Hydroxyethylated cholesterol-based cationic lipid for DNA delivery:: effect of conditioning

被引:46
作者
Percot, A
Briane, D
Coudert, R
Reynier, P
Bouchemal, N
Lièvre, N
Hantz, E
Salzmann, JL
Cao, A
机构
[1] Univ Paris 13, UFR Med, CNRS, UMR 7033,Lab CSSB, F-93017 Bobigny, France
[2] Univ Paris 13, UFR Med, EA 2360, Lab Oncol Cellulaire & Mol, F-93017 Bobigny, France
[3] Fac Sci, EA 2098, Lab Physicochim Interfaces & Milieux Reactionnels, PIMIR, F-37200 Tours, France
[4] Univ Paris 13, UFR Med, EA 3410, Lab Biotherapies Benefices & Risques, F-93017 Bobigny, France
关键词
D O I
10.1016/j.ijpharm.2004.03.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have synthesised a novel cholesterol -based cationic lipid to promote DNA transfer in cells. This lipid, dimethyl hydroxyethyl aminopropane carbamoyl cholesterol iodide (DMHAPC-Chol) contains a biodegradable carbamoyl linker and a hydroxyethyl group in the polar amino head moiety and is characterised by NMR. Liposomes prepared from this lipid and dioleoyl phosphatidyl ethanolamine (DOPE) in equimolar proportion showed a weak cytotoxicity as revealed by MTT assays and are efficient to deliver plasmids DNA evaluated by the expression of reporter genes in vitro and in vivo. In this paper, we present an original method to determine the lipid concentration based on the colorimetric detection of the colipid DOPE and the measure of the molar ratio DOPE/cationic lipid in the liposome by FTIR spectroscopy. The liposomes and lipid/DNA complexes structures were characterized by transmission electron microscopy (TEM) and by quasi-elastic light scattering (QLS). TEM indicated that the complexes correspond to aggregates containing globular substructures with liposomes size. The method of immuno-gold labelling was used to detect plasmid in the complex and reveals the presence of DNA inside the aggregates. Transfection results showed efficient DNA transfer depending on the charge ratio and liposomes conditioning. Gel retardation results indicated that at a molar charge ratio between X = 1.5 and X = 2.5 (depending on the liposome conditioning), all DNA was taken by liposomes. We showed that conditioning by freeze-drying (lyophilization) facilitates storage and improves transfection efficiency. When the liposomes were lyophilized prior to DNA addition or when the complexes were subjected to freeze-thawing cycles, the obtained complexes showed a transfection with levels enhanced up to four and five-fold respectively for the lyophilized liposomes and freeze-thawed complexes. NMR was used to characterize the modifications under freezing which showed an effect on 31 p spectra. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 163
页数:21
相关论文
共 40 条
[1]   Stabilization of lipid/DNA complexes during the freezing step of the lyophilization process: the particle isolation hypothesis [J].
Allison, SD ;
Molina, MDC ;
Anchordoquy, TJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1468 (1-2) :127-138
[2]   Stability of lipid/DNA complexes during agitation and freeze-thawing [J].
Anchordoquy, TJ ;
Girouard, LG ;
Carpenter, JF ;
Kroll, DJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (09) :1046-1051
[3]   Maintenance of transfection rates and physical characterization of lipid/DNA complexes after freeze-drying and rehydration [J].
Anchordoquy, TJ ;
Carpenter, JF ;
Kroll, DJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 348 (01) :199-206
[4]   EFFICIENT GENE-TRANSFER INTO MAMMALIAN PRIMARY ENDOCRINE-CELLS WITH LIPOPOLYAMINE-COATED DNA [J].
BEHR, JP ;
DEMENEIX, B ;
LOEFFLER, JP ;
MUTUL, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :6982-6986
[5]   Cationic lipid-mediated gene delivery to murine lung: Correlation of lipid hydration with in vivo transfection activity [J].
Bennett, MJ ;
Aberle, AM ;
Balasubramaniam, RP ;
Malone, JG ;
Malone, RW ;
Nantz, MH .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (25) :4069-4078
[6]   Delivery and pathway in MCF7 cells of DNA vectorized by cationic liposomes derived from cholesterol [J].
Cao, A ;
Briane, D ;
Coudert, R ;
Vassy, J ;
Lievre, N ;
Olsman, E ;
Tamboise, E ;
Salzmann, JL ;
Rigaut, JP ;
Taillandier, E .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 2000, 10 (05) :369-380
[7]   Stabilization of polymer-based gene delivery systems [J].
Cherng, JY ;
Van der Wetering, P ;
Talsma, H ;
Crommelin, DJA ;
Hennink, WE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 183 (01) :25-28
[8]   Biochemical and biophysical characteristics of lipoplexes pertinent to solid tumour gene therapy [J].
Dass, CR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 241 (01) :1-25
[9]   Cationic lipid-DNA complexes in gene delivery:: from biophysics to biological applications [J].
de Lima, MCP ;
Simoes, S ;
Pires, P ;
Faneca, H ;
Düzgünes, N .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 47 (2-3) :277-294
[10]   EFFECT OF CATIONIC CHOLESTEROL DERIVATIVES ON GENE-TRANSFER AND PROTEIN-KINASE-C ACTIVITY [J].
FARHOOD, H ;
BOTTEGA, R ;
EPAND, RM ;
HUANG, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1111 (02) :239-246