Development of a Two-photon 3-D Laser Scanning Cytometer

Information

  • Research Project
  • 6550210
  • ApplicationId
    6550210
  • Core Project Number
    R43CA097670
  • Full Project Number
    1R43CA097670-01
  • Serial Number
    97670
  • FOA Number
  • Sub Project Id
  • Project Start Date
    6/1/2003 - 21 years ago
  • Project End Date
    8/31/2005 - 19 years ago
  • Program Officer Name
    SWAIN, AMY L
  • Budget Start Date
    6/1/2003 - 21 years ago
  • Budget End Date
    8/31/2005 - 19 years ago
  • Fiscal Year
    2003
  • Support Year
    1
  • Suffix
  • Award Notice Date
    -
Organizations

Development of a Two-photon 3-D Laser Scanning Cytometer

DESCRIPTION (provided by applicant): This proposal describes the construction and testing of a multi-foci multiphoton laser scanning cytometer which will have superior performance in terms of speed and sensitivity in comparison to current commercial instruments, and possess the added ability to image arbitrarily large volumetric tissue samples. Image cytometry is a technique that images a population of cells on a solid substrate. It is similar to flow cytometry in that it can quickly obtain multivariate parameters data on cells and classify how these parameters are distributed across a cell population. This type of analysis is valuable in obtaining detailed information about subpopulations and in identifying rare events, and has found a number of medical and clinical applications in fields such as oncology and hematology. For the instrument in this proposal, the excitation optics will incorporate a 64 lenslet array which will allow the cytometer to scan large regions quickly and with high sensitivity. The emission optics will incorporate a dual channel detection system with a 64 PMT array on each detection channel. The laser excitation source consists of a pulsed Ti-Saph laser system that can generate 1.8 W of mode-locked power at a repetition rate of 80 MHz. The sample will be on a translation stage that is capable of movement on the range of centimeters in the x-y plane of the cytometer. This will allow the imaging of areas on the range of centimeters. Axial resolution is provided by piezo translation stage for the microscope objective. In order to extend the axial imaging depth a microtome will be incorporated into the system. This will allow imaging arbitrarily deep into tissue blocks. The performance of this system will be tested in model systems consisting of cell dilutions. Furthermore, the instrument will be used to characterize in situ tumor metastasis in a mouse model by imaging an organ that has been injected with cells transfected with GFP.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    117796
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    394
  • Ed Inst. Type
  • Funding ICs
    NCI:117796\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    TISSUEVISION, INC.
  • Organization Department
  • Organization DUNS
    606771918
  • Organization City
    SOMERVILLE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02143
  • Organization District
    UNITED STATES