4.8 Article Proceedings Paper

Polymer micelles with cross-linked polyanion core for delivery of a cationic drug doxorubicin

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 138, Issue 3, Pages 197-204

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jconrel.2009.04.019

Keywords

Block copolymer micelles; Doxorubicin; Self-assembly; Core-shell morphology

Funding

  1. NCI NIH HHS [R01 CA089225, R01 CA116590-03, R01 CA116590, R01 CA089225-07, CA116590, 2R01 CA89225] Funding Source: Medline

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Polymer micelles with cross-linked ionic cores were prepared by using block ionomer complexes of poly(ethylene oxide)-b-poly(methacrylic acid) (PEO-b-PMA) copolymer and divalent metal cations as templates. Doxorubicin (DOX), an anthracycline anticancer drug, was successfully incorporated into the ionic cores of such micelles via electrostatic interactions. A substantial drug loading level (up to 50 w/w%) was achieved and it was strongly dependent on the structure of the cross-linked micelles and pH. The drug-loaded micelles were stable in aqueous dispersions exhibiting no aggregation or precipitation for a prolonged period of time. The DOX-loaded polymer micelles exhibited noticeable pH-sensitive behavior with accelerated release of DOX in acidic environment due to the protonation of carboxylic groups in the cores of the micelles. The attempt to protect the DOX-loaded core with the polycationic substances resulted in the decrease of loading efficacy and had a slight effect on the release characteristics of the micelles. The DOX-loaded polymer micelles exhibited a potent cytotoxicity against human A2780 ovarian carcinoma cells. These results point to a potential of novel polymer micelles with cross-linked ionic cores to be attractive carriers for the delivery of DOX. (c) 2009 Elsevier B.V. All rights reserved.

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