Interactions of phospholipid- and poly(ethylene glycol)-modified surfaces with biological systems: relation to physico-chemical properties and mechanisms

被引:196
作者
Vermette, P [1 ]
Meagher, L
机构
[1] Univ Sherbrooke, Dept Chem Engn, Intelligent Mat & Syst Inst, Sherbrooke, PQ J1K 2R1, Canada
[2] CSIRO Mol Sci, Clayton, Vic 3169, Australia
[3] Univ New S Wales, Cooperat Res Ctr Eye Res & Technol, Sydney, NSW 2052, Australia
关键词
interactions; poly(ethylene glycol); biological systerns; phospholipids; mechanisms;
D O I
10.1016/S0927-7765(02)00160-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This paper critically reviews reports on the interactions of phospholipids and poly(ethylene glycol) (PEG)-also called poly(ethylene oxide) (PEO)-with biological systems (model polypeptides, proteins. macrophages. etc). The review arises from the need to rationalize the widely varying Findings reported in the literature. The paper discusses the interaction of simple polypeptides with phospholipids. followed by the interaction of proteins with supported phospholipid layers and liposomes. In addition, the interactions of liposomes with more complex biological systems, in vitro and in vivo, are discussed. Since many proposed liposome formulations contain grafted PEG molecules, a discussion of the interactions of PEG molecules and PEG surface layers with proteins is also provided as well as a substantial section dealing with the mechanistic aspects of these interactions, As well as providing an introduction to the multidisciplinary and complex literature available, we hope that this review article will provide the necessary information for more rational design of systems and devices for in vivo application. In particular. the article stresses the need for much better characterization of the systems and materials used. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 198
页数:46
相关论文
共 317 条
[1]  
Absolom D R, 1986, Methods Enzymol, V132, P281
[2]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3578
[3]   STABLE BIOMEMBRANE SURFACES FORMED BY PHOSPHOLIPID POLYMERS [J].
ALBRECHT, O ;
JOHNSTON, DS ;
VILLAVERDE, C ;
CHAPMAN, D .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 687 (02) :165-169
[4]   ADSORPTION OF CHAIN MOLECULES WITH A POLAR HEAD A-SCALING DESCRIPTION [J].
ALEXANDER, S .
JOURNAL DE PHYSIQUE, 1977, 38 (08) :983-987
[5]   POLYMER ADSORPTION ON SMALL SPHERES - SCALING APPROACH [J].
ALEXANDER, S .
JOURNAL DE PHYSIQUE, 1977, 38 (08) :977-981
[6]   In situ observation of streptavidin-biotin binding on an immunoassay well surface using an atomic force microscope [J].
Allen, S ;
Davies, J ;
Dawkes, AC ;
Davies, MC ;
Edwards, JC ;
Parker, MC ;
Roberts, CJ ;
Sefton, J ;
Tendler, SJB ;
Williams, PM .
FEBS LETTERS, 1996, 390 (02) :161-164
[7]  
Allen T.M., 1989, United States Patent, Patent No. [4,837,028, 4837028]
[8]   LIPOSOMES WITH PROLONGED CIRCULATION TIMES - FACTORS AFFECTING UPTAKE BY RETICULOENDOTHELIAL AND OTHER TISSUES [J].
ALLEN, TM ;
HANSEN, C ;
RUTLEDGE, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 981 (01) :27-35
[9]   Liposomal drug delivery [J].
Allen, TM .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1996, 1 (05) :645-651
[10]   LARGE UNILAMELLAR LIPOSOMES WITH LOW UPTAKE INTO THE RETICULOENDOTHELIAL SYSTEM [J].
ALLEN, TM ;
CHONN, A .
FEBS LETTERS, 1987, 223 (01) :42-46