Project Number
    5R44HL096170-02
  • Serial Number
    96170
  • FOA Number
    PA-08-050
  • Sub Project Id
  • Project Start Date
    9/14/2009 - 14 years ago
  • Project End Date
    3/31/2012 - 12 years ago
  • Program Officer Name
    LUNDBERG, MARTHA
  • Budget Start Date
    4/1/2010 - 14 years ago
  • Budget End Date
    3/31/2011 - 13 years ago
  • Fiscal Year
    2010
  • Support Year
    2
  • Suffix
  • Award Notice Date
    3/30/2010 - 14 years ago
Organizations

Small Diameter (3-5mm), Nanofibrous Biomimetic Vascular Graft Prosthesis

DESCRIPTION (provided by applicant): In this Fast Track SBIR application, NanoVasc (Alameda, CA) plans to use its proprietary and innovative electrospinning process (initially developed at U.C. Berkeley in Dr. Song Li's Lab) to develop small diameter vascular grafts (called NanoGrafts) for the treatment of Coronary Artery Disease (CAD) and Peripheral Arterial Disease (PAD). NanoVasc's innovation is the development of a small diameter vascular graft (3-5mm internal diameter) using a biomimetic scaffold that is both biodegradable and bioactive. This research shows great promise for the field of vascular bypass surgeries, as the structure and morphology of electrospun, nanofibrous scaffolds can be manipulated to resemble that of natural extracellular matrix (ECM), therefore creating a more "familiar" environment for the cells to migrate into. The company has preliminary evidence showing the performance and remodeling of a 1mm internal diameter, nanofibrous vascular grafts in vivo with very encouraging results. This project will focus on developing small diameter grafts, evaluating their physico-chemical properties, biological and hemo-compatibility and platelet/thrombus interactions in vitro, and then evaluating their biocompatibility and in vivo dynamics, compatibility/patency and safety in a sheep model. In Phase I, polymer selection, surface modification, and mechanical integrity will be investigated. The candidates that pass the given criteria will then be tested for thrombogenicity, biological and hemo-compatibility using an in vitro blood recirculation loop. Phase II will focus on the in vivo patency in a sheep bilateral common carotid artery model for 28 and 140 days. Controls will include commercially available, 4mm ePTFE vascular grafts.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R44
  • Administering IC
    HL
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    883936
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    837
  • Ed Inst. Type
  • Funding ICs
    NHLBI:883936\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NANOVASC, INC.
  • Organization Department
  • Organization DUNS
    796882475
  • Organization City
    ALAMEDA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    945016447
  • Organization District
    UNITED STATES