Development of efficient acid cleavable multifunctional prodrugs derived from dendritic polyglycerol with a poly(ethylene glycol) shell.

Abstract

In an attempt to explore the potential of dendritic systems for the development of effective anticancer drug delivery systems, we explored a simple modular approach of preparing polyglycerol doxorubicin prodrugs, with flexibility for drug loading using an acid-sensitive hydrazone linker and further post-modification with poly(ethylene glycol) shell. The resulting drug polymer conjugates showed optimal properties for in vitro and in vivo applications because of their high water solubility, an appropriate size for passive tumor targeting, a high stability at physiological conditions, pronounced acid-sensitive properties, cellular internalization, and a favorable toxicity profile. Doxorubicin polyglycerol conjugates with a high drug loading ratio showed clearly improved antitumor efficacy over doxorubicin in an ovarian xenograft tumor model (A2780) inducing transient complete remissions thus demonstrating the potential of developing efficient multifunctional dendritic drug delivery using our modular approach.

• Authors: Marcelo Calderón, Pia Welker, Kai Licha, Iduna Fichtner, Ralph Graeser, Rainer Haag, Felix Kratz
• Journal: Journal of controlled release : official journal of the Controlled Release Society (J Control Release) Vol. 151 Issue 3 Pg. 295-301 (May 10 2011) ISSN: 1873-4995 [Electronic] Netherlands
• PMID: 21256902 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2011 Elsevier B.V. All rights reserved.

Chemical References

• Antineoplastic Agents
• Dendrimers
• Drug Carriers
• Polymers
• Prodrugs
• polyglycerol
• Polyethylene Glycols
• Glycerol

Topics

• Animals
• Antineoplastic Agents (administration & dosage, chemistry, therapeutic use)
• Cell Line, Tumor
• Cell Survival (drug effects)
• Dendrimers (chemistry)
• Drug Carriers (chemistry)
• Drug Compounding
• Female
• Glycerol (chemistry)
• Humans
• Hydrogen-Ion Concentration
• Mice
• Mice, Nude
• Microscopy, Fluorescence
• Molecular Structure
• Particle Size
• Polyethylene Glycols (chemistry)
• Polymers (chemistry)
• Prodrugs (administration & dosage, chemistry, therapeutic use)
• Solubility
• Xenograft Model Antitumor Assays