EPR Assembly of Microgel for FRET Imaging of Breast Cancer

Abstract

The purpose of this project is to develop a new process for identifying breast cancer. This process should be at least as convenient as mammography for the patient, more sensitive for detection of even the smallest and earliest tumors, and more accurate in distinguishing tumors from normal tissue. First, the tumor site is marked by entrapment of a PEG-conjugate, due to the EPR effect. Based on the longer retention of the PEG-conjugate marker in tumor versus normal tissue, a second conjugate is administered. This second conjugate will chemoselectively interact with the first conjugate to form insoluble microgels only in tumors. Alternating cycles of the 2 conjugates should result in increasingly larger microgels. These microgels can then be used as targets to deliver another chemoselective reagent for detection (imaging) or for therapy. In this first year of the grant, we have developed procedures for synthesizing the various gelforming conjugates needed for these studies. We have also established a syngeneic mouse model assay and have carried out pilot vivo experiments.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2006
Accession Number
ADA455298

Entities

People

  • Stanley Stein

Organizations

  • Rutgers University–New Brunswick

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Chemical Synthesis
  • Chemistry
  • Detection
  • Detectors
  • Diseases And Disorders
  • Dosage Forms
  • Imines
  • Mammary Glands
  • Mass Spectrometry
  • Medical Personnel
  • Molecular Weight
  • Neoplasms
  • New Jersey
  • Organic Chemistry
  • Polymers
  • Standards

Fields of Study

  • Medicine

Readers

  • Nanocomposite Materials Science
  • Oncology
  • Oncology and Biomarker-Based Cancer Detection.