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

被引:233
作者
Kim, Jong Oh [1 ,2 ]
Kabanov, Alexander V. [1 ,2 ,3 ]
Bronich, Tatiana K. [1 ,2 ]
机构
[1] Univ Nebraska Med Ctr, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Coll Pharm, Ctr Drug Delivery & Nanomed, Omaha, NE 68198 USA
[3] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119992, Russia
关键词
Block copolymer micelles; Doxorubicin; Self-assembly; Core-shell morphology; BLOCK IONOMER COMPLEXES; POLY(ETHYLENE OXIDE)-BLOCK-POLYMETHACRYLATE ANIONS; LIPOSOMAL DOXORUBICIN; SOLID TUMOR; PHASE-I; COPOLYMER; ACID); POLYELECTROLYTE; RELEASE; TEMPLATE;
D O I
10.1016/j.jconrel.2009.04.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:197 / 204
页数:8
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