Improved Hollow Fiber Membranes for Artificial Lungs

Information

  • Research Project
  • 6932919
  • ApplicationId
    6932919
  • Core Project Number
    R43HL080771
  • Full Project Number
    1R43HL080771-01
  • Serial Number
    80771
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/29/2005 - 18 years ago
  • Project End Date
    3/28/2006 - 18 years ago
  • Program Officer Name
    HARABIN, ANDREA L.
  • Budget Start Date
    9/29/2005 - 18 years ago
  • Budget End Date
    3/28/2006 - 18 years ago
  • Fiscal Year
    2005
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/23/2005 - 18 years ago

Improved Hollow Fiber Membranes for Artificial Lungs

DESCRIPTION (provided by applicant): ALung Technologies, Inc. is developing a respiratory catheter (the Nattier Catheter) for treatment of acute and acute-on-chronic respiratory failure, which affects over 100,000 adults in the United States. A major limitation in clinical respiratory catheters and other implantable artificial lungs being developed is that commercial hollow fiber membranes (HFMs) wet after only a few hours of blood contact. In wetting, blood plasma fills the fiber wall pores and the fiber gas permeance decreases substantially causing insufficient gas exchange. This poses a serious problem because the fibers of implantable artificial lung devices cannot easily be replaced. Thus, for effective clinical use an implantable artificial lung must contain non-wetting HFMs that retain sufficient gas exchange characteristics. Phase I Goals -1) Develop non-wetting HFMs with high gas permeance. Gas-plasma phase polymerization will be used to create an ultra-thin but continuous layer of polymer with high gas permeability, sufficient to prevent liquid intrusion but thin enough to accommodate with negligible diminution the required gas exchange rates; and 2) Bench tests of candidate HFMs designed to evaluate wetting resistance and gas permeance. Tests will be performed in simple modules of candidate fiber samples throughout the optimization process. The best candidate fiber will be incorporated into the Hattler Catheter and evaluated in bench water and blood gas exchange tests. Phase II - Focuses on increased thromboresistance of fiber coatings. Polymers investigated in Phase I are generally more biocompatible than uncoated fibers, but the need for minimizing anticoagulation warrants exploring further improvements in the biocompatibility. The fibers emerging from this program will be of promise for artificial lung devices being developed for patients with lung failure.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R43
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    161854
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    838
  • Ed Inst. Type
  • Funding ICs
    NHLBI:161854\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    APPLIED MEMBRANE TECHNOLOGY, INC.
  • Organization Department
  • Organization DUNS
    089485536
  • Organization City
    MINNETONKA
  • Organization State
    MN
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    55343
  • Organization District
    UNITED STATES