CLINICAL APPLICATION OF A LASER SCANNING CYTOMETER

Information

  • Research Project
  • 3492856
  • ApplicationId
    3492856
  • Core Project Number
    R43CA055413
  • Full Project Number
    1R43CA055413-01
  • Serial Number
    55413
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/1991 - 33 years ago
  • Project End Date
    5/30/1992 - 32 years ago
  • Program Officer Name
  • Budget Start Date
    9/1/1991 - 33 years ago
  • Budget End Date
    5/30/1992 - 32 years ago
  • Fiscal Year
    1991
  • Support Year
    1
  • Suffix
  • Award Notice Date
    8/27/1991 - 33 years ago
Organizations

CLINICAL APPLICATION OF A LASER SCANNING CYTOMETER

We have developed a computer controlled laser scanning cytometer potentially capable of measuring multiple wavelength fluorescence and multiple angle scatter of cells on a solid support such as a slide, cuvette, or culture plate at rapid enough rates to process 10,000 cell samples in two minutes. In addition to the standard flow cytometry measurements, this instrument includes in its data lists and it displays interchangeably 1) course morphological properties, 2) the exact time of measurement and 3) cell position. Since cell position is recorded for each cell, cells can be visually observed during runs or retrospectively, and cells can be remeasured multiple times to follow kinetic properties of selected subpopulations. We have built two dual parameter instruments, and written software to control them and display results. We now propose to develop and evaluate techniques for measuring clinical specimens of human cancer with them as a possible aid in diagnosis and improved prognosis and treatment. This requires that we sensitively measure fluorescinated nucleic acid probes or antibodies and simultaneously and precisely measure the fluorescence of a DNA stain such as propidium iodide. Phase I aims are to test the feasibility of 1) dual fluorescence measurements on clinical specimens of human tumors in comparison with conventional flow cytometry, and 2) imaging cells or fields as they are scanned, a) to conveniently select those to be measured, or b) to view cells selected by the instrument for visual classification.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    394
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    SSS
  • Study Section Name
  • Organization Name
    COMPUCYTE CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02139
  • Organization District
    UNITED STATES