Lipid emulsions as a novel system to reduce the hemolytic activity of lytic agents:: mechanism of the protective effect

被引:68
作者
Jumaa, M [1 ]
Müller, BW [1 ]
机构
[1] Univ Kiel, Dept Pharmaceut & Biopharmaceut, D-24118 Kiel, Germany
关键词
hemolytic activity; micellar solution; lipid emulsion; protective effect;
D O I
10.1016/S0928-0987(99)00071-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The hemolytic activity of sodium oleate, a high lyric agent, was investigated in different surfactant solutions and lipid emulsion formulations. A new explanation of the protective function of these systems is proposed. It was found that the hemolytic activity of the lytic agent was greatly decreased in solutions and/or dispersions with the surfactant Cremophor EL, Solutol H16 and phospholipids, which can usually build a micellar or liposomal structure. In the case of F68, where the micelle formation is still controversial, the hemolytic activity of the lytic agent was practically not affected and complete hemolysis was observed. In contrast to this, all emulsion formulations, independent of the emulsifier type, showed a stable erythrocyte behavior. Additionally, in the case of lipid emulsions only, a larger amount of the lyric agent could be added without any remarkable increase in the hemolytic activity. As an explanation for these effects it is proposed that the lytic agent is either incorporated into the lipophilic core or intercalates between the emulsifier molecules at the interface. This decreases the direct contact of the lytic agent with the erythrocyte membrane. As a result, the erythrocytes will effectively be protected from hemolytic damage, which can otherwise be induced by such substances. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
相关论文
共 33 条
[1]   Poly(ethylene oxide)-containing amphiphilic block copolymers in ternary mixtures with water and organic solvent: effect of copolymer and solvent type on phase behavior and structure [J].
Alexandridis, P ;
Holmqvist, P ;
Lindman, B .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1997, 129 :3-21
[2]   POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) BLOCK-COPOLYMER SURFACTANTS IN AQUEOUS-SOLUTIONS AND AT INTERFACES - THERMODYNAMICS, STRUCTURE, DYNAMICS, AND MODELING [J].
ALEXANDRIDIS, P ;
HATTON, TA .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1995, 96 (1-2) :1-46
[3]  
BAHADUR PS, 1981, TENSIDE SURFACT DET, V28, P173
[4]  
BOCK T, 1994, THESIS KIEL
[5]   A NOVEL ASSAY TO DETERMINE THE HEMOLYTIC-ACTIVITY OF DRUGS INCORPORATED IN COLLOIDAL CARRIER SYSTEMS [J].
BOCK, TK ;
MULLER, BW .
PHARMACEUTICAL RESEARCH, 1994, 11 (04) :589-591
[6]  
BOGAERT R, 1980, J PHYS CHEM-US, V84, P190
[7]  
COLLINS-GOLD L C, 1990, Advanced Drug Delivery Reviews, V5, P189, DOI 10.1016/0169-409X(90)90016-L
[8]  
ELWORTHY PH, 1983, J PHARM PHARMACOL, V35, pP55
[9]   TOXICITY OF SOLUBILIZED AND COLLOIDAL AMPHOTERICIN-B FORMULATIONS TO HUMAN-ERYTHROCYTES [J].
FORSTER, D ;
WASHINGTON, C ;
DAVIS, SS .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1988, 40 (05) :325-328
[10]  
FROMMING KH, 1990, ACTA PHARM TECHNOL, V4, P214