Semiconducting Polymer Dots for Multiplexed Assays

Information

  • Research Project
  • 8646764
  • ApplicationId
    8646764
  • Core Project Number
    R43GM109564
  • Full Project Number
    1R43GM109564-01
  • Serial Number
    109564
  • FOA Number
    PA-13-088
  • Sub Project Id
  • Project Start Date
    5/1/2014 - 10 years ago
  • Project End Date
    12/31/2014 - 10 years ago
  • Program Officer Name
    HAGAN, ANN A.
  • Budget Start Date
    5/1/2014 - 10 years ago
  • Budget End Date
    12/31/2014 - 10 years ago
  • Fiscal Year
    2014
  • Support Year
    01
  • Suffix
  • Award Notice Date
    4/25/2014 - 10 years ago
Organizations

Semiconducting Polymer Dots for Multiplexed Assays

DESCRIPTION (provided by applicant): Fluorescence based techniques play an essential role in modern cell biology and biomedical research. Further development of these techniques has been hindered by the lack of suitable fluorescent probes. To overcome this challenge, various fluorescent nanoparticles have been developed. Among those, conjugated polymer dots (Pdots) exhibited superior properties such as high brightness, fast emission rate, and excellent photostability. However, a severe drawback associated with Pdots is their broad emission spectra, which significantly limit their usefulness in practical applications. This proposal describes the refinement of a new class of Pdots that emit at different wavelengths with narrow spectral bandwidth. To achieve this goal, we propose the following aims: (1) Develop multicolor bright polymer dots with emission bandwidth FWHM that is comparable to or less than 40 nm. Here, we will carry out various spectroscopic techniques to characterize the Pdot properties such as absorption cross section, emission bandwidth, fluorescence quantum yield, photostability, and fluorescence lifetime. Single-particle fluorescence imaging will also be performed to provide side-by-side brightness comparisons on Pdots versus inorganic quantum dots (Qdots) (2) Optimize nanoparticle surface properties to reduce nonspecific labeling. Here, to examine nonspecific labeling of Pdots, we will use a range of techniques, including gel electrophoresis, dynamic laser scattering, affinity chromatography, flow cytometry, and fluorescence spectroscopy/imaging. (3) Demonstrate multiplex detection of biomolecules in cellular environments. Here, we will use the bright, narrow-band Pdots for multiplex detection of biomolecules in cellular environments. Specifically, flow cytometry and fluorescence imaging will be performed to evaluate the labeling specificity and compare fluorescence brightness of the labeled targets. Reliable protocols will be established for simultaneous labeling of three or more cellular targets with multicolor Pdots. This will lay the foundation of applying these bright, narrow-band Pdots for multiplex detection and biological imaging.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    148552
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:148552\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    LAMPROGEN, INC.
  • Organization Department
  • Organization DUNS
    078456317
  • Organization City
    SEATTLE
  • Organization State
    WA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    981156005
  • Organization District
    UNITED STATES