U.S. patents available from 1976 to present.
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Poly(alkylene oxide) amino acid copolymers and drug carriers and charged copolymers based thereon

Patent 5219564 Issued on June 15, 1993. Estimated Expiration Date: Icon_subject July 5, 2011. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

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Inventors

Assignee

Application

No. 726301 filed on 07/05/1991

US Classes:

424/78.17, Aftertreated polymer (e.g., grafting, blocking, etc.)424/78.08, SOLID SYNTHETIC ORGANIC POLYMER AS DESIGNATED ORGANIC ACTIVE INGREDIENT (DOAI)424/85.5, Gamma or immune424/179.1, Conjugated via claimed linking group, bond, chelating agent, or coupling agent (e.g., conjugated to proteinaceous toxin via claimed linking group, bond, coupling agent, etc.)424/181.1, Conjugated to nonproteinaceous bioaffecting compound (e.g., conjugated to cancer-treating drug, etc.)528/310, From imide- or lactam-containing compound, or from an amino-nitrogen containing carboxylic acid, or derivative of an amino-nitrogen-containing carboxylic acid530/390.1, Removing or inactivating virus or bacterium or component or product thereof (e.g., endotoxin, etc.)530/391.7, Conjugated to a cytotoxic agent, drug, or other biologically-active substance530/810CARRIER - BOUND OR IMMOBILIZED PEPTIDES OR PROTEINS AND THE PREPARATION THEREOF, E.G., BIOLOGICAL CELL OR CELL FRAGMENT AS CARRIER, ETC.

Examiners

Primary: Page, Thurman K.
Assistant: Kulkosky, Peter F.

Attorney, Agent or Firm

International Classes

A61K 031/74
A61K 039/00
C08G 069/08

Abstract

Copolymers of poly(alkylene oxides) and amino acids or peptide sequences are disclosed, which amino acids or peptide sequences have pendant functional groups that are capable of being conjugated with pharmaceutically active compounds for drug delivery systems and cross-linked to form polymer matrices functional as hydrogel membranes. The copolymers can also be formed into conductive materials. Methods are also disclosed for preparing the polymers and forming the drug conjugates, hydrogel membranes and conductive materials.

Other References

  • Graham et al., Makromol. Chem., Macromol. Symp., 19, 255-73 (1988)
  • Imai et al., Makromol. Chem., Rapid Commun., 5, 47-51 (1984)
  • Wang et al., J. Macromol. Sci.-Chem., A26(2-3), 505-18 (1989)
  • Ouchi et al., J. Macromol. Sci.-Chem., A24(9), 1011-32 (1987)
  • Bos et al., Acta Pharm. Technol., 33(3), 120-5 (1987)
  • Pretula et al., Makromol. Chem., Rapid Commun., 9, 731-7 (1988)
  • Jeon et al., J. Polym. Sci. Part A Polym. Chem., 27, 1721-30 (1989)
  • Cho et al., Makromol. Chem., 191, 981-91 (1990)
  • Kimura et al., Makromolecules, 16, 1023-4 (1983
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