Physicochemical characterization of a synthetic lipid emulsion for hepatocyte-selective delivery of lipophilic compounds: Application to polyiodinated triglycerides as contrast agents for computed tomography

被引:25
作者
Bakan, DA [1 ]
Longino, MA [1 ]
Weichert, JP [1 ]
Counsell, RE [1 ]
机构
[1] UNIV MICHIGAN,DEPT RADIOL,ANN ARBOR,MI 48109
关键词
D O I
10.1021/js960119z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A synthetic lipid emulsion (LE) has been developed with physicochemical properties that closely resemble those of a specific class of naturally-occurring lipoproteins known as chylomicron remnants. The formulation has the potential to serve as a hepatocyte-selective delivery system for any lipophilic or amphipathic compounds that can be associated with the internal lipid phase of the emulsion. In the present studies, a lipophilic polyiodinated triglyceride (ITG) was successfully incorporated into the delivery vehicle to form a stable chylomicron-remnant-like emulsion capable of localizing material to the liver following intravenous injection. The preferred ITG-LE formulation was shown to have a mean particle diameter of less than 200 nm and a particle size stability profile in excess of 12 months. The viscosity, pH, and osmolality of the formulation also appeared favorable for safe and convenient intravenous injection. The particle size profile, chemical properties, and high degree of incorporation of ITG into the emulsion suggest that the ITG-LE formulation holds substantial promise as a hepatocyte-selective imaging agent for computed tomography of the liver. Biodistribution, elimination, and computed tomography (CT) imaging results in animals corroborated the hepatocyte-selective nature of the ITG-LE formulation.
引用
收藏
页码:908 / 914
页数:7
相关论文
共 44 条
[1]   INTRALIPID INFUSION ABOLISHES ABILITY OF HUMAN-SERUM TO CHOLESTEROL-LOAD CULTURED MACROPHAGES [J].
AVIRAM, M ;
WILLIAMS, KJ ;
MCINTOSH, RA ;
CARPENTIER, YA ;
TALL, AR ;
DECKELBAUM, RJ .
ARTERIOSCLEROSIS, 1989, 9 (01) :67-75
[2]  
COOPER AD, 1978, J LIPID RES, V19, P635
[3]   LIPOPROTEINS AS POTENTIAL SITE-SPECIFIC DELIVERY SYSTEMS FOR DIAGNOSTIC AND THERAPEUTIC AGENTS [J].
COUNSELL, RE ;
POHLAND, RC .
JOURNAL OF MEDICINAL CHEMISTRY, 1982, 25 (10) :1115-1120
[4]  
DAWES CJ, 1988, INTRO BIOL ELECT MIC, P224
[5]  
DESMIDT PC, 1990, CRIT REV THER DRUG, V7, P99
[6]   ELECTRON MICROSCOPY OF HUMAN SERUM LIPOPROTEINS USING NEGATIVE STAINING [J].
FORTE, GM ;
NICHOLS, AV ;
GLAESER, RM .
CHEMISTRY AND PHYSICS OF LIPIDS, 1968, 2 (04) :396-&
[7]  
HAMILTON RL, 1980, J LIPID RES, V21, P981
[8]   INTERCHANGE OF APOLIPOPROTEINS BETWEEN CHYLOMICRONS AND HIGH-DENSITY LIPOPROTEINS DURING ALIMENTARY LIPEMIA IN MAN [J].
HAVEL, RJ ;
KANE, JP ;
KASHYAP, ML .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (01) :32-38
[9]   THE RIPPLE PHASE OF PHOSPHATIDYLCHOLINES - EFFECT OF CHAIN-LENGTH AND CHOLESTEROL [J].
HICKS, A ;
DINDA, M ;
SINGER, MA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 903 (01) :177-185
[10]  
IVANCEV K, 1989, ACTA RADIOL, V30, P291