Spectroscopic characterization of DMPC/DOTAP cationic liposomes and their interactions with DNA and drugs

被引:10
|
作者
Labbe, Jean-Francois [1 ]
Cronier, Francis [1 ]
C.-Gaudreault, Rene [2 ,3 ]
Auger, Michele [1 ]
机构
[1] Univ Laval, CERMA, CREFSIP, Dept Chim, Quebec City, PQ G1V 0A6, Canada
[2] Univ Laval, CHUQ, Hop St Francois Assise, Ctr Rech,Unite Biotechnol & Bioingn, Quebec City, PQ G1L 3L5, Canada
[3] Univ Laval, Fac Med, Quebec City, PQ G1V 0A6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Cationic liposomes; Membranes; DNA; Arylchloroethylureas; FTIR; NMR; GENE DELIVERY-SYSTEMS; MAGNETIC-RESONANCE; CYSTIC-FIBROSIS; LIPID INTERACTIONS; BILAYER MEMBRANES; ANTICANCER AGENTS; PHASE-BEHAVIOR; DEUTERIUM NMR; PLASMID DNA; H-2; NMR;
D O I
10.1016/j.chemphyslip.2009.01.002
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
Gene and synthetic drug-delivery vectors have been developed and characterized to treat several genetic diseases and cancers. Our study aims at characterizing cationic liposomes containing the zwitterionic phospholipid DMPC and the cationic lipid DOTAP as well as their interactions with two types of DNA and a new class of antineoplastic agents derived from arylchloroethylureas (CEU). Results obtained using FTIR spectroscopy as well as P-31 and H-2 NMR indicate that DMPC and DOTAP form cationic liposomes in a highly disordered fluid phase at a molar ratio of 1:1. In addition, the FTIR results indicate that the presence of DNA or CEUs within the liposomes does not significantly affect the conformational order of both the DMPC and DOTAP acyl chains. Our results therefore provide a detailed characterization of complexes between cationic liposomes and both DNA and drugs and indicate that these complexes are stable and fluid assemblies. (c) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:91 / 101
页数:11
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