Endomyocardial Catheter Delivery of Artificial Biopolymer Matrices for Enhanced C

Information

  • Research Project
  • 7600670
  • ApplicationId
    7600670
  • Core Project Number
    R43EB008925
  • Full Project Number
    1R43EB008925-01A1
  • Serial Number
    8925
  • FOA Number
    PA-08-050
  • Sub Project Id
  • Project Start Date
    6/15/2009 - 14 years ago
  • Project End Date
    11/30/2009 - 14 years ago
  • Program Officer Name
    HUNZIKER, ROSEMARIE
  • Budget Start Date
    6/15/2009 - 14 years ago
  • Budget End Date
    11/30/2009 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    6/4/2009 - 14 years ago
Organizations

Endomyocardial Catheter Delivery of Artificial Biopolymer Matrices for Enhanced C

DESCRIPTION (provided by applicant): In the literature to date, cardiac regeneration strategies using stem cells have repeatedly had inefficient cell retention in the target zone. Our group has developed a catheter based technology that enables accurate and controlled delivery of biopolymers, with or without cells, into target zones in the myocardium. Overall procedure: Commercially available alginate and fibrin two part biopolymers will be assessed for material properties (which may be modified to keep the viscosity below a threshold to passage through a microcatheter lumen and to provide for the greatest and most uniform mechanical integrity after delivery and polymerization). Selected formulations at specific volumes (0.1ml to 5ml) will be delivered through specific flow rates (0.1ml/min to 1ml/min) and into swine left ventricular tissues ex vivo while pressure is monitored. Post delivery, three dimensional distributions within tissues will be qualitatively analyzed using sectioning and imaging. Additional testing evaluating the inclusion of bone marrow derived mononuclear cells (MNC's) from swine for viability in single part reagents and through the polymerization process will also be performed in preparation for a preliminary large animal safety study. The large animal study will evaluate a single polymer formulation and delivery protocol for safety in a healthy swine. Five formulation deliveries incorporating one of five different 15 um neutron activated microsphere populations will enable the resulting distribution of each delivery to be assessed in vivo at each of the three time points at which the animals are sacrificed (1 hour, 1 day, and 7 days). Heart, lung, liver, spleen, skeletal muscle, and brain tissue samples will be collected to assess distributions. Safety will be assessed by holter monitoring, histopathology, and biodistribution studies. Perspectives: This study is intended to establish feasibility and preliminary safety for percutaneous transendocardial delivery of two part biopolymer matrices for enhancing cell a new multi-lumen catheter at retention in vivo in large animals this goal material property analysis, flow characteristics, local tissue distribution studies, and safety parameters will be assessed in detail. using a new multiple-lumen delivery catheter. To achieve further studies will assess the safety on infarcted myocardium and assess the good conditions to avoid embolism. PUBLIC HEALTH RELEVANCE: Existing strategies for restoring heart function after myocardial injury are practically limited to cardiac transplantation. Since the supply of donor hearts is limited, tissue engineering appears to be a promising approach for the formation of new functional tissue to replace lost or failing tissue. Novel therapeutic approaches using cell therapy that may contribute to grow new vessels and repair the cardiac tissue have shown great promise and are intuitively appealing. However, successful retention of therapeutic cells in the target tissue after delivery is an important challenge that remains in that up to 98% of the cells delivered in the heart are lost very soon after delivery. The proposal here seeks to improve cell retention by incorporating biopolymer tissue matrix strategies with catheter delivery technologies appropriate for routine clinical use, with a special focus on this strategy safety. The results of this work may prove critical to enabling cardiovascular tissue engineering strategies broadly, and should also have important implications for other local tissue engineering therapies.

IC Name
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
  • Activity
    R43
  • Administering IC
    EB
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    100000
  • Sub Project Total Cost
  • ARRA Funded
    True
  • CFDA Code
    701
  • Ed Inst. Type
  • Funding ICs
    NIBIB:100000\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    BIOCARDIA, INC.
  • Organization Department
  • Organization DUNS
    122370146
  • Organization City
    SAN CARLOS
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    940702718
  • Organization District
    UNITED STATES