Pluronic® block copolymers as novel polymer therapeutics for drug and gene delivery

被引:1172
作者
Kabanov, AV [1 ]
Batrakova, EV
Alakhov, VY
机构
[1] Nebraska Med Ctr 986025, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE 68198 USA
[2] Supratek Pharma Inc, Laval, PQ H7B 1B7, Canada
关键词
block copolymers; blood-brain barrier; gene therapy; cancer chemotherapy; drug delivery;
D O I
10.1016/S0168-3659(02)00009-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pluronic((R)) block copolymers are found to be an efficient drug delivery system with multiple effects. The incorporation of drugs into the core of the micelles formed by Pluronic((R)) results in increased solubility, metabolic stability and circulation time for the drug. The interactions of the Pluronic((R)) unimers with, multidrug-resistant cancer cells result in sensitization of these cells with respect to various anticancer agents. Furthermore, the single molecular chains of copolymer, unimers, inhibit drug efflux transporters in both the blood-brain barrier and in the small intestine, which provides for the enhanced transport of select drugs to the brain and increases oral bioavailability. These and other applications of Pluronic((R)) block copolymers in various drug delivery and gene delivery systems are considered. (C) 2002 Elsevier Science BV All rights reserved.
引用
收藏
页码:189 / 212
页数:24
相关论文
共 124 条
[71]   MICELLIZATION OF POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) BLOCK-COPOLYMER IN AQUEOUS-SOLUTION - EFFECT OF POLYMER IMPURITIES [J].
LINSE, P .
MACROMOLECULES, 1994, 27 (10) :2685-2693
[72]   TEMPERATURE-DEPENDENT MICELLIZATION IN AQUEOUS BLOCK COPOLYMER SOLUTIONS [J].
LINSE, P ;
MALMSTEN, M .
MACROMOLECULES, 1992, 25 (20) :5434-5439
[73]  
MADDEN TD, 1984, J BIOL CHEM, V259, P7655
[74]  
Malmsten M, 2000, AMPHIPHILIC BLOCK COPOLYMERS: SELF-ASSEMBLY AND APPLICATIONS, P319, DOI 10.1016/B978-044482441-7/50015-3
[75]   Interaction of tumor and normal blood cells with ethylene oxide and propylene oxide block copolymers [J].
Melik-Nubarov, NS ;
Pomaz, OO ;
Dorodnych, TY ;
Badun, GA ;
Ksenofontov, AL ;
Schemchukova, OB ;
Arzhakov, SA .
FEBS LETTERS, 1999, 446 (01) :194-198
[76]   Evaluation of partition coefficients of low molecular weight solutes between water and micelles of block copolymer of ethylene oxide based on dialysis kinetics and fluorescence spectroscopy [J].
Melik-Nubarov, NS ;
Kozlov, MY .
COLLOID AND POLYMER SCIENCE, 1998, 276 (05) :381-387
[77]   Inhibition of multidrug resistance-associated protein (MRP) functional activity with pluronic block copolymers [J].
Miller, DW ;
Batrakova, EV ;
Kabanov, AV .
PHARMACEUTICAL RESEARCH, 1999, 16 (03) :396-401
[78]   Poloxamers and poloxamines in nanoparticle engineering and experimental medicine [J].
Moghimi, SM ;
Hunter, AC .
TRENDS IN BIOTECHNOLOGY, 2000, 18 (10) :412-420
[79]   STRUCTURAL STUDY ON THE MICELLE FORMATION OF POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) POLY(ETHYLENE OXIDE) TRIBLOCK COPOLYMER IN AQUEOUS-SOLUTION [J].
MORTENSEN, K ;
PEDERSEN, JS .
MACROMOLECULES, 1993, 26 (04) :805-812
[80]   POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) TRIBLOCK COPOLYMERS IN AQUEOUS-SOLUTION - THE INFLUENCE OF RELATIVE BLOCK SIZE [J].
MORTENSEN, K ;
BROWN, W .
MACROMOLECULES, 1993, 26 (16) :4128-4135