Effect of polyethyleneglycol-phospholipids on aggregate structure in preparations of small unilamellar liposomes

被引:172
作者
Edwards, K
Johnsson, M
Karlsson, G
Silvander, M
机构
[1] Department of Physical Chemistry, Uppsala University
[2] Department of Physical Chemistry, Uppsala University, Box 532
基金
瑞典研究理事会;
关键词
D O I
10.1016/S0006-3495(97)78066-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Phospholipids with covalently attached poly(ethylene glycol) (PEG lipids) are commonly used for the preparation of long circulating liposomes. Although it is well known that lipid/PEG-lipid mixed micelles may form above a certain critical concentration of PEG-lipid, little is known about the effects of PEG-lipids on liposome structure and leakage at submicellar concentrations. in this study we have used cryogenic transmission electron microscopy to investigate the effect of PEG(2000)-PE on aggregate structure in preparations of liposomes with different membrane compositions. The results reveal a number of important aggregate structures not documented before. The micrographs show that enclosure of PEG-PE induces the formation of open bilayer discs at concentrations well below those where mixed micelles begin to form. The maximum concentration of PEG-lipid that may be incorporated without alteration of the liposome structure depends on the phospholipid chain length, whereas phospholipid saturation or the presence of cholesterol has little or no effect. The presence of cholesterol does, however, affect the shape of the mixed micelles formed at high concentrations of PEG-lipid. Threadlike micelles form in the absence of cholesterol but adapt a globular shape when cholesterol is present.
引用
收藏
页码:258 / 266
页数:9
相关论文
共 29 条
  • [1] LARGE UNILAMELLAR LIPOSOMES WITH LOW UPTAKE INTO THE RETICULOENDOTHELIAL SYSTEM
    ALLEN, TM
    CHONN, A
    [J]. FEBS LETTERS, 1987, 223 (01) : 42 - 46
  • [2] Cryotransmission electron microscopy of thin vitrified samples
    Almgren, M
    Edwards, K
    Gustafsson, J
    [J]. CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1996, 1 (02) : 270 - 278
  • [3] INTERACTION OF PEG-PHOSPHOLIPID CONJUGATES WITH PHOSPHOLIPID - IMPLICATIONS IN LIPOSOMAL DRUG-DELIVERY
    BEDUADDO, FK
    HUANG, L
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) : 235 - 247
  • [4] CONTROLLED ENVIRONMENT VITRIFICATION SYSTEM - AN IMPROVED SAMPLE PREPARATION TECHNIQUE
    BELLARE, JR
    DAVIS, HT
    SCRIVEN, LE
    TALMON, Y
    [J]. JOURNAL OF ELECTRON MICROSCOPY TECHNIQUE, 1988, 10 (01): : 87 - 111
  • [5] RECENT ADVANCES IN LIPOSOMAL DRUG-DELIVERY SYSTEMS
    CHONN, A
    CULLIS, PR
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 1995, 6 (06) : 698 - 708
  • [6] COLLINS JJ, 1982, J LIPID RES, V23, P291
  • [7] CRYO-ELECTRON MICROSCOPY OF VITRIFIED SPECIMENS
    DUBOCHET, J
    ADRIAN, M
    CHANG, JJ
    HOMO, JC
    LEPAULT, J
    MCDOWALL, AW
    SCHULTZ, P
    [J]. QUARTERLY REVIEWS OF BIOPHYSICS, 1988, 21 (02) : 129 - 228
  • [8] EFFECTS OF TRITON X-100 ON SONICATED LECITHIN VESICLES
    EDWARDS, K
    ALMGREN, M
    BELLARE, J
    BROWN, W
    [J]. LANGMUIR, 1989, 5 (02) : 473 - 478
  • [9] SURFACTANT-INDUCED LEAKAGE AND STRUCTURAL-CHANGE OF LECITHIN VESICLES - EFFECT OF SURFACTANT HEADGROUP SIZE
    EDWARDS, K
    ALMGREN, M
    [J]. LANGMUIR, 1992, 8 (03) : 824 - 832
  • [10] SOLUBILIZATION OF LECITHIN VESICLES BY A CATIONIC SURFACTANT - INTERMEDIATE STRUCTURES IN THE VESICLE MICELLE TRANSITION OBSERVED BY CRYO-TRANSMISSION ELECTRON-MICROSCOPY
    EDWARDS, K
    GUSTAFSSON, J
    ALMGREN, M
    KARLSSON, G
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1993, 161 (02) : 299 - 309