Polymer micelles with cross-linked ionic cores for delivery of anticancer drugs

被引:156
作者
Bontha, Satya
Kabanov, Alexander V.
Bronich, Tatiana K.
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
基金
美国国家科学基金会;
关键词
block copolymer micelles; nanogels; template assembly; core-shell morphology; cisplatin; cancer chemotherapy;
D O I
10.1016/j.jconrel.2006.06.015
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work reports the design of polymer micelles with cross-linked ionic cores that display high stability. Block ionomer complexes of poly (ethylene oxide)-b-poly(methacrylic acid) copolymer and divalent metal cations were utilized as micellar templates for the synthesis of the crosslinked micelles. Such micelles represent hydrophilic nanospheres of core-shell morphology. The core comprises a network of the cross-linked polyanions, which is surrounded by the shell of hydrophilic PEO chains. The ionic character of the core provided for pH-dependent swelling/collapse behavior of the nanogels. Cisplatin, a potent chemotherapeutic agent, was incorporated into the ionic core of the micelles with remarkably high efficiency (22% w/w). The drug-loaded micelles were stable in aqueous dispersions exhibiting no aggregation or precipitation for a prolonged period of time. Slow release of platinum complexes was observed in sustained manner from the cisplatin-loaded cross-linked micelles in physiological saline. In vitro studies using human A2780 ovarian carcinoma cells demonstrated that the cross-linked micelles rapidly internalized and delivered cisplatin into cells. These results indicated that polymer micelles with cross-linked ionic cores are promising for further fundamental material studies and practical applications as drug delivery carriers. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 174
页数:12
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