DISTINCTION BETWEEN THE DEPLETION OF OPSONINS AND THE SATURATION OF UPTAKE IN THE DOSE-DEPENDENT HEPATIC-UPTAKE OF LIPOSOMES

被引:31
作者
HARASHIMA, H
SAKATA, K
KIWADA, H
机构
[1] Faculty of Pharmaceutical Sciences, The University of Tokush-Ima, Tokushima City, Tokushima, 770
关键词
OPSONINS; HEPATIC UPTAKE; LIPOSOMES; SATURATION;
D O I
10.1023/A:1018918623658
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Opsonins play a role in the hepatic uptake of particles such as bacteria, lipid emulsion, and liposomes. The objective of this study was to distinguish between opsonin depletion and uptake saturation in the dose-dependent hepatic uptake of liposomes. The uptake of opsonized and unopsonized liposomes was determined in the isolated perfused liver. Serum (2.9 mL) was required to opsonize 1 mumol liposomes fully, indicating that a rat (250 g with 10 mL of serum) can opsonize 3.5 mumol liposomes. Next the dose effect on hepatic uptake of opsonized and unopsonized liposomes was examined. Saturation of uptake was found only for the opsonized liposomes. On the other hand, the hepatic uptake clearance decreased dose dependently from 4.31 to 0.79 (mL/min), with increasing doses from 0.075 to 17 mumol/250 g, respectively, after i.v. administration. Thus, the decrease in the hepatic uptake clearance at the medium dose was due to the saturation of uptake alone, and at the high dose it was due to opsonin depletion as well. These results show that the saturation of liposomal uptake in the liver and the depletion of opsonins occurred at different liposome dosage levels.
引用
收藏
页码:606 / 610
页数:5
相关论文
共 30 条
[1]   LIPOSOME DISPOSITION INVIVO .3. DOSE AND VESICLE-SIZE EFFECTS [J].
ABRA, RM ;
HUNT, CA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 666 (03) :493-503
[2]  
ALLEN TM, 1983, J PHARMACOL EXP THER, V226, P539
[3]   EFFECTS OF LIPOSOME SIZE ON THE DEGRADATION OF BOVINE BRAIN SPHINGOMYELIN CHOLESTEROL LIPOSOMES IN THE MOUSE-LIVER [J].
BEAUMIER, PL ;
HWANG, KJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 731 (01) :23-30
[4]  
BEAUMIER PL, 1983, RES COMMUN CHEM PATH, V39, P277
[5]  
BECKER S, 1988, Advanced Drug Delivery Reviews, V2, P1, DOI 10.1016/0169-409X(88)90003-8
[6]   LIPOSOME DISPOSITION INVIVO .2. DOSE DEPENDENCY [J].
BOSWORTH, ME ;
HUNT, CA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1982, 71 (01) :100-104
[7]  
CHOW DD, 1989, J PHARMACOL EXP THER, V248, P506
[8]   TRANSPORT AND BINDING OF METHOTREXATE IN-VIVO [J].
DEDRICK, RL ;
ZAHARKO, DS ;
LUTZ, RJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1973, 62 (06) :882-890
[9]   CONTRIBUTION OF COMPLEMENT-SYSTEM ON DESTABILIZATION OF LIPOSOMES COMPOSED OF HYDROGENATED EGG PHOSPHATIDYLCHOLINE IN RAT FRESH PLASMA [J].
FUNATO, K ;
YODA, R ;
KIWADA, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1103 (02) :198-204
[10]   LIPOSOME FORMULATIONS WITH PROLONGED CIRCULATION TIME IN BLOOD AND ENHANCED UPTAKE BY TUMORS [J].
GABIZON, A ;
PAPAHADJOPOULOS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6949-6953