Polymeric micelles for nano-scale drug delivery

被引:374
作者
Miyata, Kanjiro [1 ]
Christie, R. James [2 ]
Kataoka, Kazunori [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Med, Ctr Dis Biol & Integrat Med, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Mat Engn, Bunkyo Ku, Tokyo 1138656, Japan
关键词
Drug delivery; Polymeric micelle; Poly(ethylene glycol); Block copolymer; Polyion complex; BLOCK-COPOLYMER MICELLES; POLYION COMPLEX MICELLES; RESONANCE ENERGY-TRANSFER; EFFICIENT GENE-TRANSFER; IN-VIVO; POLYPLEX MICELLES; PLASMID DNA; POLY(BETA-BENZYL L-ASPARTATE); SENSITIVE STABILIZATION; AQUEOUS-MEDIUM;
D O I
10.1016/j.reactfunctpolym.2010.10.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This review describes the design of polymeric micelles from block copolymers and their performances as nano-scale drug delivery systems, with emphasis on our recent work. The basic drug delivery system platform developed by our group consists of polymeric micelles comprising a core-shell structure with a versatile drug-loading hydrophobic core and biocompatible hydrophilic shell, and are several tens to one hundred nanometer in size. These characteristics are preferable to bypass both renal clearance and entrapment by the reticuloendothelial system, thus allowing subsequent accumulation within tumor tissues by the enhanced permeability and retention effect. Furthermore, polymeric micelles may be designed for enhanced biological performance by modification of the block copolymers to contain chemistries that can sense a specific biological environment. These "smart" micelles allow for target site-triggered drug release by reversible stabilization of the micelle structure and controlled intracellular trafficking (efficient endosomal release). Smart micelles designed with responsive features have demonstrated the utility in many cases compared to controls lacking such functionality. Additionally, the ability to control the size of polymeric micelles in the range of several tens to hundreds of nanometer significantly affects their longevity in the blood stream and efficiency of tumor tissue accumulation and penetration. In hypovascular tumor tissues, smaller polymeric micelles are more effective for tissue accumulation/penetration, bringing about stronger anti-tumor activity. All together, fine-tuning the structure of block copolymers enables preparation of polymeric micelles with versatile functions for treatment of many diseases including intractable cancer. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:227 / 234
页数:8
相关论文
共 92 条
[1]   Biocompatible micellar nanovectors achieve efficient gene transfer to vascular lesions without cytotoxicity and thrombus formation [J].
Akagi, D. ;
Oba, M. ;
Koyama, H. ;
Nishiyama, N. ;
Fukushima, S. ;
Miyata, T. ;
Nagawa, H. ;
Kataoka, K. .
GENE THERAPY, 2007, 14 (13) :1029-1038
[2]   Exploring polyethylenimine-mediated DNA transfection and the proton sponge hypothesis [J].
Akinc, A ;
Thomas, M ;
Klibanov, AM ;
Langer, R .
JOURNAL OF GENE MEDICINE, 2005, 7 (05) :657-663
[3]   Spontaneous Formation of Nanosized Unilamellar Polyion Complex Vesicles with Tunable Size and Properties [J].
Anraku, Yasutaka ;
Kishimura, Akihiro ;
Oba, Makoto ;
Yamasaki, Yuichi ;
Kataoka, Kazunori .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (05) :1631-1636
[4]  
Armstrong A, 2006, J CLIN ONCOL, V24, p198S
[5]   Design of aminated poly(1-vinylimidazole) for a new pH-Sensitive polycation to enhance cell-specific gene delivery [J].
Asayama, Shoichiro ;
Sekine, Takashi ;
Kawakami, Hiroyoshi ;
Nagaoka, Shoji .
BIOCONJUGATE CHEMISTRY, 2007, 18 (05) :1662-1667
[6]   CRITICAL MICELLIZATION PHENOMENA IN BLOCK POLYELECTROLYTE SOLUTIONS [J].
ASTAFIEVA, I ;
ZHONG, XF ;
EISENBERG, A .
MACROMOLECULES, 1993, 26 (26) :7339-7352
[7]   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
[8]   Intelligent polymeric micelles from functional poly(ethylene glycol)-poly(amino acid) block copolymers [J].
Bae, Younsoo ;
Kataoka, Kazunori .
ADVANCED DRUG DELIVERY REVIEWS, 2009, 61 (10) :768-784
[9]   The transport of nanosized gene carriers unraveled by live-cell imaging [J].
Bausinger, R ;
von Gersdorff, K ;
Braeckmans, K ;
Ogris, M ;
Wagner, E ;
Bräuchle, C ;
Zumbusch, A .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (10) :1568-1572
[10]   Intracellular route and transcriptional competence of polyethylenimine-DNA complexes [J].
Bieber, T ;
Meissner, W ;
Kostin, S ;
Niemann, A ;
Elsasser, HP .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (2-3) :441-454