BIODISTRIBUTION AND CLEARANCE OF LIPOSOMAL GADOLINIUM-DTPA

被引:37
作者
UNGER, E [1 ]
CARDENAS, D [1 ]
ZERELLA, A [1 ]
FAJARDO, LL [1 ]
TILCOCK, C [1 ]
机构
[1] UNIV BRITISH COLUMBIA,DEPT BIOCHEM,VANCOUVER V6T 1W5,BC,CANADA
关键词
Biodistribution; Clearance; Gadolinium-DTPA; Liposomes;
D O I
10.1097/00004424-199006000-00004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Gadolinium-DTPA (Gd-DTPA) liposomes have been studied previously as liver contrast agents and have been shown to improve the detection of hepatic metastases in rats. We synthesized 100-nm and 50-nm liposomes that encapsulated Gd-DTPA and did biodistribution and clearance studies in rats. Parallel magnetic resonance imaging (MRI) studies were also done. Biodistribution showed a prolonged blood pool phase for Gd-DTPA liposomes with a blood pool half-life of approximately 4 hours for the 100-nm liposomes. The highest uptake per gram of tissue was achieved by the spleen. Clearance of gadolinium from the liver and spleen showed a half-life of 3 to 4 days. The smaller 50-nm Gd-DTPA liposomes resulted in a longer blood pool phase and a higher delivery of gadolinium to the liver, bone marrow, and spleen. Imaging studies after intravenous (IV) administration of liposomal Gd-DTPA showed organ enhancement that paralleled the data on biodistribution studies, with appreciable hepatic enhancement at doses as low as 0.025 mm/kg of liposomal Gd-DTPA. © Lippincott-Raven Publishers.
引用
收藏
页码:638 / 644
页数:7
相关论文
共 13 条
[1]   CONTRAST-ENHANCED NMR IMAGING - ANIMAL STUDIES USING GADOLINIUM-DTPA COMPLEX [J].
BRASCH, RC ;
WEINMANN, HJ ;
WESBEY, GE .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1984, 142 (03) :625-630
[2]   GADOLINIUM-DTPA IN THE ASSESSMENT OF LIVER-TUMORS BY MAGNETIC-RESONANCE-IMAGING [J].
CARR, DH ;
GRAIF, M ;
NIENDORF, HP ;
BROWN, J ;
STEINER, RE ;
BLUMGART, LH ;
YOUNG, IR .
CLINICAL RADIOLOGY, 1986, 37 (04) :347-353
[3]   PHARMACOLOGY AND TOXICOLOGY OF RARE EARTH ELEMENTS [J].
HALEY, TJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1965, 54 (05) :663-+
[4]   GENERATION OF MULTILAMELLAR AND UNILAMELLAR PHOSPHOLIPID-VESICLES [J].
HOPE, MJ ;
BALLY, MB ;
MAYER, LD ;
JANOFF, AS ;
CULLIS, PR .
CHEMISTRY AND PHYSICS OF LIPIDS, 1986, 40 (2-4) :89-107
[5]   EFFECT OF PARTICLE-SIZE AND CHARGE ON CLEARANCE RATES OF LIPOSOMES AND LIPOSOME ENCAPSULATED DRUGS [J].
JULIANO, RL ;
STAMP, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 63 (03) :651-658
[6]  
KOHN DF, 1984, LABORATORY ANIMAL ME, P95
[7]   TECHNIQUES FOR ENCAPSULATING BIOACTIVE AGENTS INTO LIPOSOMES [J].
MAYER, LD ;
BALLY, MB ;
HOPE, MJ ;
CULLIS, PR .
CHEMISTRY AND PHYSICS OF LIPIDS, 1986, 40 (2-4) :333-345
[8]   VESICLES OF VARIABLE SIZES PRODUCED BY A RAPID EXTRUSION PROCEDURE [J].
MAYER, LD ;
HOPE, MJ ;
CULLIS, PR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 858 (01) :161-168
[9]   LIPOSOMAL GD-DTPA - PREPARATION AND CHARACTERIZATION OF RELAXIVITY [J].
TILCOCK, C ;
UNGER, E ;
CULLIS, P ;
MACDOUGALL, P .
RADIOLOGY, 1989, 171 (01) :77-80
[10]  
TILCOCK C, UNPUB BIOCH BIOPHYS