Novel drug delivery systems based on the complexes of block ionomers and surfactants of opposite charge

被引:82
|
作者
Bronich, TK
Nehls, A
Eisenberg, A
Kabanov, VA
Kabanov, AV
机构
[1] Univ Nebraska, Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
[2] McGill Univ, Dept Chem, Montreal, PQ H3A 2K6, Canada
[3] Moscow MV Lomonosov State Univ, Dept Polymer Sci, Moscow 119899, Russia
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
block copolymers; polymer-surfactant complexes; oleic acid; all-trans-retinoic acid; paclitaxel; doxorubicin;
D O I
10.1016/S0927-7765(99)00075-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this payer we have evaluated a novel family of polymer-surfactant complexes formed between block ionomers and oppositely charged surfactants. Complexes between cationic copolymer poly(ethylene oxide)-g-polyethyleneimine (PEO-g-PEI) and sodium salt of oleic acid, natural nontoxic surfactant, are prepared and characterized. These systems self-assemble in aqueous solutions into particles with average size of 50-60 nm, which can solubilize hydrophobic dyes (Yellow OB) and drug molecules (paclitaxel). The use of the biologically active surfactants as components of block ionomer complexes is demonstrated for the complexes from PEO-g-PEI and all-trans-retinoic acid. Binding of relatively soluble drugs with block ionomers is illustrated using PEO-b-poly(sodium methacrylate) and doxorubicin. Overall these studies suggest that block ionomer complexes can be used to prepare a variety of soluble and stable formulations of biologically active compounds, and have potential application as drug delivery systems (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:243 / 251
页数:9
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