Effect of composition on biological fate of oil particles after intravenous injection of O/W lipid emulsions

被引:19
作者
Sakaeda, T [1 ]
Hirano, K [1 ]
机构
[1] Shionogi & Co Ltd, Shionogi Res Labs, Fukushima Ku, Osaka 5530002, Japan
关键词
O/W lipid emulsions; drug delivery system; oil particles size; RES avoidance;
D O I
10.3109/10611869808996835
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Plasma concentrations of oil particles after intravenous injection of oil-in-water (O/W) lipid emulsions were monitored based on the plasma concentration of phospholipids (PL) and triglycerides (TG), and the light scattering intensity (LSI) of plasma. Previously, we found that their time profiles after injection of the standard O/W lipid emulsion composed of soybean oil (SO) and egg yolk phosphatides (EYP) were similar and suggested that the oil particles with diameter of about 200 nm were entrapped by reticuloendothelial system (RES). Herein, in order to develop a delivery system to avoid the RES uptake by using the lipid emulsions, biological fate of lipid emulsions with oil particles of various sizes or those emulsified by surfactants with polyoxyethylene segments were subjected to the investigations. Lipid emulsions with oil particles of various sizes (about 150-550 nm) were prepared by altering EYP content. The oil particles were stable in plasma in vitro, but oil particle size decreased time-dependently after intravenous injection. Plasma clearance of oil particles depended on their initial size and nias decreased by pretreatment with dextran sulfate 500 (DS500), a known RES suppressor, These results suggested that oil particles are still entrapped by RES, even for small-sized oil particles (about 150 nm). Lipid emulsion with small-sized oil particles was also prepared using medium chain triglycerides. The oil particles were stable in vitro, but the time profiles of plasma concentrations of PL and TG, and LSI of plasma were different, and oil particle size decreased time-dependently after intravenous injection. Plasma clearance of the oil particles also depended on their initial size and was decreased by DS500, suggesting that in vivo instability could be due to RES-mediated processes. Artificial surfactants with polyoxyethylene segments, HCO-60 (HCO60) and polysorbate 80 (PS80), were used for RES avoidance. HCO60 resulted in drastic reduction of the plasma clearance of the oil particles for both lipid emulsions composed of soybean oil and medium chain triglycerides. The lime-dependent decrease of oil particle size after intravenous injection was marginal. In contrast, PS80 could not prolong the circulation time of the oil particles, and their size decreased time-dependently after intravenous injection.
引用
收藏
页码:273 / 284
页数:12
相关论文
共 31 条
[1]  
COLLINS-GOLD L C, 1990, Advanced Drug Delivery Reviews, V5, P189, DOI 10.1016/0169-409X(90)90016-L
[2]   LIPID EMULSIONS AS DRUG DELIVERY SYSTEMS [J].
DAVIS, SS ;
WASHINGTON, C ;
WEST, P ;
ILLUM, L ;
LIVERSIDGE, G ;
STERNSON, L ;
KIRSH, R .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 507 :75-88
[3]   MICROSPHERES FOR TARGETING DRUGS TO SPECIFIC BODY SITES [J].
DAVIS, SS ;
ILLUM, L ;
MOGHIMI, SM ;
DAVIES, MC ;
PORTER, CJH ;
MUIR, IS ;
BRINDLEY, A ;
CHRISTY, NM ;
NORMAN, ME ;
WILLIAMS, P ;
DUNN, SE .
JOURNAL OF CONTROLLED RELEASE, 1993, 24 (1-3) :157-163
[4]  
DAVIS SS, 1985, ENCY EMULSION TECHNO, V2, P159
[5]   AROMATIC SUBSTITUENT CONSTANTS FOR STRUCTURE-ACTIVITY CORRELATIONS [J].
HANSCH, C ;
LEO, A ;
UNGER, SH ;
KIM, KH ;
NIKAITANI, D ;
LIEN, EJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1973, 16 (11) :1207-1216
[6]  
IGARASHI R, 1988, JPN J INFLAMM, V8, P243
[7]   THE EFFECT OF STABILIZING AGENTS ON THE ORGAN DISTRIBUTION OF LIPID EMULSIONS [J].
ILLUM, L ;
WEST, P ;
WASHINGTON, C ;
DAVIS, SS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 54 (01) :41-49
[8]   The metabolic distinctiveness of emulsified lipid particles in the bloodstream and its clinical implications [J].
Iriyama, K .
SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY, 1996, 26 (09) :673-678
[9]   CALCULATION OF HYDROPHOBIC CONSTANT (LOG P) FROM PI AND F CONSTANTS [J].
LEO, A ;
JOW, PYC ;
SILIPO, C ;
HANSCH, C .
JOURNAL OF MEDICINAL CHEMISTRY, 1975, 18 (09) :865-868
[10]   DESIGN OF NEW FORMULATIONS FOR TOPICAL OCULAR ADMINISTRATION - POLYMERIC NANOCAPSULES CONTAINING METIPRANOLOL [J].
LOSA, C ;
MARCHALHEUSSLER, L ;
ORALLO, F ;
JATO, JLV ;
ALONSO, MJ .
PHARMACEUTICAL RESEARCH, 1993, 10 (01) :80-87