Micellar formulations for drug delivery based on mixtures of hydrophobic and hydrophilic Pluronic® block copolymers

被引:204
作者
Oh, KT [1 ]
Bronich, TK [1 ]
Kabanov, AV [1 ]
机构
[1] Univ Nebraska, Med Ctr, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE 68198 USA
关键词
block copolymer; drug delivery; pluronic((R)); poloxamer; solubilization;
D O I
10.1016/j.jconrel.2003.10.018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Micelles formed by Pluronic(R) block copolymers (PBC) have been studied in multiple applications as drug delivery systems. Hydrophobic PBC form lamellar aggregates with a higher solubilization capacity than spherical micelles formed by hydrophilic PBC. However, they also have a larger size and low stability. To overcome these limitations, binary mixtures from hydrophobic PBC (L121, L101, L81, and L61) and hydrophilic PBC (F127, P105, F87, P85, and F68) were prepared. In most cases, PBC mixtures were not stable, revealing formation of large aggregates and phase separation within 1-2 day(s). However, stable aqueous dispersions of the particles were obtained upon (1) sonication of the PBC mixtures for 1 or 2 min or (2) heating at 70 degreesC for 30 min. Among all combinations, L121/F127 mixtures (1:1% weight ratio) formed stable dispersions with a small particle size. The solubilizing capacity of this system was examined using a model water-insoluble dye, Sudan (III). Mixed L121/F127 aggregates exhibited approximately 10-fold higher solubilization capacity compared to that of F127 micelles. In conclusion, stable aqueous dispersions of nanoscale size were prepared from mixtures of hydrophobic and hydrophilic PBC by using the external input of energy. The prepared mixed aggregates can efficiently incorporate hydrophobic compounds. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:411 / 422
页数:12
相关论文
共 21 条
[1]  
Alakhov V Y, 1998, Expert Opin Investig Drugs, V7, P1453, DOI 10.1517/13543784.7.9.1453
[2]   Differential scanning calorimetry investigation of the effect of salts on aqueous solution properties of an amphiphilic block copolymer (Poloxamer) [J].
Alexandridis, P ;
Holzwarth, JF .
LANGMUIR, 1997, 13 (23) :6074-6082
[3]   MICELLIZATION OF POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) TRIBLOCK COPOLYMERS IN AQUEOUS-SOLUTIONS - THERMODYNAMICS OF COPOLYMER ASSOCIATION [J].
ALEXANDRIDIS, P ;
HOLZWARTH, JF ;
HATTON, TA .
MACROMOLECULES, 1994, 27 (09) :2414-2425
[4]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[5]   SCANNING DENSITOMETRIC AND CALORIMETRIC STUDIES OF POLY(ETHYLENE OXIDE) POLY(PROPYLENE OXIDE) POLY(ETHYLENE OXIDE) TRIBLOCK COPOLYMERS (POLOXAMERS) IN DILUTE AQUEOUS-SOLUTION [J].
ARMSTRONG, JK ;
PARSONAGE, J ;
CHOWDHRY, B ;
LEHARNE, S ;
MITCHELL, J ;
BEEZER, A ;
LOHNER, K ;
LAGGNER, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (15) :3904-3909
[6]   Fundamental relationships between the composition of Pluronic block copolymers and their hypersensitization effect in MDR cancer cells [J].
Batrakova, E ;
Lee, S ;
Li, S ;
Venne, A ;
Alakhov, V ;
Kabanov, A .
PHARMACEUTICAL RESEARCH, 1999, 16 (09) :1373-1379
[7]  
Hamley I., 1998, The Physics of Block Copolymers Oxford University Press
[8]   MICELLE FORMATION AND SOLUBILIZATION OF FLUORESCENT-PROBES IN POLY(OXYETHYLENE-B-OXYPROPYLENE-B-OXYETHYLENE) SOLUTIONS [J].
KABANOV, AV ;
NAZAROVA, IR ;
ASTAFIEVA, IV ;
BATRAKOVA, EV ;
ALAKHOV, VY ;
YAROSLAVOV, AA ;
KABANOV, VA .
MACROMOLECULES, 1995, 28 (07) :2303-2314
[9]   Pluronic® block copolymers in drug delivery:: From micellar nanocontainers to biological response modifiers [J].
Kabanov, AV ;
Alakhov, VY .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2002, 19 (01) :1-72
[10]  
KATAOKA K, 1999, SPECIAL ISSUE POLYM