The Effect of Cationic Polylysine on the Release of an Encapsulated Substance from pH-Sensitive Anionic Liposomes

被引:4
|
作者
Sybachin, A., V [1 ]
Lokova, A. Yu [1 ]
Spiridonov, V. V. [1 ]
Novoskol'tseva, O. A. [1 ]
Shtykova, E., V [2 ,3 ]
Samoshin, V. V. [4 ]
Migulin, V. A. [5 ]
Yaroslavov, A. A. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Fac Chem, Moscow 119991, Russia
[2] Moscow MV Lomonosov State Univ, Fac Phys, Moscow 119991, Russia
[3] Russian Acad Sci, Shubnikov Inst Crystallog, Moscow 119333, Russia
[4] Univ Pacific, Dept Chem, Stockton, CA 95211 USA
[5] Russian Acad Sci, Zelinsky Inst Organ Chem, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
DRUG-DELIVERY; COMPLEXATION; POLYCATIONS; POLYELECTROLYTES;
D O I
10.1134/S0965545X19030179
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The formation of complexes from anionic liposomes with a pH-sensitive molecular switch (flipid) and a cationic polypeptide (polylysine) embedded in the membrane with a degree of polymerization of 90, 660, and 1360 was investigated. Liposomes in the complex retain their integrity in a buffer solution with a pH of 7; The resulting complexes are resistant to dissociation in a physiological solution containing 0.15 M NaCl. Lowering the pH of the solution to 5 causes the formation of defects in the lipid bilayer by changing the conformation of the flipid, which leads to the release of the encapsulated substance from the liposomes into the surrounding solution. In this case, complexation increases both the rate of release of the encapsulated substance and the amount of the substance moving from the liposomes to the external solution. The results obtained are of interest for encapsulation and controlled drug delivery.
引用
收藏
页码:308 / 316
页数:9
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