Core cross-linked block ionomer micelles as pH-responsive carriers for cis-diamminedichloroplatinum(II)

被引:86
|
作者
Oberoi, Hardeep S. [1 ,2 ]
Laquer, Frederic C. [3 ]
Marky, Luis A. [1 ,2 ]
Kabanov, Alexander V. [1 ,2 ,4 ]
Bronich, Tatiana K. [1 ,2 ,4 ]
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] Univ Nebraska, Dept Chem, Omaha, NE 68182 USA
[4] Moscow MV Lomonosov State Univ, Fac Chem, Lab Chem Design Bionanomat, Moscow, Russia
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Cisplatin; Block copolymers; Cross-linking; Drug delivery; Micelle; INCORPORATED POLYMERIC MICELLES; CISPLATIN; DNA; NANOPARTICLES; DELIVERY; STABILITY; COMPLEXES; PLATINUM; NEPHROTOXICITY; CONFORMATION;
D O I
10.1016/j.jconrel.2011.03.028
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Benefits of the frequently prescribed platinum (II) chemotherapy drugs are compromised by undesirable side effects, poor pharmacokinetics and development of drug resistance. Polymer micelles derived from amphiphillic block copolymers, offer a novel macromolecular platform for carrier based delivery of such compounds. Soft polymeric nanocarriers were synthesized by template-assisted method involving condensation of the poly(ethylene oxide)-b-polymethacrylate anions by metal ions into core-shell block ionomer complex micelles followed by chemical cross-linking of the polyion chains in the micelle cores. The resulting micelles can efficiently incorporate cisplatin with a high loading capacity (up to 42% w/w). Core cross-linking stabilized the micelles against structural disintegration and prevented premature drug release. The reversible cisplatin entrapment involved the carboxylate groups of the micellar core. The drug was released in a pH-responsive manner, without loss of its biological activity. The stable cross-linked polymer micelles can potentially improve platinum (II) drug disposition with improved therapeutic potential. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 72
页数:9
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