AMPHIPATHIC POLY(ETHYLENE GLYCOL) 5000-STABILIZED DIOLEOYLPHOSPHATIDYLETHANOLAMINE LIPOSOMES ACCUMULATE IN SPLEEN

被引:57
作者
LITZINGER, DC
HUANG, L
机构
[1] UNIV PITTSBURGH,SCH MED,DEPT PHARMACOL,PITTSBURGH,PA 15261
[2] UNIV TENNESSEE,DEPT BIOCHEM,KNOXVILLE,TN 37996
关键词
POLY(ETHYLENE GLYCOL); PHOSPHATIDYLETHANOLAMINE; LIPOSOME; SPLEEN; DRUG DELIVERY;
D O I
10.1016/0005-2760(92)90228-N
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Relatively small liposomes (d < 200 nm) composed of dioleoylphosphatidylethanolamine (DOPE) and cholesterol (Chol) and containing dioleoyl-N-(monomethoxypoly(ethylene glycol)succinyl)phosphatidylethanolamine (PEG-PE), with PEG of M(r) 5000 (PEG5000-PE), accumulate in the spleen (approximately 40% i.v. injected dose), unlike dioleoylphosphatidylcholine (DOPC)/Chol/PEG5000-PE liposomes of similar size, which show prolonged circulation in the blood. Spleen accumulation was dependent on the injection dose, PEG-PE concentration, and the PEG chain length. The DOPE/Chol/ PEG5000-PE liposomes are plasma stable and morphologically indistinguishable from DOPC/Chol/PEG5000-PE liposomes. These results reveal the significance of the matrix lipid in determining the circulation time of PEG-PE-containing liposomes, and are relevant to the design of liposomes which avoid or accumulate in the spleen.
引用
收藏
页码:249 / 254
页数:6
相关论文
共 22 条
  • [1] LIPOSOMES CONTAINING SYNTHETIC LIPID DERIVATIVES OF POLY(ETHYLENE GLYCOL) SHOW PROLONGED CIRCULATION HALF-LIVES INVIVO
    ALLEN, TM
    HANSEN, C
    MARTIN, F
    REDEMANN, C
    YAUYOUNG, A
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1066 (01) : 29 - 36
  • [2] LIPOSOMES FOR THE SUSTAINED DRUG RELEASE INVIVO
    BLUME, G
    CEVC, G
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1029 (01) : 91 - 97
  • [3] LIPID POLYMORPHISM AND THE FUNCTIONAL ROLES OF LIPIDS IN BIOLOGICAL-MEMBRANES
    CULLIS, PR
    DEKRUIJFF, B
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 559 (04) : 399 - 420
  • [4] HIGHLY EFFICIENT IMMUNOLIPOSOMES PREPARED WITH A METHOD WHICH IS COMPATIBLE WITH VARIOUS LIPID COMPOSITIONS
    HOLMBERG, E
    MARUYAMA, K
    LITZINGER, DC
    WRIGHT, S
    DAVIS, M
    KABALKA, GW
    KENNEL, SJ
    HUANG, L
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (03) : 1272 - 1278
  • [5] GADOLINIUM-LABELED LIPOSOMES - TARGETED MR CONTRAST AGENTS FOR THE LIVER AND SPLEEN
    KABALKA, G
    BUONOCORE, E
    HUBNER, K
    MOSS, T
    NORLEY, N
    HUANG, L
    [J]. RADIOLOGY, 1987, 163 (01) : 255 - 258
  • [6] GADOLINIUM-LABELED LIPOSOMES CONTAINING VARIOUS AMPHIPHILIC GD-DTPA DERIVATIVES - TARGETED MRI CONTRAST ENHANCEMENT AGENTS FOR THE LIVER
    KABALKA, GW
    DAVIS, MA
    MOSS, TH
    BUONOCORE, E
    HUBNER, K
    HOLMBERG, E
    MARUYAMA, K
    HUANG, L
    [J]. MAGNETIC RESONANCE IN MEDICINE, 1991, 19 (02) : 406 - 415
  • [7] ACTIVITY OF AMPHIPATHIC POLY(ETHYLENE GLYCOL)-5000 TO PROLONG THE CIRCULATION TIME OF LIPOSOMES DEPENDS ON THE LIPOSOME SIZE AND IS UNFAVORABLE FOR IMMUNOLIPOSOME BINDING TO TARGET
    KLIBANOV, AL
    MARUYAMA, K
    BECKERLEG, AM
    TORCHILIN, VP
    HUANG, L
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1062 (02) : 142 - 148
  • [8] AMPHIPATHIC POLYETHYLENEGLYCOLS EFFECTIVELY PROLONG THE CIRCULATION TIME OF LIPOSOMES
    KLIBANOV, AL
    MARUYAMA, K
    TORCHILIN, VP
    HUANG, L
    [J]. FEBS LETTERS, 1990, 268 (01) : 235 - 237
  • [9] LIS LJ, 1982, BIOPHYS J, V37, P657
  • [10] BIODISTRIBUTION AND IMMUNOTARGETABILITY OF GANGLIOSIDE-STABILIZED DIOLEOYLPHOSPHATIDYLETHANOLAMINE LIPOSOMES
    LITZINGER, DC
    HUANG, L
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1104 (01) : 179 - 187