Micelles from lipid derivatives of water-soluble polymers as delivery systems for poorly soluble drugs

被引:538
作者
Lukyanov, AN [1 ]
Torchilin, VP [1 ]
机构
[1] Northeastern Univ, Bouve Coll Hlth Sci, Sch Pharm, Dept Pharmaceut Sci, Boston, MA 02115 USA
关键词
amphiphilic polymers; polymer-lipid conjugates; micelles; poorly soluble drugs; anticancer drugs; solubilization; enhanced permeability and retention effect; anticancer antibody; immunomicelles; tumor drug-delivery;
D O I
10.1016/j.addr.2003.12.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polymeric micelles have a whole set of unique characteristics, which make them very promising drug carriers, in particular, for poorly soluble drugs. Our review article focuses on micelles prepared from conjugates of water-soluble polymers, such as polyethylene glycol (PEG) or polyvinyl pyrrolidone (PVP), with phospholipids or long-chain fatty acids. The preparation of micelles from certain polymer-lipid conjugates and the loading of these micelles with various poorly soluble anticancer agents are discussed. The data on the characterization of micellar preparations in terms of their morphology, stability, longevity in circulation, and ability to spontaneously accumulate in experimental tumors via the enhanced permeability and retention (EPR) effect are presented. The review also considers the preparation of targeted immunomicelles with specific antibodies attached to their surface. Available in vivo results on the efficiency of anticancer drugs incorporated into plain micelles and immunomicelles in animal models are also discussed. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1273 / 1289
页数:17
相关论文
共 85 条
[61]  
SHABNER BA, 1990, CANC CHEMOTHERAPY PR
[62]  
Sharma D, 1996, ONCOL RES, V8, P281
[63]   CRITICAL MICELLE CONCENTRATION OF L-ALPHA-DIPALMITOYLPHOSPHATIDYLCHOLINE IN WATER AND WATER/METHANOL SOLUTIONS [J].
SMITH, R ;
TANFORD, C .
JOURNAL OF MOLECULAR BIOLOGY, 1972, 67 (01) :75-&
[64]  
TANNOCK IF, 1989, CANCER RES, V49, P4373
[65]  
Teicher B.A., 1997, ANTICANCER DRUG DELI
[66]  
THOMPSON D, 2000, DRUG DELIV TECHNOL, V2, P34
[67]   AMPHIPHILIC VINYL-POLYMERS EFFECTIVELY PROLONG LIPOSOME CIRCULATION TIME IN-VIVO [J].
TORCHILIN, VP ;
SHTILMAN, MI ;
TRUBETSKOY, VS ;
WHITEMAN, K ;
MILSTEIN, AM .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1195 (01) :181-184
[68]   TAT peptide on the surface of liposomes affords their efficient intracellular delivery even at low temperature and in the presence of metabolic inhibitors [J].
Torchilin, VP ;
Rammohan, R ;
Weissig, V ;
Levchenko, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8786-8791
[69]   Immunomicelles: Targeted pharmaceutical carriers for poorly soluble drugs [J].
Torchilin, VP ;
Lukyanov, AN ;
Gao, ZG ;
Papahadjopoulos-Sternberg, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :6039-6044
[70]   POLY(ETHYLENE GLYCOL) ON THE LIPOSOME SURFACE - ON THE MECHANISM OF POLYMER-COATED LIPOSOME LONGEVITY [J].
TORCHILIN, VP ;
OMELYANENKO, VG ;
PAPISOV, MI ;
BOGDANOV, AA ;
TRUBETSKOY, VS ;
HERRON, JN ;
GENTRY, CA .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1195 (01) :11-20