Physical stability of liposomes bearing hemostatic activity

被引:40
作者
Casals, E
Galán, AM
Escolar, G
Gallardo, M
Estelrich, J
机构
[1] Univ Barcelona, Fac Farm, Dept Fisicoquim, Catalonia 08013, Spain
[2] Hosp Clin Barcelona, Serv Hemoterapia & Hemostasia, Barcelona, Spain
关键词
stability; liposomes; zeta-potential; aggregation; size;
D O I
10.1016/S0009-3084(03)00086-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The physical stability of six liposome systems designed as platelet substitutes was determined on storage at 4 degreesC over a 3-month period under quiescent conditions. Liposomes used were large unilamellar vesicles. Correlation of the n-average mean diameter, polydispersity, zeta-potential and the presence of aminophospholipid on liposome surface (in those preparations which contain phosphatidylethanolamine (PE) and phosphatidylserine (PS)) led to the conclusion that liposomes that mimicked the composition of platelets were the most stable. When a net charge was present in the vesicles (liposomes with PS), the likelihood of aggregation was extremely low. In the period studied, a proportion of 25% of charged lipid (PS) conferred sufficient electrostatic stabilization to prevent vesicle fusion. An increase in this charge did not modify the stability characteristics. PE-containing liposomes behaved in a particular way: when PE content was 50%, the stability of the preparation was limited to 1 month; whereas if the content was 25%, the;zeta-potential rose with time, as did the presence of PE in the liposome surface. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:139 / 146
页数:8
相关论文
共 25 条
[11]   FORMATION AND REGULATION OF PLATELET AND FIBRIN HEMOSTATIC PLUG [J].
HAWIGER, J .
HUMAN PATHOLOGY, 1987, 18 (02) :111-122
[12]  
HOPE MJ, 1985, BIOCHIM BIOPHYS ACTA, V812, P55, DOI 10.1016/0005-2736(85)90521-8
[13]  
HUNTER RJ, 1988, ZETA POTENTIAL COLLO, P69
[14]  
LEE LH, 1995, BRIT J HAEMATOL, V89, P131
[15]  
LIS LJ, 1982, BIOPHYS J, V37, P657
[16]   Bilayer distribution of phosphatidylserine and phosphatidylethanolamine in lipid vesicles [J].
Roy, MT ;
Gallardo, M ;
Estelrich, J .
BIOCONJUGATE CHEMISTRY, 1997, 8 (06) :941-945
[17]   Influence of size on electrokinetic behavior of phosphatidylserine and phosphatidylethanolamine lipid vesicles [J].
Roy, MT ;
Gallardo, M ;
Estelrich, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 206 (02) :512-517
[18]   Damage to liposomal lipids: protection by antioxidants and cholesterol-mediated dehydration [J].
Samuni, AM ;
Lipman, A ;
Barenholz, Y .
CHEMISTRY AND PHYSICS OF LIPIDS, 2000, 105 (02) :121-134
[19]  
Senior J., 1984, LIPOSOME TECHNOLOGY, VIII, P264
[20]  
Silberman S, 1999, ARCH PATHOL LAB MED, V123, P889