New Method For Protein Sampling and Delivery in Brain

Information

  • Research Project
  • 6833009
  • ApplicationId
    6833009
  • Core Project Number
    R43NS049714
  • Full Project Number
    1R43NS049714-01
  • Serial Number
    49714
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/15/2004 - 20 years ago
  • Project End Date
    8/31/2005 - 19 years ago
  • Program Officer Name
    PANCRAZIO, JOSEPH J.
  • Budget Start Date
    9/15/2004 - 20 years ago
  • Budget End Date
    8/31/2005 - 19 years ago
  • Fiscal Year
    2004
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/18/2004 - 20 years ago
Organizations

New Method For Protein Sampling and Delivery in Brain

[unreadable] DESCRIPTION (provided by applicant): The objective of this Phase I SBIR proposal is to develop a novel in vivo method for collecting and delivering proteins to the extracellular volume in the central nervous system (CNS). Physiologically significant extracellular proteins include neurotropic factors, cytokines, extracellular enzymes and hormones, of which the pathophysiologic roles are mostly unknown. The immediate application of the proposed method will enable determination of protein function in neurochemical and neuropharmacological research in the brain and spinal cord of whole animals. Potential human applications include drug development and testing, along with clinical diagnostics and drug delivery for alcoholism, Alzheimer's, analgesics, brain tumors, epilepsy, multiple sclerosis and stroke. Specific aims for this novel method are to: 1) develop an optimal LaPP microtube; 2) develop a compatible push-pull microperfusion pump, 3) test the LaPP microtube and push-pull microperfusion pump capability to collect and deliver proteins in vitro. [unreadable] [unreadable] The central element of the technology is a Laser-perforated, Push-Pull Perfused (LAPP) microtube having a protein-exchange zone at the functional end, comprising an array of 10 to 1000 holes of diameters ranging from 1 to 20 microns, and having a bifurcated tubing connection to allow the continuous push-pullregulated perfusion of the outer lumen and inner cannula of the microtube. Semi-automated laser fixturing will be developed to enable fabrication of replicate microtubes having hole arrays of various configurations. In vivo animal experimentation and potential diagnostic applications will be explored in Phase II. [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R43
  • Administering IC
    NS
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    132000
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:132000\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    LENOX LASER
  • Organization Department
  • Organization DUNS
    178597142
  • Organization City
    GLEN ARM
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    21057
  • Organization District
    UNITED STATES