Drug delivery by phospholipase A2 degradable liposomes

被引:40
作者
Davidsen, J
Vermehren, C
Frokjaer, S
Mouritsen, OG
Jorgensen, K
机构
[1] Royal Danish Sch Pharm, Dept Pharmaceut, DK-2100 Copenhagen, Denmark
[2] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark
关键词
drug-delivery; PEG liposomes; phospholipase A(2); lipopolymer; liposomes; degradation;
D O I
10.1016/S0378-5173(00)00634-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of poly(ethylene glycol)-phospholipid (PE-PEG) lipopolymers on phospholipase A(2) (PLA(2)) hydrolysis of liposomes composed of stearoyl-oleoylphosphatidylcholine (SOPC) was investigated. The PLA(2) lag-time, which is inversely related to the enzymatic activity, was determined by fluorescence, and the zeta-potentials of the liposomes were measured as a function of PE-PEG lipopolymer concentration. A significant decrease in the lag-time, and hence an increase in enzymatic activity, was observed with increasing amounts of the negatively charged PE-PEG lipopolymers incorporated into the SOPC liposomes. The enhancement of the PLA(2) enzymatic activity might involve a stronger PLA(2) binding affinity towards the negatively charged and polymer covered PEG liposomes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:67 / 69
页数:3
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