Design of soluble conjugates of biodegradable polymeric carriers and adriamycin
- 1 May 1993
- journal article
- research article
- Published by Wiley in Makromolekulare Chemie. Macromolecular Symposia
- Vol. 70-71 (1), 119-136
- https://doi.org/10.1002/masy.19930700115
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis and biodistribution of immunoconjugates of a human IgM and polymeric drug carriersJournal of Controlled Release, 1992
- Polymers containing enzymatically degradable bonds, XII. Effect of spacer structure on the rate of release of daunomycin and adriamycin from poly [N-(2-hydroxypropyl)-methacrylamide] copolymer drag carriers in vitro and antitumour activity measured in vivoJournal of Controlled Release, 1992
- Passive immunotherapy of cancer: perspectives and problemsJournal of Controlled Release, 1991
- Optimization of macromolecular prodrugs of the antitumor antibiotic adriamycinJournal of Controlled Release, 1985
- The synthesis and characterization of polypeptide-adriamycin conjugates and its complexes with adriamycin. Part IJournal of Controlled Release, 1985
- A novel method of conjugation of daunomycin with antibody with a poly(L-glutamic acid) derivative as intermediate drug carrier. An anti-.alpha.-fetoprotein antibody-daunomycin conjugateJournal of Medicinal Chemistry, 1984
- Effect of the chemical structure of N- (2- hydroxypropyl) methacrylajnide copolymers on their ability to induce antibody formation in inbred strains of miceBiomaterials, 1984
- Alkylating Prodrugs in Cancer ChemotherapyPublished by Springer Nature ,1983
- Cis-aconityl spacer between daunomycin and macromolecular carriers: A model of pH-sensitive linkage releasing drug from a lysosomotropic conjugateBiochemical and Biophysical Research Communications, 1981
- Immunological Studies with Synthetic PolypeptidesAdvances in Immunology, 1966