Skip to main content

POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY.

Publication ,  Journal Article
Pitha, J; Caron, MG; Lefkowitz, RJ
Published in: American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
January 1, 1979

Water-soluble polymeric drugs are often prepared by complex procedures. The same applies to the preparation of resin-anchored drugs used in the affinity chromatogrphy of drug receptors. In some instances a more direct approach may result in a considerable improvement. The authors found that inclusion of some drugs or polymeric drugs into a suitable monomer mixture and subsequent polymerization results in a useful incorporation of the compound into the newly formed polymer. The incorporation of an allyl-group containing drugs into polyacrylamide formed by a free radical polymerization was an effective process. The compounds containing quinonoid-type grouping or aromatic amines can also be incorporated into polyacrylamide; the process probably occurs by a radical substitution. Incorporation of a drug into a polymer generally changes its distribution in cells and body and their biological effects change accordingly. The direct polymerization of the drug in addition to this change leads to a further modification of properties. The main additional effects observed are based on a considerable decrease of steric accessibility of the drug after the direct incorporation into the polymeric chain. Experimental procedure is briefly described. It is concluded that the direct co-polymerization of drugs may yield products in a nearly effortless way; the resulting polymers can be easily tagged by fluorescent moieties. The process furthermore may potentially increase the specificity of a drug.

Duke Scholars

Published In

American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

ISSN

0032-3934

Publication Date

January 1, 1979

Volume

20

Issue

2

Start / End Page

652 / 653

Related Subject Headings

  • Polymers
  • 3403 Macromolecular and materials chemistry
  • 1007 Nanotechnology
  • 0912 Materials Engineering
  • 0303 Macromolecular and Materials Chemistry
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Pitha, J., Caron, M. G., & Lefkowitz, R. J. (1979). POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY. American Chemical Society, Polymer Preprints, Division of Polymer Chemistry, 20(2), 652–653.
Pitha, J., M. G. Caron, and R. J. Lefkowitz. “POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY.American Chemical Society, Polymer Preprints, Division of Polymer Chemistry 20, no. 2 (January 1, 1979): 652–53.
Pitha J, Caron MG, Lefkowitz RJ. POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY. American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 1979 Jan 1;20(2):652–3.
Pitha, J., et al. “POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY.American Chemical Society, Polymer Preprints, Division of Polymer Chemistry, vol. 20, no. 2, Jan. 1979, pp. 652–53.
Pitha J, Caron MG, Lefkowitz RJ. POLYMERIC DRUG BY DIRECT CO-POLYMERIZATION: POLYMER OF beta -ADRENERGIC ANTAGONIST AND ITS BINDING TO RECEPTOR AND ANTIBODY. American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 1979 Jan 1;20(2):652–653.

Published In

American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

ISSN

0032-3934

Publication Date

January 1, 1979

Volume

20

Issue

2

Start / End Page

652 / 653

Related Subject Headings

  • Polymers
  • 3403 Macromolecular and materials chemistry
  • 1007 Nanotechnology
  • 0912 Materials Engineering
  • 0303 Macromolecular and Materials Chemistry