SOLUBILIZATION AND SUSTAINED DELIVERY OF ANTITUMOR AGENT

Information

  • Research Project
  • 3492201
  • ApplicationId
    3492201
  • Core Project Number
    R43CA049346
  • Full Project Number
    1R43CA049346-01A1
  • Serial Number
    49346
  • FOA Number
  • Sub Project Id
  • Project Start Date
    5/10/1990 - 34 years ago
  • Project End Date
    3/31/1991 - 33 years ago
  • Program Officer Name
  • Budget Start Date
    5/10/1990 - 34 years ago
  • Budget End Date
    3/31/1991 - 33 years ago
  • Fiscal Year
    1990
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    5/11/1990 - 34 years ago

SOLUBILIZATION AND SUSTAINED DELIVERY OF ANTITUMOR AGENT

The overall objective of this study is to provide a new drug delivery system and to enhance the solubility of existing compounds which exhibit excellent antitumor properties but are insoluble in water. Aqueous' solubility is essential for iv administration of antitumor drugs. Phase I research will solubilize diammineplatinumhydroxymalonate, 2, and (trans-1,2-diaminocyclohexane)platinumhydroxymalonate,2, complexes by conjugating them to hydrophilic and biodegradable polymeric ligand, carboxydextran; and to monomeric glucopyranose ligand. Complexes 1 and 2 were selected for solubilization studies because they are sparingly soluble but stable in aqueous solution, and exhibit different spectra of antitumor activity than cisplatin. Conjugation of these complexes to carboxydextran may provide a mechanism for the sustained delivery of antitumor agents. The merits of conjugating polymeric or monomeric ligands will be assessed from the antitumor data of the conjugates. Initial screening of the new conjugates will be done against L1210. Tumor will be injected ip and the treatment will be iv. Selected candidates will also be screened against a panel of solid tumors. Preliminary nephrotoxicity and hepatotoxicity studies will also be undertaken. The success of this program will provide expanded use of platinum complexes in cancer chemotherapy and this approach will be extended to the solubilization of other insoluble antitumor platinum and organic drugs in Phase II research.

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
    395
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ET
  • Study Section Name
    Experimental Therapeutics Subcommittee 2
  • Organization Name
    ANDRULIS RESEARCH CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    BETHESDA
  • Organization State
    MD
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    20814
  • Organization District
    UNITED STATES