Supramolecular assemblies of block copolymers in aqueous media as nanocontainers relevant to biological applications

被引:365
作者
Harada, Atsushi
Kataoka, Kazunori
机构
[1] Univ Tokyo, Grad Sch Engn, Dept Mat Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Osaka Prefecture Univ, Dept Appl Chem, Grad Sch Engn, Naka Ku, Sakai, Osaka 5998531, Japan
关键词
block copolymer; self-assembly; polymeric micelle; polyion complex micelle; drug delivery system; non-viral gene vector;
D O I
10.1016/j.progpolymsci.2006.09.004
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Multimolecular assemblies of block copolymers have received considerable attention from both fundamental and applied standpoints. These assemblies are formed in selective solvents based on the different solubilities of constitutent segments; for example, hydrophilic and hydrophobic segments in an aqueous medium. Although the assemblies may assume various morphologies, including spherical, rod and lamellar structures, spherical micelles have been most extensively investigated. Polymeric micelles have a fairly narrow size distribution and are characterized by their unique core-corona structure. Their physicochemical properties have been extensively studied and higher-order controlled association has also been attained. This review highlights the recent progress in physicochemical characterization of the polymeric micelles and their applications as functional materials. Particular focus is placed on their applications in drug delivery systems, capillary electrophoresis and surface modification. Further, novel polymeric micelle formation through electrostatic interaction in aqueous medium is reviewed from the standpoint of their utility as bioreactors, diagnostic tools and non-viral gene vectors. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:949 / 982
页数:34
相关论文
共 148 条
[91]   Lipid fusion in oligonucleotide and gene delivery with cationic lipids [J].
Mönkkönen, J ;
Urtti, A .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 34 (01) :37-49
[92]   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
[93]   Structural studies of aqueous solutions of PEO-PPO-PEO triblock copolymers, their micellar aggregates and mesophases; A small-angle neutron scattering study [J].
Mortensen, K .
JOURNAL OF PHYSICS-CONDENSED MATTER, 1996, 8 (25A) :A103-A124
[94]   INVERSE MELTING TRANSITION AND EVIDENCE OF 3-DIMENSIONAL CUBATIC STRUCTURE IN A BLOCK-COPOLYMER MICELLAR SYSTEM [J].
MORTENSEN, K ;
BROWN, W ;
NORDEN, B .
PHYSICAL REVIEW LETTERS, 1992, 68 (15) :2340-2343
[95]   Sugar-installed block copolymer micelles: Their preparation and specific interaction with lectin molecules [J].
Nagasaki, Y ;
Yasugi, K ;
Yamamoto, Y ;
Harada, A ;
Kataoka, K .
BIOMACROMOLECULES, 2001, 2 (04) :1067-1070
[96]   PRIMARY AMINO-TERMINAL HETEROBIFUNCTIONAL POLY(ETHYLENE OXIDE) - FACILE SYNTHESIS OF POLY(ETHYLENE OXIDE) WITH A PRIMARY AMINO GROUP AT ONE END AND A HYDROXYL GROUP AT THE OTHER END [J].
NAGASAKI, Y ;
IIJIMA, M ;
KATO, M ;
KATAOKA, K .
BIOCONJUGATE CHEMISTRY, 1995, 6 (06) :702-704
[97]   FORMYL-ENDED HETEROBIFUNCTIONAL POLY(ETHYLENE OXIDE) - SYNTHESIS OF POLY(ETHYLENE OXIDE) WITH A FORMYL GROUP AT ONE END AND A HYDROXYL GROUP AT THE OTHER END [J].
NAGASAKI, Y ;
KUTSUNA, T ;
IIJIMA, M ;
KATO, M ;
KATAOKA, K ;
KITANO, S ;
KADOMA, Y .
BIOCONJUGATE CHEMISTRY, 1995, 6 (02) :231-233
[98]   The reactive polymeric micelle based on an aldehyde-ended poly(ethylene glycol)/poly(lactide) block copolymer [J].
Nagasaki, Y ;
Okada, T ;
Scholz, C ;
Iijima, M ;
Kato, M ;
Kataoka, K .
MACROMOLECULES, 1998, 31 (05) :1473-1479
[99]   Development of the polymer micelle carrier system for doxorubicin [J].
Nakanishi, T ;
Fukushima, S ;
Okamoto, K ;
Suzuki, M ;
Matsumura, Y ;
Yokoyama, M ;
Okano, T ;
Sakurai, Y ;
Kataoka, K .
JOURNAL OF CONTROLLED RELEASE, 2001, 74 (1-3) :295-302
[100]   Evaluation of polyether-polyethyleneimine graft copolymers as gene transfer agents [J].
Nguyen, HK ;
Lemieux, P ;
Vinogradov, SV ;
Gebhart, CL ;
Guérin, N ;
Paradis, G ;
Bronich, TK ;
Alakhov, VY ;
Kabanov, AV .
GENE THERAPY, 2000, 7 (02) :126-138