Amphiphilic block copolymer micelles for nanoscale drug delivery

被引:122
作者
Kwon, GS [1 ]
Forrest, ML [1 ]
机构
[1] Univ Wisconsin, Sch Pharm, Div Pharmaceut Sci, Madison, WI 53705 USA
关键词
micelles; drug delivery; poly(ethylene oxide); nanotechnology;
D O I
10.1002/ddr.20063
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Amphiphilic block copolymers can assemble into supramolecular core-shell structures, termed ABC micelles, that have proven utility in drug delivery, particularly for drug solubilization. Several examples have entered clinical trials, attesting to the biocompatibility of ABCs and the potential advantages for drug delivery, e.g., low toxicity relative to Cremophor (R) EL, a surfactant commonly used for drug solubilization. Several examples of ABC micelles demonstrate potential for prolonged circulation in blood. Coupled with novel strategies toward controlled release of drug, nanoscale ABC micelles have tremendous potential for the targeting of antitumor agents, many of which are poorly water soluble and possess dose-limiting toxicity.
引用
收藏
页码:15 / 22
页数:8
相关论文
共 37 条
[1]   Relative aggregation state and hemolytic activity of amphotericin B encapsulated by poly(ethylene oxide)-block-poly(N-hexyl-L-aspartamide)-acyl conjugate micelles:: effects of acyl chain length [J].
Adams, ML ;
Kwon, GS .
JOURNAL OF CONTROLLED RELEASE, 2003, 87 (1-3) :23-32
[2]   Amphotericin B encapsulated in micelles based on poly(ethylene oxide)-block-poly(L-amino acid) derivatives exerts reduced in vitro hemolysis but maintains potent in vivo antifungal activity [J].
Adams, ML ;
Andes, DR ;
Kwon, GS .
BIOMACROMOLECULES, 2003, 4 (03) :750-757
[3]   Block copolymer-based formulation of doxorubicin. From cell screen to clinical trials [J].
Alakhov, V ;
Klinski, E ;
Li, SM ;
Pietrzynski, G ;
Venne, A ;
Batrakova, E ;
Bronitch, T ;
Kabanov, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :113-134
[4]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[5]   Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change [J].
Bae, Y ;
Fukushima, S ;
Harada, A ;
Kataoka, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (38) :4640-4643
[6]  
BAE YS, 2005, POLYM DRUG DELIVERY, P489
[7]   Optimal structure requirements for pluronic block copolymers in modifying P-glycoprotein drug efflux transporter activity in bovine brain microvessel endothelial cells [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Miller, DW ;
Kabanov, AV .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (02) :845-854
[8]   ONE-SIDED ACTION OF AMPHOTERICIN-B ON CHOLESTEROL-CONTAINING MEMBRANES IS DETERMINED BY ITS SELF-ASSOCIATION IN THE MEDIUM [J].
BOLARD, J ;
LEGRAND, P ;
HEITZ, F ;
CYBULSKA, B .
BIOCHEMISTRY, 1991, 30 (23) :5707-5715
[9]   Carrier effects on biological activity of amphotericin B [J].
Brajtburg, J ;
Bolard, J .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (04) :512-+
[10]   Alteration of the intravenous pharmacokinetics of a synthetic ozonide antimalarial in the presence of a modified cyclodextrin [J].
Charman, SA ;
Perry, CS ;
Chiu, FCK ;
McIntosh, KA ;
Prankerd, RJ ;
Charman, WN .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (02) :256-267