I-Corps: Thermo-responsive biopolymers for tumor targeted delivery

Information

  • NSF Award
  • 1264214
Owner
  • Award Id
    1264214
  • Award Effective Date
    10/15/2012 - 12 years ago
  • Award Expiration Date
    9/30/2013 - 11 years ago
  • Award Amount
    $ 50,000.00
  • Award Instrument
    Standard Grant

I-Corps: Thermo-responsive biopolymers for tumor targeted delivery

This project builds on prior studies that were designed and conducted by researchers to significantly reduce or remove key limitations to most current cancer treatment processes. A crucial limitation has been that most current therapies cannot effectively restrict drugs to tumor cells. The drug delivery system designed through this work may accomplish a selective targeting and delivery of anticancer drugs to solid tumors. This targeted delivery, achieved via a thermally responsive, biopolymer, elastin-like polypeptide (ELP) of a pre-determined molecular weight, can facilitate drug aggregation in tumors exposed to an externally applied, clinically utilized heat source. The proposed biopolymer carrier can exploit the passive targeting properties of macromolecular carriers and the Enhanced Permeability and Retention effect, along with active targeting properties that make use of heat at the tumor site. Through this cell penetrating peptide?s mediation, an efficient, intracellular delivery of chemotherapeutics to the tumor can be achieved. Researchers have applied this approach in the lab within several experimental cancer models to confirm its potential for clinical use as a human therapeutic. <br/><br/>Cancer, a leading cause of morbidity and mortality worldwide, has been difficult to treat through therapies targeted at specific tumor sites. A tremendous need exist for therapeutic approaches that both increase treatment specificity and efficacy within tumors and reduce cytotoxicity in healthy tissues. This proposed tumor-targeting drug delivery system uses a biopolymer ELP in tandem with hyperthermia techniques to augment standard-of-care by selectively inducing intra-tumoral accumulation of a broad range of anti-cancer therapeutics. This treatment methodology may allow doctors to administer chemotherapeutics at doses sufficient for tumor reduction without also harming healthy tissue, thereby enormously impacting treatment success. Moreover, this therapy, although new, is cost-effective: it can be readily integrated into systemic therapies and harnesses hyperthermia and standard-of-care techniques already common in cancer clinics. Successful completion of this project and its clinical translation may lead to greater health and cost effectiveness in cancer treatment.

  • Program Officer
    Rathindra DasGupta
  • Min Amd Letter Date
    10/11/2012 - 12 years ago
  • Max Amd Letter Date
    10/11/2012 - 12 years ago
  • ARRA Amount

Institutions

  • Name
    University of Mississippi Medical Center
  • City
    Jackson
  • State
    MS
  • Country
    United States
  • Address
    2500 North State Street
  • Postal Code
    392164505
  • Phone Number
    6018155000

Investigators

  • First Name
    Drazen
  • Last Name
    Raucher
  • Email Address
    draucher@umc.edu
  • Start Date
    10/11/2012 12:00:00 AM

Program Element

  • Text
    I-Corps
  • Code
    8023

Program Reference

  • Text
    EXP PROG TO STIM COMP RES
  • Code
    9150